did you ignore 90% of this video? The vaccine is causing worse damage to people because it creates antibodies mimicking the spike protein... I understand that a cure for EBV would be ideal, but Im not going to be rushing in for an EBV vaccine for quite some time myself. EBV and LC are being cured through things like anti-viral + dry fasting therapy.
I have fibromyalgia and dormant EBV. After covid in fall of 2021, I experienced a wave of almost unbearable symptoms about three weeks after I recovered from Covid. I was beyond exhausted, my cold sore virus woke up and I had very bad cold sores (I hadn't had even one in years), my skin hurt, my body hurt, it felt like even my bones hurt. Even though I was not hospitalized with Covid, I considered going to the hospital at this point. Everything started smelling like garlic and onions. This has since improved but I still can't smell parts of the mint smells. I told my husband that I felt like I was being spiritually attacked. Like my whole body was being attacked. I felt then that every dormant virus in my body was awake and my fibromyalgia was flaring up like I had never had before. My head hurt horribly. I am sure my eastern barr woke up too. Between the fibromyalgia, eastern barr and long covid....I slept and slept and slept. My kidney function showed a 16 point drop in my next annual blood work in April of 2022. By altering my diet and losing close to 60 pounds I have reversed this damage. I was obese and pre-diabetic and had high cholesterol at the time I contracted covid. This is not the case anymore. But this video just confirmed my suspicions.
I haven't had Epstein-Barr (to my knowledge) but when I got Covid the 1st time in Jan 2021 all this happened to me, too. It seemed to travel through my body & hit every system one-by-one, everything I have had an issue with in the past seemed to reactivate. I had a strong case of mumps when I was 13 (even with being vaxxed for mumps) & it seemed to "wake up" again for a full 6 weeks, the regular time frame for mumps. I felt spiritually attacked, too, I had bad dreams for weeks until Covid ran its course. I had long-Covid, as well, and it finally went away after I got a long break from work & was able to sleep for a few weeks. Hope you're doing better now, going thru all that isn't fun!
A lot of people with Ehlers-Danlos were originally misdiagnosed with Fibromyalgia. Chronic or reactivated EBV seems to be more common in the Ehlers-Danlos community. Take a look at the 2017 Hypermobile EDS Diagnostic Checklist.
@@leslietascoff9784 thank you. I will look into that. I do not have full confidence that the medical field has fibromyalgia figured out much at all. My doc told me it isn't caused by inflammation also but I tell you, from experiencing the pain, that feels like inflammation related to me. Aleve seemed to help minimize the pain (likely contributed to kidney issues also). But I also noticed that anytime I was over weight I was in more pain. After losing all that weight my pain level went down 95 percent and my energy skyrocketed. So what I have been told about fibromyalgia from doctors just doesn't add up to me. Something is off.
@@AJ_SouthernGal Thank you 😊 I am doing much much better now. I can smell mint again also! I hope you are recovering well from Covid also. BTW, I don't know when I had Epstein Barr. I was chronically fatigued while in the military and being a new mom...twice. I suspect it happened somewhere in that time frame and I just passed the overwhelming fatigue off as being the usual overwhelming fatigue from that life style. The military is good at making you feel like you are a whimp if you need sleep so we push through it to very unhealthy levels. My doc told me after labs once that I had the antibodies for Epstein Barr. That was a shock to me.
My family has been so sick with this for the last three months. Three of us are so sick. Headaches, soar throats and nausea and it never goes away. The headaches are unbearable.
yes, but you didn't have to take it..may of us got abused for saying no....for our health and safety. Glad I didn't take the shot. I had severe covid and with how they neglected basic care to me (a nurse who treated thousands with this before it had name and did it well and fine!), I would trust them to care about me if things got worse from a shot? I was killed by their neglect , survived by God's grace but still dealing with EBV, mold, etc. Sadly, I didn't choose this :(
Doc, thank you. Look into DesBio homeopathic for this. I'm doing it. I'm a long time longhauler from initial infection, critical are patient who was never admitted since I refused the vent, and then they refused care to me. What a hot mess. Anyway, I did all the flccc protocols for longhaul since I was busy dying and surviving on my own in my house, complete with clots flying through a PFO I had to find later myself too, stroke and seizures, no help. Yes, there is ptsd and yes, I'm talking to a ptsd therapist (good and thankful). I also wanted to ask you if MTHFR plays a role ..I'm pos for the copies.
@@sherrainehiggs7380 that's good quick question was your appetite affected at all like loss of appetite or no appetite. Bloated. Digestion issues Etc. Also have you been on any meds or just diet change ? Thanks, im glad your better ..
May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
The second paper discussed stated about a 30% incidence for LC. Shouldn't we keep in mind that the study looked at papers prior to Feb 2022. "A systematic literature search was conducted using multiple electronic databases (MEDLINE and The Cochrane Library, Scopus, CINAHL, and medRxiv) until January 2022." I wonder what the incidence of people getting LC from a covid infection is since Jan 2022, considering the trend is generally less serious cases.
