From ME Association

If you took part in the PACE Trial, would you be willing to revisit your experience for research for a TV medical show? Details on the ME Association's Facebook page | 6 August 2023:

https://www.facebook.com/meassociation/posts/pfbid02gWE5yWK7441mPBiQTJfKSNc7gVxDrqkvW5QQkqHGpT1NoFuDooj5vweEjMhKNEsl

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #MyalgicE nostr:npub1gxp6qn9ehf92pmvy7cl2r5l04vdctls6sr7gn3csf60ap65qdapsr58dpd

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nostr:npub1pmxc6x4m8cf2gemjktdhu7vmf87kaprlq8t88fm2n25pzyp5sf9qdzexkq nostr:npub1gxp6qn9ehf92pmvy7cl2r5l04vdctls6sr7gn3csf60ap65qdapsr58dpd This sounds like it could be good, but people should be very wary about these television show people. I don’t remember the name of that awful series on Netflix where they claimed they were spreading awareness about invisible illnesses, but what they were really doing was just ridiculing people who suffered from them. It was gross and we don’t want more of that.