Good luck having your DNA modified, you've all been warned but you didn't listen ! I don't have to choose, l choose sanity and normality, my vaccine is my immune system and a 99.97% survival rate lab made virus won't boder me at all ! You don't think that this was a real pandemic right ? It was all for…..you will see !
Wonderful interview! I often reference Dr.Offit when I’m asked about Covid vaccines, and I encourage everyone to watch these videos. And if that was a Boston Terrier walking in the background, I’m an even bigger Offit fan! Lol
@@patriciahoke4722 Mr personally I listen to Sirius xm. I'm a big fan of Howard stern lol, I know he is not everyone's cup of tea but I enjoy it. I like Sirius xm cause I can listen to liberal conservative neutral and plain conspiracy idiots. But at the end of the day I create my own opinion on my daily struggles and what I see witg the people around me. The media and the internet cannot change your mind!
Thank you for this interview. It was very helpful and informative. I wasn't hesitant to get the vaccine, but I like a deeper understanding of things especially why we need 2 doses. I got my first dose of the Pfizer vaccine yesterday. I'm excited to get my next dose in 3 weeks. It's been feeling so dismal and hopeless for so long, it's nice to see a glimmer of hope on the horizon.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
That slimebag might be some combination of stupid and arrogant enough to actually show up, but personally I think he is just an evil racist that pushes antivax because he knows it hurts minorities the most and that of the non-minorities harmed, the damage is mostly limited to people many racists think should not reproduce.
Another great video! Z, I know what you're doing in trying to educate people in an objective way with videos like this, and you are totally nailing it to the wall. What I don't know is how effective you really are with this kind of format, but at least for people like me - you are killing it. Please don't think that you or your guests are getting 'too technical'. I'm not even a medical professional (though I am somewhat of a science nerd), and I got some tingly feelings in my special place - ESPECIALLY when Offit said, "OK, I'm about to bore your listeners with some math...". Please keep doing this kind of stuff! You're doing EXACTLY what you want to do to a greater extent than you might imagine.
So thankful for the clarification on Biden’s announcement. I’ve been so concerned that second doses would be given very late due to the poor messaging. Thanks for being clear! 😊
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Yes it was an absolute messaging problem. One of my Patients refused the vaccination when offered because they thought they would not be able to get the second dose. I am sure he is not the only one.
I have seen several episodes and I'm subscribed and liking. Thank you. You are sincere and doing a great job of respecting and sharing the information. Great job ZDoggMD!
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).When we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane?(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ) Especially when we consider the fact that CDC confirmed cross recognition of existing SARS-COV antibodies to this novel coronavirus, this means that so long as we have a strong and appropriate T-cells immune respond, our evolutionary adaptive immune system is more than enough to handle this virus during low viral inoculation. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
@@DomFortress Thankyou. Thorough & informative. Antivirals exist for fractions of vax billions. Think how the money could've been used ..All critical thought, absent in covidiom Blatant media bias and lies
@@DomFortress 🤔maybe you need to do more research on where you are getting your info. You do know that there is a lab who have already made a vaccine that has just went in to human trial studies that has already tested their vaccine in animals who's lung are quite similar to our own. The US, China and Britain are not be all end all of medical studies.
@@susanpick2382 I don't care about all vaccinations that still depends on a strong and appropriate T-cells immune respond from the host, when I care about therapeutic lifestyles as holistic preventive cares that can prime and optimize human autoimmune functions, period. Medications thus big pharmas be damned.
Prepared this summary for my colleagues, posting here for those who don’t want to sit through 48 minutes and rather read, some portions are skipped that aren’t applicable to us. Enjoy! My notes and highlights from the video to keep in your back pocket for those who are strong with the cognitive dissonance: Paul Allan Offit (bio paraphrased from Wikipedia): pediatrician, co-inventor of rotavirus vaccine, professor at UPenn SOM, founding member of autism science foundation (ASF) has been on CDC’s ACIP, was on FDA advisory committee for covid vaccine approvals, one of the most public faces of the scientific consensus that vaccines have no association with autism, for which he has been a frequent target of hate mail and death threats. ⁃ Maurice Hilleman (father of modern vaccination, helped create 9/14 childhood vaccines now given out), won’t breath a sigh of relief till the first 3 million doses. - 7 million given out so far - No Bell’s palsy reported yet - Pfizer Anaphylaxis: 11 cases per million doses (higher than other vaccines 1 out of 1 million, though we are looking closer at this data and could cause observer bias), good news happens immediately, treatable w/ epi, no cases w/ moderna vaccine (possibly one with a physician who gave himself an epi dose because he was probably having a panic attack...) - One report of an obstetrician dying 3 days after he got the vaccine and his platelets went to zero (possible ITP, MMR vax can cause it 2 weeks out and usually transient, incidence 1 out of 20k-30k, though wild type measles also causes it) hard to sort out coincidental from causal associations, still under investigation - Natural viral infection can cause some of the same side effects as the vaccine, e.g. flu and the vax can cause guillain barre (though natural infection has a 17x higher rate than vax) - Other vaccines (N/A, skipped, watch video if interested) ⁃ Pfizer vs moderna preferences (N/A, skipped, watch video if interested) ⁃ Vaccine efficacy inflated conspiracy (BMJ article by someone who speaks at antivaxxer conferences, watch video if interested) ⁃ Asymptomatic spreaders, theoretically less contagious if vaccinated as they would make less of a viral load because of an immune response faster (example rotavirus vaccine, does not stop asymptomatic spread, still virtually eliminated disease) ⁃ Why do we still need to wear masks? (Skipped, you know, watch video if interested) ⁃ Civilian vaccine logistics, Biden rollout mess up, and why two doses (N/A, skipped, watch video if interested) ⁃ Variants: UK variant still neutralized with natural immunity of vaccination (no response difference from original); South African variant, study still pending (convalescent serum vs Pfizer vaccinated serum) ⁃ Any test to see if you’re a nonresponder to the vaccine? Currently no specific antibody test, Pfizer didn’t have that data yet at the FDA committee meeting, pending results ⁃ Previously/currently infected, should I get it? (mostly skipped, you know, interestingly there were 8 people in the Pfizer study who were previously infected and got vaccinated, 7 people in the placebo group got sick, 1 in the vaccine group did not, possible booster effect, need to check the numbers on this, he may have misspoke) ⁃ Monoclonal antibody treatment -> wait 3 months before getting vaccine ⁃ Are they unblinding vaccine groups from studies so they can get vaccine? Short answer yes, watch vid for long answer ⁃ Can you mix vaccines, e.g. Pfizer dose 1, moderna dose 2? No ⁃ Pregnancy/lactating? (mostly skipped, you know, of note: one episode of spontaneous abortion in each trial Pfizer and moderna, both cases in placebo groups) ⁃ Hesitancy in healthcare professionals? Not enough data, or don’t know the data -> convinceable; believe in conspiracies, trust issue -> difficult/lost cause, if they refuse tell them to stop complaining about PPE, there is a ready solution, vaccinate, don’t go to social media and say you’re not getting vaccinated, spreads distrust; public value the opinion of nurses (medics) more than us (which is true) ⁃ PSA: covid is now a preventable disease ⁃ Hope: Could stop the spread by early summer (mostly skipped, can watch for the math on existing community immunity, herd immunity and number needed to vaccinate and logistics going forward) ⁃ Ghostbusting
Fam phys in Florida with high 65+ pt demographic. I have seen very little vaccine hesitancy in my patients. We are bombarded with calls daily to get it asap. I’ve had Pfizer vax, both doses, and make it widely known. Great information! Finally, I’m seeing some optimism! Thanks Z!
