Dr. Tina Peers from UK Discusses the Management of Long Haul Syndrome
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- Опубліковано 20 тра 2021
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. Dr. Tina Peers from UK Discusses the Management of Long Haul Syndrome
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Disclaimer:
This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only.
Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional. ...
Disclaimer:
This video is not intended to provide assessment, diagnosis, treatment, or medical advice; it also does not constitute provision of healthcare services. The content provided in this video is for informational and educational purposes only.
Please consult with a physician or healthcare professional regarding any medical or mental health related diagnosis or treatment. No information in this video should ever be considered as a substitute for advice from a healthcare professional.
Brilliant Doctors asking all the important questions and serving humanity! Merci!!!!!!
Thank you 🙏
Yes thank you so much for addressing this you two. You are both great ..
Special spot in heaven for Doctors like her.
Its definitely is a light in the darkness when two very intelligent doctors talk openly and with so much passion, I wish you the very best Doctor Peers with your research and hopefully many many people will get the treatment that they so desperately need .As always a big thank you DrBeen as Dr Peers says your a rock star
My gp has always treated me like I'm a hypochondriac, but especially post covid. Very frustrating! Thank you all who are speaking out!
Was treated the same for 30 years until a mri finally showed my dics in c spine were bulging, spinal stenosis and degenerative disc disease! They all thought I was a pill junkie. Never gave me any until mri. I blame big pharma because they control what Dr's are taught. Fund, own med schools and give huge incentives to get their "legal dope" prescribed. More ppl die of side effects from prescription drugs than most could fathom. Nutrition hours for Dr's are about 4 and maybe 1 hour a year after graduating. When I started to see through the facade was mom took 35 different supplements for many years. Dr's said its junk! Dont waste your money. Next breath, please list them all because they can interfere with prescribed medications! If its junk, why list?
Beautiful. helpful, Whole hearted talk. Thank you.
Thank you 🙏
Gratitude and appreciation for excellence, diligence, intelligence! Thank you for your service Dr. Peers, Dr. Been🙏🏽❤️
You are welcome 🙏
My mother has been in this state since about 1976 when she collapsed and fell into a semi-sleep for 2 weeks. No cause was found. She has many diagnosis (hypertension, arthritis, fibromyalgia, bouts of angina, ibs, kidney disfunction, elevated ldl, osteoporosis) & her quality of life is very low. No treatment has ever helped. I will be taking this information to her & see if we can get better care for her. Thank you so much Dr.s for this talk.
I have ME/CFS which is similar to LH Covid and I am hoping this will help me.
God be with your mama and heal her!
Heather I am praying this will be an answer for your Mother.
It sounds like insulin resistance to me my friend..not medical advice. Go research Dr jason fung, nina teicholz big fat lie, dr berry-- that will get you started. We need to lower insulin for most chronic health issues (diabetes, fatty liver, many neurological diseases, metabolic syndrome (high BP, high insulin, high blood glucose, often obese or high abdomen to height ratio) pcos, osteoporosis, even most cancers are sugar loving..the list is long. Eating a clean diet low in omega6s, high in nutrient density and you'll see you don't need to eat every 4 hrs keeping us all in fat storage mode. Our mitochondria should be able to use sugar and fat but cant use fat efficiently always being in high insulin storing sugar as fat mode.. The mitochondria are not efficient. Search what diseases have mitochondrial dysfunction and youll see.. Its crazy.
Have a Look at Grassroots Health, Nonprofit Informations about Vitamin d3!
Thank u so much DrMobeen and DrPeers ❤️🌷🧚🏼♀️ (from Paris)
You are welcome 🙏
So thankful for both these doctors! I'm super happy I live in the UK where Dr Peers is!
"Brain the size of a planet!" For sure!! Such a great talk. I am sharing it with everyone I think will benefit from it. =)
Thank you 🙏
Dr, please please please look at the work of Dr Ron Davies at standford. He is way beyond where this nice capable lady us.
He's totally cutting edge.
@@69birdboy this is really interesting that he developed a test for CFS and potential for drugs to help. I do think taking things back to basics like Dr. Peers is doing is a very good approach too. Changing diet and trying different stabilizers helps so much!
Gratitude and appreciation for excellence, diligence, intelligence! Thank you for your service Dr. Peers, Dr. Been!