I couldn't remember(brain fog) where I learned about EBV reactivation by stress which is why I added a long post to your review of the Yale study preprint. My apologies; and thank you so much for this body of papers. I would like to add a clinical trial paper "Results of Open-Label Non-randomized comparative clinical trial: 'Bromhexine and Spironolactone for Coronavirus Infection Requiring Hospitalization(BISCUIT) a Russian study Kardiologiia (2020); 60(11): 4-15. Caught my eye not only because of spironolactone but I remember finding an Australian cough syrup with bromhexine in it during my first researches on the cellular entry attachment mechanism which included 2 steps, binding to ACE2 receptor and then a serine protease(like endogenous TMPRSS2) or furin protease facilitated second attachment to the outer cell membrane. I never understood why no one seemed to consider preventing COVID19 infections with repurposed drugs. In the Russian hospital study, even delayed treatment with Brom/Spirono was effective in lowering temperatures, decreasing viral load and shortening hospital stays. From 2016 comes a paper "Specific inhibition of HIV infection by the action of spironolactone in T cells". Spironolactone is a potassium-sparing drug used as a diuretic, it's also an aldosterone antagonist in the mineralcorticoid family and a mild androgen antagonist. In this report it "blocks viral Tat-dependent transcription, thereby inhibiting both HIV-1 and HIV-2 infection of permissive T cells." In Cardiovascular Research(2018)114, 65-76, Elinoff et al demonstrated an anti-inflammatory role for spironolactone delineating its ability to suppress both NFKB and AP-1 signalling, NFKB being a massively studied inflammatory player. Of note: "Spironolactone blocks Epstein Barr Virus production by inhibiting EBV SM protein function" Verma et al 2016 and in May, 2021 "When Off target effects are on target: the role of spironolactone in patients with COVID-19" a preprint from Wilcox at Georgetown who concludes that "physicians might consider using spironolactone initially twice daily in doses of 12.5 to 25mg for patients at high risk for SARS-COV-2 infection" to prevent infection; and "in higher doses of 100-200 mg daily in those infected with the virus." Having grown cell lines for drug discovery, I understand why inexpensive, "safe and effective" treatments are ignored, it's greed...and that makes me incredibly sad.
This video has changed my life, I have been saying this was the cause of my return of partial paralysis for 18 months ( I haved partial transverse myelitis in 2003 from EBV) - I was called a too "medically minded social worker" at a major institution and received "unfortunate care". If you go back to my chart when I was non-ambulatory, bladder and bowel dysfunction of a severe nature it was called "anxiety:. I have shown doctors this article 5-7 weeks ago and was told "everyone has EBV". Mine was from the Moderna vaccine, and in fact when I got covid and when on Paxlovid I felt it was the best I have had felt in months and shared it was diagnostic, and also still neglected even with BP 257/132 to 80/47 and abnormal CSF from LP, hypoxia with carbon monoxide with central sleep apnea - and then 6 months later totally different finding.
The Covid vaccine reactivated my EBV a few years ago and I’m still struggling with it, sometimes it’s terrible and sometimes it’s just feels like the flu.
I got EBV last April. I was so sick and my mouth and throat were so full of sores, that if it wasn’t for IV I would have starved to death. 104+ fever for weeks. Lost 40lbs. I never wished I was gone more than that month.
Um, not for all, Norten. I'm a nurse - never had a flu shot, not 'vaccinated' with anything. I got sevre covaids in march 2020 when the mask went on in our workplace which was full of mold, along with my HVAC at home. It's not "the jab" for many of us who got infected before the shot was even out.
I wasn’t vaccinated but caught Covid from someone who was. It was severe even though I was in perfect health. Now I’ve suffered for a year with EBV reactivation .
Thank you very much d for your kindness, your passion to help people and in Arendt searching for truth.🙏💖 I avoided allopathic doctors all my adult life b/c they were a product of the big P. We need doctors like you to work with alternative medicine approaches, and I know that this time is coming. It’s been 60 years that I have been waiting for that for humanity.
Do I understand correctly that ROS can play a role as a signal to affect apoptosis? If so, could it be that older people are susceptible to recurring herpesvirus infections because of diminished glutathione levels that are typical of older adults. Should we all be taking gly-nac supplements?
Exactly the same as my experience with M.E. I had glandular fever in 1999, fully recovered within two weeks, but somehow the EBV reactivated, possibly because of acute stress, and I developed M.E. which I still have 20 years later. I was vaccine injured in 2021. It feels like the EBV was reactivated, once again, my the vaccine.
@@myyoutubechannel3161 The same. Things that have helped over the past year or two were a steroid injection, pine needle tea and nicotine patches. But still very poorly. Thanks for asking.
@Michelle-72 steroid injection? For the ebv, I didn't know that was a thing for people suffering from it. The question I had was, do you think there is a connection between ebv/mono and COV-19 reactivation from COV-19? I'm just asking to better understand. I got covid 2 years ago and never really recovered. My digestion has been off for two years bloated belly, weight loss, my appetite sucks!! Hurts to eat. Tested positive for covid 2 month's straight at the time.
@@myyoutubechannel3161 No, sorry, I had the steroid injection for shoulder impingment caused by the vaccine, but it helped eventually including the M.E. I'm sorry you arw so poorly. I definitely think there is a link between EBV and covid/vaccine.
What about copper (and especially the copper/zinc /iron /mag combo) to help as does the vit C ? I have noticed a good impact by focusing on food with this combo . And it is amazing in results.
Can anyone here please tell me how to keep living and working and still enjoying life with long Covid and EBV. The fatigue is unbearable at times. Any natural options?
I had a reactivation long before Covid, about 6 years prior. Now I have had a bad case of Covid and was wondering if Paxlovid helps on both? Or is there studies on that??
