You can Still Help Madeline!

“Madeline” is a woman who has been suffering with a post viral syndrome for 40 years which includes Severe Myalgic Encephalomyelitis (ME) and fibromyalgia. Madeline  lives in British Columbia, Canada and she urgently needs your help. There is a need to seek alternative medical treatments due to the lack of…

Continue ReadingYou can Still Help Madeline!

Join Action for M.E.’s online self-advocacy workshop

You are invited to join us for a Self-Advocacy workshop online via Zoom live on Friday 18th March 2022 12:30 pm-2:30 pm hosted by our team of Advocacy officers. The workshops will centre around 'Accessing social care in England'. We welcome people with M.E. or those affected by M.E., whether…

Continue ReadingJoin Action for M.E.’s online self-advocacy workshop

L’AQEM réagit à un article controversé sur l’encéphalomyélite myalgique dans la revue de la Fédération des Médecins Omnipraticiens du Québec (FMOQ)

L’AQEM a réagi à un article controversé sur le syndrome de fatigue chronique paru dans Le Médecin du Québec, revue officielle de la Fédération des médecins omnipraticiens du Québec... AQEM reacted to a controversial article on chronic fatigue syndrome published in Le Médecin du Québec, official journal of the Federation…

Continue ReadingL’AQEM réagit à un article controversé sur l’encéphalomyélite myalgique dans la revue de la Fédération des Médecins Omnipraticiens du Québec (FMOQ)

First World ME Day and theme launched by alliance members

The World ME Alliance, a collaborative of organisations from across the globe, is launching World ME Day on 12th May this year. This new initiative aims to bring together organisations and unify efforts to raise awareness and campaign together on Myalgic Encephalomyelitis (ME). Through collective action, we will step closer…

Continue ReadingFirst World ME Day and theme launched by alliance members

Un programme virtuel d’ergo thérapie pour aider les gens atteints d’encéphalomyélite myalgique

Après avoir accueilli deux groupes entièrement constitués de membres PAEM de l’AQEM durant leur phase pilote l'an dernier, le programme virtuel d’ergothérapie est de retour en 2022 de façon officielle... After welcoming two groups made up entirely of PAEM members of AQEM during their pilot phase last year, the virtual…

Continue ReadingUn programme virtuel d’ergo thérapie pour aider les gens atteints d’encéphalomyélite myalgique

#MEAction Continues to Get Press for ME

#MEAction continues to prioritize getting ME in the press. We are very thankful to be featured in USA Today, North Jersey, New York Times, Infection Control Today, Times-Herald and Well+Good, all in the last few weeks!  Our press reach continues to focus on multiple audiences, including scientists and medical practitioners,…

Continue Reading#MEAction Continues to Get Press for ME

Lessons from ME/CFS for long COVID: “Energy System First Aid” for people with PESE (aka PEM)

Lessons from Myalgic Encephalomyelitis/Chronic Fatigue Syndrome for Long COVID Part 3: “Energy System First Aid” for People With Post Exertional Symptom Exacerbation, by Todd E Davenport, Staci R Stevens, Jared Stevens, Christopher R Snell, J Mark Van Ness in JOSPT, February 16, 2022 [https://doi.org/10.2519/jospt.blog.20220216] Blog post extract: In a previous post,…

Continue ReadingLessons from ME/CFS for long COVID: “Energy System First Aid” for people with PESE (aka PEM)