Our Papers: 1. www.frontiersin.org/articles/10.3389/fimmu.2021.700782/full 2. www.biorxiv.org/content/10.1101/2021.06.25.449905v1

As someone who's suffered with ME/CFS for the past decade, and having followed the scientific research on a weekly basis, I can say that this is by far and away the biggest breakthrough in understanding chronic illnesses. We're not far now. Thank you so much for your (and your team's) hard work Dr Patterson.

@olivertruswell

2 жыл бұрын

@Azul Amigo First they have to understand the complete mechanism of the disease(s), and then do clinical trials to prove those theories. So it'll take some time. I've lived with this illness where there's been no biomarker and doctors called me crazy, depressed or lazy. So me having a diagnosis with a biomarker will be a huge day for me.

@teddybearroosevelt1847

2 жыл бұрын

@@olivertruswell What a horrible thing to go through. The people who are supposed to help you get better are just insulting you.

@TheBushRanger.

2 жыл бұрын

10 years? I have had post covid for 6 weeks and want to die. There is no way I can go a decade with this. How did you cope mentally for that long? I will give this a year tops and then sayanara I’m out.

@olivertruswell

2 жыл бұрын

@@TheBushRanger. it's a lot of things. 1 is accepting it. Sounds cheesy but it's true. Then it'd adjusting expectations. My 6/10 is my new 10/10. Then comes rest, good sleep, cut out extreme exercise and eat healthy. My life balanced itself out. I have a good job and I'm luckier than others. Some are bed bound forever. I feel like shit most of the time but it's manageable. Go easy on yourself. You'll also find a tolerance you never knew you had. Once they cure this the world has a bunch of super humans on its hands. If you can make it through this you can make it through anything.

@TheBushRanger.

2 жыл бұрын

@@olivertruswell I have a tbi from 5 months ago and now developed long covid. No hope for me

2 months into COVID. Have all the symptoms especially fatigue, vertigo And Tinnitus( vestibular neuritis /Labyrithitis). I want my life back and for doctors to stop dismissing me and say that I just have anxiety. I’m really excited about your research and possible ways to beat this disease 🦠. Thank you for your work.

@jac1161

2 жыл бұрын

I didn't find these guys until 1.5 years later!! Finally heading in the right direction! Plus HBOT

@robertharris4661

2 жыл бұрын

I'm 2 months after COVID as well. Been having extreme charlie horse pain in all of my muscles, spasms everywhere, tingling, numbness, etc. My doctor also said it's anxiety and just wanted to prescribe cymbalta. Pisses me off

@marionharris5952

2 жыл бұрын

I have exactly the same symptoms. I am severely depressed because of the persistent symptoms and how it is interfering with life in general. Don't wish this even on my worst enemies.

@lukesmith3283

2 жыл бұрын

Hey Danny have been struggling for 46 days now post infection from Jan 2022. My symptoms are headaches/head sinus throbbing, head fullness, fatigue, GI discomfort, upper back/spine discomfort, pots, heart palpitations, tremors in central nervous system, water/air sensitivity. Anxiety-insomnia. I go to doctor’s offices or hospitals with my symptoms they just blow me off. This is horrible.

@lukesmith3283

2 жыл бұрын

@@jac1161 that’s great, how are you improving?

16 month long hauler here. Grinding my teeth through every day. Been on the Patterson protocol for 3 months. I’m holding on for my family and my love of music. Hopefully they figure this thing out .

@CarmenLopez-ge3bw

2 жыл бұрын

You’ve been on his protocol for 3 months and still no relief?

@tfouto

2 жыл бұрын

Any improvements after 3 months?

@cryptoaddicted5419

2 жыл бұрын

dam. he spoke like he's treatment was the cure

@ladybug5859

2 жыл бұрын

@@cryptoaddicted5419 I've heard doctor Patterson speak before several times and he's BRILLIANT of course but also he's an optimist. So I have heard similar things to what u said from people who tried his protocol and it was not actually working. So I guess it's not 100% but I would persist as he is persisting and hopefully something better will come along. I wouldn't exactly fault him because it looks like to me he's a super Optimist I'm a realist and so the two shall never meet but they can coexist. AND sometimes being an optimist is better because they carry on ignoring the bumps in the road or figuring they'll get all smoothed out in the end which we do hope they will. I treat a mild 😤tendonitis in an interesting Way by taking two 5 inch seashells and applying them to each🐚👂🐚 👂ear as I relaxed in my Epsom salt filled bathtub and it's nice IN the days of old I used to hear the sound in the seashells and I don't hear it anymore which is sort of sad but actually there's a certain type of quiet that comes from holding them to my 🙉ears. IT'S not exactly silent but something is happening and so I give that to you as an idea for those of you who have tendonitis🤙I also breathe VERY deeply thru my 👃

@cryptoaddicted5419

2 жыл бұрын

@@ladybug5859 Hi thanks for reply, I'm actually not on he's treatment yet I was replying to someone else. But great sounds a bit like myself an optimist lol. I've just had he's blood panel done so hoping it shows something so I can try the treatment I had Lyme and now long covid on top of it so really hoping something shows up.aha Thank you I shall give that a go maybe one day.

Thank you to Dr Patterson and the team. I’ve been suffering from LC for almost a year now. It’s been hell and I say that with no exaggeration…

@MDBYSL

11 ай бұрын

How are you feeling now

Thank you Dr Patterson! I am a long time healthcare worker in Nashville. I am almost full recovered from long covid but not alot of doctors know how to help around here. No one gets it until it happens to them. Thank you!

@mva3845

Жыл бұрын

How r u recovered? Teen needs help!

As a Rheumatologist, this data is remarkable regarding a systems approach of putting needed focus as to immunological marker's with pathophysiological findings and strong clinical correlations. Like HIV, COVID is and will further expand our understanding of autoimmune illnesses/diseases. I wish to hear more detail in regards to therapies as in why Statins? Mechanisms of selecting therapies? How do we refer our Long Covid/Long Vax patient's to a defined site? How does one find such? Keep Educating us...we need more specific/targeted therapies in autoimmune disease.