Thank you for an important talk. At last - some helpful information on EBV. It is a really nasty virus I had EBV in 1989, very severe (my Dad, a GP, said he had never seen such bad liver function tests). But I recovered really quickly and got normal liver function tests in a month. However 11 years later I developed chronic fatigue and have had recurrences - extreme stress reactivated each time (eg death of parent, work, caring for a parent with Parkinsons). Also damaged my thyoid gland and then caused choroiditis in my right eye. nasty virus. Am doing really well now because I did a hair mineral analysis test and found that magnesium and potassium levels really low. Feel so much better on sorting that out. I also take NACA and glutathionine among other nutrients. Also helps to take nutrients to support mitochondrial health and gut health As I knew I had issues with that virus, I avoided the Covid jab - knew that I did not want a virus with adjuvents which would play around with my immune system managed to have Covid - delta and omicrom with just a hint of a symptom which wiped out with 3g vit C - and repeat if the symptom returns. As a result - had Covid but no illness - just a mild sore spot in the centre of my lung which cleared and then a sore throat, which also cleared. Only knew I had had Covid by tiaking blood test for anti bodies which was positive. I have been lucky in that I saw Doctors trained in Integrated Medicine ( Lucky to see Prof Lewith) - they understand EBV and chronic fatigue and use nutritional support. No point in seeing GP in the UK - they were happy to see me bedridden and just confirm that it was ME - one would have prescribed anti depressants - even though I was not depressed!!! Pissed off at my body being unable to sustain any physical activity - but not depressed. From my experience the big thing to take away - we are all different - EBV has been said elsewhere to block the uptake of certain nutrients (I think zinc, vit A and D) From personal experience I have known that zinc was an issue over the last 20 years - I have to take zinc or I get white spots on my nails). I really recommend a hair analyisis test - better than blood test as it shows how the body is handling the nutrients, not what is floating around in the blood stream. In addition - if you are low in magnesium - read levy's book on magnesium there are loads of different types of magensium - and the bioavailbility vareis - find what works best for you - and inlcude magnesium threonate as that corsses the blood brain barrier. And keep searching - as someone said to me - you won't get better until you have learned everyting you need to know. ALl the best on your healing journey - it has taken me 20 years - but I am doing the best and feel the energy levels are more reliable than ever before.,
Hello M J, your story sounds so familiar to me. Have EBV for many yrs. Don't know when I contracted it. My docs never tested for it until 2016 (!??), then my lightbulb went on and my thinking cap and so I'm much much more educated, thanks to Docs like Dr. Been and so many online physicians who truly care about ill people. I also got CV in Aug and now my energy is much more diminished with PEM plus other neuro symptoms. Yes, the stress incidents do definitely seem to trigger my fatigue and then I'm down for days. Am 71 yo now but in younger times I'd just have long 3 hour naps at end of work week. You reminded me on the zinc. Same here. My nails got almost completely white after the birth of my son. I'll check into the mag issue. Thanks for your post. Stay strong in the fight!
Yes, and I like you got quite tired of seeing the practitioners eyes glaze over and then prescribe an anti- depressant. I never took bcuz I was not depressed only frustrated with my body not cooperating with me to do necessary life chores. This illness forces you to cultivate patience! And also to be kind and understanding of yourself. To not be so proud as to continue to push thru. I'm still working on that one, hence my sleep deprived status. Needing sleep is not a sign of laziness!!
I got Mono in 2010 at age 40 and it morphed into ME/CFS… Since having covid once I fight EBV symptoms weekly. I am on disability. Being out for 3+ hours wipes me out for days. It is frustrating, and fighting all the heavy metals we are bathed and marinated in (which is part of what caused this I believe) i feel like my immune system system will never recover 😏
I agree re: the metals. I had severe covaids in 2020...no hospital help and I was a critical care patient. It was HELL on earth. Thanks to a nurse practitioner who checked this, I am over 600 IgG every time. I also had mold toxicity from work, the gym HVAC and my house HVAC! It activated lyme too. I"m still out on disability from 2020...ME/CFS. I REFUSE to believe I will continue this way. Being on disability is very hard on my mental health but I'm also working on other things that I didn't work on before, like lowering my tolerance to stress. It was too high and I was living a very hectic life, but I had such a joyful energetic life! This is so, so hard and lonely. I WILL recover, God willing. EBOO, HBOT, Sauna, clean foods, the right supplements, but....anyway though. I"m also doing DesBio homeopathics.....pretty good!
Couldn't watch last night. Watching this afternoon until rain clears. A reactivation question: If EBV and Lyme reactivation can occur, then it's possible that zoster varicella (shingles) could be triggered, right? A family member had that happen after Covid took up residence in his home.
anecodotally, I have heard of shingles occurring after jabs. A friend is currently ill with shingles 0 still believes in the jab and had the over 75 booster offered in the UK. There is no point discussing any of this with him - just gets angry! Just have to accept people have to learn the hard way, if at all!!! Hope they get well soon. All the best
I started having an inflamed toe, turning purple from damage. Got antibiotics twice, didn't work. Other toes started to swell and also my forefoot. From flaming hot to icey cold, not being able to stand on the foot anymore and the other foot started having symptoms too. Low grade fever and swollen glands. Went to a rheumy and they took blood. Turned out I had active EBV infection. And the foot is explained as arthritis, enthesitis, dactylitis. Did the ebv cause the arthritis (reactive) or the other way around, did the ebv somehow trigger a form of rheuma? Nobody seems to know. Taking prednisone, but still it flares and flares. Been 2,5 months now. Tuesday my blood will be checked for the ebv igm, to see if it lowers. The fever is gone, never had other symptoms besides that, feeding tired and having swillen glands. It's the inflammation in my feet that's killing me man!
These symptoms could be the damage from the spike protein that was injected into you. May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
@@sarahwalkerbeach6985 I had 2 doses back in 2021. Never any issue. I always take my supplements and eat healthy (not too many carbs and refined sugars and lots of anti inflammatory foods) Don't think there's much to do about a damaged immune system due to the vaccine (2 doses back in 2021) and 2 rounds of covid.
@@rememberallah5201 Your post says "nobody knows". But we do know that EBV can be triggered by a lowered immune system. The spike that was injected into you can compromise your immune system. The FLCCC has a protocol for detoxing from the spike protein. May God give you strength.
Don't give up. You sound like you have micro clotting from CV. Check out Dr. Resia Pretorius and Dr. Jordan Vaughn. Dr. Resia proved the microclots were in CV patients blood and Dr. Vaughn can treat. Also much good info on Gez Medlinger's You Tube channel. Best wishes for your recovery.