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I work in in home healthcare and I'm scheduled to get the pfeizer vaccine next week. I hate shots and I've never been so excited for a shot in my life. Listen to the science. Listen to the experts. I'm so ready for us to get to herd immunity so we can all get back to normal life.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
@@laurelpearse179 before the invention of vaccine as intentional infection, low viral inoculation is how we achieved herd immunity. And this is how some nations gained herd immunity with both high viral infection rate, and some mild symptoms, while in an absent of vaccine. The mask wearing doesn't eliminate viral infection, but instead it causes low viral inoculation. www.nejm.org/doi/full/10.1056/NEJMp2026913 However, a history of autoimmune diseases rooted in a weaken and inappropriate regulatory T-cells anti-inflammatory respond(onlinelibrary.wiley.com/doi/full/10.1002/mco2.12 ), which is a common comorbidity factors such as chronic inflammation, obesity and fatty liver disease rooted in metabolic imbalance(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), and high blood pressure rooted in systemic endothelial glycocalyx damages(www.sciencedirect.com/science/article/pii/S2319417020301414 ), are strong indicators for a severe outcome during any viral infection, regardless of age. And historically with the majority of the adult population in the Western world were already trending to overweight or obesity at 2018(www.medpagetoday.com/primarycare/obesity/90142 ), we're not gonna be fine by ourselves just vaccinating millions. Especially when the vaccine had never been tested for antibodies in its 2 months long safety and efficacy trials(www.medpagetoday.com/primarycare/obesity/90142 ), nevermind that the manufacturers prescreened all test subjects for autoimmune diseases, and reinterpreted mild symptoms as evidence to prove that it offers some protection. And if we're good at studying the medical history of overdiagnosis(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), then we could've known that within the context of psychoneuroimmunoloy, overdiagnosis can cause irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ), and this can disrupt our parasympathetic nervous system that regulates our T-cells immune response(www.ncbi.nlm.nih.gov/pmc/articles/PMC5050399/ ), due to overt activation of our sympathetic nervous system by our irrational fear. And if we're better at studying legal history still, then we could've known that DNA forensics scientists had been warning since 2016, about just how molecular PCR test was misused to convict the innocent to serious crimes like murder(www.sciencemag.org/news/2016/03/forensics-gone-wrong-when-dna-snares-innocent ), yet the exact same molecular PCR misuse is now the sole justification(www.cebm.net/covid-19/infectious-positive-pcr-test-result-covid-19/ ) for the dangerously autoimmune health damaging social isolation caused by just such policies as mandatory social distancing and worst, lockdown.
I am glad to listen to your programs, thank you. I am disappointed that you said you were going to discuss autoimmune disorders at the beginning of this program and then did not do so. I hope that you actually address that issue at some point
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I received the 1st dose. The day after, I had so much pain on my left arm. I was not able to lift it up, my fingers hurt when I tried to close my hand. I had a horrible pain on the left back and front of my head, worse than a migraine headache that wouldn't go away. When I receive the vaccine, minutes later I felt a numbing sensation that radiated from my left arm down to my fingers then up to my left side of my face and to the back of my left side of my head. I have been having chills after that and I lost my appetite for 5 days. I'm not getting the 2nd dose.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Fake news, you are a liar, an ativax to say you have pain, you want to scare peoples....Moderna & Pfizer are our new churches and we need to follow without question.
Why wouldn't the primo-infection not result in a longlasting cellular and humoral immunity for the SarsCov2?? It does for the other coronaviruses including SarsCov1 from 2013.
Why is it taking so long to approve the AstraZenica vaccine. Cheap effective and only requires fridge temp. Already approved by the UK can you not share date
That first scratch analogy. The only new car I ever bought was delivered at 10pm. The next morning I bought paper towels and glass cleaner because the car had been driven 200 miles to get it to me. While paying, March winds blew a shopping cart uphill into my car. Six months later I almost totalled it in a ice storm. The only panel not repaired was the one that shopping cart hit...
“COVID NOW IS A PREVENTABLE DISEASE.” - the most understated but impactful statement I heard online on COVID this year! And I heard lots. Thanks ZDOGGGGG
I guess we don’t trust what the British decided after they looked at the studies. We need our own because we are smarter. Look how successful we were initially with our own tests(not). Plus they are very cheap, no money to be made there. It’s not like 1 in 1000 Americans have died so far.
No mention of cross-immunity? From the BMJ : "But memory T cells are known for their ability to affect the clinical severity and susceptibility to future infection,25 and the T cell studies documenting pre-existing reactivity to SARS-CoV-2 in 20-50% of people suggest that antibodies are not the full story."
So if there is no antibodies detected after having both covid and first dose of Pfizer, it does not mean there is no immunity? What is your opinion on getting the second dose and getting it a few weeks late due to lack of availability?
@@mariamamiri2257 After a (mild) Covid you can be immune without the presence of ( detectable levels of ) antibodies. An IM injection of a vaccine should always result in the production of antibodies (which can take a week or two ) otherwise it's ineffective. A second dose will boost the immunesystem and Ab-production and provide a stronger and longer lasting protection.
If a patient stays in a area or waiting room waiting to be vaccinated that was occupied 5 minutes previous to appointment by someone that tests positive , without cleaning and disinfecting as usual, could going to be vaccinated cause someone to get infected?
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
HIM Coder here, even though I work from home, the wonderful peds institution that Dr Offit and I work for placed the coders in phase 2, so I've recently received my 1st dose. I still feel some type of way that I've gotten it before other people who work outside of the home but on the other hand I also want to set an example and protect others like Z said.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Great interview. He really dismissed your question on Doshi's BMJ piece. We don't have privy to the study but Doshi did. He wrote about suspected but not confirmed covid cases which would decrease the efficacy of the vaccines had they been tested. "category of disease called “suspected covid-19”-those with symptomatic covid-19 that were not PCR confirmed. According to FDA’s report on Pfizer’s vaccine, there were “3410 total cases of suspected, but unconfirmed covid-19 in the overall study population, 1594 occurred in the vaccine group vs. 1816 in the placebo group.” With 20 times more suspected than confirmed cases, this category of disease cannot be ignored simply because there was no positive PCR test result. Indeed this makes it all the more urgent to understand. A rough estimate of vaccine efficacy against developing covid-19 symptoms, with or without a positive PCR test result, would be a relative risk reduction of 19% (see footnote)-far below the 50% effectiveness threshold for authorization set by regulators. Even after removing cases occurring within 7 days of vaccination (409 on Pfizer’s vaccine vs. 287 on placebo), which should include the majority of symptoms due to short-term vaccine reactogenicity, vaccine efficacy remains low: 29% (see footnote)."
Why not have Peter Doshi on for another perspective? If you are trying to have open discussion, why shun such an important voice just because he questions vaccines? As we all should be to have a clearer understanding. Science begs and demands curiosity. You cany have it both ways.
I understand the rotavirus parallel, but the mode of transmission is a bit different. This is aerosol and airborne. Asymptomatic transmission is much easier in this mode. So I as a vaccinated family member could become an asymptomatic spreader and not know until my wife or children are infected. That is a concern in being the only one of 7 eligible for the shot.
It would be interesting to see a breakdown of vaccine hesitancy in health care workers and in what sectors these health care workers are employed. An RN friend at UC Irvine ER and her colleagues (from what I understand) are eager to get vaccinated. Also, my colleagues and I in the ER I am working in Canada are eager to get this done and are not hesitant in the least. From what I understand, our ICU workers are also on board. I wonder if the hesitant are those that work in areas where covid has been of little concern? Just would be great to see how the data all breaks down. If possible
I joined the Pfizer vaccine trial in August. Lots of nasal swabs and blood draws over the last few months. They unblinded me on Jan 18 and I had received a placebo. They offered me the chance to join the vaccine group and I received my first dose shortly thereafter.
