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??
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!
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.
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.
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.
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.
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.
Thank you for your excellent work. ME for decades.
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??
Thank you David PutHERO. I love the fact that you are in the field. Please stay!
Thank you 55 yrs here in Australia
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!
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.
Been suffering with ME for over 35 years. Glad to see some progress. Hope to find cause and cure very soon.
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.
I'm into year 32 so know exactly how you feel!
Thank you for all your hard work
What’s the treatment?
Could treatment with immunology intravenous help?
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.
Why no Immune Repertoire Sequencing?
Would be easy then to find the specific 'auto-immune' antibody in the IgG bulk sample.
Any updates on BC007 from Berlin Cures? They have an aptamer in stage two clinical trials to neutralize autoantibodies
Is there any hope for muscle wasting after cv and vac? 39 and recliner bound from mysterious wasting. Every test comes back fine
Have you done TCR/BCR sequencing? Still have peripheral blood samples to gather that info? We may collaborate.
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.
Thank you for your work.
I wish I could participate in one of these studies, but I don't live in America, lel :/
Thank you.
The Ugg in mice says it all….balance, pain extremities…yahoo……get on it everyone……we are desperate….xxx
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.