Good evening sir I have exposure,,, get lymphocytosis as also leicoocytosis, ebv igg positive, igm negative, tuberculosis goldferon positive, having symptoms i.e Foggy urine traces protein , oral candiadis, weight loss, having liver granuloma Please advice treatment
There is a possibility the vaccines have caused this. Not being a smart alec, just what I'm seeing with my own eyes. Post vaccine followed by infection.
Your symptoms could be the damage from the spike protein that was injected into you. May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
This is very interesting. I got the JJ vaccine 2021 and basically immediately got horrible fatigue that never truly went away. 6 months post vaccine, I caught COVID which retriggered the fatigue that had slightly improved. Never got any boosters. Fatigue is still debilitating, but have since been diagnosed with MS. Diagnosis process started w optic neuritis end of 2022. Diagnosed Jan of 2023 at 23 y/o. I don't think COVID or the vaccine gave me MS because I had symptoms back in 2016 (numbness in limb that lasted half a year) and had what I retrospectively realize was a milder optic neuritis in 2020. But the vaccine/COVID 100% triggered the current fatigue that I am struggling with. Likely triggered my current MS relapse. Not surprising as EBD is thought to contribute to MS. When I try to find any research about MS and COVID, all I can find is "people with MS can safely get the vaccine". I'm not convinced. Would love a video on the subject if you had any insight
That’s a terrible shame in one so young. Low Dose Naltrexone has been very effective for many with MS in stopping the progress especially in relapsing remitting MS. Look into it there’s plenty of information online to review and it is very cheap.
@@nonpareilstoryteller5920 I honestly feel very lucky. Could have gone on a lot longer w/o diagnosis. The vague fatigue left me undiagnosed until the more obvious optic neuritis which led to diagnosis. I'm blessed that it was identified instead of going undiagnosed for decades like for some. Otherwise minimal disability. I took a look and I'll keep it in mind. It's not a medication that has crossed my path in my research thus far. I'm on ocrevus rn which has high efficacy. I'm glad that there are now so many effective options for MS when 30 years ago there were literally zero.
This is such a huge thing, research needs to find cures for EBV/Long Covid. And release EBV vaccine sooner.
Are you suffering from EBV reactivation From COV-19? Any updates
did you ignore 90% of this video? The vaccine is causing worse damage to people because it creates antibodies mimicking the spike protein... I understand that a cure for EBV would be ideal, but Im not going to be rushing in for an EBV vaccine for quite some time myself. EBV and LC are being cured through things like anti-viral + dry fasting therapy.
There are theories that EBV is only reactivated because other viruses are as well. 90% of people have EBV but only 1-2% has problems
dry fasting is one of the best solutions@@maxjames00077
NO vacc1ne. They damaged us enough with the C jabs
Thank you... Kinesiologists are aware EBV being set off from covid and vax exposure too.
So COV-19 is reactivating ebv in people correct? Did this happen to you ?? Any updates?
I have fibromyalgia and dormant EBV. After covid in fall of 2021, I experienced a wave of almost unbearable symptoms about three weeks after I recovered from Covid. I was beyond exhausted, my cold sore virus woke up and I had very bad cold sores (I hadn't had even one in years), my skin hurt, my body hurt, it felt like even my bones hurt. Even though I was not hospitalized with Covid, I considered going to the hospital at this point. Everything started smelling like garlic and onions. This has since improved but I still can't smell parts of the mint smells. I told my husband that I felt like I was being spiritually attacked. Like my whole body was being attacked. I felt then that every dormant virus in my body was awake and my fibromyalgia was flaring up like I had never had before. My head hurt horribly. I am sure my eastern barr woke up too. Between the fibromyalgia, eastern barr and long covid....I slept and slept and slept. My kidney function showed a 16 point drop in my next annual blood work in April of 2022. By altering my diet and losing close to 60 pounds I have reversed this damage. I was obese and pre-diabetic and had high cholesterol at the time I contracted covid. This is not the case anymore. But this video just confirmed my suspicions.
Epstein barr, sorry auto correct is a pain.
I haven't had Epstein-Barr (to my knowledge) but when I got Covid the 1st time in Jan 2021 all this happened to me, too. It seemed to travel through my body & hit every system one-by-one, everything I have had an issue with in the past seemed to reactivate. I had a strong case of mumps when I was 13 (even with being vaxxed for mumps) & it seemed to "wake up" again for a full 6 weeks, the regular time frame for mumps. I felt spiritually attacked, too, I had bad dreams for weeks until Covid ran its course. I had long-Covid, as well, and it finally went away after I got a long break from work & was able to sleep for a few weeks. Hope you're doing better now, going thru all that isn't fun!
A lot of people with Ehlers-Danlos were originally misdiagnosed with Fibromyalgia. Chronic or reactivated EBV seems to be more common in the Ehlers-Danlos community. Take a look at the 2017 Hypermobile EDS Diagnostic Checklist.
@@leslietascoff9784 thank you. I will look into that. I do not have full confidence that the medical field has fibromyalgia figured out much at all. My doc told me it isn't caused by inflammation also but I tell you, from experiencing the pain, that feels like inflammation related to me. Aleve seemed to help minimize the pain (likely contributed to kidney issues also). But I also noticed that anytime I was over weight I was in more pain. After losing all that weight my pain level went down 95 percent and my energy skyrocketed. So what I have been told about fibromyalgia from doctors just doesn't add up to me. Something is off.
