www.theguardian.com/commentisfre...
'The research team utilized and investigated the role of a protein called SMPDL3B as a therapeutic target.'
montreal.citynews.ca/2025/07/25/m...
It feels like this year, we’ve made a significant step towards understanding the pathophysiology of ME/CFS.
A brief overview of the studies that caught our eye.
Packed a lot of important info in: Pace Trial, GET harms, benefit cuts, insurance etc. It was like a potted history and didn't mince words about how awful it is.
Listen back! #MEcfs
#MyalgicEncephalomyelitis
Packed a lot of important info in: Pace Trial, GET harms, benefit cuts, insurance etc. It was like a potted history and didn't mince words about how awful it is.
Listen back! #MEcfs
#MyalgicEncephalomyelitis
This clip is from his closing comments, which I thought were very powerful.
Actually, I burst into tears 😭
Thank you both 💙 #MyalgicEncephalomyelitis
#GreatestMEdicalScandal #LongCovid
This clip is from his closing comments, which I thought were very powerful.
Actually, I burst into tears 😭
Thank you both 💙 #MyalgicEncephalomyelitis
#GreatestMEdicalScandal #LongCovid
@meassociation.org.uk
@actionforme.bsky.social
#prime26 #PRIMEsymposium #pwme #me/cfs #mecfs #MyalgicEncephalomyelitis #buildingcapacity
#MEKills #HumanRights
#pwME #MyalgicEncephalomyelitis #MECFS #LongCovid #ChronicIllness #NIH
Opening: Amy Adams of NINDS wonders if the same "butler did it" in each of the multi-system diseases covered by the conference.
Adams discusses her appreciation for people with lived experience,the "true experts", hopes to continue to learn from them. 🧪
In-person tomorrow; reporting from home, today! 🧪
#pwME #MyalgicEncephalomyelitis #MECFS #LongCovid #ChronicIllness #NIH
@georgemonbiot.bsky.social discusses #MyalgicEncephalomyelitis.
@georgemonbiot.bsky.social discusses #MyalgicEncephalomyelitis.
He has multiple sclerosis himself rather than ME/CFS.
Note that the F word is used.
#MEcfs #PwME #MyalgicEncephalomyelitis
He has multiple sclerosis himself rather than ME/CFS.
Note that the F word is used.
#MEcfs #PwME #MyalgicEncephalomyelitis
Non disabled people can’t understand how much independence and autonomy means to us. Whatever small amount we have left - is priceless.
That’s why we don’t take necessary risks. We know what’s at stake.