ME Association
@meassociation
We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RTs do not necessarily mean endorsement.
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https://linktr.ee/meassociation 04-12-2009 20:38:02
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ME Association Collins Primary Thanks so much for featuring me and my book! And thank you for your help in reviewing the story before it went to publication ☺️
Thanks so much to the ME Association for featuring this! Please read the blog below if you'd like to find out more about how and why I wrote Max and Monty: The Raven Thief with a protagonist who has #MECFS 👨🦽🐕🍦💰🦅 Shares appreciated
.SciTechDaily Long Covid Still a Mystery: Routine Labs Show No Reliable Biomarkers "A new study found that most routine laboratory tests are not reliable for diagnosing #LongCovid......" scitechdaily.com/long-covid-sti… #pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #PostCovid
Parliamentary Question To ask the Secretary of State for Health and Social Care, what steps he is taking to support biomedical research into (a) long covid and (b) myalgic encephalomyelitis. See the answer here: questions-statements.parliament.uk/written-questi… #pwME #MECFS #MyalgicEncephalomyelitis
#Research Preprint: How Long is #LongCovid? Evaluation of Long-Term Health Status in Individuals Discharged from a Specialist Community Long COVID Service (Sivan et al 2024) preprints.org/manuscript/202… Please also see the ME Association website blog - Professor MANOJ SIVAN to
. Nation.Cymru Long Covid treatment guidelines are three years out of date says Doctor "Doctors, charities, and victims of Long Covid are calling for “outdated” NHS guidelines on #LongCovid to be updated." nation.cymru/news/long-covi… #MECFS #MyalgicEncephalomyelitis #LongCovid