@@AJ_SouthernGal Thank you 😊 I am doing much much better now. I can smell mint again also! I hope you are recovering well from Covid also. BTW, I don't know when I had Epstein Barr. I was chronically fatigued while in the military and being a new mom...twice. I suspect it happened somewhere in that time frame and I just passed the overwhelming fatigue off as being the usual overwhelming fatigue from that life style. The military is good at making you feel like you are a whimp if you need sleep so we push through it to very unhealthy levels. My doc told me after labs once that I had the antibodies for Epstein Barr. That was a shock to me.
My family has been so sick with this for the last three months. Three of us are so sick. Headaches, soar throats and nausea and it never goes away. The headaches are unbearable.
Also jaw pain and teeth. It’s three generations. Please help us!!❤
It's called vaccine adverse reactions, you were fooled.
Consider medicinal cannabis concentrates for the pain.
@@mg4mg281 agree
Check for carbon monoxide in your home
S9 basically, my job who forced me to get the vaccination to keep my job basically injected me with EBV.
yes, but you didn't have to take it..may of us got abused for saying no....for our health and safety. Glad I didn't take the shot. I had severe covid and with how they neglected basic care to me (a nurse who treated thousands with this before it had name and did it well and fine!), I would trust them to care about me if things got worse from a shot? I was killed by their neglect , survived by God's grace but still dealing with EBV, mold, etc. Sadly, I didn't choose this :(
Yes! Dr. Been continue with the Lecture on EBV please
Yes Dr. Been I second that! Would love to learn more. Thank you. You are great!
Please share mgs of nac, vit c i awesome liposomal? How much, gluathione mgs?? I use nano gluathione but unsure if enough?
Doc, thank you. Look into DesBio homeopathic for this. I'm doing it. I'm a long time longhauler from initial infection, critical are patient who was never admitted since I refused the vent, and then they refused care to me. What a hot mess. Anyway, I did all the flccc protocols for longhaul since I was busy dying and surviving on my own in my house, complete with clots flying through a PFO I had to find later myself too, stroke and seizures, no help. Yes, there is ptsd and yes, I'm talking to a ptsd therapist (good and thankful). I also wanted to ask you if MTHFR plays a role ..I'm pos for the copies.
I’m busy dying in my house too!
Ive suffered from EBV reactivations on off for many many years. Had Covid in May '22. Got EBV more often since then. 😢
Stress has been definitely a factor, Mom, had Cancer, died in March '22 ,
@@sherrainehiggs7380 So sorry for your loss. Stress is such a big trigger!
@@sherrainehiggs7380hope your feeling somewhat better, what were your symptoms what have you been feeling with mono ?
Im doing better this year...thank goodness 😅
@@sherrainehiggs7380 that's good quick question was your appetite affected at all like loss of appetite or no appetite. Bloated. Digestion issues Etc. Also have you been on any meds or just diet change ? Thanks, im glad your better ..
Yes please Dr.Been I also would love to learn more from the extra EBV information. Thank you!
I have this with my vaccine injury too 😢
May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
You a not alone - Vax injured too. Reactivated EBV
Me too…in my nervous system. Have you found any help?
Me too! Severe exhaustion and weakness gets worse as the day goes on@DaylanTheAngrySauerkraut
Me tooooo! It's terrible!
I tested positive for EBV after Covid and my numbers keep going up instead of down.
In terms of EBV, I recommend Anthony William's books. These might help you further.
All the best!
@@semperveritas3 Thank you.
I have ebv igm for 4 months now, so still active. I feel so bad.
I’ve had ebv active since December 2020 and my numbers are very high
@@rememberallah5201how are you feeling now ? Any update?
Yes please, I’d like to see the more detailed videos.
Proton pump inhibitors actually made my EBV worse with severe Chronic Fatigue Syndrome symptoms. I felt like hell.
The second paper discussed stated about a 30% incidence for LC. Shouldn't we keep in mind that the study looked at papers prior to Feb 2022. "A systematic literature search was conducted using multiple electronic databases (MEDLINE and The Cochrane Library, Scopus, CINAHL, and medRxiv) until January 2022." I wonder what the incidence of people getting LC from a covid infection is since Jan 2022, considering the trend is generally less serious cases.
I wonder if !vermectin would be effective for treating EBV?
I've had EBV recently (2018) and no there's no drug treatement, only time off to rest and recover.
@@LeePatekar acyclovir has some anti-EBV action, doesn’t it?
I think it's possible
And can't hurt.
No try instead Homeopathic Gelsemium CMK and treat aggressively for one year.
@@calderhouse2403 is this also for ebv have had for years?
I couldn't remember(brain fog) where I learned about EBV reactivation by stress which is why I added a long post to your review of the Yale study preprint. My apologies; and thank you so much for this body of papers.
I would like to add a clinical trial paper "Results of Open-Label Non-randomized comparative clinical trial: 'Bromhexine and Spironolactone for Coronavirus Infection Requiring Hospitalization(BISCUIT) a Russian study Kardiologiia (2020); 60(11): 4-15. Caught my eye not only because of spironolactone but I remember finding an Australian cough syrup with bromhexine in it during my first researches on the cellular entry attachment mechanism which included 2 steps, binding to ACE2 receptor and then a serine protease(like endogenous TMPRSS2) or furin protease facilitated second attachment to the outer cell membrane. I never understood why no one seemed to consider preventing COVID19 infections with repurposed drugs. In the Russian hospital study, even delayed treatment with Brom/Spirono was effective in lowering temperatures, decreasing viral load and shortening hospital stays.
From 2016 comes a paper "Specific inhibition of HIV infection by the action of spironolactone in T cells". Spironolactone is a potassium-sparing drug used as a diuretic, it's also an aldosterone antagonist in the mineralcorticoid family and a mild androgen antagonist. In this report it "blocks viral Tat-dependent transcription, thereby inhibiting both HIV-1 and HIV-2 infection of permissive T cells."
