The Latest Research into Abnormal Clotting in Long Covid | With Dr Jordan Vaughn
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- Опубликовано: 1 июн 2024
- In part 2 of my interview with Dr Jordan Vaughn we talk about the latest research on abnormal clotting in Long Covid, whether viral persistence may be driving the problem - and if so, what do we do about it? We also talk a little about Long Covid-like symptoms after vaccination.
Part 1 can be viewed here:
• The Genetic Link to Ab...
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Before I caught Covid in March 2020 I was a filmmaker. I’m not well enough to go back to work yet (shoot days are brutal), but I’ve decided to indulge my passion by breaking down the hottest recent films and TV shows (from an insider’s perspective with 20 years in the industry) to describe exactly how they work. Sound interesting? Then subscribe to my second channel! ( @thescriptflip )
Here are some links:
5 Reasons Why Top Gun Maverick Crushes the Original | Film Director Breaks it Down:
• 5 Reasons Why Top Gun ...
Why Succession Shouldn't Work at All, But is Somehow the Best Show on TV:
• Succession Shouldn't W...
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The Long Covid Handbook (Feb 2023) by Gez Medinger & Professor Danny Altmann (and published by Penguin Books) is now available in paperback, ebook and audiobook. A singular resource that brings together everything patients, clinicians and academics have learnt about the condition to date, as well as lessons from sufferers and researchers of ME/CFS and other chronic conditions. It offers world leading expert advice on understanding, managing and treating Long Covid. It is available from the following links.
US: a.co/d/0gvkJCU
UK: amzn.eu/d/9KjurGb 
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If most of these Long Covid people had just had access to EARLY treatment with repurposed drugs, they would not have gotten Long Covid. Kick down the viral load from DAY ONE and you’re ahead of the game. For me, taking HCQ and IVM with the FLCCC protocol, made my Covid illness a 3 day mild event and I’m an older woman. It’s critically important to treat this disease on DAY ONE of symptoms.
I wish other medical practitioners were putting in their spare time to read up the studies on Covid and LC 😔
Unfortunately, medicine is a political endeavor, so no doctors will come out unless they have political backing. Doctors who have come out with this kind of information have all been stripped of their license by the pharmaceutically backed drug companies and their cronies in gov't and media. The only doctors I have seen come out are the ones who were either old enough not to care about their careers, or the ones who did lose their licenses so had nothing to lose by spreading the truth. Too many of the best doctors in the country lost their license for asking questions, and now those bright doctors around the world are banding together and pushing back, so that less people will die from COVID in the long run. Big pharma and healthcare is a broken system at this point, choosing to suppress truth seeking doctors, which is tantamount to negligence at best, homicide at worst, when you are covering up life saving medicines in favor of the vax.
Thank you Gaz. There aren’t enough words to adequately thank you for all you are doing for our Long Covid community
I’m a patient of Dr. Vaughn. I’ve just started treatment for mast cell. Doctor Vaughn is the ONLY doctor that’s given me hope…best part is it’s not just hope…he’s saving people and giving them their lives back. I can’t wait to see my progress. I’ve learned So much about my allergies and have changed my diet to the anti inflammatory diet.
update pls
would love to hear how its going - I am struggling with MCAS and long covid for 8 months. some days I think Im going to die.
There are a lot of doctors doing this work. They are called functional medicine doctors, and if big pharma would just get out of the way and let doctors determine what is right for their patients, we would not be in the mess we are in.
This is my doctor. Him and his staff are the ONLY doctors in our country doing anything for patients. Our government has abandoned us. Thank you dr Vaughn and everyone at lakeshore!
I’m a patient of his too! They’re so amazing!
I’m all signed up and waiting for my test to arrive and the hopefully will get into seeing him by the end of January. I have been suffering and seen 7 or 8 doctors and therapists.
My first visit with him was Jan 25th. I was put on 5 meds and they took 22 tubes of blood. I go Thursday to get my results. I'm anxious to know how did yall blood work come back and how are you now?
I love the shower pipes/plumber analogy. That's exactly how it feels when the doctor does a load of unrelated test then tells me it's all fine.
I’m convinced this is a major factor. Covid in April 2020. Slow steady recovery until visiting Andrew Greenland in Aug 21, for Redlight/Supplements/diet etc therapy that really help over the following twelve months. Six weeks of serapeptise/Nattokinase at the end of 2022 really seemed to clean up whatever problematic thing was inside me and have made a dramatic almost full recovery since touch wood.
There is a randomized control trial of an anti-coagulant beginning in Canada led by Dr. Angela Cheung--it has approval already and last I heard already has patients that have started to receive the treatment.