Thank you both for this information!! I have had all of these symptoms and have been referred to a variety of specialists to no avail. I have truly felt that I should just give up on life completely. This program came as a blessing and a reason to keep going with a hopeful heart and spirit.
How are u now
Thank you so much for this, I know someone who has long COVID and is miserable.
BRILLIANT ! Great discussion with our phenomenal Dr Been and the wonderful Dr Tina Peers. So much valuable information. Thank you both so much.
Thank you 🙏
Incredible talk & brilliant information. Thank you so much to you both for sharing x
Your guests are always so fascinating. Thank you for all that you do!
Seriously I've had ALLLLLLLLLL of these symptoms.... slowly losing my hearing, brain fog, tingling in hand and feet after temp changes, anxiety, vision change, ALLLLLLL the GI symptoms, all the respiratory issues including waking up in the middle of the night coughing/wheezing, super increased sensitivity to odors, migraines, and so on and so forth.... I've had many of these symptoms off and on over the last two decades but all have increased exponentially since I was sick in Feb 2020.
I now have HOPE that I can help heal myself because for years doctors have given me generic solutions and none of them have really helped.
I'm so tired of being unwell, I look forward to restoring my health 💯
I've had quite a bad day today but listening to you 2 "superdocs" really improved my mood. Thanks for all that you are doing. 💜
I have now subscribed. Thank you so much for putting this information out there. I have been searching for answers for my 79 yr old mother, following Dr. Peers and Dr. Patterson. So wonderful to confirm I am on the right track with my research. Now I pray her Doctor will be onboard…
Thank you both from the bottom of my heart 🙏 This interview made me tear up ❤️❤️❤️
Thank you so much Dr Been and Dr Peers. Saving this one to my favorites!
Amazing video Dr's. Thank you. I think I know a few people who need to see this including myself.
Thank you for this presentation, this makes me feel validaded!
What an awesome feeling to hear there are doctors who really listen and really take the time to understand what the patients are going through. Just like Dr.Been said: THINKERS. Thank you for that and thank you for sharing all that knowledge!
Thank you for having this talk!
Great work! Thank you both so much!❤️🙏
Fantastic discussion and creates so much hope for me personally. Especially the comments on resuming exercise. That would be a dream come true.
Can you ask the medical student who got better on Ivermectin in 3 days to do a testimonial for the FLCCC? They have created a wonderful series of quick video testimonials that really get the information out to the general public in a fantastic way. She would be a perfect candidate for creating a testimonial. If you could ask Dr. Kory how those get made and connect her with the way that could be created, I think it would be helpful for the public to hear.
How do we get our doctors to check us for this as mine think I'm just overreacting,could the vaccine make us worse
@@lynlawley8903 I got JnJ vaccine on 7/8 from 7/9 to present day 8/6 I have had terrible side effects. First 2 weeks I couldn't function. Headache, SOB, Pain bones joints. Muscles. N/V, feet, hips, can hardly walk.
Absolutely.
@@francesthompson4276 I bet you could take human Ivermectin right now & be well in 3-4 days or @ least on the mend! No doubt your symptoms are directly caused by the 1 vaccine.
@@naomifortune2707 I know this comment is late, but that side effect is from the shot not Covid symptoms
LOVE THIS !!!!!💜👍 have a wonderful weekend Dr. Been and also Dr. Peers 💜🙏🌈☀️💕
Thank you. You have a great weekend as well 🙏
You two are the kind of doctors I hope to meet if I need help. Bright lights indeed.
This is a lasting thread. Thanks soooo much for this info Doctors
Thank you Dr Been for having Dr Peer on your show. I agree with you. Mast cell is my least favorite cell after seeing your drawing on them. I don’t know anyone personally that is a long hauler, but know plenty with IBS, food allergies and fibromyalgia. I’ll be passing along this lecture.
Blessings. Also, Strongly urge you to read Dr Broda Barnes book, HYPOTHROIDISM: The unsuspected illness. You will find many other answers.
