ME/CFS is a life altering disease. Your support will fund crucial research into the energy crash in ME/CFS, and give hope to the hundreds-of-thousands with this devastating illness in the UK. Donate now, and have your amount doubled! https://meassociation.org.uk/BigGive2025 #MECFS #MyalgicEncephalomyelitis #LongCovid #BigGive2025 #ChristmasChallenge #WhenRestIsntEnough #DoubleYourDonation | ME Association
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Clarke et al (2025) The search for a blood-based biomarker for ME/CFS: from biochemistry to electrophysiology Recent studies have found measurable differences in the blood of people with ME/CFS compared to those without it. These differences show promise to help diagnose ME/CFS. The ME Association and ME Research UK will jointly fund a 12-month study (2025-26) further exploring electrical differences in blood cells from people with ME/CFS. Read the paper: https://doi.org/10.1186/s12967-025-06146
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Knowing This Can Change Everything About Healing – CFS, Long Covid How do you approach your movement and activity? 📝 Grab a pen and paper – take a moment just for you. Tune in. No judgement, just gentle curiosity. Rate yourself from 0 to 10 in these areas: 🌿 Physical health 💚 Self-compassion 🌊 Calm score 🤝 Supportive thoughts ⌛ Patience with yourself 🌟 Trust in your recovery ⚠️ Stress kills healing. So, what did you score the lowest in? 🎯 That’s your focus. That’s where the work begins. B
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