tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

Latest
e-newsletter is here:
https://s4me.info/threads/uk-decodeme-recruitment-open-online-questionnaire-postal-spit-kit-12pm-12th-sept-2022.29463/page-30#post-494577

It shows they have less than 16,000 DNA samples (they have funding for 25,000). Hopefully the ME community will make a big effort to reach more people in next 8 weeks.

@mecfs

IrishMECFSAssociation, to mecfs

ME Association

Decode ME Study - "Join the world’s largest ME/CFS study!"

Are you aged 16 or over, live in the UK, and have had an ME/CFS diagnosis from a healthcare professional?

If so, please take part (if you haven't already) here:

https://www.decodeme.org.uk/portal/

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #LongCovid #DecodeME #DecodeMEStudy #DNAresearch #Research @mecfs

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