Fantastic. I love these programs as it’s nearly impossible to see a doctor these days . Thank you 🙏 🙏🙏🙏🙏🙏♥️
Amazing. 62 with lifetime history of disability from so much pain from GI to suicidal migraines every 3 weeks anaphylaxis, severe allergies to long list of drugs and environmental things which have disabled me for up to a year, twice. I have a new avenue to research and hope when all was lost. Fear the vaccine but this gives something to try to get through even that. Thank you Dr. Been and Peers and all the Coolbeens commenting.
Thank you Dr.'s. Very informative
I am so encouraged for help with my daughter who has had life long issues. I do believe these are therapies that will help her.
Thank You both for this excellent educational information.
Thanks Dr Been ...great show...
Thank you 🙏
Amazing program. So helpful. So much information.
Dr Tina, superb presentation. Thank you very much.
It was great.Thank you.
Excellent point about the titration between diet and exercise to avoid an episode 💯
That makes so much sense, I have experienced this and just chalked it up to either something I ate OR overexertion outside.... and waking up the next day feeling like my insides (trunk) were very angry plus the other symptoms. Now I put the two together and bam that's it!
I'm going on all the way on the low histamine diet 💯 and gonna make my family eat this way also 💯
??? I have had symptoms labled Post Viral Syndrome since a severe CMV infection in 2011 and have been to a myriad of specialists .
PE's, neuropathy, myopathy, brain fog, imbalance, SIB0, 'non-diffrentiated rheumatologc syndrome', etc. No diagnosis.
This is the first I've heard of this
For me, it was EBV plus CMV. I saw the light when I listened to Dr. Tina Peers
Yes. Me too. EBV and CMV. Later " Chronic fatigue and Fibromyalgia diagnosed tovether. Treatment: many drugs. No cure.
Quit the drugs years ago.
What’s your symptoms
🙏🏼 Dr Mobeen, thank you for posting these videos on UA-cam for the general public to see. It has been such a valuable resource for trying to understand wth is going on. The standard mainstream media has done a despicable job of keeping the public informed of the truth of what’s going on with Covid. I think I’m dealing with long haul (1 yr) and I did do the Ivermectin recently. It helped and I had one day where I got to see what it was like to feel normal and have lots of energy. I ran out of Ivermectin and I’m back to feeling exhausted, heavy and brain foggy. I’m going to keep learning and trying to find Drs that will work with me to fix this because I can’t live like this for years on end. It’s torture. My partner is the only one who understands, everyone else thinks I’m just being lazy, exaggerating and that I need to “suck it up”. Anyway, sincere gratitude and blessings to you and the few Drs that are actually digging into this mismanaged Covid mess and trying to help all the suffering people.
Thank you Dr. Peers and Dr. Syed both for your brilliant and absolutely pro human work.
"Nothing is a waste of time if you use the experience wisely."
Auguste Rodin
Thank you 🙏
Dr. Syed my humble wish is more and more will become your patreons as an appreciation for your true compassion sharing your wisdom and observations for the benefit of all. Also the excellent networking with other professionals you host and offer for all is in the very special format you do unique. Thank you :)
@Cyberfunk...maybe you can go through some other lectures of Dr. Syed which topic immune aspects in general and find something which you could adapt together with your Dr. to your personal situation. Dr. Syed has a lot lectures about general supplements, Ivmc is an other story, within the European Union it is banned for off label use and you will finde nearly no doctor which is prescribing it. I should maybe say, no doctor.
@@cyberfunk3793 I advise you to join the group on Facebook called "Long Haulers on Ivermectin and beyond". They discuss all the questions you have. It's International group you can ask questions in English, and Russian, and, perhaps, Estonian.
@Cyberfunk..... "The thing I have is so rare typical doctors don't know much about it so better to do study yourself also."
I can feel exactly your situation. The next is, if you then researched yourself through all the informations, at the end you need a doctor who is with you and then also is willing to sign the developed protocol. Further guides you and gives you his lab assistance, and is then finally in his mindset pro you. The doctor develops integrative his own thoughts in the whole process and observes the results unbiased and acts like a partner. What we saw through the last months was, that some treatments like Ivmc just were used in a sinister run for powerplays. I would also say you get in direct contact with Dr. Peers, as you already found out what could help you.
Wonderful talk, thank you doctors😃
Some doctors here are still treating long haulers as patients w psychological problems and others say it‘s no big deal, just like any other long haul from viral infection, so they are telling their patients that it‘s nothing out of ordinary and they should just have some patience and everyth. will be good soon again! So ignorant!! Thanks for this talk!! All the best for you both, Dr.Been and Dr. Peers!