We believe in you, Dr. Vaughn. So thankful for you. Keep going!!!
It’s the dizziness with activity that presents itself as vestibular migraine that’s the worst , lack of blood flow / oxygen deprivation makes sense for sure and I’m a professional plumber so clogged pipes makes even more sense . Going on 3 years of this lovely issue
I pray this helps me. It's a crime what they did to us. You are amazing man.
Here's hoping this dedicated man gets the funding pretty soon for his RCT and paper gets published with good peer reviews, and that this then rapidly translates into treatment from primary care givers . Thank you for putting it out there Gez( so eloquently ) for all of us to benefit from .😊
It’s looking positive on the research front atm!
@@RUNDMC1 Great news ! 😊👍
The who will step in and stop him on the orders of the elitist wef sadly..what a great dr
😮
Looking forward to hearing more research results in regards to long covid induced by the vaccine.
Diagnosed by cardiology in July 2021, I'm a previously fit, healthy, healthcare worker suffering with vaccine induced long covid for 28mths now. In addition to this and my myocarditis diagnosis, I've have recently been diagnosed with mylagic encephalomyelitis. Although I do suffer with neuropathies as mentioned I'd say my main symptoms are still cardiac issues, cognitive dysfunction, autonomic issues, PEM and myalgia, so mostly housebound still. Thank you so much Gez and The #teamclots for updating us with this research and keeping the hope alive
2 years, 3 months. Thank you Dr. Jordan for your passion and persistence.
I also suffer from malaise post effort from a tick bite. It's devastating. My body is a prison and I have to be very creative to not die from this evil mess. I was very active, rollerblade, ski, natation, dancing and so on. Now, hamac and books.
Me too! Had Lyme and Bartonella. Treated with antibiotics. Then got Covid. Now I feel like I have CFS. Some days are okay and some days I struggle to walk and feed myself.
That's the plan..YOU ALL DIE!!!
I also have lyme disease plus longhauler hell on earth
I recently went through having clots in both lungs and right leg which the doctors tell me was Unprovoked. This is overwhelming interesting to me as it may be the answer to my hospitalizing.
Yes, I am a marathon runner as well and haven't been able to run for a year now without laying around for days gasping for breath afterwards. It's horrible.
LifeWithKyle offers some great specific information on how he used Meditation to have a breakthrough on Recovery when he experienced Post Exertion Malaise. His main idea is that the Fear of onset Symptoms causes the Body to go into Fight or Flight mode, exacerbating the Symptoms. Instead, he discusses how he reframed PEM to be more Accepting of what was taking place and examining how he felt about it. In a sense, giving himself PERMISSION to be sick. Eliminating his Fear of the Symptoms calmed his Nervous System and helped to Prevent Symptoms.
JUST ROB and Raelan Agle had similar Attitude Adjustments that helped them recover from Long COVIDand CFS respectively.
The Mind is a very powerful thing regarding its effect on the Body. I believe Long COVID, Chronic Fatigue Syndrome/ME, Fibromyalgia, Post Lyme Disease, POTS, and MCAS are chronic dysfunctions of the Immune System that are the end stage results of Chronic Stress.
In addition to becoming a Student of how to reduce Chronic Stress through Improved Sleep Habits, BREATHWORK (Andrew Huberman on the Physiological Sigh), and Meditation, Recovery also requires becoming a Student on Pacing, to give the Body time to properly recover before the next Training Session, as well as a Student of Proper Nutrition, FASTING, and Supplementation to reduce inflammation, properly supply the Body with Essential Nutrients to prevent or correct deficiencies, and Optimize the Immune System.
same here, but then suddenly i felt like i could run again almost over night , i was doing small beach jogs/walks "checking in" into my body for months then suddenly i could get a proper breath like i remember from pre covid. i would have paid a million dollars to get that months ago!!!
Now i can breath normally, run and not gasp for breath on a jog and i have lost my fear of a re lapse after breaking out in a sweat.
but its taken me 3 years to get this far :(
@@marky5493 long covid is so strange, I've heard that story multiple times where people just randomly feel normal after years of long covid symptoms
@@xGlobs yeah me too, I think it's more to do with timing than some magic supplement hidden under a rock in deepest darkest, snow capped mountain somewhere.
I do belive a full recovery is possible for majority of people out there if they stay on the parth.
The other thing is you'll never get back to your TRUE pre covid level ever as you've aged a couple of years in the process so its abit of an illusion to strive for ha ha ha
Your vo2max, etc drops off over the years which just sucks man.
Bring on the old 20 year old in me!!