In Cardiovascular Research(2018)114, 65-76, Elinoff et al demonstrated an anti-inflammatory role for spironolactone delineating its ability to suppress both NFKB and AP-1 signalling, NFKB being a massively studied inflammatory player.
Of note: "Spironolactone blocks Epstein Barr Virus production by inhibiting EBV SM protein function" Verma et al 2016
and in May, 2021
"When Off target effects are on target: the role of spironolactone in patients with COVID-19" a preprint from Wilcox at Georgetown who concludes that "physicians might consider using spironolactone initially twice daily in doses of 12.5 to 25mg for patients at high risk for SARS-COV-2 infection" to prevent infection; and "in higher doses of 100-200 mg daily in those infected with the virus."
Having grown cell lines for drug discovery, I understand why inexpensive, "safe and effective" treatments are ignored, it's greed...and that makes me incredibly sad.
This video has changed my life, I have been saying this was the cause of my return of partial paralysis for 18 months ( I haved partial transverse myelitis in 2003 from EBV) - I was called a too "medically minded social worker" at a major institution and received "unfortunate care". If you go back to my chart when I was non-ambulatory, bladder and bowel dysfunction of a severe nature it was called "anxiety:. I have shown doctors this article 5-7 weeks ago and was told "everyone has EBV". Mine was from the Moderna vaccine, and in fact when I got covid and when on Paxlovid I felt it was the best I have had felt in months and shared it was diagnostic, and also still neglected even with BP 257/132 to 80/47 and abnormal CSF from LP, hypoxia with carbon monoxide with central sleep apnea - and then 6 months later totally different finding.
That's wonderful to hear that you have such a donation! You deserve it.
The Covid vaccine reactivated my EBV a few years ago and I’m still struggling with it, sometimes it’s terrible and sometimes it’s just feels like the flu.
Me too. Any luck with treatments?
I got EBV last April. I was so sick and my mouth and throat were so full of sores, that if it wasn’t for IV I would have starved to death. 104+ fever for weeks. Lost 40lbs. I never wished I was gone more than that month.
Are you also insulin resistant?
@@aveccoeur3874 I am realising I had this. Could you tell me why you asked about insulin resistance because I do have that.
David any update? How are you now ?
Its the jab!!
it was for me - after i got the shots it basically destroyed my immunity :/
Um, not for all, Norten. I'm a nurse - never had a flu shot, not 'vaccinated' with anything. I got sevre covaids in march 2020 when the mask went on in our workplace which was full of mold, along with my HVAC at home. It's not "the jab" for many of us who got infected before the shot was even out.
I wasn’t vaccinated but caught Covid from someone who was. It was severe even though I was in perfect health. Now I’ve suffered for a year with EBV reactivation .
@@Emily-cl1yfwhat kind of symptoms you have?
Oh, WOW! Thanks for this one, Dr. Mobeen - makes so much sense!
Thank you very much d for your kindness, your passion to help people and in Arendt searching for truth.🙏💖 I avoided allopathic doctors all my adult life b/c they were a product of the big P. We need doctors like you to work with alternative medicine approaches, and I know that this time is coming. It’s been 60 years that I have been waiting for that for humanity.
Amen to that!
I agree. We need more Dr's like Dr. Syed.
Do I understand correctly that ROS can play a role as a signal to affect apoptosis? If so, could it be that older people are susceptible to recurring herpesvirus infections because of diminished glutathione levels that are typical of older adults. Should we all be taking gly-nac supplements?
how do we test for reactivation ? i know i had ebv in the past .
IGG test ( VCA or EBNA )
@@misovuletic of these 2, if one is positive or negative what is the interpretation ?
Exactly the same as my experience with M.E. I had glandular fever in 1999, fully recovered within two weeks, but somehow the EBV reactivated, possibly because of acute stress, and I developed M.E. which I still have 20 years later. I was vaccine injured in 2021. It feels like the EBV was reactivated, once again, my the vaccine.
Any update?? How are you feeling?
@@myyoutubechannel3161 The same. Things that have helped over the past year or two were a steroid injection, pine needle tea and nicotine patches. But still very poorly. Thanks for asking.
@Michelle-72 steroid injection? For the ebv, I didn't know that was a thing for people suffering from it. The question I had was, do you think there is a connection between ebv/mono and COV-19 reactivation from COV-19? I'm just asking to better understand. I got covid 2 years ago and never really recovered. My digestion has been off for two years bloated belly, weight loss, my appetite sucks!! Hurts to eat. Tested positive for covid 2 month's straight at the time.
@@myyoutubechannel3161 No, sorry, I had the steroid injection for shoulder impingment caused by the vaccine, but it helped eventually including the M.E. I'm sorry you arw so poorly. I definitely think there is a link between EBV and covid/vaccine.
During the different peaks of Covid Sweden experienced surges of shingles in children due to reactivation of varicella.
My sister-in-law contracted shingles after the first dose of the moderna vaxcine.
I got shingles after a mandated flu vacc1ne@jerryerickson9921
What about copper (and especially the copper/zinc /iron /mag combo) to help as does the vit C ? I have noticed a good impact by focusing on food with this combo . And it is amazing in results.
What food please
Yes I remember seeing a literature on copper
Wow wow! This is amazing! Thank you for this research and theraputics for help!
Hmmm think about it. Long covid might be ebv. Not long covid. Hmmmm
@Drbeen Medical Lectures are you saying to reduce Glutathione- or Glutathione is beneficial?
Yup, Jun, 2021; jab and booster; MS progression; Fall 2022 ever since, plus Optic Neuritis. ..😮
Can anyone here please tell me how to keep living and working and still enjoying life with long Covid and EBV. The fatigue is unbearable at times. Any natural options?