@@daviddeavours4909 unless he is prepared to say the UK health officials are incompetent, there is no reason not to approve it based on their approval.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
@@buckcampbell4292 😂😂😂 yes, sure is about this. FDA change the rules to allowed 2 experimental vaccine that NEVER use until now on humans and now they talk about safety...this is a good on. Personally I will wait for „classic vaccine approach“, they are few in phase 3: www.covid-19vaccinetracker.org/
These interviews have helped me stay informed and more confident about getting the vaccine. Thank you, Dr. Z for doing them!! 🥰Ultimately, I got the vaccine because I didn’t want to run the risk of being a long-hauler. I have autoimmune diseases and my immune system is good at overreacting. I’d rather not give it anything else to overthink about. Lol. 😏
Did you get the vaccine already? Asking because I'm 63 years old and have to autoimmune diseases and one of them is an inflammatory muscle illness which is already giving me a lot of problems. They did not test it yet on people with autoimmune illnesses and don't know how they are immune system will react or whether it will overreact so I was wondering how you did after the vaccine? I will be speaking with my rheumatologist next week though
@@pokerlover16 Yes, I received the vaccine. (2nd shot was just yesterday). My arm was sore like usual after you have a needle stuck into it. About a week later, I noticed a systemic inflammatory response- meaning swollen lymph nodes, cold/flu symptoms, increased joint pain, etc. All my usual suspects acted up. I have alopecia as well, so I couldn’t really tell if that was affected because there’s no hair growing anyway. I was pretty tired for a couple of days as well. I took the time to get extra rest. It resolved after that. I expect to see the same this week with a bit more intensity since I got the vaccine booster yesterday. I still think it would be better than risking being a long-hauler after enduring an actual infection of covid.
This was an AMAZING information. I am one of the nurses that is hesitant about getting the vaccine, not because I don't trust the science, scientists, or pharma, but because I would like to see how effective the vaccine is long term, don't want to create an immune response that could potentiate the risk of developing an autoimmune disorder that I or my spouse may have already been genetically predisposed to. One question that I would like answered, which may not be available at this time is whether or not there is a chance that this mRNA vaccine could possibly potentiate the onset of some of those diseases such as SLE, RA, or others. Maybe I'm thinking outside of my realm of knowledge as I don't know if that is even a possibility, but I do believe that stressors can trigger an autoimmune disease. THANKS!! Hope you actually are able to catch this question in the midst of all of the other response. In the mean time, I guess I need to be doing some personal searching on this topic, but do trust your and Dr. Offit's input... for the record, I am NOT anti-vaccines, I am simply questioning still if it is too soon... I know there are minimal immediate risks, but as for long-term... i don't quite understand the nature of mRNA vaccines and what they may be capable of especially if put out there so rapidly.
This might be a long shot, but can someone provide a journal article, or other evidence based link for NOT taking an antipyretic before/after the vaccine as Dr. Offit advises? My facility’s vaccine providers are telling those receiving the vaccines they can take Tylenol. I’ve been searching the Cochrane Library without much luck so far.
@zdoggmd Can you make a video on the Global Times vaccine article about a 19% to 95% efficacy rate on the Pfizer vaccine due to eliminating "suspected" cases from the trial data. I love your analysis and background! Thank you!!
I am a health care worker and I had my first vaccine on 12/30. I tested positive yesterday for Covid. Now I'm on a z-pack, prednisone, and an inhaler. I hope my breathing gets better.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Thank you for all the info and I am finally getting my vaccine shot tomorrow. I am tier A but they asked if I worked in a purple tier school district and I live in a purple tier for 6 months now. I am a school nurse and my families are really suffering, been doing covid tracing and it started with just parents and now it’s the whole families. So thankfull. I am getting it at disneyland employee parking lot!
It was well done. They had a waiting area in the last tent for 15 minutes to observe for any adverse situations. They had EMTs and it was really safe. @Christine, I do not have allergies and no adverse issues. I am fine for this. I am post cancer 6 years out and well in general. I have an RN, BSN, PHN, M.Ed. I got the shot and fine. I felt hope.
By no means am I a medical expert in any shape or form. I appreciate your videos and knowledge coming from a rational point of view. I have a question about the formula determining herd immunity, should there be a variable taking into account effective treatments? To me if we have that factored in, it would reduce the amount of vaccines needed for herd immunity because we could better treat the infected, ultimately reducing their sickness (symptoms, spreadability, etc) but those who have been infected would carry antibodies for their own protection and not need vaccinated as quickly. Thoughts?
I would like to know how long do the antibodies from the covid vaccine last? Also is there any evidence so far that mutant strains will be covered by current vaccine?
I had Bell’s palsy in March 2020. It resolved, but i worry that the vaccine will cause a resurgence of the Bells. I work for the health department and now we are required to staff these vaccine sites. We can get vaccinated on the day of working at the point of dispensing event. Shouldn’t i wait about 10 days for an effective immune response before i work at these events? Would certainly appreciate your expert recommendation.
Very disappointed he didn’t talk more about the Oxford/AstraZeneca vaccine. To not even acknowledge there is another vaccine out there, approved by many countries and already being given to people, is shameful.
You still have to wear a mask and social distance. Even after years of flu shots, they are only effective 25-35%. I don't believe in less than a year that these vaccines are 95% Effective.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I don't know why anyone should agonize over those who don't wish to be vaccinated. There are lots of people what DO want to be vaccinated. Focus on people who don't have access because of the slow distribution.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
thank you for keeping up with these videos. I trust you and Dr. offitt. I'm one of those 30% of nurses who aren't getting the vaccine for now. I DO hope to get one just not the current two MRNA vaccines. I have a severe anaphylaxis to shellfish so I'm afraid of the allergic reaction with the two available right now. I'm hoping the J&J one will be a better choice for me and then I can be immunized as well.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I got the Pfizer vaccine and then had symptoms related to covid 3 days later. Tested positive for covid next day. Did I just cancel out the vaccine effect? Due for 2nd dose next week.
They say even if you had Covid I still need to get the vaccination. When you get the vaccination you still have to wear your mask stays social distancing and yes you do have to get the second part of the vaccine. Good luck
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs. What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age. Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I want to get the shot, but I don't want to get it in the arm. I have thoracic outlet compression syndrome. 20 years ago, I got a vacc, my shoulder swelled. Ended up with 6 weeks of therapy (that's all you get with insurance) and 7 months of excruciating pain. Can I get, to put it nicely, in the hip instead?
Do we know what the percentage of people who refuse the vaccination is? Just curious. And what is the main reason? I know you have touched on this in your videos....wondering about %'s.
Not this nurse! Got the vaccine the first day it was available to me! Feeing great and less anxiety caring for my covid patients! Thank God for modern science!
What about Dr. Fuller’s caution in waiting for long term safety data? I know 7 million have the vaccine, but that comment about 3 million was made when the development cycle was much longer . When you ask what people are waiting fir, it is the longer term safety data. When will it be available. The 7 million provide very short term observation.
I wonder if our reaction to the first vaccine can determine our reaction to the 2nd vaccine. Just had some mild injection site soreness for 2 days after the first vaccine.
My experience has been that way too many people I see when in a shopping centre still have their noses hanging out of those masks. Honestly, don't know why they bother if they don't wear it properly anyway.
Can you get some info and share on the Sinopharm vaccine? My older parents are US citizens in Jordan and they have approved Pfizer and Sinopharm there. It looks like they may only be able to get the Sinopharm this week and it makes me nervous. Should it?
Sorry, don't mean to interrupt, but if you goggle that vaccine it has articles. Seems Taiwan is not very high on it for the side effects. Have a good day
Would love to hear the differences, in efficacy and in approach between the different vaccines across the world.. American Pfizer/Moderna, Russian Sputnik V , British/Sweden AstraZeneca Chinese Sinovac/Sinopharm India's Bharat Biotech Covaxin and Oxford/AstraZeneca Do they all use mrna? If so, do they just differ in the lipid encapsulation technique?
I did the same as you and refused my vaccine at first feeling people more exposed to the virus should get it first. After hearing how many people were turning it down including my sister who works in food service at a hospital & my 80 year old mother who I help care for, I changed my mind. When I signed up there were so many spots open for Tues & Thursday which confirmed I wasn't taking it from anyone who was in line & wanted to get it.