@@marky5493 thank you for your comment, it gives us all hope. 🙏🏻🙏🏻🙏🏻
Have to add something here regarding athletes appearing to be more affected. I am not the athlete now at 70, I was until 50ish, but not to the iron man degree. I have long covid, and been referred to this states Long Covid clinic. Can’t get in, two doctors working one afternoon a week. That schedule is the problem and there doesn’t appear to be the interest Dr. Vaughn has, so pretty helpless here in this state, Colorado. This channel and the information has helped me inch forward and finally have hope, utilizing the information from Gez and his guests. Dr. Vaughn, by far, is tackling the far end of LC and not still stuck at the beginning of Covid, etc. There is a strong focus on recent Ironman type athletes and I am wondering if they get more attention because their lifestyles, vs people like me, older and we get put aside just for that reason. Not accusing here, but it’s a thought worth consideration and probably plenty of others my age, who also have LC but our doc’s don’t specialize in it and refer out. If this clinics are not actually up to speed, then we are on our own. I don’t know what I would have done without this channel and Gez and now Dr. Vaughn. I am improving after one month of switching from 1000 units Vit-E daily, which was like a pain reliever pre-Covid, to Tocotrienols @300 mg daily, along with Nattokinase/Serrapeptase @ 3000FU a day. A real difference in endurance, improving mental clarity, improving energy, and pacing with better sleep. Just want to share this with those who don’t fit the triathlete type, but still suffer w/LC and older. Thank you Gez and Dr. Vaughn for offering information and options to try. Doubt I am the only one and hope others begin to recover! Love Dr. Vaughn’s approach to cleaning up the mess and learning what got us here after getting some solutions to recovery! ❤ to all sufferers.
I'm an old guy too but was very active nonetheless. Time is of the essence to get this solved.
@@kapaul1584 Agree, good luck to you.
Yes im taking natto 2x per day and just got my 2nd bottle of tocotrienols..feeling better already but im also taking a ton of other supps, following flccc protocol and some herbs that were shown to bind to and expell the spike protein. Not sure when to decrease or stop some of this cuz i dont know if its all necessary anymore...not sure when to quit...
@@PureExistence1 Well it sounds like good progress. I trust you will know when and then if needed, can go back on, one at a time to figure it out. Happy for you.
Thanks for all your hard work, Gez! Just ordered your book and am looking forward to reading through your findings. Keep fighting! My wife is at almost 3 years of long covid. She used to run every day before covid but has been gradually getting worse over those years to now being bed bound since January due to leaving the house for blood work. We are praying daily for a breakthrough for all who are suffering.
I’m so sorry to hear about your wife. I hope there are some nuggets in the book that help you make a difference to her quality of life and recovery.
The idiot pulmonologist who didn't believe in long covid, just dismissed my obscenely high D-Dimer rate as due to obesity. Pre -covid levels, at the same weight, were normal. Then my cardiologist dismissed them as well. Sooooo frustrating and outright scary.
Sadly, it is no secret why they pigeon-holed you with such mundane explanations: they know they can't help but don't want to say so. The big problem with the way you were handled is that you are expected to just stay away from recovery because they can't be the one to lead you there. You could do them a big favor by being hit by a meteor... but somehow that does not sound like medicine either.
My d diner was 4885, my doctor got me straight to AE for 22 hours every test under the sun, but no answers they called it dirty blood, been nearly a year now with long covid, not vaccinated and it’s getting worse, now taking NAC
@@flagmichael At least I fought back verbally. The pulmonologist mocked videos I quoted about long covid, by saying I shouldn't listen to YT. I was able to advise him the names of the Yale educated physicians and show him that the video was from CDC - not some yahoo in their mother's basement. Then I challenged him as to where he got HIS information. Needless to say, we're not seeing each other anymore 😄 He told me I needed to get a referral from my primary doc to see a shrink about my anxiety. I was due to see the primary, who laughed, said I had long covid. He said that the pulmonologist's suggestion I join a gym likely would have killed me. A rare moment of validation from the medical field.
Yup..ive had similar reactions..my doctor keeps asking me if Im depressed!!!. Oy!
@@samanthapurcell3125nattokinese and serrapeptase. Both have fibrinolytic properties. Aspirin when things get bad.
Also, get on an anti-inflammatory diet (no gluten, sugars, processed foods, vegetable oils, dairy, high FODMAP foods), try fasting (intermittent and prolonged). Controlling stress is also a huge part of it. Stress reduction, meditation, slight exercise, spend time in nature...
My treatment so far is only half way successful. It costs me a fortune in supplements every month but if I don't take them, I can't get by. The clotting issue is definitely only half of the story.
