Here’s a hearty hello from the Medieval Town of Medical Education! Lords and Ladies, We did it!… we got over $75,000 (£56,781) which means we have arrived at this new land on our Giving Adventure Map. I’m Laurie Jones, the Managering Elf, and I am going to tell you what…
Two NICE ME/CFS guideline committee members joined #MEAction for a community call, to provide their insight into the guideline process and answer questions. Adam Lowe is a person with ME and has been supporter of various ME organisations, including #MEAction UK and Science for ME. He was one of five…
Being part of an association like AQEM is much more than filling out a membership form and supporting a cause ... We emphasize the sending of greeting cards between members! Find out more... This post first appeared on AQEM. Read More
Incredible news! Thanks to the generosity of a first-time donor, we are so thrilled to announce a new matching challenge. This donor has a passion for our Solve M.E. research... The post New Matching Challenge: Triple Your Donation! appeared first on Solve ME/CFS Initiative. Read More
In advance of next week’s CDC ME/CFS Stakeholder Engagement and Communication (SEC) call, #MEAction has sent a letter to Chronic Viral Diseases Branch Chief Dr. Elizabeth Unger requesting her to clearly and directly address our four key objections to publishing a flawed evidence review of ME/CFS treatments that CDC commissioned.…
On November 12th, just a few days after our launch of the Dear Doctor Campaign, @NICEGetInvolved retweeted our campaign and shared their thanks in our work to educate the medical establishment about the new guideline. This is cause for celebration! This is the start of a real change that has…
Over 1,700 people have now voted for their top ten ME/CFS research priorities in the UK. With the deadline fast approaching this is your last chance to join them and vote. Deadline Monday 13th December 5pm Vote now This process gives greater voice to people affected by ME/CFS to decide…
December 09, 2021 The M.E./CFS Priority Setting Partnership (PSP) is giving you the opportunity to define your top ten priorities for future M.E./CFS research. Over 1,700 people have now voted for their… This post first appeared on Action for M.E. Read more >>
In survey, 19% of people with ME/CFS said health worsened after vaccination compared to 4% reported by controls. A recent survey conducted by our You + ME Registry found that the health... This post appeared first on Solve ME/CFS Initiative. Read More
In the spirit of giving and giving back this holiday season, we’re excited to launch our #MEAction 2022 Board of Directors Recruitment Campaign! If you are curious about Board Service or want to use your skills to help a growing nonprofit or know someone who would be a great Board…