Kristina Braly is an anesthesiologist who has youtube channel, is pregnant and went over why she got vaccinated. Not research per se, but a physician who is pregnant her perspective.
My mom is in South Africa and works as a medical professional there. She is therefore signed up to receive one of the first Oxford-AstraZeneca vaccine's from India. Should I be concerned? My mom is 61
I am 7 days post Pfizer vaccine. I started with fevers last night, today I’m up to 101.2. I have a test pending and should know tomorrow what the results are. Also my MIL received her first Moderna injection and now has tested positive. We are both totally bummed about this. Should we get the second vaccine? I’m sure my symptoms are less severe than had I not had it..
I am hearing, from Nurses that have been vaccinated, that if you have been Covid positive the vaccine hits you a bit harder in respect to side affects.
@@monykalynf3604 well as long as they get the vaccine. Thought they said immunity from getting infected is equal to the 1st dose with about 60% effectiveness. Maybe this is stretch but if you increase the chance of the elimination variation with just a single vaccine dose, it seems to follow those with prior infections that don’t get vaccinated may be responsible for virus mutations that yield the vaccine impotent. It is important they get the vaccine, I have many RT and Nurse friends in ICU that have been vaccinated, it seems people that have had the infection respond differently, by way of side effects, than those that do not. It is notable that in the, placebo group, more got reinfected than those that got vaccinated after infection. Take away: those with past infections should get both shots.
@@OceanFrontVilla3 listen to the whole broadcast...that is not true. I know health care workers that are taking the vaccine with a past Covid infection. It is also unknown wether or not past infection keeps you from spreading it.
did I misunderstand what the guest said here? Did I hear him say that once you get the disease that you are immune? And then he said you need to get the vaccine even if you've had it? I am confused.
Please talk about this important issue Zdogg. If you have recovered from covid and are a plasma donor for antibodies, once you get the vaccine you can no longer donate antibodies. I think this is a very serious issue. Recovered people are being urged to be vaccinate. Most of the time having a disease gives more immunity than a vaccine does so why such a hurry to vaccinate people already recovered from CoVid. Perhaps, there is some research that shows the vaccine is better at protecting from other strains, because if that is the case I would like to hear about this. The problem is if everyone that is recovered gets vaccinated, what happens to our store of convalescent plasma? It's seems unlikely the vaccine will put an end to its necessity. Some people will still get sick. More importantly, these vaccines may not work for future mutant strains that perhaps convalescent plasma might still treat. Would love to hear thoughts on this.
After 10 month of people dropping dead everywhere, strict measures are finally in place here in Stockholm. As of this week, we have to wear face masks in buses and trains during rush. For as long in public transit, it has to to be on from 7am and may not be removed until 9am. Must be put on again from 4pm until 6pm. Thank goodness for our decisive government.
I wish the Belgian "experts" had as much common sense. We have to wear masks everywhere, sometimes even outside, in the city centres or during a stroll along the seaside! Sweden doesn't seem to have any excess deaths in 2020 and half the deathtoll compared to Belgium. Only elderly frail people in carehomes dropped dead in spring around here.
@@guidospanoghe8896 Yes, I have been wondering about you guys, how things are in Belgium. You're right, Sweden is only average in Europe. Infact, I'm not even sure how big of a difference there would have been if we had kept everthing totally open, sports, concerts etc. Our second wave curve is already flattening. Same thing here, most of the deaths occurred among the elderly.
Dr. Z, I had Bells Palsy when I was a child. Have you heard anything about people getting Bells again? I got the first Moderna vaccine before I heard this. So far so good. But I have heard the second round has kicked people in the butt.
Im an EMT and I was 100 percent against this vaccine. Thanks to your videos I changed my mind and got the Pfizer one last week. So far so good
Good luck having your DNA modified, you've all been warned but you didn't listen ! I don't have to choose, l choose sanity and normality, my vaccine is my immune system and a 99.97% survival rate lab made virus won't boder me at all ! You don't think that this was a real pandemic right ? It was all for…..you will see !
@@ghitaciprian Keep reading. That's not how mRNA vaccines work.
@@ghitaciprian Please explain how DNA will be modified...genuinely asking.
@@ShimmyMD do your diligence, l did mine
@@paulmaximus3975 didn't mention something about that....
Paul Offit is awesome!
I always love your interviews with Dr. Offit. Thanks so much to both of you!
Wonderful interview! I often reference Dr.Offit when I’m asked about Covid vaccines, and I encourage everyone to watch these videos. And if that was a Boston Terrier walking in the background, I’m an even bigger Offit fan! Lol
❣️👍
And if the dog is a Boston Terrier/ Chihuahua mix, it will look like a Chihuahua on steroids. Pump me up!
"The older I get, the more I listen to talk radio. I don't know if that's a good thing." Lol... Truth!
You are not alone!!
@@edmondbilbili567 But is PBS really talk radio??
@@patriciahoke4722 Mr personally I listen to Sirius xm. I'm a big fan of Howard stern lol, I know he is not everyone's cup of tea but I enjoy it. I like Sirius xm cause I can listen to liberal conservative neutral and plain conspiracy idiots. But at the end of the day I create my own opinion on my daily struggles and what I see witg the people around me. The media and the internet cannot change your mind!
As always, great analysis. I just love that you call Dr. Paul Offit "Dude."
Slowly changing my mind! Thank you both! So much great info.
Paul off it books are a must read for medical providers , thanks God for his life.
Love you ZDogg!
ua-cam.com/video/M0A8e6_8SQE/v-deo.html
I love listening to Paul Offit. What an educational and encouraging video. Thank you to both of you for all you do.
Thank you for this interview. It was very helpful and informative. I wasn't hesitant to get the vaccine, but I like a deeper understanding of things especially why we need 2 doses. I got my first dose of the Pfizer vaccine yesterday. I'm excited to get my next dose in 3 weeks. It's been feeling so dismal and hopeless for so long, it's nice to see a glimmer of hope on the horizon.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I want to see a discussion with
RFK Jr.
I want JFK Jr to be jailed and never hear about this disgusting nubjob ever again
That slimebag might be some combination of stupid and arrogant enough to actually show up, but personally I think he is just an evil racist that pushes antivax because he knows it hurts minorities the most and that of the non-minorities harmed, the damage is mostly limited to people many racists think should not reproduce.
Why? It's not like he has any scientific expertise, just a famous (and famously unlucky) family name.
Another great video!
Z, I know what you're doing in trying to educate people in an objective way with videos like this, and you are totally nailing it to the wall.
What I don't know is how effective you really are with this kind of format, but at least for people like me - you are killing it.
Please don't think that you or your guests are getting 'too technical'. I'm not even a medical professional (though I am somewhat of a science nerd), and I got some tingly feelings in my special place - ESPECIALLY when Offit said, "OK, I'm about to bore your listeners with some math...".
Please keep doing this kind of stuff! You're doing EXACTLY what you want to do to a greater extent than you might imagine.
So thankful for the clarification on Biden’s announcement. I’ve been so concerned that second doses would be given very late due to the poor messaging. Thanks for being clear! 😊
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Yes it was an absolute messaging problem. One of my Patients refused the vaccination when offered because they thought they would not be able to get the second dose. I am sure he is not the only one.
I have seen several episodes and I'm subscribed and liking. Thank you. You are sincere and doing a great job of respecting and sharing the information. Great job ZDoggMD!
Thank you for bringing the T. Really appreciate you both. God bless
I hope lots of people see this. We need good vaccine info out there to combat the misinformation.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).When we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane?(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ) Especially when we consider the fact that CDC confirmed cross recognition of existing SARS-COV antibodies to this novel coronavirus, this means that so long as we have a strong and appropriate T-cells immune respond, our evolutionary adaptive immune system is more than enough to handle this virus during low viral inoculation.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
@@DomFortress Thankyou. Thorough & informative. Antivirals exist for fractions of vax billions. Think how the money could've been used ..All critical thought, absent in covidiom Blatant media bias and lies
?,?