@zlnine8272

2 жыл бұрын

Agree! Appreciate his work greatly. But, would appreciate a little more specific details, I, for one am not a virologist or immunologist. So, I’d like to know exactly how to interpret my cytokines panels as well as differentiating my S1 protein results

@Jennifer-gr7hn

Жыл бұрын

It's great that you are open and seeking outside the mainstream, Dr Vansant. I'm a nurse, but also a covaids longhauler and the reason I use "covaids" is because what I went though after the early acute phase, felt like HIV -- 100% of the symptoms (mixed with radiation poisoning, stroke, seizures, and all in the [dis]"comfort" of my own home, rejected over and over by the hospital because I refused their "protocol." I live to tell, but live with many disabilities now which is hard for a 40 something year old active nurse, zumba instructor, hiker, skier hater of couches and potatoes. The more you do, the worse you feel. AWFUL. From the devil, to be honest. Anyway, what's been helping me? Anything and everything outside the system! Nutritional chiropractor to get vitamins and nutrients replenished, IV vitamin C, NAD, NAC, high dose melatonin as anti-oxidant, HBOT, and now IV ozone and chelation. There is SO much about these viruses but also, much more surrounding that I encourage doctors to consider. Other variables to increase viral load and cortisol, inflammation, etc. What should also be discouraged is the covaidshot! It's NOT good to increase spike load. Thanks for being humble and inquiring. My antibodies are still over 2,000 from march 2020 and I'm still harassed about getting a shot despite autoimmunity. Maraviroc was SOOOOOO helpful. Wonderful drug. I was willing to take it - black box warning and all. That's what you'll do when you feel regrets of survival at times.

Thank you, Dr. Patterson. I’ve had CFS/ME for over 30 years. I contracted covid early on.March 16, 2020 in England. Was alone and isolated in a rural area for 6 months. Took me 10 weeks to recover on my own. Since no one knew what this was, they kept sending me home from the hospital! I decided to take matters into my own hands and decided to double the doses I take daily for CFS (vitamins and herbs that boosted my immune system). It took a while, but it worked. I felt better after 10 weeks. Then 2 months later, long covid symptoms remained, and unfortunately, I’ve had these symptoms since September 2020. The good news is..I have started to feel better and better over time, but it has been a very slow process. I still have shortness of breath, fatigue, aches and energy comes and goes. I’m currently in Europe.I’d say I’m about 75% back now to where I was b4 covid. I have specific breathing exercises I keep doing, and I’m still doubling my CFS regime to stay on top of this. I am very grateful for your research. Feels like FINALLY people are seeing that there are parallels between CFS and long covid. Thank you for all you are doing. A grateful survivor, Monica

@solids1451

2 жыл бұрын

Do you get weird stomach feeling connected to your eye ?

@whome5810

2 жыл бұрын

Glad you are feeling a bit better! Could you please tell me what vitamins etc that you take for CFS? Cheers! :)

@susanwoodward7485

2 жыл бұрын

Have had CFS/ME since having mono when 16 - am now 70 - episodic, worsening over the years. Severe long-covid since October 2020, on top of pre-existing chronic kidney disease and severe resistant hypertension. Recurrent mast cell activation, GI issues, severe insomnia, brain fog and fatigue, crazy fluctuation in blood pressure and heart rate, and loss of appetite and weight loss post-covid. I am very interested in what supplements you have found to work. I take a ridiculous amount, but not seeing progress. Many thanks.

@JayTsay

2 жыл бұрын

Hi Monica. Did you take the vaccines?

@JayTsay

2 жыл бұрын

@@susanwoodward7485 Hi Susan. Have you taken the vaccines?

Thank you so much for the incredible work you guys are doing!

Thank you all so much for your hard work! I'm almost a year into my health journey that began the day I received the 2nd dose of Moderna with no end in sight. I have been unable to work, unable to do much most days. It's a good day, when I can make it through a video like this. This gives me so much hope! I'm also inspired by what your research will mean for everyone experiencing similar chronic health issues. Great things are happening, thanks to your care and diligence! Hoping we all get the medical and financial help we need very soon.

@rulingmoss5599

2 жыл бұрын

I'm also having a bad adverse reaction from moderna, for me it was the booster that made me sick, been going on for exactly one month now.

@sgleason8115

2 жыл бұрын

@@rulingmoss5599 I am so sorry to hear you're going through it. And please don't let my experience scare you! Some people are feeling better much faster than some of us long haulers. I hope you are one of them, and you feel better very soon. In the meantime, you have my empathy and sympathy! It took me 11 months, but I finally found a neurologist who believes me. You have the advantage of time and experience, at least. I couldn't even find information online about us, until 8 months into my event. Now there's research and support online, though still not always easy to find. Please let me know if you would like me to direct you anywhere. I know exactly how isolating and frightening this all can be.

@rulingmoss5599

2 жыл бұрын

@@sgleason8115 Thank you for the kind words, I did in-fact find a doctor who took me seriously and had even mentioned that she saw similar cases regarding vaccine reactions, I am trying to see a neurologist myself and fingers crossed they'll believe me too. Best of wishes to you, glad you've found some help!

@ClorisKylie

2 жыл бұрын

@@sgleason8115 what helped you the most? It's been 10 weeks for me

@golfrepcitizen

2 жыл бұрын

i developed irregular heartbeat after my pfizer booster back in November 2021. i am glad i came across this video

Thanks for sharing this and thank you guy for all your hard work 🙏

Thanks Dr Patterson. You are amazing

this is giving me so much hope

This gives me so much hope. Two years into this pandemic not only have a lot of studies been done, he’s also able to put a lot of the pieces together already. It really gives me a sense of there finally being light at the end of the tunnel.

@whisperingdeath308

2 жыл бұрын

I've been wanting answers to my dilemma. I hope it truly brings hope to all that suffer from LC.

On behalf of those of us who've had CFS, prompted by elevated levels of EBV, HHV-6, and CMV, and many years and/or decades before there ever was a virus called CoV2, thank you for continuing your research in this area.

@judymiller5154

2 жыл бұрын

I had CFS 15 years ago with the same viral components a couple of bacteria also! My hubby had chronic Lyme for 25 years. Now I have long covid, tho doing better than many. I am so appreciative of the research as well as support groups now available online. God bless ❤🙏❤

@le_th_

2 жыл бұрын

@@judymiller5154 Wishing you well as you continue along the path of restoring your health.

