If one more person claims it’s all deconditioning… papers.ssrn.com/sol3/papers.cf…

Siri, can dogs have hysteria?

New preprint of a #longCOVID study from us: biorxiv.org/content/10.110… "Neuroinflammation in post-acute sequelae of COVID-19 (PASC) as assessed by [11C]PBR28 PET correlates with vascular disease measures"

Yup

Yes! Thank you thank you! So incredible to see

Since the NIH clearly isn’t going to help us and I know so many #pwLC and #pwME are paying an arm and a leg for their own copious testing is there any patient led research database where we can upload our own test results in a standardized manner? #LongCOVID #ME/CFS

On Long Covid Awareness Day, we recognize the millions still living with the disabling effects of COVID-19. I am committed to fighting for the federal funding necessary to better diagnose, treat, and support them.

I’ve been making a lot of writing errors (email, texts, longer works too) lately where I substitute a word with another that sounds similar. Today in a text I wrote “wish” instead of “which” and “strange thing” instead of “strengthen.” What is this called? #MECFS #LongCovid

“I wish I could rest as much as you do” Please remember that disabled people are not home relaxing. We are sick. We are in pain. We are still exhausted while resting. We are bored. It’s not a fun little vacation. We are miserable.

Any #pwLC or #pwME tried the herbal blend ITIS? Recently prescribed by my functional med Dr and haven’t seen any benefit so far but wondering if others have? #LongCovid

How much accumulating evidence will be enough for people to actually take this seriously?

How many more articles are needed until people take this seriously?

Danielle Beckman whenever someone tells me they dont know anyone with LC I tell them I technically dont know anyone with erectyle disfunction either but that doesnt exactly mean no one has it

Do any other people with ME or LC get headaches with nattokinase? Wondering if I just need to ramp up even slower or if it’s not for me #MECFS #LongCovid #pwME

Routine blood panel yet again shows low ALP - consistent over a decade and no provider concerned. Fellow #pwme or others with chronic health issues - anyone else have this finding or know what to make of it. Guessing would be associated with chronic malabsorption? #ME/CFS

Following the work of Dr. Tyna Moore and others to learn more about benefits of micro dosing GLP-1 for neuroinflammation. Seems like that might be useful for Long COVID. Any insight Danielle Beckman?

Say whaaaaat??