@@DomFortress 🤔maybe you need to do more research on where you are getting your info. You do know that there is a lab who have already made a vaccine that has just went in to human trial studies that has already tested their vaccine in animals who's lung are quite similar to our own. The US, China and Britain are not be all end all of medical studies.
@@susanpick2382 I don't care about all vaccinations that still depends on a strong and appropriate T-cells immune respond from the host, when I care about therapeutic lifestyles as holistic preventive cares that can prime and optimize human autoimmune functions, period. Medications thus big pharmas be damned.
Prepared this summary for my colleagues, posting here for those who don’t want to sit through 48 minutes and rather read, some portions are skipped that aren’t applicable to us. Enjoy!
My notes and highlights from the video to keep in your back pocket for those who are strong with the cognitive dissonance:
Paul Allan Offit (bio paraphrased from Wikipedia): pediatrician, co-inventor of rotavirus vaccine, professor at UPenn SOM, founding member of autism science foundation (ASF) has been on CDC’s ACIP, was on FDA advisory committee for covid vaccine approvals, one of the most public faces of the scientific consensus that vaccines have no association with autism, for which he has been a frequent target of hate mail and death threats.
⁃ Maurice Hilleman (father of modern vaccination, helped create 9/14 childhood vaccines now given out), won’t breath a sigh of relief till the first 3 million doses.
- 7 million given out so far
- No Bell’s palsy reported yet
- Pfizer Anaphylaxis: 11 cases per million doses (higher than other vaccines 1 out of 1 million, though we are looking closer at this data and could cause observer bias), good news happens immediately, treatable w/ epi, no cases w/ moderna vaccine (possibly one with a physician who gave himself an epi dose because he was probably having a panic attack...)
- One report of an obstetrician dying 3 days after he got the vaccine and his platelets went to zero (possible ITP, MMR vax can cause it 2 weeks out and usually transient, incidence 1 out of 20k-30k, though wild type measles also causes it) hard to sort out coincidental from causal associations, still under investigation
- Natural viral infection can cause some of the same side effects as the vaccine, e.g. flu and the vax can cause guillain barre (though natural infection has a 17x higher rate than vax)
- Other vaccines (N/A, skipped, watch video if interested)
⁃ Pfizer vs moderna preferences (N/A, skipped, watch video if interested)
⁃ Vaccine efficacy inflated conspiracy (BMJ article by someone who speaks at antivaxxer conferences, watch video if interested)
⁃ Asymptomatic spreaders, theoretically less contagious if vaccinated as they would make less of a viral load because of an immune response faster (example rotavirus vaccine, does not stop asymptomatic spread, still virtually eliminated disease)
⁃ Why do we still need to wear masks? (Skipped, you know, watch video if interested)
⁃ Civilian vaccine logistics, Biden rollout mess up, and why two doses (N/A, skipped, watch video if interested)
⁃ Variants: UK variant still neutralized with natural immunity of vaccination (no response difference from original); South African variant, study still pending (convalescent serum vs Pfizer vaccinated serum)
⁃ Any test to see if you’re a nonresponder to the vaccine? Currently no specific antibody test, Pfizer didn’t have that data yet at the FDA committee meeting, pending results
⁃ Previously/currently infected, should I get it? (mostly skipped, you know, interestingly there were 8 people in the Pfizer study who were previously infected and got vaccinated, 7 people in the placebo group got sick, 1 in the vaccine group did not, possible booster effect, need to check the numbers on this, he may have misspoke)
⁃ Monoclonal antibody treatment -> wait 3 months before getting vaccine
⁃ Are they unblinding vaccine groups from studies so they can get vaccine? Short answer yes, watch vid for long answer
⁃ Can you mix vaccines, e.g. Pfizer dose 1, moderna dose 2? No
⁃ Pregnancy/lactating? (mostly skipped, you know, of note: one episode of spontaneous abortion in each trial Pfizer and moderna, both cases in placebo groups)
⁃ Hesitancy in healthcare professionals? Not enough data, or don’t know the data -> convinceable; believe in conspiracies, trust issue -> difficult/lost cause, if they refuse tell them to stop complaining about PPE, there is a ready solution, vaccinate, don’t go to social media and say you’re not getting vaccinated, spreads distrust; public value the opinion of nurses (medics) more than us (which is true)
⁃ PSA: covid is now a preventable disease
⁃ Hope: Could stop the spread by early summer (mostly skipped, can watch for the math on existing community immunity, herd immunity and number needed to vaccinate and logistics going forward)
⁃ Ghostbusting
Fam phys in Florida with high 65+ pt demographic. I have seen very little vaccine hesitancy in my patients. We are bombarded with calls daily to get it asap. I’ve had Pfizer vax, both doses, and make it widely known. Great information! Finally, I’m seeing some optimism! Thanks Z!
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I work in in home healthcare and I'm scheduled to get the pfeizer vaccine next week. I hate shots and I've never been so excited for a shot in my life. Listen to the science. Listen to the experts. I'm so ready for us to get to herd immunity so we can all get back to normal life.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Unfortunately what is pushed here is not science nor are these experts.
@@laurelpearse179 before the invention of vaccine as intentional infection, low viral inoculation is how we achieved herd immunity. And this is how some nations gained herd immunity with both high viral infection rate, and some mild symptoms, while in an absent of vaccine. The mask wearing doesn't eliminate viral infection, but instead it causes low viral inoculation. www.nejm.org/doi/full/10.1056/NEJMp2026913
However, a history of autoimmune diseases rooted in a weaken and inappropriate regulatory T-cells anti-inflammatory respond(onlinelibrary.wiley.com/doi/full/10.1002/mco2.12 ), which is a common comorbidity factors such as chronic inflammation, obesity and fatty liver disease rooted in metabolic imbalance(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), and high blood pressure rooted in systemic endothelial glycocalyx damages(www.sciencedirect.com/science/article/pii/S2319417020301414 ), are strong indicators for a severe outcome during any viral infection, regardless of age.
And historically with the majority of the adult population in the Western world were already trending to overweight or obesity at 2018(www.medpagetoday.com/primarycare/obesity/90142 ), we're not gonna be fine by ourselves just vaccinating millions. Especially when the vaccine had never been tested for antibodies in its 2 months long safety and efficacy trials(www.medpagetoday.com/primarycare/obesity/90142 ), nevermind that the manufacturers prescreened all test subjects for autoimmune diseases, and reinterpreted mild symptoms as evidence to prove that it offers some protection.
And if we're good at studying the medical history of overdiagnosis(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), then we could've known that within the context of psychoneuroimmunoloy, overdiagnosis can cause irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ), and this can disrupt our parasympathetic nervous system that regulates our T-cells immune response(www.ncbi.nlm.nih.gov/pmc/articles/PMC5050399/ ), due to overt activation of our sympathetic nervous system by our irrational fear. And if we're better at studying legal history still, then we could've known that DNA forensics scientists had been warning since 2016, about just how molecular PCR test was misused to convict the innocent to serious crimes like murder(www.sciencemag.org/news/2016/03/forensics-gone-wrong-when-dna-snares-innocent ), yet the exact same molecular PCR misuse is now the sole justification(www.cebm.net/covid-19/infectious-positive-pcr-test-result-covid-19/ ) for the dangerously autoimmune health damaging social isolation caused by just such policies as mandatory social distancing and worst, lockdown.
I am glad to listen to your programs, thank you. I am disappointed that you said you were going to discuss autoimmune disorders at the beginning of this program and then did not do so. I hope that you actually address that issue at some point
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
What do people want? Long-term data.