I had a reactivation long before Covid, about 6 years prior. Now I have had a bad case of Covid and was wondering if Paxlovid helps on both? Or is there studies on that??
What is the duration of spironolactin 25mg treatment?
What is reduced Glutathione?
I have all of the above and would like to know more about reducing spike protein and /ebv as I have had both since second vaccine 2 years ago
Me too
Thank you for an important talk. At last - some helpful information on EBV. It is a really nasty virus
I had EBV in 1989, very severe (my Dad, a GP, said he had never seen such bad liver function tests). But I recovered really quickly and got normal liver function tests in a month. However 11 years later I developed chronic fatigue and have had recurrences - extreme stress reactivated each time (eg death of parent, work, caring for a parent with Parkinsons). Also damaged my thyoid gland and then caused choroiditis in my right eye. nasty virus. Am doing really well now because I did a hair mineral analysis test and found that magnesium and potassium levels really low. Feel so much better on sorting that out. I also take NACA and glutathionine among other nutrients. Also helps to take nutrients to support mitochondrial health and gut health
As I knew I had issues with that virus, I avoided the Covid jab - knew that I did not want a virus with adjuvents which would play around with my immune system
managed to have Covid - delta and omicrom with just a hint of a symptom which wiped out with 3g vit C - and repeat if the symptom returns. As a result - had Covid but no illness - just a mild sore spot in the centre of my lung which cleared and then a sore throat, which also cleared. Only knew I had had Covid by tiaking blood test for anti bodies which was positive.
I have been lucky in that I saw Doctors trained in Integrated Medicine ( Lucky to see Prof Lewith) - they understand EBV and chronic fatigue and use nutritional support. No point in seeing GP in the UK - they were happy to see me bedridden and just confirm that it was ME - one would have prescribed anti depressants - even though I was not depressed!!! Pissed off at my body being unable to sustain any physical activity - but not depressed.
From my experience the big thing to take away - we are all different - EBV has been said elsewhere to block the uptake of certain nutrients (I think zinc, vit A and D) From personal experience I have known that zinc was an issue over the last 20 years - I have to take zinc or I get white spots on my nails).
I really recommend a hair analyisis test - better than blood test as it shows how the body is handling the nutrients, not what is floating around in the blood stream. In addition - if you are low in magnesium - read levy's book on magnesium there are loads of different types of magensium - and the bioavailbility vareis - find what works best for you - and inlcude magnesium threonate as that corsses the blood brain barrier.
And keep searching - as someone said to me - you won't get better until you have learned everyting you need to know.
ALl the best on your healing journey - it has taken me 20 years - but I am doing the best and feel the energy levels are more reliable than ever before.,
Sad, similar experiences.
🙏
@@aveccoeur3874 Thank you all the best to you and yours
Hello M J, your story sounds so familiar to me. Have EBV for many yrs. Don't know when I contracted it. My docs never tested for it until 2016 (!??), then my lightbulb went on and my thinking cap and so I'm much much more educated, thanks to Docs like Dr. Been and so many online physicians who truly care about ill people. I also got CV in Aug and now my energy is much more diminished with PEM plus other neuro symptoms. Yes, the stress incidents do definitely seem to trigger my fatigue and then I'm down for days. Am 71 yo now but in younger times I'd just have long 3 hour naps at end of work week. You reminded me on the zinc. Same here. My nails got almost completely white after the birth of my son. I'll check into the mag issue. Thanks for your post. Stay strong in the fight!
Yes, and I like you got quite tired of seeing the practitioners eyes glaze over and then prescribe an anti- depressant. I never took bcuz I was not depressed only frustrated with my body not cooperating with me to do necessary life chores. This illness forces you to cultivate patience! And also to be kind and understanding of yourself. To not be so proud as to continue to push thru. I'm still working on that one, hence my sleep deprived status. Needing sleep is not a sign of laziness!!
I got Mono in 2010 at age 40 and it morphed into ME/CFS… Since having covid once I fight EBV symptoms weekly. I am on disability. Being out for 3+ hours wipes me out for days. It is frustrating, and fighting all the heavy metals we are bathed and marinated in (which is part of what caused this I believe) i feel like my immune system system will never recover 😏
I agree re: the metals. I had severe covaids in 2020...no hospital help and I was a critical care patient. It was HELL on earth. Thanks to a nurse practitioner who checked this, I am over 600 IgG every time. I also had mold toxicity from work, the gym HVAC and my house HVAC! It activated lyme too. I"m still out on disability from 2020...ME/CFS. I REFUSE to believe I will continue this way. Being on disability is very hard on my mental health but I'm also working on other things that I didn't work on before, like lowering my tolerance to stress. It was too high and I was living a very hectic life, but I had such a joyful energetic life! This is so, so hard and lonely. I WILL recover, God willing. EBOO, HBOT, Sauna, clean foods, the right supplements, but....anyway though. I"m also doing DesBio homeopathics.....pretty good!
Has anyone tried the antivirals? TDF AND TAF that Dr is reading off the study?
Thank you,you are appreciated...God✝️Bless
I'm unvaccinated, the woman I was sleeping with got vaccinated and I got Mononucleosis the following week I did not have COVID.
Does consuming almond trigger EBV reactivation in a highly stressed body?