@judymiller5154

2 жыл бұрын

@@le_th_ thank you 😊

@le_th_

2 жыл бұрын

@@judymiller5154 : )

@scriabina

2 жыл бұрын

@@judymiller5154 how did you get over CFS? I'm desperate to get my life back after 5+ yrs, exacerbated by flu or covid in feb 2020....

Amazing information! Great work.

Thank you for your research in EBV! You are a life saver. Help us heal.

Thank you, Dr Yo!

Awesome job and information. Thank you so much ❤

Thank you. Love, longhauler from March 2020 and proudly on your precision care program :) LH panel #4 on Monday; 4 months on treatment. Help and hope are attributed to you guys!

@boxer1639

2 жыл бұрын

Has it helped?

@whome5810

2 жыл бұрын

Is the treatment working?

@justinvaughnatx

2 жыл бұрын

@jac any update

@mva3845

Жыл бұрын

Whats healing solution?

So good to understand 😌

Headache/migraines, brain fog, depression/anxiety, nausea, vomiting, diarrhea, LOSS OF SMELL AND TASTE, coughing, tachycardia/POTs, chest pain, fatigue, seizures/tremors, vision disturbances, palsies, tinnitus, shortness of breath, muscle and joint aches, skin rash, immune cell activation, changes to bone marrow and white blood cells, changes in menstruation, lung scarring/coughing, atrophy of saliva glands leading to sore/dry throat, numbness, tingling, nerve pain, hair loss... = 5mm radiation exposure symptoms = “Long Covid” symptoms

I am a healthcare professional and am a ping pong ball in our medical system. Despite my education, I am still looked at like I’m just anxious/crazy or jump to managing one part of my PASC dx. Thank you so much for your work and presenting this information so I can further prove the need for intervention beyond a beta blocker that worsens my symptoms

@Yazzie101

2 жыл бұрын

Same here! My dr is lost when I see her!

@Jennifer-gr7hn

Жыл бұрын

Same here, but thanks be to God I learned as soon as I was able to breathe better and think...what an AWESOME thing......outside the system. Functional medicine, nutritional chiropractor, FLCCC and ChronicCovid treatment center. Beta blocker is not the answer.

So proud of you Dr Patterson and Dr Yo, and all of your team behind the scenes. Your hard work and integrity have given me hope, and some improvement in my post vax long haulers'. I was so happy to be feeling better, and not going blind, I got up on my roof to do maintenance, and could do garden maintenance without gasping for breath and having to go and sleep. I stopped taking statins and had a relapse within a week, the rash on my face returning too. I'm back on Atorvastatin 20 and feeling improvement again after two weeks. Rash clearing. Oral Melatonin and basking in infrared sunshine has helped switch on my mitochondria again, along with the nutriceutical cocktail I take, and Fluvoxamine. Prior to that, I was preparing for death. I felt like I was circling the drain. We need to be patient with our healing and health. God bless you and thank you.🇦🇺

@dcuste

2 жыл бұрын

I spent two month in the hospital and now 10 weeks home on 3L/min O2 all the time except sitting. I have been taking low dose statin for 20 years, Melatonin 3mg since I came down with COVID. I took fluvoxamine while in the hospital, but stopped when I went home. I haven't seen any improvement with O2 requirements for weeks. Is your nutraceutial cocktail creatine monohydrate, coQ10, alpha-lipoic acid? What strengths? How much lung improvement did you see?

@lunatremolsaries8027

Жыл бұрын

How I can contact this doctor 👨‍⚕️ or other doctor can help me

Dr Yo and Dr Patterson- Thank you so much for your amazing minds and findings! I've had severe ME/CFS for over a decade and just had my test done from IncellDx and got my results back. I had 3 that were high. IL-10, VEGF and CD40L. I'm sure the LDN I've taken for 4 years has kept alot of the IL's low. I'm looking forward to getting a video consult, getting started with treatment and hopefully getting parts of my life back!!🙏 My 13year old daughter has never seen me healthy and able to live life outside of my home and bed. I pray that this may be the end of this nightmare journey that God has given me the strength to endure. May God continue to bless you in every way as you help so many who need it!!💙

@robertharris4661

2 жыл бұрын

I got mine back and had high VEGF and sCDL40L as well. I've been in a lot of pain for the last 2 months after COVID. I'm not sure what these mean, but hope there is treatment for the muscle pain, spasms, etc

@jessedwards2912

2 жыл бұрын

@@robertharris4661hey! yes I hope we both have success with this treatment. Dr Patterson just put out a video from his presentation at George Washington University and has a chart on it that shows what meds address what cytokines. It looks like for VEGF and CD40L, it's Maraviroc, statins, fenofibrate and aspirin (from what I can read). My doctor is ready to get rolling with things. I pray that God gives us all the healing we are searching for🙏💙 best of luck to you, stay strong

@robertharris4661

2 жыл бұрын

@@jessedwards2912 My doctor isn't willing to work with them on the video consult. I don't know how I"m going to get treatment, but feel like I"m dying and running out of time.

@jessedwards2912

2 жыл бұрын

@@robertharris4661 I'm so sorry to hear that. I will be the first patient that my doctor will do this with. I'm not sure where you live. I live in Illinois. Assuming this goes well, I'm sure my doctor would be willing to help others with this journey too. I'm not sure if you can find a willing doctor in your area? I'm sure my doctor would wanna see you in person atleast once, but he would also be cool with video appointments too. Let me know how I can get you my doctor's info if it's an option🙏 don't lose hope. Please keep fighting. There's a whole army here fighting along side you too. 💙

@robertharris4661

2 жыл бұрын

@@jessedwards2912 thanks for responding. I live in Texas. My sCD40L levels were 37,000. Supposed to be lower than 9,000. My VEGF was 57.6 and supposed to be less than 12.3. My IL-8 was at the top of the range at 20.21. I dont know how bad that is. My doctor has no idea what he’s looking at. What do you know about these markers

Thank you so much to Dr Patterson, Dr Yogendra and teams. I was fortunate enough to be in your trial in London in July 2021. At that point I had LC since March 2020. Maraviroc and possibly a higher dose of statin (I was already on 20mg statins because of high cholesterol) had a posititive effect within 2 weeks and I have only gone upwards since. I am 90% of my pre covid self. I applaud you and will be forever grateful. I do wonder though if I should have a booster in the fall....?

