Comparing immunological signatures between Long Covid and ME/CFS

[@pattysmith5989]

Thank you for your excellent work. ME for decades.

[@davidburian5095]

Thank you David PutHERO. I love the fact that you are in the field. Please stay!

[@Gina-dn6xm]

Wow! I feel like we are finally getting somewhere with these conditions! In the last 8 years, I have been diagnosed with chronic lyme ( positive test), reactivated Epstein Barr, ME/ CFS, and long covid. Thank you so much!

[@riptaylor5862]

Yeah right. We”ll be dead by the time they figure this out. Every week there is a new theory, a new presentation with a bunch nonsense. In two months this presentation will be invalidated when another study finds something completely unrelated. You can find hundreds of “hopeful” articles and videos which all point to a different root cause, and they come out every week. It’s been like this for years! Are you better? No. Will you be better in 5 years? I doubt it. I hope you are better. But guess what? The solution won’t come from these dummies at Solve Nothing. Some brilliant person from Sweden, the UK or China will figure it out. We just need to pay that person a lot of money and he/she could figure this out in a week. Think about it…these dopes won’t be able to make videos if there is a cure. Then what will they do to pass the time? Actually do work? C’mon!

[@maryreid2282]

Very interested in this research. After being ill in 1980 I was left with M.E./Chronic Fatigue and would love to know some answers for my illness and symptoms. Thank you for doing your research.

[@annabeldean8276]

Thank you 55 yrs here in Australia

[@rrrrrulo]

Been suffering with ME for over 35 years. Glad to see some progress. Hope to find cause and cure very soon.

[@dansmith9724]

Maybe it wasn't mentioned, but many previous studies on mecfs have shown low natural killer cell function. Was nk function testing done in these long covid studies??

[@jewelleryaddict]

30 years of CFS this should have been done for us after first outbreaks of CFS at Incline Village. Has surely wasted some of my best years of life with a myriad of horrible symptoms and so much disbelief. Not sure which was the worst.

[@ShadowMan66]

I'm into year 32 so know exactly how you feel!

[@HarryJensen-kr4qz]

Was 68, now 71. Had covid in 2020 & 2021. Had brain fog/vertigo, had what I believed to be shingles in right arm. Was several years ago, seem fine now. Best luck to anyone still struggling.

[@jakeclarke8706]

Thank you for all your hard work

[@RowOfMushyTiT]

Why no Immune Repertoire Sequencing? Would be easy then to find the specific 'auto-immune' antibody in the IgG bulk sample.

[@valerielord1088]

I need to share this with a family member. In place of the usual icons, there is ink a link to an ad by the CDC, stating that the vaccine is safe and effective.

[@Swansue]

What’s the treatment?

[@janisedmondson7132]

Could treatment with immunology intravenous help?

[@davidkohl8962]

Any updates on BC007 from Berlin Cures? They have an aptamer in stage two clinical trials to neutralize autoantibodies

[@polyrhythmnix9723]

Thank you for your work. I wish I could participate in one of these studies, but I don't live in America, lel :/

[@lmr3639]

Thank you.

[@ashantimatthewson1702]

Is there any hope for muscle wasting after cv and vac? 39 and recliner bound from mysterious wasting. Every test comes back fine

[@jianhan3538]

Have you done TCR/BCR sequencing? Still have peripheral blood samples to gather that info? We may collaborate.

[@justcees]

Sadly, dr. Putrinos efforts maybe thwarted due to staffing issues. I waited more than 2 mos. For a scheduled APPT. only TO BE cancelled 1 week before the visit. The group running these studies don't respond to emails or telephine calls. It is atrocious how ME/CFS/LC people are being treated STILL. @Dr. Putrino, IF he is truly interested should look into what is going on with this study n STAFF.

[@omygod9062]

The Ugg in mice says it all….balance, pain extremities…yahoo……get on it everyone……we are desperate….xxx