@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.

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

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.

@@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.

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

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

Any improvements after 3 months?

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

@@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 👃

@@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.

How r u recovered? Teen needs help!

How are you feeling now

And what about now ?

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

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.

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

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

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.

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.

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

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

Do you get weird stomach feeling connected to your eye ?

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

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.

Hi Monica. Did you take the vaccines?

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

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.

@@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.

@@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!

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

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

Has it helped?

Is the treatment working?

@jac any update

Whats healing solution?

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 ❤🙏❤

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

@@le_th_ thank you 😊

@@judymiller5154 : )

@@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....

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?

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

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

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.

Noooooo

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.

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

@@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.

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 .

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.

God heals through doctors also.

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

What did he say the treatment was?

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

I agree and understand completely.

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.

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

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.

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!

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

@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'.

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

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

Mine started 2 wks ago Praying to god for healing

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

@@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

@@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.

@@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. 💙

@@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

@@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

Exactly what I think.

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?

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

Please help!!!

@@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.

Samantha , what therapies did they recommend?

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

What treatment

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

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

i like him but lets not jump the gun yet

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

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

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!

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

@@AA-mf7si me too!!!

@@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 need take it I have problems

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

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.

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.

@@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.

there is no good thing about the pandemic fonzi hay

What huge leap lol. Prescribing statins & steroids? 😂

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

Has ivermextine helped.

I had c19 and I contracted it from vaxxed family

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.

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

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

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

Maravoric made you feel worse? How?

Those were my two elevated numbers as well.

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

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

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

Did you take the jabs?

I am severly injured after vaccination 😭

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

And my lymphocytes T: CD 4, CD 8, were normal. And NKH 1 (CD3+CD56) also normal. PCR protein C reactive: is always high but decreases if I'm lying down all day. Thanks

What kind doctor 👨‍⚕️ do I need in order to do all blood test , here where I live any doctor want help me , there are criminals

Yes they have seen post vax long haulers but apparently its very rare

@@FixedWing82 Not rare, they now have over 4000 post vax injured patients enrolled in the program.

@@FixedWing82 it's not THAT rare unfortunately... In Germany alone there are about 500'000 such cases (more or less severe).

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.

Great question, I’m suffering from that as well along with a plethora of other symptoms.

Same horrible insomnia

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

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

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

@@MegaEpicGamingGuy what were your symptoms

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

@@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

www.covidlonghaulers.com to get more info

I’m going on two years buckle up…

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

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

@@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.

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

@@DoctorYogendra Thankyou!

Email nursing@immunotrak.org

Alieta Eck or her husband excellent Drs and they understand