@adonnaprice9676

Жыл бұрын

Noooooo

Thanks for sharing this interesting video 😊📸

Yo, dude. This is awesome!

All doctors must go through these videos to understand patients rather than just dismissing . It’s so discouraging when they do that . Such doctors have bought me down more .

PLEASE APPROVE THE CURE FDA WE NEED THE CURE GLOBALLY PLEASE

What is so strange is that these doctors should have recognized a pattern by now . There are so many it seems with these problems I find it hard to believe a doctor has only run into this with you once. I've seen 3 doctors all who recommended psychiatric help and ignored the tachycardia, elevated troponin, and myriad of other symptoms. It's very discouraging .

@cryptoaddicted5419

2 жыл бұрын

Its a joke they all need to be held accountable. I'm almost certain that most diseases are caused by a virus,infection,mold toxin, heavy metal, pesticides along with all the rest of the toxins the immune system doesn't over react for no reason.

@euneadventure3112

2 жыл бұрын

@@joeboss4410 are u saying in all that time,nothing got better ?? im 2 months in and im fcking struggling

@SimplyNailArt

2 жыл бұрын

@@euneadventure3112 I got COVID in october 2021, with no symptoms at all. I was doing just fine. Got dizzy in november, from december till february I was doing fine again with no symptoms. Then I got really sick in february/march/april; heart palpitations, dizziness and short of breath. Been doing slightly better since then, but definitely not my old healthy self. It just comes and goes.

@williamgrimberg2510

Жыл бұрын

My wife and I got Covid from sick vaccinated family members while visiting us . Since we don’t believe in taking a non long term tested new vaccines and we are older and have had past and on going health compilations , we treated ourselves with the suggested vitamins to boost our immune systems. So when we got Covid our temperature and oxygen levels stayed close or in the normal ranges with different but short lived ailments at about a week . After that, I myself became better and stronger while my wife though not seemingly having the effects of the virus as far as lung problems, now is having very long lasting problems with her fibromyalgia since she had Covid back in January of 2022 . We are desperately looking for help (the local doctors and doctors assistance after examining her , seem to have no clue of what’s really going on with her)since she is in a very bad state loosing weight (134lbs. to 103 Ibs.)and lose of sleep which is affecting her mental state of mind . I am hoping through this podcast we will find some relief for her .

@Sally-ej5xp

Жыл бұрын

Agreed! Why has it taken so long for doctors to treat the cause not symptoms. I understand people want a quick fix. Our medical system is so broken.

An outstanding presentation. I am very interested to know more about the role of statins in other autoimmune diseases like MS that might have an overlap with long Covid. Multiple Sclerosis has very similar symptoms. He makes an excellent of tackling the root cause not just treating the symptoms. Also As he mention, symptoms are important not biomarkers.

11 months after severe Delta, 5 lobe pneumonia and pulmonary emboli, my brain was just beginning to wake back up. Mood was improving, palpitations, adrenaline dumping improved, activity level increasing, and peripheral neuropathy post Covid was beginning to improve. Then 12 days ago caught omicron. Set my head and brain back severely, head pressure and severe tiredness and fatigue returned with a vengeance. So frustrating. I'm so afraid my brain will never be normal again.

@mzman4183

2 жыл бұрын

You might want to ask your Dr. if it is ok to take Black Cumin Seed Oil (40mg/ KG body weight, daily). It has worked for others and appears to be a strong natural anti-inflammatory.

@djmotise

2 жыл бұрын

@@mzman4183 of course it's okay. It's a great product for covid inflammation

@djmotise

2 жыл бұрын

I had a similar experience. Recent covid brought back some older symptoms of long covid. Are you doing anything to treat your long covid now? Do something this time. If you throw some treatments at it now, there is a good chance you can reduce inflammation in the brain and other organs. And it could help your prior case of LC. Don't let this latest covid bout turn into another long haul syndrome. I would do the FLCCC protocol. (If you've not tried already.) Or something similar. Low dose prednisone. Naltrexone. Ivermectin. Anti histamines. NAC, aspirin, lumbrokinase, serrapeptase and nattokinase. (Latter enzymes are natural supplements for circulation to prevent clotting) Order from Amazon. "Doctor's Best" brand.

@paulah.9415

2 жыл бұрын

Same thing happened to me after Omicron. I had the original virus in April 2020 and had virtually recovered. Now sicker than with first bout of long covid. This video is incredibly encouraging!

Good work

Thousands are suffering with Dysautonomia (POTS,Ehlers Danlos, Mast Cell activation syndrome and other under the umbrella of Dysautonomia). Long Covid symptoms are the same. We need a cure to prevent extreme daily suffering for all these patients.

@TheBushRanger.

2 жыл бұрын

I have covid symptoms for weeks and got pots now along with a concussion syndrome. There will be no cure for this In my lifetime and I’ve heard this conditions are lifelong. Get the noose ready

@crazycarlitropro2450

2 жыл бұрын

What did he say the treatment was?

@Sally-ej5xp

Жыл бұрын

Big Pharma will fight this because it doesn’t bring them profits.

Is anyone having issues with their eras? I’ve since I got covid back in 2020,my ears have never been the same. Ringing,echoing and a feeling of fullness.

@edwinolvera15

2 жыл бұрын

Yes it's called tinnitus..i get that symptom its a ringing...mine comes and goes.

@caroliner2029

2 жыл бұрын

@henry Yes, me too. I'm also having problems with my eyes. I had night blindness and peripheral sparkling, like flash blindness during the day. The statins and Melatonin have helped to settle it, (with the other nutriceutical agents I take too) I'm delighted to report. My skin stings less too. The nerves in my arms don't feel like they're being intermittently crushed, and my hands aren't going numb with use. My heartbeat is less erratic. I have post vax long haulers'.

@henrypolanco9719

2 жыл бұрын

@@caroliner2029 yes. I haven’t felt the same since covid. My ears have just been getting worst.