I agree. I had symptoms after my AZ jab that lasted for almost a half year, after which they went away by themselves. Now it’s been 16 months after I contracted the virus that I’ve had my current symptoms for and they go up and down and up and down: do there is something that’s driving this. I think it’s viral persistence or autoantibodies.
Shots ruined our immune system and only god knows what else . Forever. I am injured from 20 months, from 2nd dose of pfizer... Was really fit and healthy... Some days are better other worse, but never good. They ve made it by purpose...we ruined our life signing for it.
Are you taking any antifibrinolytics like natto etc?
Try anti histamine diet and see if it helps you even 5 percent . Anti histamines help too. Quercetin helps me
@@shilk4301 I'm already on an anti histamine diet and it does help a lot. I'm just worried about the long term effects of staying on this diet indefinitely as it is so very restrictive. I was using Quercetin for a long time but it stopped working for some reason and then started to have a detrimental effect. Now I am using Curcumin C3 and it is making a significant difference.
Truly believe what he is speaking to is what I am dealing with post covid infection. Curious about connection to Connective Tissue Vascular pre-existing underlies susceptibility.
That connection to Mast Cell Activation and connective tissue and vascular inflammation. Maybe pairing up with mast cell and connective tissue experts for trials and research.
Blurred vision, inflamed veins, neurological to the point of presenting as mild dementia, environmental exposures inflaming all the blood vessels causing pain and dysautonomia with sweats and blood pressure not regulating.
I had pre-existing mass cell activation got Covid and everything just went off the rails. Leveled up man.
The mast cell issue makes access to care so challenging when just going in for diagnostics and treatment sets you back to critical state.
Just looking at the bulging veins at this point makes me feel like bride of Frankenstein. 😢
It seems the skin just keeps getting more translucent and the veins more bumpy lumpy larger. Can’t retain any weight despite eating therefore it’s more like chicken woman bride of Frankenstein. Feeling like I look so ugly and unhealthy on top of it all just kinda sucks .
Hi, I completely agree. I have a connective tissue disorder as well, and am also wondering about the connection.
I am a patient of Dr. Vaughn, just getting started, hoping our blood vessels can still heal even if the deck is stacked against us.
Ehlers Danlos Syndrome?
It’s interesting to read your comments on connective tissue issues; I accompanied a friend with EDS to see Dr. Vaughn today and he explained how long Covid has exacerbated her condition. He has a particular interest in this and it may be worth it to you to call Medhelp and make an appt with him for treatment of long Covid. He is doing telehealth.
The "something there" with Paxlovid is the same as what's "there" with Ivermectin. (Both meds have same mechanism of action). It acts like an immune modulator\anti-inflammatory while taking it... Unfortunately symptoms often return after discontinuing use... However Paxlovid\Ivermectin does seem to resolve or lessen some ongoing symptomology and can help with nerve repair in neurological cases of Long Covid.
The problem still persist; GPs dont want to or dont have access to ivermectin.
Heck no that paxlovid is not good! I read it causes recurrence of covid. Ivermectin is good. Please don't compare!
@@stephangauthier911 You can get it from abroad
He is my doctor for Long Covid and he is great! I am on TT right now, just passed month 3!
How are you
how r u doing now
How is it going? I’ve also started TT, it’s tough…
@@o.udolph8086 how r u doing o.u? Why is it tough? Any improvement? Who r u doing it with?
@@phantomtr1 too early to tell, I can keep you posted if you want. The apixaban is quite tough on the body. Are you planning to do TT yourself?
I showed my dr your video and now she is treating me with 3 different things you mentioned. I was walking funny now I’m not. My heart is starting to feel better.
Thank you for doing this. I have had Covid 3 times and have breathing issues ever since and with all the test my Doctor did blood and ex rays he say's nothing is wrong but with everything Dr, Vaughn had said it's all clear now. Thank you for sharing this and thank you Dr, Vaughn and a big thank you to Sharyl Attkisson of Full Measure for doing the interview with Dr, Vaughn.
Excellent discussion. Good to know people like this are out there still searching for answers.
We are a community of understanding and support now.
Brilliant video. Thank you both for keeping me hopeful
Thank you Gez for continuing hard work
I love this approach. This is about investigation; looking into what is actually happening rather than relying on theory of how we got here. I think many people in a position of finding "what the Sam Hill is going on" continue to look for the best-lighted path even though that is where everybody else goes, and they never found the answer. To those who do not take the risk of failure comes the risk of more likely failure. The task is to solve a deep mystery, not to try to make the solution fit what has already been tried.
Following COVID, with long-COVID, I've always felt GREAT, as if I'd never had long-COVID, for ~ a week following covid vaccinations!
