C19
Scientists are exploring how inflammation and sleep are connected. “But this wasn’t a restful sleep. Infected people had difficulty falling asleep, woke up more, and had a more restless sleep especially when they were most symptomatic.” “Up to six months after an infection, 41 percent reported sleep disturbances; an additional 7 percent reported disturbances that were severe.”
The problem is when you have a marginally better day or days, the temptation to do more is just unavoidable. You just want to feel normal, to be able to do normal things, desperate to just have a normal life. #pwME #MECFS #LongCovid
+ But this world is not big corp-owned, is about communities, rewards authenticity over celebrity (so far), and encourages conversations rather than fuelling the Outrage Economy.
Perhaps those who want a Birdsite clone will hop on and hop off. For me, this feels like a healthier way to be on socmedia.
I had huge "follower" numbers on the other site, but very shallow engagement. It's not about numbers. It shouldn't be. I feel freer here, connected, and more creative. Thanks for listening!
"Long Covid: What's changed, and what we know now"
Includes a mention of our 56k-strong, compassionately-moderated Long Covid Support group on Facebook, link in bio.
https://www.bbc.co.uk/news/uk-england-london-63546138
ME/CFS and Long COVID: Q&A With the CDC's Dr Jennifer Cope
excellent article from the perspective of a reporter who fell ill with Long Covid. and it explicitly connects it to ME/CFS. there's an accompanying video too.
https://news.sky.com/story/how-long-covid-ruined-my-life-from-crushing-fatigue-to-brain-fog-12744444
RT @lisa_iannattone@twitter.com
It’s so strange to see public health officials and institutions adopt libertarian phrases. “Wearing a mask is a personal choice” is political phrasing. That’s not a sentence that would ever be used in public health messaging normally. “Brushing your teeth is a personal choice.”
🐦🔗: https://twitter.com/lisa_iannattone/status/1593239179181363201
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a severe condition characterized by post-exertional #Neuroimmune exhaustion (PENE) accompanied by #Neurological, #Immunological, #Gastrointestinal (GI), & #Mitochondrial disturbances […]i affecting 17 million to 24 million people (2). ME/CFS is heterogeneous not only in Sx presentation but also illness trajectories, which can be worsening, plateauing, improving, or relapsing-remitting”
https://www.science.org/doi/10.1126/science.abo1261
#MECFS #ChronicIllness
The audiobook version of Ryan Prior's The Long Haul is now available for pre-order, with delivery on Nov. 29. Ryan himself is doing the narration, and if you've heard him on podcasts you know he made a great choice. #LongCovid #mecfs
Highly recommend all #DisabledSocial and new Mastodon users read the following tips on how to stay safe in the #Fediverse
Given that we are rapidly trying to build community here…
Can I ask you to do two key things:
1) Reshare other people’s posts - so your timeline is rich with other people’s posts for anyone browsing your content to discover.
2) Follow, follow, follow. That goes for following those posting good stuff - and also following those that follow you (as much as practically possible/sensible).
If you do these things, you’ll help us all network up at fast pace - and we all grow our voices & reach. ✌️
@mikegalsworthy Yes definitely, and well done for putting in so much work on this.
People new to this might not realise that likes/favourites work like a "thank you" but do nothing to make the post more visible. There is no algorithm. Use the button that looks like retweet, which is called either "boost" or "reblog" depending on which app you're using.
Author Spotlight: Fiona Lowenstein, Dona Kim Murphey and "The Long Covid Survival Guide"
Nov 22, 2022 10:00 AM
#LongCovid #mecfs #LongCovidKids
https://us02web.zoom.us/webinar/register/WN_rBZZcTFCQzq1H7ru7y4Epg
Full title is "The Long Haul: Solving the Puzzle of the Pandemic's Long Haulers and How They Are Changing Healthcare Forever" by Ryan Prior
So proud of my friend Ryan Prior who just published his book on the patient movement to understand & research long covid. Ryan developed serious chronic illness in high school, made a documentary about it, improved enough to finish college & land a job at CNN, where he wrote two of the most read stories on CNN's website. Now he's written the definitive account of how people who never recovered from covid have built a movement. #covid #longcovid #bookstodon #books https://www.amazon.com/Long-Haul-Pandemics-Changing-Healthcare/dp/1637581416?ref=d6k_applink_bb_dls&dplnkId=67995777-948a-488e-af06-c08b7936d0ed
I highly recommend that people watch Unrest by Jennifer Brea.
This documentary gives a glimpse into what it’s like to live with M.E. It’s sensitive, powerful and the best piece that I’ve seen on the subject. Such an important film. Especially no, as the number of people that are being disabled by Long Covid & M.E are rapidly rising.
#UnrestFilm #MECFS #MillionsMissing #LongCovid #ChronicIllness #NEISVoid
Is anyone creating a #LongCovid documentary film similar to how #unrest was created for #mecfs ?
Reposting a photo of my little friend. This time, I've used the caption feature for the benefit of the visually impaired. Will remember to do this in the future. #millionsmissing #mecfs #pwme #LongCovid
New York Magazine have published an outrageous article on #LongCovid , claiming post-viral illnesses such as #MECFS are treatable using #psychotherapy - implying such illnesses are driven by psychological factors not physical dysfunction.
This outdated view is widely discredited #pseudoscience. Shocking to see it rehashed in 2022.
Here, journalism professor David Tuller, who was mentioned in the article (but not interviewed for it), reports on some of the reaction.
Husband, Father, former software developer with myalgic encephalomyelitis, Living a limited life, missing from many places. #mecfs #pwme #longcovid #neisvoid
#MyalgicEncephalomyelitis #MyalgicE