Thank you both....🙏🙏
This has been great to hear. I'm relating to all of these especially the nerve twitching but cannot see. Coincidentally I stopped taking my anti histamine then go all the symptoms post covid.
Fantastic. Thank you so much 😊
Thanks very much for your work and for this very interesting and helpful discussion on MCAS! I am interested in the conference that wil be held in June? - Could you please post a link to that? - It would also be useful, if you could post the suggested medication below the presentation a link to the slides with the suggested medications, if possible. Thanks!
Amazing thank you
Remarkable presentation.
God bless you both!
I am a pathologist who strongly believe in mast cell activation disorders. My experience is that most physicians reject the mechanism/diagnosis. In its treatment I have found that humic acid/fulvic acid is very effective as it stabilizes mast cells. Mast cells are long lived and once activated do not become inactivated. Instead they must be replaced over time in an environment that does not allow the mast cell to become activated. For IBS, butyrate is also hellpful.
Very informative thanks! So how do you create this new environment?
@@sjfuqua I think the idea is to create a low histamine environment (via low histamine diet, type 1 & type 2 anti-histamines, etc. - all the basics that she uses in ALL her MCAS patients, and potentially some of the others as needed.)
@@sjfuqua Go to 1:16 for the brief discussion on this. She mentions that mast cells live a few months and in some cases (I think when riled up,) can even last a couple years. Like what Path doctor above says.
Finding mcas knowledgeable drs in any country is ver difficult for all with MCAS. Would you mind adding your location to your comment so that ppl could contact you to see if you knowledgeable drs in their particular areas? We as patients have been gas lit for over a decade (those of us who had mcas prior to covid). As recently as 2022, I was told by immunologists in my area who denied mcas existing. ...when patients knew full well it exists but we were told that this belongs with the immunologists 'wheelhouse'. In fact if a full research paper would be written to actually tell everyone in medicine are affected by mcas.
If there is any sort of database of knowledgeable mcas providers...in every country...would be very helpful.
I am so grateful to hear this. It resonates from my continuing experience as truth. I had COVID twice and then was affected by the second Pfizer vaccine.
You are so correct Dr Mobeen! The Doctors you showcase are thinkers! And so many patients are victims of Doctors! "Go home there's nothing we can do". How many times I have been told that! There is such an awakening in medical Fields at the moment!
Wonderful presentation ❤🙏💖
So helpful thank you!!
This was a very interesting talk,quite early on Dr Peers spoke of the increasing number of allergies and at the end she also spoke of the importance of diet if anyone reads this comment please listen to a talk by Dr Stephenie Seneff on the growing effects of glyphosate in the food chain
Pfizer shot gave me long haul symptoms. Every single doctor has talked to me about mental health.
Yay! 🥳🎉❤️
Thank you Dr. Peers!!!!!
You just gave me all the tools aside from prescriptions that I need to implement TODAY in addition to confirming what measures I have already undertaken. You mentioned a lady that had stools 8 times daily..... that would be me 🙋♀️
One of the things I can confirm that you said is that the day to day presentation of this syndrome is variable and I think changes between the trigger and the hormone production. I have increased symptoms close to my menses schedule.
What can we do to explain to many GPs that THEY ACTUALLY DO NOT KNOW EVERYTHING??? Not that specialists do much better... The cause of a lot of illnesses are often just lain at the feet of patients... as if it's in your head... When actually it is the "doctor" who DOESN'T KNOW EVERYTHING!!! Medical doctors often portray an arrogant air of omni-knowledge, when they should be acknowledging their many shortcomings and delve into constructive research... something it seems 90%+ of medically trained people are very unfamiliar with.
I really despise people who think they know everything even when everyone else knows for sure that they are making a fool of themselves!
That's why it is so important to find a Doctor, that cheers one on! One that is not condescending, and listens and will accept articles and discuss it with you?
@@judyprior9231 Yes, I agree wholeheartedly! Medicine is supposed to be a holistic practice. A doctor who takes time to address a patient's concerns (other than the normal physical/emotional matters), will have a very devout patient and is likely to get many referrals. But even a very well trained professional cannot know everything. Acknowledging when this is the case and hopefully trying to obtain an answer, is likely to gain even more respect from the patient.