I've had long covid for 2 and 1/2 years, and I'm out of airspeed, altitude, and ideas. I'm getting progressively more ill and unable to think clearly, and I lack the energy to seek out more doctors. I don't have the strength to answer my phone and talk or respond to messages, emails, or texts. All this pain is too much for a human being to endure. Went to a long covid clinic, and they said I have one of the worst cases he's treated. Blood work shows abnormal clotting, but I'm too ill to return to doctor's appointments. My children are estranged and care nothing about me. I'm not going to survive long covid and not afraid to die, just not in so much pain and recently having lost my mind. In addition I'm so depressed that I can't stand it. This state of my physiology without the ability to think clearly compels me to ask you what should I do? I'm a retired lawyer, former prosecutor, judge followed by years of private practice. My children want me to die and not contact them, my wife wants me to die. Are there not physicians to help us pass with some measure of dignity? Bobby
If you lived in Canada or Washington state.
thanks for sharing your experience, bob. really. i'm sure i'm not alone in saying i'm right there with you (minus the family stuff). i keep coming back to these videos a few times a week hoping i'll find the ones that apply to me and give me some clear steps to take. This is purely anecdotal, but i recently got my hands on an injectable blood thinner (heparin?), 2 syringes, and for 2 days i was able to taste food again for the first time in 3 years. I consider it a minor victory but it at least gave me some hope and helps me continue my pursuit of any possible treatment. good luck to you. gene
Thanks Gez.
Thanks once again Gez for taking on these topics and keeping this illness before the public. Seems like many just have shuffled it under the carpet so to speak. I was curious as to whether you or your colleague have tried the triple therapy? If not how about the Natto/Serapetase combo? How would you rate the positive or negative effects these may have had? Thank you
I’m the first to comment… finally after years of seeking
In reference MRIs and small chronic ischemias, how would I get neuros and Drs onboard with that kind of treatment when it IS overlooked due to being younger or it labeled as "normal"?
I was one of the original infected with Co19 and still have major LongC. Another question is because of the effects to vascular and coagulation, does LC weaken arteries overtime? I had a VAD in January 2023 after a chiro visit and instincts are telling me LC was also to blame. I had an MRI due to the VAD and feel gaslighted when i bring up the small chronic ischemia in my brain.. Help
I am 72 years old and made it through covid without masks and social distancing because I never believed it and simply trusted my ammine system. In August of 22 me and my wife got covid (I tested the both of us) but very mild cases in my view. We recently moved to SC in Feb of 2021 and I was having a great time both of us very active building things and enjoying our retirement. After my covid illness the only way I can describe it is I feel everyday and getting worse, like I weigh a thousand (1000) pounds. I have had some good days but always exhausted and quite irritable and am fighting it as hard as I can. I have been to doctors and when I tell them my problem they tell me it was from the covid but have no diagnosis or cure. Can you help direct me to someone near Conway SC That could help me like you do for your patients. I'm so glad I found you on you tube and are very thankful and blessed to find you. Thank you for everything you do.
dr Jordan vaughn treats people out of state as well. just look on his website, medhelp, to sign up for out of state treatment
Thank you for your work!
It’s a pleasure :)
I refused the shot was healthy until I went to Austria/Germany for 3 weeks in July 2023. 4 days after arriving in Austria I got sick. I didn't have all of my COVID meds such as ivermectin, nebulizer, vit D, C, quercitin and the rest. I was never bedridden so I didn't think it was COVID bit here I am 6 weeks later with a persistent cough. My doc said it is bronchitis but it's not. I have started Nattokinase and other supple,ents but I want to go to Alabama to see Dr. Vaughn because the docs in my area are daft.
Thank you! Ive been getting odd internal bruises. This makes sense. Id be amenable to doing a trial..where do I sign up? Tx.
Thank you, Gez, for your videos!
The only thing I wish to point out is that PEM/PESE is part of the symptomatology of more than 40% of LongCovid patients. This means that for us advice like "go out of the house to take sun" or going towards some normality or any activity to boost immunity is not possible, not without serious relapses that can leave us bedridden. Many of us have rashes from sun even with sunscreen, sunlight can trigger sensorial sensitivities, we cannot regulate body temperature, and even dressing up or eating leaves us in extreme pain.
Also, as someone with autoimmunity due to Covid-19, it works better when my immune system is not boosted.
I would like to get back to some normality, but other than Stop. Rest. Pace, nothing else works. Looking forward to seeing research narrowing on mechanisms, biomarkers and treatment.