Given the circumstances, what do they want, realistically?
ua-cam.com/video/scfIOl3rt4o/v-deo.html
Thank you
I received the 1st dose. The day after, I had so much pain on my left arm. I was not able to lift it up, my fingers hurt when I tried to close my hand. I had a horrible pain on the left back and front of my head, worse than a migraine headache that wouldn't go away. When I receive the vaccine, minutes later I felt a numbing sensation that radiated from my left arm down to my fingers then up to my left side of my face and to the back of my left side of my head. I have been having chills after that and I lost my appetite for 5 days. I'm not getting the 2nd dose.
I had the Moderna
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Fake news, you are a liar, an ativax to say you have pain, you want to scare peoples....Moderna & Pfizer are our new churches and we need to follow without question.
@@MrOvidiuk I did have pain and i know what I felt.
@@MrOvidiuk and we had to call a code blue when a nurse was unresponsive after getting the vaccine
Why wouldn't the primo-infection not result in a longlasting cellular and humoral immunity for the SarsCov2?? It does for the other coronaviruses including SarsCov1 from 2013.
This was a wonderful video! Thanks so much!!!
Why is it taking so long to approve the AstraZenica vaccine. Cheap effective and only requires fridge temp. Already approved by the UK can you not share date
Can’t make money off of it 🤷🏼♂️ everything is profit driven in the USA
No money in it obviously
That first scratch analogy. The only new car I ever bought was delivered at 10pm. The next morning I bought paper towels and glass cleaner because the car had been driven 200 miles to get it to me. While paying, March winds blew a shopping cart uphill into my car. Six months later I almost totalled it in a ice storm. The only panel not repaired was the one that shopping cart hit...
“COVID NOW IS A PREVENTABLE DISEASE.” - the most understated but impactful statement I heard online on COVID this year! And I heard lots. Thanks ZDOGGGGG
Well, that comment certainly didn't age well.
Why another two dose trial of Astrazen vaccine. It has already been studied and approved by UK who are not slouches
I guess we don’t trust what the British decided after they looked at the studies. We need our own because we are smarter. Look how successful we were initially with our own tests(not). Plus they are very cheap, no money to be made there. It’s not like 1 in 1000 Americans have died so far.
No mention of cross-immunity?
From the BMJ :
"But memory T cells are known for their ability to affect the clinical severity and susceptibility to future infection,25 and the T cell studies documenting pre-existing reactivity to SARS-CoV-2 in 20-50% of people suggest that antibodies are not the full story."
That the same article that found reactivity in Sars COV 1 17 years later? yet the headlines only ever say "limited immunity long term without vaccine"
So if there is no antibodies detected after having both covid and first dose of Pfizer, it does not mean there is no immunity? What is your opinion on getting the second dose and getting it a few weeks late due to lack of availability?
@@mariamamiri2257 After a (mild) Covid you can be immune without the presence of ( detectable levels of ) antibodies. An IM injection of a vaccine should always result in the production of antibodies (which can take a week or two ) otherwise it's ineffective.
A second dose will boost the immunesystem and Ab-production and provide a stronger and longer lasting protection.
If a patient stays in a area or waiting room waiting to be vaccinated that was occupied 5 minutes previous to appointment by someone that tests positive , without cleaning and disinfecting as usual, could going to be vaccinated cause someone to get infected?
Dr. Drew Pinsky says he got Covid when he went to a hospital get vaccinated. (He wasn't actually able to get the vaccine.)
@John Doe right, cleaning and disinfecting won't help, is this common practice, this is 1 for the books
Gentlemen, THANK YOU!!💯💯💯
Thanks,I feel better.gonna go for it!
yes! thanks for this! been reading up CDC guidelines today, and this pops up. i'm grateful.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Are you really not aware of the CDC criminal history?
This was excellent. Thank you.
HIM Coder here, even though I work from home, the wonderful peds institution that Dr Offit and I work for placed the coders in phase 2, so I've recently received my 1st dose. I still feel some type of way that I've gotten it before other people who work outside of the home but on the other hand I also want to set an example and protect others like Z said.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I love you both! Thank you for sharing!
thank you thank you thank you .....
Need this.
Why aren't we authorizing the Oxford vaccine?!
What? A $6 vaccine that works about as well when corporations want to charge over $35 here? Shuuush.😉
@@OceanFrontVilla3 is the evidence out yet?
Thank you ❤️
Great interview. He really dismissed your question on Doshi's BMJ piece. We don't have privy to the study but Doshi did. He wrote about suspected but not confirmed covid cases which would decrease the efficacy of the vaccines had they been tested. "category of disease called “suspected covid-19”-those with symptomatic covid-19 that were not PCR confirmed. According to FDA’s report on Pfizer’s vaccine, there were “3410 total cases of suspected, but unconfirmed covid-19 in the overall study population, 1594 occurred in the vaccine group vs. 1816 in the placebo group.”
With 20 times more suspected than confirmed cases, this category of disease cannot be ignored simply because there was no positive PCR test result. Indeed this makes it all the more urgent to understand. A rough estimate of vaccine efficacy against developing covid-19 symptoms, with or without a positive PCR test result, would be a relative risk reduction of 19% (see footnote)-far below the 50% effectiveness threshold for authorization set by regulators. Even after removing cases occurring within 7 days of vaccination (409 on Pfizer’s vaccine vs. 287 on placebo), which should include the majority of symptoms due to short-term vaccine reactogenicity, vaccine efficacy remains low: 29% (see footnote)."
36:00 You understood but it wasn't clear what you understood.
Why not have Peter Doshi on for another perspective? If you are trying to have open discussion, why shun such an important voice just because he questions vaccines? As we all should be to have a clearer understanding. Science begs and demands curiosity. You cany have it both ways.
Great video! Very informative
Love this❣️ Thank you, thank you, thank you!
Message of Hope💛🙏
I understand the rotavirus parallel, but the mode of transmission is a bit different. This is aerosol and airborne. Asymptomatic transmission is much easier in this mode. So I as a vaccinated family member could become an asymptomatic spreader and not know until my wife or children are infected. That is a concern in being the only one of 7 eligible for the shot.
It would be interesting to see a breakdown of vaccine hesitancy in health care workers and in what sectors these health care workers are employed. An RN friend at UC Irvine ER and her colleagues (from what I understand) are eager to get vaccinated. Also, my colleagues and I in the ER I am working in Canada are eager to get this done and are not hesitant in the least. From what I understand, our ICU workers are also on board. I wonder if the hesitant are those that work in areas where covid has been of little concern? Just would be great to see how the data all breaks down. If possible
THIS exactly-remember HCW include janitorial, support services, food service, housekeeping, laundry etc. It is NOT just nurses and doctors!!!!
I joined the Pfizer vaccine trial in August. Lots of nasal swabs and blood draws over the last few months. They unblinded me on Jan 18 and I had received a placebo. They offered me the chance to join the vaccine group and I received my first dose shortly thereafter.
Should you get tested for covid-19 antibodies before you take this vaccine?
How long does the 95% efficacy last? I month? 3 months? 1 year? We are part of the trial.
Yes we are the trial last stage.
Can you ask Dr Offit why the FDA hasn’t approved the Oxford vaccine? I assume there’s a reason, but the UK and India approved it awhile ago
That's covered in this video - it is still in phase 3 trial in the USA.
@@daviddeavours4909 unless he is prepared to say the UK health officials are incompetent, there is no reason not to approve it based on their approval.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Simple, it is all about money and share the profits...in not about safety.
@@buckcampbell4292 😂😂😂 yes, sure is about this. FDA change the rules to allowed 2 experimental vaccine that NEVER use until now on humans and now they talk about safety...this is a good on. Personally I will wait for „classic vaccine approach“, they are few in phase 3:
www.covid-19vaccinetracker.org/
These interviews have helped me stay informed and more confident about getting the vaccine. Thank you, Dr. Z for doing them!! 🥰Ultimately, I got the vaccine because I didn’t want to run the risk of being a long-hauler. I have autoimmune diseases and my immune system is good at overreacting. I’d rather not give it anything else to overthink about. Lol. 😏
Me too immune compromised had to get rid of flu shot 20 years ago so no thanks.
