If you are a #LongCovid patient with #MECFS , have you been offered:

'It's still not discussed enough how the majority of practicing physicians worldwide, particularly in sub-specialties frequently interacting with #MECFS patients, have a considerable conflict of interest, leading to an inherent bias against updating their knowledge base.'

ME/CFS:  Top Tips Handout for Doctors doctorswith.me/me-cfs-top-tip…

Reality of life for a medical doctor with #LongCovid #MECFS

“Why can't we use encephalomyelitis? That means inflammation of the brain and spinal cord. When will we be able to use the name ME instead of ME/CFS and get rid of CFS? That's my main comment.' Dr. Maureen Hanson, from today’s NIH meeting #MECFS #longcovid #longcovid kids

I highly advise against doing this. I’m an exercise scientist. This is WHY I am here.

I’ve learned this from Long Covid patients, clinicians and exercise physiologists.

In rare circumstances, some have bounced back… and some athletes have pushed through. But the overwhelming…

Triple anticoagulant therapy, day 50. For a week, I've seen marked improvement in ortostatic intolerance but none in exertion intolerance. I don't crash anymore but I get dead tired. If you are on triple, I wonder if you experience the same. #LongCovid #MECFS

#LongCovid

Hairdo for the friend's costumed party this evening; if I had been born half a century earlier, I could have worne this all of the time and avouded #LongCovid too.

We still urgently need 30 more healthy volunteers to carry out the study as planned. Please share with anyone eligible/who can spread the word in Sheffield! Volunteers get a £25 shopping voucher.

Thanks to all who signed up & shared so far, every sample makes a huge difference!

Please sign and share this petition to help us reach a wider audience. As a neurologist, I advocate for the reclassification of ME/CFS in medical textbooks from psychiatry to neurology. I'm confident that my psychiatrist friend Marya Alexander, MD will agree as well.

ME/CFS:…

PLEASE sign, Retweet & Share as much as you can to help people with #ME ( #ME CFS) in Australia. 👇👇👇

We need updated medical guidelines to remove harmful #GET & #CBT , Dr education, easier access to social services & so much more.

#StopTheHarm

change.org/p/harm-caused-…

10% of children whose mothers had COVID during pregnancy had an abnormality on ultrasound of the head.

10%

#CovidIsNotOver #Covid_19 #childhealth

Absolutely, Putrino Lab. CBT and GET for post-viral diseases like LongCOVID and ME/CFS should be seen as malpractice. In time, the psychosocial label and those driving that agenda will also be proven wrong.

I should probably have added that I am trying to convince a big PR agency to work pro bono on our cause. I told them, 'we get the numbers on Twitter.' So please hit the button, folks. 😄

How many #MECFS , #LongCovid , post-infectious disease patients, and their respective loved ones are active on Twitter? It would be great to get a rough estimate of how many folks we can mobilize. Please like and RT. Let's see if this works.