This is one of the main reasons people are suffering years or even decades. The psychological weaknesses are in the doctors head and not the patients. I saw well over 20 specialists over 7 years; because of multiple organ damage due to inflammation. Only 3 told me my problem was well over their head and they haven't got a clue what to do, these were the good doctors, the ones who helped me find a solution. The rest fobbed me of with complete nonsense, incoherent answers, which contradicted themselves and other specialists. They just couldn't cope with the fact that they didn't have a clue.
@@robinhood4640 What was your diagnosis you came to at the end? I am trying to become my own Doctor. I can't rely on GPs anymore.
@@elenalepotova6623 I have no complaints about my GP, she tried her hardest to help. The specialists she sent me to, were the disappointing ones.
After being suspected of having systemic sjogren's, it was found to be secondary to an undifferentiated autoimmune disease.
It all boils down to fancy names for toxic overload. We live in a very toxic environment, and some of us cannot cope as well as others. We just don't realise how toxic it is, until our immune system can't take any more of it. We eat toxins, drink them, put them on our skin and most importantly, we breathe them 24/7.
AMAZING!!!! THANK YOU!!! I am vaccine injured, not caught covid ...yet and thanks to you, have self diagnosed myself with MCAS because the flare-ups correlated to a change in diet on Mondays! Oats, dairy,strawberries,spinach, tuna, avocado and lots of green tea ! By the afternoon my body was raging. I was eating ALL the foods I was not supposed to. I was diagnosed with anxiety..😃 NO Dr, rheumatologist, nor the ED department could help. So thank you both for this! It will be up to me to educate my 70 year doctor so that he can help others. Strangely enough, in 2015 after keyhole surgery, I started suffering from burning mouth disease and sort of worked out that it was related to food but I have not been able to be rid of it but I have learned to live with it. I have found a functional doctor who is treating my gut, along with other protocols mentioned. I hope this 9 Month nightmare will be over soon and pray for others, going through this as well.
As a medical professional, I did deep research 25 years ago for another patient. Burning mouth syndrome can be very low vitamin b-12 deficiency.
Just looking today, I am also seeing burning mouth syndrome can also be pernicious anemia.
Have you dr do blood test for b-12 level.
Wishing you healing.
Hi Dr Mobeen, can you bring on Dr Peter McCullough on your show?
My 🙏🙏🙏🙏🙏🙏🙏 Dr. Peers and Dr. Been you all the light 🕯️🕯️🕯️🕯️🕯️ at the end of Covid 19 tunnel.
Bless you all x x x x
The deficiency of VitD results in mast cell activation. The data demonstrate that VitD is required to maintain the stability of mast cells. The deficiency of VitD results in mast cell activation. Vitamin D contributes to mast cell stabilization. All the more reason to take vitamin d
There are so many reasons to ensure a good vitamin D status. I am reading Michael Holicks book 'The Vitamin D solution'. It's a real eye opener.
@@helenporter7584 I agree and will also look for that book. Thanks for the information Heather.
Daughter with Ehler-Danlos having headaches.
@@lcunningham1776 I am sorry your daughter is having headaches. You probably already know of L carnitine, magnesium, and MSM and vitamin c supplements under a doctor or nutritional advice. And vitamin d deficiency seems to be a pandemic and we know that can be a cause for many disease. Although it seems some are said to be genetic. I hope your daughter's headaches will improve. Best to you.
Can be said, that the amount and maybe the activity of mast cells in one could be also used as indicators for the personal true biological age of one's body?
Thank you, I will look into MCAS. I have had chronic IBS. I am otherwise known/physical tested as healthy and was exercising etc. I did not get covid, however I got the Pfizer vaccine and since that day I have had full body paresthesia, the vibrating nerves or tremors your long covid patients described, partial numbness in face, neck, head and nerve pain in sciatic, fingers and toes. I tried to exercise and this made the symptoms worse. My Eustachian tubes have been blocked for over 2 weeks, before that I had some episodes of tinnitus. It has been over 40 days since the vaccine and the symptoms persist. I’ve found many others going through these symptoms across the different covid vaccines.