Did you get the vaccine already? Asking because I'm 63 years old and have to autoimmune diseases and one of them is an inflammatory muscle illness which is already giving me a lot of problems. They did not test it yet on people with autoimmune illnesses and don't know how they are immune system will react or whether it will overreact so I was wondering how you did after the vaccine? I will be speaking with my rheumatologist next week though
@@pokerlover16
Yes, I received the vaccine. (2nd shot was just yesterday). My arm was sore like usual after you have a needle stuck into it. About a week later, I noticed a systemic inflammatory response- meaning swollen lymph nodes, cold/flu symptoms, increased joint pain, etc. All my usual suspects acted up. I have alopecia as well, so I couldn’t really tell if that was affected because there’s no hair growing anyway. I was pretty tired for a couple of days as well. I took the time to get extra rest. It resolved after that. I expect to see the same this week with a bit more intensity since I got the vaccine booster yesterday. I still think it would be better than risking being a long-hauler after enduring an actual infection of covid.
This was an AMAZING information. I am one of the nurses that is hesitant about getting the vaccine, not because I don't trust the science, scientists, or pharma, but because I would like to see how effective the vaccine is long term, don't want to create an immune response that could potentiate the risk of developing an autoimmune disorder that I or my spouse may have already been genetically predisposed to. One question that I would like answered, which may not be available at this time is whether or not there is a chance that this mRNA vaccine could possibly potentiate the onset of some of those diseases such as SLE, RA, or others. Maybe I'm thinking outside of my realm of knowledge as I don't know if that is even a possibility, but I do believe that stressors can trigger an autoimmune disease. THANKS!! Hope you actually are able to catch this question in the midst of all of the other response. In the mean time, I guess I need to be doing some personal searching on this topic, but do trust your and Dr. Offit's input... for the record, I am NOT anti-vaccines, I am simply questioning still if it is too soon... I know there are minimal immediate risks, but as for long-term... i don't quite understand the nature of mRNA vaccines and what they may be capable of especially if put out there so rapidly.
Wow! That was good...understatement of the year!
This might be a long shot, but can someone provide a journal article, or other evidence based link for NOT taking an antipyretic before/after the vaccine as Dr. Offit advises?
My facility’s vaccine providers are telling those receiving the vaccines they can take Tylenol.
I’ve been searching the Cochrane Library without much luck so far.
@zdoggmd Can you make a video on the Global Times vaccine article about a 19% to 95% efficacy rate on the Pfizer vaccine due to eliminating "suspected" cases from the trial data. I love your analysis and background! Thank you!!
I am a health care worker and I had my first vaccine on 12/30. I tested positive yesterday for Covid. Now I'm on a z-pack, prednisone, and an inhaler. I hope my breathing gets better.
That's terrible timing. I hope you recover quickly.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Thank you for all the info and I am finally getting my vaccine shot tomorrow. I am tier A but they asked if I worked in a purple tier school district and I live in a purple tier for 6 months now. I am a school nurse and my families are really suffering, been doing covid tracing and it started with just parents and now it’s the whole families. So thankfull. I am getting it at disneyland employee parking lot!
It was well done. They had a waiting area in the last tent for 15 minutes to observe for any adverse situations. They had EMTs and it was really safe. @Christine, I do not have allergies and no adverse issues. I am fine for this. I am post cancer 6 years out and well in general. I have an RN, BSN, PHN, M.Ed. I got the shot and fine. I felt hope.
By no means am I a medical expert in any shape or form. I appreciate your videos and knowledge coming from a rational point of view. I have a question about the formula determining herd immunity, should there be a variable taking into account effective treatments? To me if we have that factored in, it would reduce the amount of vaccines needed for herd immunity because we could better treat the infected, ultimately reducing their sickness (symptoms, spreadability, etc) but those who have been infected would carry antibodies for their own protection and not need vaccinated as quickly. Thoughts?
Thank you for the update- agree that getting the vaccine out there is a priority vs sub-grouping risk categories.
I would like to know how long do the antibodies from the covid vaccine last? Also is there any evidence so far that mutant strains will be covered by current vaccine?
I had Bell’s palsy in March 2020. It resolved, but i worry that the vaccine will cause a resurgence of the Bells. I work for the health department and now we are required to staff these vaccine sites. We can get vaccinated on the day of working at the point of dispensing event. Shouldn’t i wait about 10 days for an effective immune response before i work at these events? Would certainly appreciate your expert recommendation.
Very disappointed he didn’t talk more about the Oxford/AstraZeneca vaccine. To not even acknowledge there is another vaccine out there, approved by many countries and already being given to people, is shameful.
Great interview, thanks!
I had a question on the vaccination and rituximab treatment. Can I still get the vaccination even though I’m undergoing rituximab treatment?
Dr paul when do i check for my antibody or antibody surveillance after my second vaccine
Should i expect positive result in antibody test correct?
I was wondering this too
There isnt currently a test available to test this after vaccination.
You still have to wear a mask and social distance. Even after years of flu shots, they are only effective 25-35%. I don't believe in less than a year that these vaccines are 95%
Effective.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
I don't know why anyone should agonize over those who don't wish to be vaccinated. There are lots of people what DO want to be vaccinated. Focus on people who don't have access because of the slow distribution.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Got my vaccine today!
Are you okay Heather
thank you for keeping up with these videos. I trust you and Dr. offitt. I'm one of those 30% of nurses who aren't getting the vaccine for now. I DO hope to get one just not the current two MRNA vaccines. I have a severe anaphylaxis to shellfish so I'm afraid of the allergic reaction with the two available right now. I'm hoping the J&J one will be a better choice for me and then I can be immunized as well.
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
ua-cam.com/video/M0A8e6_8SQE/v-deo.html
I got the Pfizer vaccine and then had symptoms related to covid 3 days later. Tested positive for covid next day. Did I just cancel out the vaccine effect? Due for 2nd dose next week.
They say even if you had Covid I still need to get the vaccination. When you get the vaccination you still have to wear your mask stays social distancing and yes you do have to get the second part of the vaccine. Good luck
When I can ramp up antibodies production with high intensity training alone(www.ncbi.nlm.nih.gov/pmc/articles/PMC7351507/ ), while the vaccine never tested for antibodies in the blood during its 2 months long safety and efficacy trails(www.nejm.org/doi/full/10.1056/NEJMoa2034577 ), why should I get vaccinated/intentionality infected? Furthermore, when our T-cells can only respond to acute inflammation caused by viral infection on the cellular level, in the absence of antibodies, while the B-cells can only produce specific antibodies for the aforementioned viruses after they've been informed and maturated by helper T-cells, then there's a literal gap from an empty shell of mere spike proteins, not an actual virus that can cause infection on a cellular level, to even cause an acute inflammation via cytokine signaling, to start mobilize the T-cells in the first place(www.cebm.net/covid-19/what-is-the-role-of-t-cells-in-covid-19-infection-why-immunity-is-about-more-than-antibodies/ ). Also, this novel coronavirus isn't literally novel at all, when CDC knew since last year that old antibodies from the first SARS-COV outbreak can recognize and respond to this one too(wwwnc.cdc.gov/eid/article/26/6/20-0516_article ). Let's also consider the fact that when we didn't cultivate any live SARS-COV-2 virus from within the lungs of severely ill COVID-19 patients, while we only cultivated a novel coronavirus from the nasal and oral swap samples of someone with only mild COVID-19 symptoms, how then do we know for certain that this vaccine is even immunizing us from a viral infection of the lungs, through the ACE2 receptors on the cell membrane? Especially since naval nitric oxide in our nose has antiviral property(www.ncbi.nlm.nih.gov/pmc/articles/PMC7200356/ ), this means what's in our nose isn't the same as in our lungs.
