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This magazine collects helpful resources. Please visit mecfs at the following links:...
This magazine collects helpful resources. Please visit mecfs at the following links:...
Link to DePaul questionnaire on ResearchGate
We often hear from people with ME seeking our support because they have to see a physiotherapist for a problem other than ME. This could be something like a shoulder injury, or following knee surgery, or neck pain etc....
This is the new Mayo Clinic Proceedings on ME/CFS...
National and local support agencies and groups for people with ME/CFS in New Zealand.
Please note this is a pdf
Carruthers BM, van de Sande MI, De Meirleir KL, Klimas NG, Broderick G, Mitchell T, Staines D, Powles ACP, Speight N, Vallings R, Bateman L, Baumgarten-Austrheim B, Bell DS, Carlo-Stella N, Chia J, Darragh A, Jo D, Lewis D, Light AR, Marshall-Gradisbik ...
The American ME and CFS Society is dedicated to serving the needs of patients and caregivers through support, advocacy, and education. We seek to channel patient perspectives to government agencies, committees and initiatives, and to unify the ME and CFS community by pursuing the common goals of expanding research, increasing...
European ME Alliance
ME/FM Action Network is a Canadian, registered, non-profit organization dedicated to advancing the recognition and understanding of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Syndrome (FMS) through education, advocacy, support, and research. Copyright 2020 National ME/FM Action Network
Associated New Zealand ME Society (ANZMES), serving New Zealanders with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome since 1980. ANZMES objects in the constitution are:...
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Abstract (link goes to full text)...
Abstract (link goes to full text)...
CDC's ME/CFS Resources - toolkit and resources on page
ME/CFS resources for researchers and patients.