Dear @PaulGarnerWoof as a doctor myself, who’s been on same journey, it’s been interesting to read the evolution of your thoughts on experiencing #Covid_19 viral/postviral fatigue & then on Sx experienced by those who develop #ME/CFS . People who are so often wrongly disbelieved.
@PaulGarnerWoof to read u say,
“I am reading materials about pacing and CFS/ME and listening to the CFS/ME community. I am taken aback that doctors have been so dismissive of what these patients have been saying for so long” & to hear youve spoken to Charles Shepherd too is great
“I am reading materials about pacing and CFS/ME and listening to the CFS/ME community. I am taken aback that doctors have been so dismissive of what these patients have been saying for so long” & to hear youve spoken to Charles Shepherd too is great
@PaulGarnerWoof so much work is being done by charities & individuals to advocate for patients but also to teach, educate & convince many doctors that these symptoms are REAL, debilitating & MUST be believed & correctly advised & managed.
@MEAssociation @MEActNet @actionforme
@MEAssociation @MEActNet @actionforme
Thank you also to @bmj_latest for publishing important and eye-opening thoughts from @PaulGarnerWoof on his learning & experience of significant, debilitating viral/postviral #Fatigue after #Covid_19 and how experience & learning from #pwme #ME/CFS can help #rehab & 🤞recovery
@PaulGarnerWoof as your experience of viral/post #Covid_19 viral fatigue & learning from #pwme #ME/CFS grows & ur acknowledgement of the authenticity & validity of range of symptoms, will you also follow up on this in @guardian as u did with your BMJ post?
theguardian.com/world/2020/may…
theguardian.com/world/2020/may…