@edwinolvera15

2 жыл бұрын

Does anybody have coughin, difficulty breathing,fast heartbeat and lump feeling in throat??...besides the tinnitus I'm dealing with those symptoms.

@makhines431

2 жыл бұрын

Mine started 2 wks ago Praying to god for healing

4 weeks into treatment no symptoms have changed. I have another appointment Tuesday excited to see if we just need to change some medication. 🤞🏼🤞🏼🙏🏼

@AA-mf7si

2 жыл бұрын

Samantha , what therapies did they recommend?

@lukesmith3283

2 жыл бұрын

Hey Samantha what were your full list of symptoms? Also how long past infection did you start with the medication.

@crazycarlitropro2450

2 жыл бұрын

What treatment

@Liliarthan

Жыл бұрын

@samantha r - have you had any improvements from the treatment?

@samanthar5123

Жыл бұрын

@@Liliarthan no it didn’t work. I wasted thousands of dollars like so many people. 🥺

Deserving of a nobel prize for his work! Thank you Dr Patterson and collegues ,God bless you for helping humanity on this war! Are physicians allowed to prescribe this regimen or it is just experimental?

Long covid for 2 yrs but moved from reactivated EBV symptoms to MCAS! Vertigo for 4 months! Drs are not being told.. I research myself and let my dr know possible treatments but I don’t know enough! A million sensitivities I can’t take meds 🤷🏻‍♀️ I agree with disability that needs to be recognized.. treatments need to be given free.. LC can’t work so how do we pay for treatments.. we don’t get any🤷🏻‍♀️ Just an update I am taking xyzal 1/2 tab at night and it has stopped the daily headaches migraines.. 🙏 still struggling but with less pain!

@djmotise

2 жыл бұрын

I agree and understand completely.

Best video I ve ever seen as a chronic Lyme patient with Bartonella and babesia. Ever. I have pots and dysautonomia, PEM, as well as wel as atheroscleroses and severe MCAS plus endometriosis stage 4. I wish there will be help for us too now. I do have activated ebv as well. Will there be help for us post/chronic Lyme sufferers too? Most of us are suffering for decades. Since Lyme comes usually with coinfections from the tick it might give a more diffuse image and therefore more difficult to categorize by biomarkers alone. Bartonella is notoriously hard to test. But you got rickettsia, erlichia, babesia and many others there too.

@melanievesters5473

2 жыл бұрын

I ve read about the cell danger response (CDR). This might be where it all starts. Suramin is supposed to dampen the CDR. How do we get suramin. Can research be done re Suramin?

@juliemaxwell6902

2 жыл бұрын

I'm really hoping that we can get some help for this! I've been suffering from Cfs and cytomegalo viral and epstein barr for 30 yrs now. After having a bout of covid and now been called a long hauler I've never been so unwell! It's been such a long time since I've ever felt healthy! Down depressed and lifeless and don't have the energy to look for help! I've truly had enough.... my heart truly doesn't want to continue on if this is not going away! My kids and grandkids keep any will I have left going

@juliemaxwell6902

2 жыл бұрын

Please help!!!

@cryptoaddicted5419

2 жыл бұрын

@@juliemaxwell6902 i feel your pain! Diagnosed with all the same viruses and now covids totally ruined me but yet cov antibody tests come back negative so doctors don't believe lol. I had mild covid i know that for a fact then from that day on things went down hill by the week. Of course the already immune suppressed wont have antibodies for covid that's prob why covids done all the more damage with us. Not sure if you've looked into SOT therapy there's some groups on fb lots having success with ebv lyme ect, my next try.

Dr Paul Benson in Michigan, I am sure is just as well versed. However his "a" team missed and dismissed my complaints of shortness of breath and other fatigue syndromes I explained. It's a good thing I know how to care for myself for the most part.

It would be lovely if he would speak in a way that regular people like me suffering from this condition could understand. He speaks for those with education in biology etc.

@petrarushing

2 жыл бұрын

@@skellington2000 yes, but since other people have also access, it should be covered in their professional lingo as well as making understandable for your every day Joe

@billielewis535

2 жыл бұрын

Exactly what I think.

ok you talk about s-1 being the same in longcovid and post vaccine well is it possible to rid the spike out of the body ??????

My prayers are with humanity. Our lack of trust and faith in God and our blind trust in man is what is responsible. For a corrupt tree cannot bring forth good fruit.. Yet out of fear you'all submitted to man's deception. Now submit to Jesus Christ and ask God to heal you. Have faith for it is possible~

@teejayangel6638

2 жыл бұрын

God heals through doctors also.

İ am 44 and have been a CFS patient for around 15 years now. Recently, a month ago, I got covid and still did not recover and showing long covid symptoms alongside with my CFS symptoms. Great huh! Having both CFS/ME and long covid at the same time chrrently, İ guess İ would be a great case to study for researchers.

2021 August 28th diagnosed with long covid symptoms from SAR-2 Delta Strain mutation! Long covid left me on total disability! I’m not vaccinated and won’t get vaccinated! Had 3 positive tests to date! When do we all get treatment for long covid??

Thankyou so much for your work. Will this treatment be available in Australia?

Thank you Dr. Patterson for the advances in Precision Therapy, wow! Can you provide studies that show the content presented in the slides ? Thanks !

This man deserves a Nobel Prize. I hope I can use this to cure my suspected cfs. Thank you Dr Patterson.

@cryptoaddicted5419

2 жыл бұрын

i like him but lets not jump the gun yet

@jone-nc1di

Жыл бұрын

Yes he does and with this research it will hopefully help alot of people with alot of different diseases

Thank you do much for this will join the incell long covid program. You have given me hope after w4 mo ths of suffering and invalidation

The ethical and valuable use of AI.....thank you for your research and development of therapeutic intervention

Thanks for posting this, Dr Yo. A lot of new information here. Will you also post the round-table discussion?

@DoctorYogendra

2 жыл бұрын

If that is available, I'll make sure to post it!

@lvaleiron

2 жыл бұрын

Hey @loopduplicate! I remember you from the been fluvox video, how are you feeling? I know you were better under flvx, wondering how things have progressed with you. Hope you are all recovered now!