Unfortunately the problem with any advice is that the severity of the condition is on a spectrum, so what is good advice for someone on one end is terrible for someone at the other end - makes it very hard saying anything generally useful!
great video and great questions. thank you. look forward to the follow up. After my 2nd infection, I exercised 3 times in 2 months, then saw the widespread advice to let your body rest extra long. So I waited 1 more month and at the end of 3 months started to ramp up exercise. I was doing well for about a month then I started to come down (5 months after 2nd infection) with frequent malaise and flu-like symptoms and abdominal pain/gastrointenstinal issues. I wonder if the exercise brought these on or if they were going to happen anyway. Sadly, I've had to stop exercising
Stopping exercising very important!!
I had covid back in 2021 and it lasted very long. Then after going to the ER many times they said i have long covid. Racing heart , fatigue, nausea, weak muscles, etc.... after abiut 7 months i started getting better with the fatigue, and was on BP meds for racing heart. Seem to be doing better but not able to work out anymore. As i
am a ex athlete and dont perform anymore but am very active. Or was active befire covid. Now this last year in December got sick again and think it was a new strain of covid. Had very bad fatigue and muscle weakness the worst ive ever had was very scary. Alonf with racing heart and i knew this was covid or long covid relapes. I am doing better, but this round i have alot of body pain and my right leg is always bothering me. Muscle weakness if i do too much, but not as bad as the beginning. I did have the symptoms of dysautonomia for sure but they are getting better. But it's the dont feel good every other day. No energy. And then i injured my knee i guess doing practically nothing, now its hurting along with my hip and foot if the right leg. I feel like its vascular as my leg hurts if i keep it bent to long in a weird position. I feel the tightness in that leg and see my veins more prominent. I dont know what else to do, my doctors are helping me, but only to keep me comfortable they dont know any treatments. I am doing everything from the flccc protocol. Ive done ivermectin this 2nd time of covid and it seem to work. But i still have this vascular issue i think thats causing the weakness in my legs. I dont know but i hope it goes away. I am getting very uoset and concerned i will not recover. I wish i had a dr. Like you dr. Vaughn it would be nice to have someone try medication or treatment of some sort. Gez has been so helpful to me and i have gotten all my info from his videos and people he has interviewed. He has been a blessing to us all. I am taking aspirin and thats it for blood thinning. If dr. Vaughn reads my post, please reach out to me as i need help. Thanks Gez again for all your help you are such a sweet soul!!!❤❤
We all need help hun. That's the problem. No one wants to tackle this global recovery. First they'd have to admit there's a problem. 🙄
I know I'm not here for vengeance or recompense. I just want some freaking help to get better. 😢
Omg !!! This is exactly what I'm dealing with !!! Is there anything that is working ???
Love love his analogies. I had forgotten I had a blood clotting disorder until my Looong Covid. Inherited from my mother I have Factor V Leiden. Recently relapsed. Hurting. Dr told me I need to work out more eat fish take Omega 3’s. Lol
Do you think the UK will have the necessary equipment to test us for long haulers for clots / hyperactive platelets soon ? So that we then have the " evidence" to trial the triple therapy ?
Three jabs and two rounds of covid have certainly had an adverse effect on my coagulation and blood . I have purple toes and fingers , eye damage and freezing extremities as proof ! . However I remain optimistic that we are getting closer to treatment
It’s coming!
Great content and life changing! Can you do a video recapping some of the best advice you’ve gathered so we can see all viable treatments in a consolidated way?
Good shout! That does currently exist in the form of the Long Covid Handbook, by the way :)
I had it 3 times in less than 18 months and had many post symptoms but no vax .... I had to rebuild my gut biome....completely change my diet with supplements and no sugar or flour it was crazy but i am feeling better and my immune is back on deck
It will eventually get better, Karen. Ypu will move on in health. Have ypu tried Gez's supplement stack ( see his video on this ). Have you tried an alkalising diet to shift blood pH towards greater alkalinity because hypoxia ( due to poor vascular perfusion and micro clots ) shifts it towards abnormal acidity ? These 2 changes plus low histam8ne diet ( helps dial down Mast Cell Activation ) and finally get some sunshine...that'll boost immune system , regulate inflammation ( bt vit D production ) and raise dopamine and estrogen levels making you feel good !
Did he mention which anti viral to take with the triple anticoagulant therapy to eliminate viral reservoirs?
First i have never tested positive for covid i had one JNJ shot in 2022. Rewind i got really really sick in OCT 25- 31 2019 the 1st report case in the US was JAN 21ST 2019 . Im almost certain i had covid. ....i am struggling with many many symptoms. Csn i find out with antibodies or something if i ever had covid? All the typical symptoms x10 im 49 now
The test is invalid and produces false positives.
How do we get ahold of Dr. Vaughn?
Given the rate of reinfection and viral evolution it is inevitable that LC will eventually affect the majority. Perhaps once people wake up we will see progress.