What's more, when the majority of the Western world population was steadily trending towards obesity since 2018(www.medpagetoday.com/primarycare/obesity/90142 ), while fatty liver disease can still develop in people that are "skinny fat" with otherwise normal BMI(www.ncbi.nlm.nih.gov/pmc/articles/PMC3959355/ ), then autoimmune diseases caused by comorbidity factors rooted in metabolic diseases, can still make all vaccinations useless, regardless of age.
Finally, when people are still suffering socioeconomically from lockdown, while overdiagnosis of COVID-19(www.bmj.com/content/370/bmj.m3374/rr-1 ) can cause real psychological harms due to fear of labeling(www.ncbi.nlm.nih.gov/pmc/articles/PMC6135119/ ), according to psychoneuroimmunoloy we're only making our immune system weaker with our own irrational fear(www.ncbi.nlm.nih.gov/pmc/articles/PMC1299209/ ).
Will you let us know if you are okay
I want to get the shot, but I don't want to get it in the arm. I have thoracic outlet compression syndrome. 20 years ago, I got a vacc, my shoulder swelled. Ended up with 6 weeks of therapy (that's all you get with insurance) and 7 months of excruciating pain. Can I get, to put it nicely, in the hip instead?
Do we know what the percentage of people who refuse the vaccination is? Just curious. And what is the main reason? I know you have touched on this in your videos....wondering about %'s.
Not this nurse! Got the vaccine the first day it was available to me! Feeing great and less anxiety caring for my covid patients! Thank God for modern science!
Thanks for such an informative discussion.
Lol
What about Dr. Fuller’s caution in waiting for long term safety data? I know 7 million have the vaccine, but that comment about 3 million was made when the development cycle was much longer . When you ask what people are waiting fir, it is the longer term safety data. When will it be available. The 7 million provide very short term observation.
I wonder if our reaction to the first vaccine can determine our reaction to the 2nd vaccine. Just had some mild injection site soreness for 2 days after the first vaccine.
I
Phrase the question properly: Is it utterly insane to require masks for vaccinated people.
Vaccinated people still carry the virus in the nose etc they just dont get sick.
Vaccination will not prevent reinfections.
My experience has been that way too many people I see when in a shopping centre still have their noses hanging out of those masks. Honestly, don't know why they bother if they don't wear it properly anyway.
Duh it is a bunch of bullshit these vaccine pushers are desperate the word is out
Danger ! Danger! these guys are Lost in Space because the truth is out there you are desperate to push these deadly death shots.
An excellent talk😎
Just got my first Pfizer dose today! Zero side effects so far except extremely subtle injection site soreness.
As Dr Fauci ? ua-cam.com/video/scfIOl3rt4o/v-deo.html
Hope you are fine, and will keep your health.
Watching these Paul Offit talks is a trip because i almost died from rotavirus when I was a kid. Thank you Paul!!!
Can you get some info and share on the Sinopharm vaccine? My older parents are US citizens in Jordan and they have approved Pfizer and Sinopharm there. It looks like they may only be able to get the Sinopharm this week and it makes me nervous. Should it?
Sorry, don't mean to interrupt, but if you goggle that vaccine it has articles. Seems Taiwan is not very high on it for the side effects. Have a good day
Would love to hear the differences, in efficacy and in approach between the different vaccines across the world..
American Pfizer/Moderna,
Russian Sputnik V ,
British/Sweden AstraZeneca
Chinese Sinovac/Sinopharm
India's Bharat Biotech Covaxin and Oxford/AstraZeneca
Do they all use mrna? If so, do they just differ in the lipid encapsulation technique?
Go on ZDogg take 10,000 vaccines.
Prove that the Offit is right.
" let me love your child "
What about the people dying from it?
I did the same as you and refused my vaccine at first feeling people more exposed to the virus should get it first. After hearing how many people were turning it down including my sister who works in food service at a hospital & my 80 year old mother who I help care for, I changed my mind. When I signed up there were so many spots open for Tues & Thursday which confirmed I wasn't taking it from anyone who was in line & wanted to get it.
When should we expect to see some more information on research on the people who are pregnant and have already received the vaccine?
Kristina Braly is an anesthesiologist who has youtube channel, is pregnant and went over why she got vaccinated. Not research per se, but a physician who is pregnant her perspective.
My mom is in South Africa and works as a medical professional there. She is therefore signed up to receive one of the first Oxford-AstraZeneca vaccine's from India. Should I be concerned? My mom is 61
What about Radiation Therapy ( cancer) patients ?Currently taking radiation for stage 1 cancer? - Thanks !
Depends where you are having the radiotherapy. But it doesn't generally badly affect the immune system. So you'll likely be ok.
I am 7 days post Pfizer vaccine. I started with fevers last night, today I’m up to 101.2. I have a test pending and should know tomorrow what the results are. Also my MIL received her first Moderna injection and now has tested positive. We are both totally bummed about this.
Should we get the second vaccine?
I’m sure my symptoms are less severe than had I not had it..
I am hearing, from Nurses that have been vaccinated, that if you have been Covid positive the vaccine hits you a bit harder in respect to side affects.
Yeah the first dose seems to be acting like the "booster" that the 2nd shot for everyone else who hasn't had covid.
@@monykalynf3604 well as long as they get the vaccine. Thought they said immunity from getting infected is equal to the 1st dose with about 60% effectiveness. Maybe this is stretch but if you increase the chance of the elimination variation with just a single vaccine dose, it seems to follow those with prior infections that don’t get vaccinated may be responsible for virus mutations that yield the vaccine impotent. It is important they get the vaccine, I have many RT and Nurse friends in ICU that have been vaccinated, it seems people that have had the infection respond differently, by way of side effects, than those that do not. It is notable that in the, placebo group, more got reinfected than those that got vaccinated after infection. Take away: those with past infections should get both shots.
@@OceanFrontVilla3 listen to the whole broadcast...that is not true. I know health care workers that are taking the vaccine with a past Covid infection. It is also unknown wether or not past infection keeps you from spreading it.
Hey, maybe interview Dr. Michael Yeadon? Give your followers actual informed consent.
did I misunderstand what the guest said here? Did I hear him say that once you get the disease that you are immune? And then he said you need to get the vaccine even if you've had it? I am confused.
Please talk about this important issue Zdogg. If you have recovered from covid and are a plasma donor for antibodies, once you get the vaccine you can no longer donate antibodies. I think this is a very serious issue. Recovered people are being urged to be vaccinate. Most of the time having a disease gives more immunity than a vaccine does so why such a hurry to vaccinate people already recovered from CoVid. Perhaps, there is some research that shows the vaccine is better at protecting from other strains, because if that is the case I would like to hear about this.
The problem is if everyone that is recovered gets vaccinated, what happens to our store of convalescent plasma? It's seems unlikely the vaccine will put an end to its necessity. Some people will still get sick. More importantly, these vaccines may not work for future mutant strains that perhaps convalescent plasma might still treat. Would love to hear thoughts on this.
Filipina friend said they have to take Sinovac. Any comments?
After 10 month of people dropping dead everywhere, strict measures are finally in place here in Stockholm. As of this week, we have to wear face masks in buses and trains during rush. For as long in public transit, it has to to be on from 7am and may not be removed until 9am. Must be put on again from 4pm until 6pm. Thank goodness for our decisive government.
I wish the Belgian "experts" had as much common sense. We have to wear masks everywhere, sometimes even outside, in the city centres or during a stroll along the seaside!
Sweden doesn't seem to have any excess deaths in 2020 and half the deathtoll compared to Belgium. Only elderly frail people in carehomes dropped dead in spring around here.
@@guidospanoghe8896 Yes, I have been wondering about you guys, how things are in Belgium. You're right, Sweden is only average in Europe. Infact, I'm not even sure how big of a difference there would have been if we had kept everthing totally open, sports, concerts etc. Our second wave curve is already flattening. Same thing here, most of the deaths occurred among the elderly.
Dr. Z,
I had Bells Palsy when I was a child. Have you heard anything about people getting Bells again? I got the first Moderna vaccine before I heard this. So far so good. But I have heard the second round has kicked people in the butt.