@AA-mf7si

2 жыл бұрын

@@DoctorYogendra where can I get the watch? Looking for more information

@juliemaxwell6902

2 жыл бұрын

@@AA-mf7si me too!!!

@abstuli1490

Жыл бұрын

@@DoctorYogendra There are many indications that this is a Mast Cell problem. Mast cells can release more than 1,000 different types of mediators, including all types of cytokines. Mast cell activation syndrome (MCAS) is a new, little-known autoimmune disease where mast cells become hypersensitive and release too much and the wrong type of mediators. MCAS is suspected to be linked to ME/CFS, POTS, IBS, Fibromyalgia, Post-Lyme syndrome, CIRS, MCSS, IC/BPS, PTSD, GWI, Kounis syndrome, Hypermobile EDS and many more. Mast cells as sources of cytokines, chemokines and growth factors on NCBI The Role of MCAS in Long Covid | With World Leading Specialist Dr Lawrence Afrin Dr. Tina Peers from UK Discusses the Management of Long Haul Syndrome (Long Covid) Mast cell activation symptoms are prevalent in Long-COVID on NCBI Recent advances in our understanding of mast cell activation - or should it be mast cell mediator disorders? on NCBI Mast Cells and Irritable Bowel Syndrome (IBS) on NCBI Mast Cells, Neuroinflammation and Pain in Fibromyalgia Syndrome on NCBI Mast Cell Activation Disorder and Postural Orthostatic Tachycardia Syndrome: A Clinical Association on NCBI The relationship between mast cell activation syndrome, postural tachycardia syndrome, and Ehlers-Danlos syndrome on NCBI Post-HPV-Vaccination Mast Cell Activation Syndrome on NCBI Mast Cell Activation Syndrome: An Alert to Psychiatrists

I believe the viral load is correlated to the degree of disease. You all have my prayers.

WOW! I forgot to tell my doc that I had mono as a kid. 6 months post COVID and still struggling.

@dianemckenzie9669

Жыл бұрын

Me too i had mono age 17. I still coughing 4 months. Negative for copd and asthma.

Thanks Dr. Yo Is there a list of Doctors you collaborate with world wide that believes, and follows the research that you can provide? I reside in Namibia.

Micro-clotting is mentioned as significant in treatment decisions with these ailments. It is noteworthy to address treatment with HCQ. It has effects on both micro vascular anti-clotting and anti- inflammation.

@lunatremolsaries8027

Жыл бұрын

I need take it I have problems

@chrodriguezmarydown

Жыл бұрын

So does high doses of immediate flush Niacin about 500mg-1g daily

@leezap

6 ай бұрын

I had covid but I treated it with Ivermectin. I didn't take any quackzines. I'm doing Nattokinase now to prevent micro-clotting as I want to get back into exercise. The jabbed has much higher risk of micro-clotting than the unjabbed.

Any active trials going on in the US that are accepting applicants?

The best thing about this pandemic is this huge leap forward in treating immune system illness and sharing your findings with the world I admire you tremendously Dr Patterson and also your colleagues You have been there from the start helping people

@toby621

Жыл бұрын

there is no good thing about the pandemic fonzi hay

@MDBYSL

11 ай бұрын

What huge leap lol. Prescribing statins & steroids? 😂

I get relapses some lasting longer than others..same exact symptoms of when I had covid last year..its horrible..a constant reminder of the hell I went through..I get breathlessness, fatigue,my mouth gets inflamed, my stomach gets crazy..iv been to sooo many drs..noooobody can help me..I was a pretty healthy 58 year old b4 I got covid...

@gaelicjane1613

2 жыл бұрын

I hate to say but I'm like that too, I caught covid in March 2020 and still have symptoms which come and go, flare up, especially following physical activity. I hope they can find some form of treatment as I want my normal life back. Havent been able to work for the last 6 months. I'd struggled to work before that but couldn't cope with it physically. Its a never ending nightmare.

@djmotise

2 жыл бұрын

@@gaelicjane1613 There is treatment. Go search it. Start with the FLCCC website and its Wednesday night weekly updates online. Or go into their archive. There is someone near you who can treat you, I'm sure. If not, have a telemed visit with a doctor. Or contact My Free Doctor site.

The last version of the Covid booster seemed to have gotten my immune system to recognize remnants of Covid virus and it’s been 10 months of recovering since. I’m finally able to go through days without falling asleep in the afternoon. My breathing seems normal, no more gasping for air when taking a walk. Extra B12 helped. Hopefully, in a couple more months I’ll be 100%.

@user-vx7ni2kz7v

2 ай бұрын

The last version of the Covid booster what？？？tell me！！

Wonderful work. I thank you so much. Many of us are not being heard by family or our doctors. Your videos are far too technical for many. It would help us to have a summary especially for family. I’d love to go to a long Covid clinic but won’t get family support. There’s serious denial in my case there was denial that Covid is nothing but a bad flu. Has been the same for my family from start even until now. Thanks for your hard work.

Thank you Dr Patterson for your research. It’s a tremendous breakthrough to rescue the COVID-19 Long Haulers. How can I have access to your treatment. I live in Los Angles county, Ca. and I’ve struggled with Long haul COVID for almost 2 years. Thank you.

@angeminc

Жыл бұрын

Did you find out where he practices, did you get the treatment? Please share info.

Long hauling with a gut permanently damaged from covid, not much shows up on tests, three years later plus 4 vaccines, got insomnia, now add Chronic Regional Pain Disorder, really intense pains 24/7, neuropathy intensely shocking and squeezing my chest, major inflammation, hair, nails and skin problems, weakness, no pain meds work, getting frequent bacterial infections, immune system shot, heart a bit tachy, lots of other weird symptoms, now on off label treatments costing lots. Helping a little only. I'm in Austin Texas. Being as proactive as possible in search of an approach to multiple symptoms and pathologies and I'm so very frustrated. Where's that kind of team care anymore? Or, is there one place could I go to? I can't drive. Doctors don't communicate with each other or give referrals. They're stressed too, I know. In my case, all the above just may stress me to death. I'm a shell of my former self. Any ideas anyone? I've found nothing. This stuff needs a lot of medical attention from a steady source in a community of practitioners. It's piecemeal approaches that don't help; rather have contributed to getting steadily more incapacitated. Help, people, please...,