The difference is immune dysfunction and other pre-existing abnormalities that allow the virus to wreak havoc in some people while not doing much in others.
2019 COVID and 3 Moderna shots. Veins are gone. Was super vascular - can’t get a pump anymore even.
Veins are gone? :(
I used to be a bodybuilder.
I have the same phenomenon! What are things like for you now.
Can we exchange notes?
Dr vaughns podcast/ radio show is on 'America out loud pulse'
With regards to capping heart rate, you said "not the 95 that it should have been." Do you have a reason to believe that it's an intensity thing rather than a duration thing?
It’s both
I have off and on neuropathy in my feet. Has anyone had an emg for that from Covid? If so what did they do for it? My is getting better now. 🙏. I also have dizziness now and it’s like being on a boat and it’s getting a little better I think. These symptoms don’t happen every day now.
How do we just get treatment.
Been loads of research now
Money needs to go on treatments..
Film coming to talk about this very soon
Can you ask your Doctor Friend . . Does augmented nac work ?
Not a biology student :( don’t understand what he means wrt vital persistence . Anyone can summarize ? Thsi is so complex and I wish I could find out in simple terms so I can go and tell my dr
Is there anyone here who has gotten rid of small fiber neuropathy (eg, burning, tingling, and spasms of limbs and face)? What did you do for it? Greetings from Germany and God's blessings to you fellow sufferers!
I suffer from this 3 years. My face is numb and burning at this very moment. Never got rid of it. German born in USA.
I get high-dose vitamin C infusion and that helps against the tingling.
German: Die hochdosierten Infusionen (7,5g) senken nachgewiesener Maßen den Histaminspiegel. Ich mache das beim Heilpraktiker. Der Hausarzt hat es abgesegnet. Ich versuche damit, und mit anderen Mitteln, die Entzündungskaskade zu unterbrechen. Nach der Infusion bin ich oft einige Tage fast symptomfrei.
Alpha lipid acid, boswellia and lion's mane.
I have neuropathy ie tingling and burning in my feet after the vaccine :( I was very fit and healthy before. I have tried everything recommended in LC community and although I have seen improvement its still there 22 months post vaccine
This is also one of my symptoms (covid not vaccine). I’m trying R ala, benfotiamine, b12/b6 and a b complex. Seems to be helping a bit.
Thanks- I have started benfotiamine and LDN about two months ago and I havent seen a huge difference yet. Still get electric shocks and burning when walking . But last year I also had dizziness , muscle twitching and POTS which thankfully all improved a lot. I am only stuck with neuropathy in my feet
I had the neuropathy for about 15 months post delta. Got better. Now here I am with covid again. Sure hope it doesn't return.
I had the tingling feeling a lot of the time especially at night if I happened to bend my arms for too long while asleep. I upped my omega3 intake and it seemed to go away, every time I reduced it the numbness came back after a couple of days, now I just stay on it.
the other thing was, I take vit K and my joint pain also vanished, but its works against the blood by thickening it!! which is a double edged sword.
Where can I get some Rapamycin and some N-acetyl Cysteine? I can get Ivermectin and Nattokinase. The biggest problem I have is my microbiome. Where can I get food?
Probiotic from biotiquest is important
I have trouble breathing , pain in my neck for almost 2 years since my vaccine. I've tried natto but I don't know if it works very well. The only thing that seems to help is vitamin b1 and aspirin
What helps against these microclots? Best regards
Have a look at what COMUSAV do.....
No one’s talking about the difference between people that got the magic bullet and people that did not as far as clotting and heart attacks like endocarditis and stuff. I’d really like to see the numbers on that but apparently nobody has those numbers!? Is anyone talking about that!? No! This needs to be answered!
Anyone try Wormwood?
Yes. Every time I run out and forget I have ever taken it, within about a week I "coincidentally" am swamped with a really bad flare. Then I wrack my brains to what I am doing differently, remember the wormwood, start taking it again, and "coincidentally" experience lessening of intensity within a few days. Not cured, not even remotely!, but I now take wormwood regularly and "coincidentally" experience more stability overall. That said, it hasn't prevented acute covid round 4, which I am currently trying to recover from.🙄
Sleep would be great. Since Covid I don't sleep.
Raelan Agle offers some good tricks that helped her get through insomnia with CFS. I also recommend Raelan’s interview Claudia’s ME/CFS and FM Full Recovery. You’ll learn what you need to know in the last 1/3 of this video.
My sleep has been off too
Same here until I tried otc generic liquid for nighttime flu relief. Huge difference while suffering so many painful symptoms and the sleep really helped face the non-productive day, but helped my mood. It was one tiny step. I guess the antihistamines helped with inflammation, but not fatigue and about 20 other symptoms. Sleep cannot be underestimated. Tiny steps.