TS sorry that you are suffering from this. Would you consider reporting to the Vaccine adverse events reporting system? Also, would you consider giving a testimonial to children health defense to raise awareness of these issues?
Thank you. Canada is completely clueless about long Covid, we don’t even have more than 2-3 clinics. None of which are in my province so nowhere for my GP to refer me, and she hasn’t been very helpful either.
I am ar the same point... so frustrating to see how we are far behind
Dr Mobeen ? A rock stsr and artist. Wow
Cycling and Spag Bol (and red wine) - YES please :)
I have mthfr...arthritis, sleep apnea, anxiety, tinitus, vertigo, extreme fatigue, more joint and muscle pain, migraines, extreme tmj, wheat allergy and gluten intolerance. My gp prescribed a steriod pk 3 times in 8 months for tmj. I believe it's why I got covid! My covid was mild. Post covid has been much worse than the virus itself. Watching this video helps me to understand why.
Blessings. Strongly urge you to read Dr Broda Barnes book, HYPOTHROIDISM: The unsuspected illness. You will find many answers.
Blessings. Strongly urge you to read Dr Broda Barnes book, HYPOTHROIDISM: The unsuspected illness. You will find many answers.
How are you doing?
52:00 yes! Thank You👏👏 Dr Peers
I have recently seen some shocking eye problems following a COVID injection
Good morning from Louisiana
Thank you for the video. Dr. Tina Peers was my first information about long covid. In my country most of the doctors do not even know abut long covid. Finally I went to the neuro covid clinic and they are helping me, but invermentin isnºt disponible here.
go to the flccc dot net website to find a prescriber of IVM if that is what you are looking for.
@@eugeniebreida1583 I agree
This is so interesting. I've suffered with stomach issues for years not knowing what exactly causes it, chest pain, intolerances, skin pain, tingling , headache.. I just want to be well. 🙏😇
I totally believe I have MCAS. I caught a bad virus a few years ago and have never been the same
We are 74 n 80 yrs old and we tested positive for Covid after our grand daughter was very sick with it. We barely had any symptoms but we continue to have the liquids seemingly pouring out our nostrils and sneezing like it’s spring allergies. I’m glad to get your info as we must find out which foods trigger us.
Is this treatment just for long haul Covid patients or would it be helpful for those of us with Chronic Lyme/Fibromyalgia/CFS/IBS?
Yes! The landscape will change
Some doctors are saying it’s ME/Chronic Fatigue syndrome which you get after a virus
how many weeks can you do this protocol, specifically I'm referring to cetirizine and famotidine daily? Thanks, I've been having an awful time in the last couple of months (after I assume having covid last march) and so far I've been slightly better due to using some of this protocol.
Thanks
So using antihistamines parallels with Dr. Shankara Chetty in South Africa.
QQQ Could this condition possibly cause Depression because of the inability to resume with their normal past activities?
I was diagnosed with a major depressive disorder 40 years ago after being diagnosed with RA (rheumatoid arthritis). Depression is often explained in relation to another chronic disease but after 40 years of observation I have a different idea
I believe depression is often the result of an autoimmune process. I don't have the background to explain how it happens but the correlations with RA flares are unmistakable
Dr Tina Peers is on to something. I believe I contracted CoV 2 two years ago. initially I thought I had Arthritis and long haul. Now, after doing my own research, discovered I have Ehlers-Danlos Syndrome Hypermobile Type. I am now clinically diagnosed by genetics department.
I suspect there are going to be a lot of people who will also come to realise they have genetic conditions.
I had a bad case this summer. Quercetin, 1 gram 4x a day helped. If I missed a dose, I would get worse. I started to feel better and then I upped my vit D, too high. All symptoms returned. I quit d for a few days and I’m getting better. I think that too much d activated mast cells. I was addicted to Benadryl in the past so I don’t take antihistamines. I have had so many symptoms. I recently moved across the country and I struggled and paced myself to be able to function due to my high activity level, lifting things, etc. itching commences as a harbinger of relapse. I can’t concentrate. I’m an artist and I have a lot of trouble drawing when activated!