he should win the nobel

What if I was never tested? I had extreme fatigue for 2 weeks and about 4 days of watery stool in early Sept 2020. No treatment. Late October my infrequent and short bedtime tachycardia I've had for 30+ years became daily, longer, and anytime of the day. ER visit diagnosed anxiety after high bp and heartrate resolved without treatment and CT scan was clear. Also fatigue, insomnia, head pressure, suspicion of food sensitivity, then heat/sun sensitivity, lung ache, no capacity for exercise, no motivation for relationships or activities. Feb 2021 addressed histamines and got huge relief. Almost normal thru summer/fall of 2021. Jan 2022 sick again - fever, headache, runny nose, cough that moved into chest. I got hcq for a week, then ivm, budesonide, prednisone, azithromycin which helped a lot except for persistent fatigue. Slowly regaining energy after 2 months but sensing increased heartrate when getting out of bed, or just walking from couch to bathroom...not always, but I'm aware at these times. Is this POTS? Am I still long hauling? Would this testing be helpful? BTW 15 years ago I was dx with CFS, overgrowth of EBV, CMV, HHV-6, and 2 bacteria, plus adrenal insufficiency. Treatment lasted about 2 years, since then I've taken armor thyroid, female hormones, lots of vits, and low carb diet. Very active, outdoorsy lady till covid.

Hello. In a subgroup of patients with POTS and ME/ CFS, elevated autoantibodies to β2-adrenoreceptors and muscarinic 3rd and 4th acetylcholine receptors were observed. Can maraviroc with pravastatin neutralize these autoantibodies?

Waited to get covi 2 years. Then 5 days ill. Got it back after 2 month. Noted. I met fully vaccinated people 3 times. All of them have had covi. 3 times about 4 hours in same room with 5..6..8 people. B days and stuff. Every time i was with them i started feel bad. More and more. Last time met family where children where bit ill. All vacced. After that meeting i got more and more ill. 4 weeks. And started with ivermectin. Almost fine now. And will never be in one room with vacced covi people ever again. 3 times exact same shit. I learned.

@evo8power228

2 жыл бұрын

Has ivermextine helped.

@youflatscreentube

Жыл бұрын

I had c19 and I contracted it from vaxxed family

@dianemckenzie9669

Жыл бұрын

Hi are you taking the horse o r s e paste or the pills? I tried the paste for 2 months but still have cough which is my main symptom.

Dr. Yo, are there any patients with ME/CFS who have improved their health according to Dr. Patterson's protocol? Does the improvement persist after discontinuation of therapy?

I've been following Dr. Bruce Patterson and Dr. Yo's work from the beginning. Astonishing to see where it has lead. The magic and promise of bioinformatics being realized. You can see the excitement of the commenters at the end of the presentation who are from a larger audience on autoimmunity. Goosebumps! If you can comment on whatever happened to Leronlimab, an alternate option to Maraviroc, that would interesting.

The beginning of hope to this eternal nightmare.

Where can we find out about the treatment that was mentioned that is based in the UK please?

6months of long covid still have issue in breath, tinnitus, fatigue 😭 covid ruin my life everyday suffer

@MDBYSL

2 жыл бұрын

Did you take the jabs?

@dianafrancisspencer

2 жыл бұрын

I am severly injured after vaccination 😭

@youflatscreentube

Жыл бұрын

Speaking for myself, I had a significant reduction in the cardiopulmonary areas of symptoms after two months of hiking for 600+ miles. Still fatigued at times, tinnitus increases, etc. But, It seems that the continuous exercise helped “reset” the neurological pathways associated with CO2 detection, baro receptors with autonomic nervous system. The hike seem to cause a small patch of neuropathy on my left thigh, very strange

I just received my results from IncellDX lab and am going to schedule a video consult. I started having charlie horse type pain starting in the bottom of my feet and moved up to my calves, thighs, hamstrings, then my biceps, triceps, shoulders and pecks. The pain is excruciating and have muscle spasms. This has been going on for 2 months. I'm missing work now and depressed. I have the Covid antibodies but never had classic symptoms. I'm also suspect of campolybacter jejuni because I have a chicken coop at home I've cleaned without a respirator. I've had diarrhea for 2 months. My doctor just thinks it's anxiety. My C Reactive proteins were at 15.3 but have come down to 4.4 thankfully. However, my sCD40L levels were 37,000 and supposed to be under 9,000 and my VEGF were elevated at 57.3 above the 12.3 Do you think my symptoms have anything to do with these elevated cytokines? And if so, is there any help for me? Thank you

@ks5924

2 жыл бұрын

Those were my two elevated numbers as well.

@robertharris4661

2 жыл бұрын

@@ks5924 Can I ask what symptoms you had? If any.

When will these tests be available for us in the UK?

Try L Arginine for CFS trying it for my dad seems to help

Hi, I tried to do your protocol for long covid, but couldn't tolerate Maravoric, is there any other medications I could take that won't feel like I cannot even function? Was on your service site, and you have to pay to still be in touch with your network of doctors.

@Liliarthan

Жыл бұрын

Hi Heather, have you received support from Incelldx since? Any changes to your symptoms? I hope you’re doing better

@heatherlomaxmusic4776

Жыл бұрын

@@Liliarthan hi, yes but no new protocol yet :/

@user-hv8jw1fx7x

Жыл бұрын

Maravoric made you feel worse? How?

I wish I could find a doctor that would prescribe the medications. I am an ME/CFS patient. I have been diagnosed by Incell and am ready to try the medications. I've have been turned down by four doctors. Maybe the problem is I live in the Midwest which is usually the last to keep up with medical advances.

@DoctorYogendra

2 жыл бұрын

Email the nurses. I think I know of someone who can help.

@gmbowdle

2 жыл бұрын

@@DoctorYogendra Thank you

@djmotise

2 жыл бұрын

Go to My Free Doctor. Or FLCCC practitioner list.

@Liliarthan

Жыл бұрын

@@gmbowdle did you manage to try the treatment protocol by Incelldx?

@gmbowdle

Жыл бұрын

@@Liliarthan No, I can not find a doctor in Missouri that will treat me. Thanks for asking...