Melatonin!
Yes, i have tried magnesium and melatonin with no luck.
What antibody? Anyone caught it?
Do people recover from the CFS/ME version of long Covid ?
Experience reports that is still possible. But it is important to fight the disease on all fronts immediately.
Thanks Gez for the video. What supplements were/are you taking for the gut microbiome? I think you were taking 2 different supplements, one was polyphenols? Ive forgotten the names
Phyto V and Your Gut +
@@RUNDMC1 thanks, do you think they have helped you ?
Why does tylenol 8 hr exstended release ease my covid induced tinnitus?🤔
Aspirin gets me back to 80% as soon as I take it (only when it's bad). Has to do with inflammation and blood thinning.
@@stephangauthier911 Tylenol isn't a blood thinner though or an anti inflammatory
Do you take aspirin for tinnitus ?
@@MissKrisLoves wow ur right! "Instead, acetaminophen works by blocking your brain from releasing substances that cause the feeling of pain." So why is it labeled as anti arthritic? Its the only thing that helps my pulsatile T! I guess its just numbing the brain so i do not notice the tinnitus as much....hmmmm asprin actually MAKES me have ringing always has...wierd.
I don't think monoclonal antibodies exist in my country. I've never heard of anyone having taken them here (South Africa). Personally I've been wanting to at least give Ivermectin a shot (to address viral persistence), but no doctor will prescribe it for me.
Why don’t you fly out to one of the African or Asian countries where they give away any type of medicine just like that? I know you can pick it up just like that in Egypt from one of the pharmacies by the hotels in those resort towns.
Ive had the 125bpm walking up the stairs.
Still LC since March 2020.
How does long COVID affect reproductive health?
I made a film about it! Scroll back through the archive :)
I’m not sure what the test is called exactly. The captions have it down as “pile 4g5g” - is that right? Or is it pilo or pile one 4g5g? My long covid appointment is tomorrow so quick answers are muchly appreciated! Also, anyone else testing positive for covid for 7months?
I think my partner just found it so I’m sharing it here in case it helps anyone else out.
I think it’s: PAI-1 gene 4G/5G genotype.
Have a scan through the comments on here, it’s spelled out a few times
@@RUNDMC1 That’s good to know. I did scan through but I must have missed it. Will check again, thanks for such a quick response!
Plasminogen Activator Inhibitor (Pai-1) 4G5G
labcorp tells you the amount of spikes in your blood the only lab that does it
Who is Jocko?
Dr Jaco Laubscher
@@RUNDMC1who is Reisha?
@@RUNDMC1also have you had any of the microscope testing done? Or the triple therapy?
Has fasting helped anybody?
I am trying... 20 months of pain, life ruined after 2nd dose of pfizer, same syntoms of long covid (i am sure 99 cases out 100 comes from shots, doctors lie to us). Now i am trying fasting... Just done 3 days... I ll do 1 day a week... Last chance to recover a little. Was fit and healthy, now life ruined signing for it... Damn the day i trusted doctors.. They lied to us from the beginning
I'm doing it now with thre eof the suggested supplements and I forgot to mention I have oxygen cans I use. I am feeling better in the first time in three years!
@@MinouMinet what supplements ?
For me fasting was very bad. I need to be gentle with my body, to let it recover. I did 2x per week a 24h fast. It has made me worse. The thing is that some people on the internet have been pushing this idea, while not understanding adequately the state of LC people body.
@@alexandrecouture2462everybody has a different body, genes and reaction to virus/vax. I struggled with fasting, too. So I do intermittent but the important part is to listen to your body (not.your hunger tho lol). You'll know when to fast and when to break it. Also, what you consume after a fast is as important as the fast itself.
Thank God someone with a brain instead of gov and pharmaceutical propaganda. Vac wrecked me took a year to come right
His wife doesn’t understand that he is passionate. This is normal among gifted people many times.
💉💉☠️👈🏻we tried to warn YOU.
"Safe and effective"....
3 years 4 months 😑🫣🫣😶🌫️😶🌫️
This thing is a bioweapon...vaxx is 100x worse. Follow Karen Kingston. Monsters who did this to us.
Long Covid or Long Vax?
They are afraid
Vax damage
I am shocked 😳 there are still people on the loose who chew this covid sh@te! Thought everybody woke up from this bs? You are all adorable 😅 🎉
Hate to break the news to you, but millions of people are having chronic symptoms after having been exposed to the virus (and this is a continuing trend). It isn’t exactly over and more and more people are developing symptoms.
you are all being lied to.