Support Research, Support Patients A recent survey from our friends at Research!America found that over 80% of Americans believe our government should fund “basic scientific research that advances the frontiers... This post appeared first on Solve ME/CFS Initiative. Read More
In honor of Women’s History Month, #MEAction asked our community to share which woman or women have inspired them in their advocacy work. The responses are heartfelt, moving, and inspiring. We hope you enjoy reading them! "This Women's History Month, I like many others, will be thinking about the contribution…
The need for official data from the Centers for Disease Control (CDC) is crucial to the study of Long Covid, as well as the effort to fund the Long Covid... This post appeared first on Solve ME/CFS Initiative. Read More
Welcome to our second Facets of ME! This is an educational feature in which we choose one aspect of ME to dive into and explore more in-depth once a month. Our goal is to keep it understandable while still providing a great overview and links to even more detailed information. …
By Emily Taylor, Vice President of Advocacy and Community Engagement, Solve M.E. This essay was originally published as a blog for Cumberland Advisors Market Commentary “I just got a virus... This post appeared first on Solve ME/CFS Initiative. Read More
“THAT’S WHY THEY DON’T BELIEVE YOU, YOU DON’T LOOK SICK!”: FICTIONAL REPRESENTATIONS OF ME/CFS by Giada Da Ros Sociologists emphasize the importance of social and cultural representation of social and cultural representation of chronic and emerging disease, both for individual and collective behavior. “(T)he fact that people are able to…
The following speech was delivered by Solve M.E. Board Member and person with Long Covid, Cynthia Adinig, during a Covid-19 memorial event hosted by Rami’s Heart Memorial and COVID-19 Hope... This post appeared first on Solve ME/CFS Initiative. Read More
As our team at Solve M.E. continues to make breakthroughs possible in research into ME/CFS, Long Covid, and other post-infection diseases, we also stand firm in our commitment to ensuring... This post appeared first on Solve ME/CFS Initiative. Read More
The National Institutes of Health (NIH) recently published a long-expected request for applications (RFA) for the Collaborative Research Centers (CRCs) for ME/CFS, announcing that the funding levels for the centers... This post appeared first on Solve ME/CFS Initiative. Read More
“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…