This is super interesting to me ive been upping my d thinking it will help not even dreaming it could be making me worse
I have the tachacardyia after COVID. Standing , walking, sitting and folding shirt or cutting vegetable for a salad was all a struggle. But slowly I got better. Happened to be taking a lot of the supplement you recommend. Also took quercetin and glutathione. Now I am back to teach my low impact aerobics. HR still goes higher then it would have. Can ride a bike. Still struggle to play softball or pickle ball. Starting the low histamine diet yesterday and added some more of the supplements. I have a dr who will give me iver, but appointment is not till end of aug. here’s hoping that is the other missing piece.
How did it go? Did you take ivermectin? Do you feel any better?
Thank you very much indeed for this fruitful presentation. Cetitizin has been very helpful in combatting my congestion and allergic rhinitis now and then. Due to a persistent tinnitus and vertigio with imbalance am taking Betavert 6mg 3xdaily since mirth of Sept. The vertigio has improved a bit, although not completely gone. My eartinging is as high as before (since May 22).would appreciate your opinion on this issue.
Dr. Tina Peers should get an OBE!
Studying the anti histamines available I really liked the profile of Desloratadine and it's many other effects on white cell activity, inflammation, IL and cytokines. a really interesting profile for MASC. I found it to be less metabolized by caucasians (2% of them) and 18% of African descendants, but these low metabolizers didn't exhibited a worse security profile, with opens up speculation to make tests with slightly increased dosage of what is one of the most powerful anti histamines known. it also is an inverse agonist instead of receptor blocker, which decreases the basal "constitutive activity"of histamine receptors that may be self activated even without histamine agonism present. Hope you test it more extensively on long haulers. I'm just about to test it on a refractory long hauler evolving to obliterates bronquiolittis and pulmonary fibrosis proven by biopsy, which negated the presence of germs and CMV cytomegalic incursions... last attempt for a great man also known as Father for me...
I have had these 'long haul' symptoms since a severe infection with CMV.
I dont understand why the name is long haul vs a more accurate name of Post Viral Syndrome.
I have had the same symptoms since 2008. The diagnosis in 2011 was chronic fatigue syndrome, done by primary care doctor without doing a single test. Been bed bound, house bound since 2017. Fully disabled. I am watching these videos hoping to find some answers.
Exactly! This is not a new phenomenon.
@@taradrolma2774 I have had these symptoms since Epstein Barr Virus in the 80's. no help from doctors. Only from studying vitamins and nutrition.
@@horbour7 sorry to hear that. What a nightmare. Have you been diagnosed? If you were it would probably be CfS. CFS patients are neglected and maligned by medical professionals. I finally saw a functional medicine doctor and he did some tests for coq10, creatine, carnitine etc. i was deficient. It helped but didn't cure 🌸
I have the same symptoms with chronic Lyme. I was diagnosed with Chronic Fatigue Syndrome and Fibromyalgia. It’s so frustrating trying to get help.
Please comment on how i can manage the after vaccine effects on my MCAS condition
First, this woman doesn't look old enough to have a 33 year old son! Second, she has unshrouded a mystery I've been dealing with, the complex of problems that apparently suggest MCAS as an underlying condition. So it makes sense that I got the long haul COVID. Truly, at first COVID didn't feel much worse than I would feel after a Thanksgiving dinner (given all the food sensitivities I deal with, among other things) then it took a nasty turn that I have only barely emerged from with help from my naturopath. My doctors certainly did nothing to help, except to tell me to take lots of ibuprofen (and kill my liver). Thank you Dr. Peers and Dr. Mobeen for being among the thinkers, a couple of real Human Beens! One would think anyone who could get through medical school should be a thinker, but sadly, experience shows otherwise. Maybe med school used up all those energies for some, or maybe my dad was right when he pointed out the sad truth that half of all doctors graduate at the lower end of their class!
I'm not a doctor, but the suggested dosage of fexofenadine anti histamine sounds high, if it is 3 times daily. The 180mg is normally a once daily. The 12-hour version is 60mg every 12hrs. I guess you can consult with your doc and listen to what your body wants / can handle. I'd think start with the lower 12hr dose.
Thinking doctors ?? If only the U.S.would legalize thinking and real scientific medicine , so wonderful to hear !! Thank you both .
Please can we have info about the conference on 19 June?
A friend got a posterior vitreous detachment in one eye and a retinal detachment in the other within 5 months of Covid with conjunctivitis. Have seen this in others?