European ME Alliance 🇪🇺
@euromeall
The European ME Alliance is a grouping of European organisations who are involved in supporting patients suffering from myalgic encephalomyelitis (ME or ME/CFS)
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https://www.europeanmealliance.org 25-12-2011 12:34:14
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"Nothing for us without us." Genuine inclusion of persons with disabilities is vital if policies impacting their health and wellbeing are to be of genuine value. At WHO/Europe we take this mission very seriously - advocating with our Member States to strengthen
For #InternationalDayOfPersonswithDisabilities EMEA joins over 100 organisations to urge EU Commissioner Lahbib to “keep the momentum” on disability rights European Disability Forum statement- europeanmealliance.org/news-Q42024-00… #MEawareness #DisabilityRights #mecfs
Young EMERG workshop 26-27 May 2025 youngemerg.com/yemerg05.shtml We have also announced Young EMERG workshop 2026 - now full two-day workshop youngemerg.com/yemerg06.shtml The future for research into ME #mecfs #research Young European ME Research Group European ME Research Group (EMERG)
On #InternationalMEawarenessDay the European ME Alliance member societies are extremely grateful to Dr. Kluge Hans Kluge for his support & meeting with us in Oct 2024 to discuss future collaboration to address this devastating illness x.com/hans_kluge/sta… #mecfs #MedEd
In May the European ME Alliance was accepted as a full member of the European Patients' Forum (European Patients' Forum), the leading umbrella organisation representing patients across Europe europeanmealliance.org/news-Q22025-00… #mecfs