Thanks to my mum for getting everything ready for our family #TeaPartyForME2025 on #BlueSunday2025 (tomorrow).
We’re doing it in aid of the Irish ME/CFS Association
https://www.idonate.ie/event/BlueSunday2025fortheIrishMECFSAssociation but other worthy charities are available (see...
With Andy retiring, I wasn’t sure if this was being done:
https://bsky.app/profile/tomkindlon.bsky.social/post/3lkja4u3zzc2y
https://www.threads.net/@tomkindlon/post/DHRQzCpsiAr
https://disabled.social/@tomkindlon/114173442330353132
P.S. I’m not going to do one for the published papers.
Not sure if I have said this much but this was written for the PACE Trial special issue. The original title had the PACE Trial in it because that is what it focuses on but then the editor asked me to shorten it. If I was writing something from scratch on “Do graded activity therapies cause harm...
A reply:
Mads
@blueforpwme.bsky.social
Meant to add that I also tried the LP back in 2010/11 and felt like a superhero for a few weeks then crashed badly with awful flu symptoms, fever, swollen lymph nodes etc
https://bsky.app/profile/blueforpwme.bsky.social/post/3ljn5ypzyl22s
Adverse reaction following the Lightning Process shared today on my FB page
Because participants are programmed to say they are well and not mention symptoms & impairments, positive testimonials are very unreliable
We have been on previous committees the HSE have had including one that ran from 2019 for a few years that led on to this process. But weren’t invited to this. I think there aren’t many patient representatives on this. Don’t know whether the Irish ME Trust are on this. They are closer to ME...
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