If I were let's say hypothetically having tinnitus and only that, could I get drugs over the counter or order legally from other countries that could help with tinnitus? And there is no option to use your service here in my country.

One year and a half.... They think its only panic attacks.... I can't walk more than 5 minutes, my body just shut down and react in crazy way... Potassium is mild low.

I've been sick with this before they even announced covid 19. I think as of today I am closer to being back to myself. 4,16,2022

@djmotise

2 жыл бұрын

When do you think you first contracted the virus/toxin?

9:21 So vindicating to hear a medical researcher confirming long covid-like reactions from vaccination! Hope the vaccine injured can have more visibility and help.

Is this treatment protocol available in the UK? Long covid since March 2020, only help here is "pacing and resting"? Please suggest anyone who could help in the UK? Thanks very much.

How I wish those providing these super videos would learn to enlarge their charts & graphs so we can actually read the info! Instead, we get a huge video of the presenter's head and tiny charts...

@paulah.9415

2 жыл бұрын

I wish the journals in which Dr. Patterson's research is being provided could be accessed by the general public. There is so much new research on LC just coming out, but I can only access a limited amount of it. Even that has been enlightening though.

You could have also included CIRS in your dataset ? would be interesting to see how it compared to CFS, we need a simple biomarker that distinguishes between both.

I have long covid, from ,2020 and then got worse after vaccination. Thank you for this.

Does anyone know of any.Drs following this protocol in NYC and or Westchester County NY?

@lunatremolsaries8027

Жыл бұрын

I m Looking help too , we other let’s know about this

I’m a long Covid-19. It’s been 2 month. I wish I could contact this Doctor to see what he recommended for my case. I seen Doctors and they don’t seem to have a answer for me. I feel alone and no hope through this long covid situation.

@DoctorYogendra

2 жыл бұрын

www.covidlonghaulers.com to get more info

@mrsancheezee4793

2 жыл бұрын

I’m going on two years buckle up…

@luisnueces23

2 жыл бұрын

@@mrsancheezee4793 Wow, what kind of symptoms do you have?

@lukesmith3283

2 жыл бұрын

Hey Luis I’m on day 42 with covid. Following symptoms Fatigue/lethargy Severe headaches/throbbing/head fullness Headache sensitivity to temp water and vents. Stomach/GI issues Upper back discomfort Muscular warmness in the legs Dizziness

@shelleylannon2245

2 жыл бұрын

@@DoctorYogendra Why are they treating long covid with liptor as one drug when it causes Intestinal lung disease. I took a liptor and it opened up something I could breath so much better but then pain in my lungs started and I became sob. It was weird.

i find it very risky, to show such a colour-oriented graphic with such low resolution like in 25:44. Vor example i see in orange "prednison" but its not be associated to one of the cytokiks. Maybe i'm confused by the similar colours yellow, orange and brown. Is ther a possibility to show this matrix without any doubts? Or is ther a link wher i can find it?

I had Epstein Barr so bad my doctor said I had liver damage and an enlarged damaged spleen. Fast forward: I was having these weird exhaustion episodes where I couldnt even lift a comb to my head, and when I tried to take a shower I had to sit down in the tub. I didnt have enough energy to stand up. Lab tests showed I was having relapses of Mono. Fast forward I was diagnosed with fibromyalgia and CFS. Fast forward: I have been ill since my 2nd (mandated) C0vid jab. I recognized right away I was having an Epstein Barr relapse. I cant live a normal life anymore. I only have so much energy a day and the exhaustion gets worse as the day goes on and my muscles get weaker. I have to save my energy like an "energy bank" every day

I've done alot of research on this and it appears alot of long haulers are having issues due to microclots and reactivation of dormant viruses that They caught before like cytomegalovirus and ebstein barr virus

@rubymuasya3531

2 жыл бұрын

So what do you suggest we do ?.. I’ve been having joint pains and I keep stretching my hands and legs cause I feel I just need to stretch and I keep massaging my butt and I also see mirages

@angela1981

2 жыл бұрын

@@MegaEpicGamingGuy yup last month just found out I had ebv and had covid end of Dec then last month developed neuropathy in my feet

@angela1981

2 жыл бұрын

@@MegaEpicGamingGuy what were your symptoms

@joeorlando94

2 жыл бұрын

Thanks to the “vaccines” that suppress the immune system.

@youflatscreentube

Жыл бұрын

@@angela1981 I just hiked for over 500 miles 6 months post c19 infection, and long covid I was improving before the hike After several weeks of hiking I had improvement in cardio pulmonary regulation issues related to post covid long haul But, I had a very strange return of neuropathy on my left thigh… And only there! Very weird. And an increase in head “fullness” with increased tinnitus

Where are the Centers. Great study . My friend has post vaccination Long Covid.

how can i i get a hold of the doctor because i have all of these crazy symptoms

Dr. Patterson, can you help me? Are you taking new patients. I have not been able to work for 15 months. I have chronic lyme, and went back on treatment but it didn't work. I also tested positive for ebv years ago but didn't know you could treat it. I also moved out of a moldy house 6 months ago. My worst symptom is anxiety, depression, brain fog and heart issues. I also covid 15 months ago and never felt the same. I live in Maine can you take me as a patient.

@DoctorYogendra

2 жыл бұрын

We have a doctors in Maine collaborating with us. Email nursing@immunotrak.org to get information about our program.

@hilarymurray7800

2 жыл бұрын

@@DoctorYogendra Thankyou!

Is there anything on the rest????

What is the name of the watch and where is it available?

two mth after mild Covid I experienced digestive problems inflammation on the face rash on the palms and acid reflux . it's still present 4 mths later. any advice will be welcomed.

Why isn't this treatment going national???

@godfamilycountry2785

8 ай бұрын

Follow the money 💰

I had mononucleosis/EBV in October 2019 (after a trip in Asia) and was devastated with all covid symptoms in 2020 and then I got two jabs of vaccination in 2021 and I collapsed again for two and a half years ! Please help !

Merci pour la traduction!!!

Can anyone summarize the video? My brain isn’t taking anything in. What are the recommended treatments?

@hejjjj7210

Жыл бұрын

Basically ivermectin, hydroxychloroquine, maraviroc, Fluvoxamine, vitamin d 10000 iu with k2. That's the most important.