@cochranecollab How can @cochranecollab claim to stand for evidence-based decision making when the flawed Cochrane review of exercise in ME/CFS continues to be used as justification for harmful, poorly-evidenced treatments, not only for ME/CFS but now for Long Covid as well?
Hello all, my personal account, @SockFoam has been suspended and I can't figure out how to un-suspend it. This is really difficult for me as a disabled person who struggles to leave the home and depends on social media to stay connected to the world. I have a favour to ask.
🎉 Antrim Library invites you to an unforgettable event on May 29th from 10-11am! 🎉
Step into the world of virtual reality with Discover ME, an eye-opening film raising awareness for M.E., Fibromyalgia and Long Covid.
#Hope4Me#DiscoverME#AntrimLibrary@LibrariesNI
Learn about the pathophysiology of ME/CFS and Long Covid, clinical presentation, making a diagnosis, & POTS at our webinar on ME/CFS and Long COVID. More info here: https://t.co/U3Kl7lcQ4O #MillionsMissing#MEAction#rcpeMECFSLC
Learn about the pathophysiology of ME/CFS and Long Covid, clinical presentation, making a diagnosis, & POTS at our webinar on ME/CFS and Long COVID. More info here: https://t.co/U3Kl7lcQ4O #MillionsMissing#MEAction#rcpeMECFSLC
Learn about the pathophysiology of ME/CFS and Long Covid, clinical presentation, making a diagnosis, & POTS at our webinar on ME/CFS and Long COVID. More info here: https://t.co/U3Kl7lcQ4O #MillionsMissing#MEAction#rcpeMECFSLC
Learn about the pathophysiology of ME/CFS and Long Covid, clinical presentation, making a diagnosis, & POTS at our webinar on ME/CFS and Long COVID. More info here: https://t.co/U3Kl7lcQ4O #MillionsMissing#MEAction#rcpeMECFSLC
This video series on post-exertional malaise (PEM) in ME/CFS from the Bateman Horne Center is a fantastic resource - I've watched it several times and learned something new each time. #MedTwitter#MedicalEducation#MedEd
Discover ME, a groundbreaking VR film is coming to a city near you!
The Discover ME Experience is a unique, two-part awareness and educational introduction to M.E.
All you have to do is show up to experience the VR film.
#Hope4Me#DiscoverME@LibrariesNI
🎉Portstewart Library welcomes you on May 21st from 10-11am for an enlightening experience! 🎉
Join us for Discover ME, a powerful VR film raising awareness for M.E., Fibromyalgia and Long Covid.
See you there!
#Hope4Me#DiscoverME#PortstewartLibrary@LibrariesNI
Find out how to take part in our ‘Postcards to Doctors’ campaign as part of #TeachMETreatME for #MillionsMissing 2024. Send postcards to your doctors or local GP surgeries asking them to learn more about ME.
https://t.co/JUC1Bdr9JH
From our free event in Dublin yesterday. In photo is the speaker, Dr Nigel Speight with Association Chairperson, Vera Kindlon, & her daughter, Deirdre Kindlon Murphy, both of whom hosted the event.
We have received some positive feedback about the event.
#MEcfs#CFS#PwME
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Day 8 ME Awareness
“People with Severe ME will do almost anything to avoid hospital; they are not safe places for patients. The noise, lights, lack of knowledge by medical staff etc puts patients in harms way”
5 Caring Lessons
https://t.co/nUw9soYutE
#Call4Protocol4SevereME
At our webinar on ME/CFS and Long COVID talks include:
>POTS and Dysautonomia- what, tests, current treatments – Dr Nicholas Gall
>Severe ME/Feeding – Jaime Seltzer
More info here: https://t.co/U3Kl7lcQ4O @UKPoTS@exceedhergrasp1#rcpeMECFSLC
Our hot topic webinar on ME/CFS and Long COVID will explore these complex multi-system illnesses. More info here: https://t.co/U3Kl7lcQ4O #MillionsMissing#MEAction#rcpeMECFSLC