Almonds contain arginine which may cause cold sores due to same pathway competition for lysine. (Lysine helps prevent cold sores)
Couldn't watch last night. Watching this afternoon until rain clears. A reactivation question: If EBV and Lyme reactivation can occur, then it's possible that zoster varicella (shingles) could be triggered, right? A family member had that happen after Covid took up residence in his home.
anecodotally, I have heard of shingles occurring after jabs. A friend is currently ill with shingles 0 still believes in the jab and had the over 75 booster offered in the UK. There is no point discussing any of this with him - just gets angry! Just have to accept people have to learn the hard way, if at all!!! Hope they get well soon. All the best
I started having an inflamed toe, turning purple from damage. Got antibiotics twice, didn't work. Other toes started to swell and also my forefoot. From flaming hot to icey cold, not being able to stand on the foot anymore and the other foot started having symptoms too. Low grade fever and swollen glands. Went to a rheumy and they took blood. Turned out I had active EBV infection. And the foot is explained as arthritis, enthesitis, dactylitis. Did the ebv cause the arthritis (reactive) or the other way around, did the ebv somehow trigger a form of rheuma? Nobody seems to know. Taking prednisone, but still it flares and flares. Been 2,5 months now. Tuesday my blood will be checked for the ebv igm, to see if it lowers. The fever is gone, never had other symptoms besides that, feeding tired and having swillen glands. It's the inflammation in my feet that's killing me man!
These symptoms could be the damage from the spike protein that was injected into you. May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
@@sarahwalkerbeach6985 I had 2 doses back in 2021. Never any issue. I always take my supplements and eat healthy (not too many carbs and refined sugars and lots of anti inflammatory foods) Don't think there's much to do about a damaged immune system due to the vaccine (2 doses back in 2021) and 2 rounds of covid.
@@rememberallah5201 Your post says "nobody knows". But we do know that EBV can be triggered by a lowered immune system. The spike that was injected into you can compromise your immune system. The FLCCC has a protocol for detoxing from the spike protein. May God give you strength.
Don't give up. You sound like you have micro clotting from CV. Check out Dr. Resia Pretorius and Dr. Jordan Vaughn. Dr. Resia proved the microclots were in CV patients blood and Dr. Vaughn can treat. Also much good info on Gez Medlinger's You Tube channel. Best wishes for your recovery.
Has it gone dormant? I suspect not. EBV is secondary to the thing compromising your immune system.
Will this show positive in a blood test? The reactivación
Yes
Would it be the viral capsid antigen igm? Sorry I’m a bit illiterate when it comes to this stuff lol
Yes as Igm in blood test as doctor said in other lecture.
Thank you so much for this information.
Good evening sir
I have exposure,,, get lymphocytosis as also leicoocytosis, ebv igg positive, igm negative, tuberculosis goldferon positive, having symptoms i.e
Foggy urine traces protein , oral candiadis, weight loss, having liver granuloma
Please advice treatment
No issues after my vaccines. Got covid for first time Valentines day. My life has been miserable ever since. Can't breath can't focus. Can't live.
There is a possibility the vaccines have caused this.
Not being a smart alec, just what I'm seeing with my own eyes. Post vaccine followed by infection.
Don’t give up , you have people who love you and people you love 💕 will pray for you
Your symptoms could be the damage from the spike protein that was injected into you. May I suggest you take a look at the FLCCC protocol online, to find ways to boost natural immunity. It includes, vit c, vit d, zinc, quercetin, magnesium, nattokinase, and N-acetylcysteine. And intermittent fasting. I wish you well.
Methlene. blue, nitric oxide inhalers..
Quantum NAC and nattokinaise if not histamine intolerant
Can radiation from a stress test trigger EBV ?
How to overcome Chronic active ebv (CAEBV) would be blessing!
How did you get diagnosed with chronic active
Antiviral dosage?
Could you explain about immunoblot IgM for EBV versus the standard one?
No, IGG is very important. IgM is acute infection, IGG is chronic
AMAZING NEWS! 🥳🎉
Candida. Auris. Shigulla. Nori. Çovid. Adenovirus. Conora. All. Still. Out there. Some. Old. Still. Dieing. Of. Çovid. And. Combanations
Any updates? How are you feeling from this ...
I sleep all the time..😢
So valuable
very helpful
This is very interesting. I got the JJ vaccine 2021 and basically immediately got horrible fatigue that never truly went away. 6 months post vaccine, I caught COVID which retriggered the fatigue that had slightly improved. Never got any boosters. Fatigue is still debilitating, but have since been diagnosed with MS. Diagnosis process started w optic neuritis end of 2022. Diagnosed Jan of 2023 at 23 y/o. I don't think COVID or the vaccine gave me MS because I had symptoms back in 2016 (numbness in limb that lasted half a year) and had what I retrospectively realize was a milder optic neuritis in 2020. But the vaccine/COVID 100% triggered the current fatigue that I am struggling with. Likely triggered my current MS relapse. Not surprising as EBD is thought to contribute to MS.
When I try to find any research about MS and COVID, all I can find is "people with MS can safely get the vaccine". I'm not convinced. Would love a video on the subject if you had any insight
That’s a terrible shame in one so young. Low Dose Naltrexone has been very effective for many with MS in stopping the progress especially in relapsing remitting MS. Look into it there’s plenty of information online to review and it is very cheap.
@@nonpareilstoryteller5920 I honestly feel very lucky. Could have gone on a lot longer w/o diagnosis. The vague fatigue left me undiagnosed until the more obvious optic neuritis which led to diagnosis. I'm blessed that it was identified instead of going undiagnosed for decades like for some. Otherwise minimal disability. I took a look and I'll keep it in mind. It's not a medication that has crossed my path in my research thus far. I'm on ocrevus rn which has high efficacy. I'm glad that there are now so many effective options for MS when 30 years ago there were literally zero.
@@nonpareilstoryteller5920 Yes look at LDN use for MS in Scandinavia!
My friend had similar issues. After third jab, bedriden....Diagnosed with MS....
Please do lecture !
Thanks Doc
Vitamin D and Zn, Diet, and virus will go away 🤗
Did you go on keto?
@@stellaancimer8505yes
@@stellaancimer8505 yes
@@AdventureWithPrinces did you also have ebv?
@@stellaancimer8505 yes, and ebv will always be there...
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