All-Hands-On-Deck Time To Double ME/CFS Funding at the NIH
Please note this is an action for U.S. residents. HR 7057: The Understanding COVID-19 Subset and ME/CFS Act HR 7057 is the ME/CFS community’s first ever attempt to fulfill a dream: a House Congressional bill that begins to address the decades of neglect from the...
The Solve ME/CFS Initiative Goes All In on First Ever Patient Registry for ME/CFS
The Fixer Often when I communicate with the Solve ME/CFS Initiative (SMCI), I end up with Allison. She seems to have her fingers in everything. She seemed to know the nuts and bolts of just about everything. I knew that Sadie Whittaker, the SMCI’s Chief...
Genetic Study Finds Mitochondrial Link to Fibromyalgia
A surprise finding suggests that a small alteration in their mitochondrial DNA may greatly increase some women's risk of getting fibromyalgia.
An Open Letter to the COVID-19 Long Hauler Community From a Person with ME/CFS
“If you look anecdotally, there is no question that there are a considerable number of individuals who have a post-viral syndrome that in many respects incapacitates them for weeks and weeks following so-called recovery. They report symptoms such as brain fog,...Lives Interrupted Latest Story
Megan
Randolph, United States
Former occupation: Day care worker
$562,824
StudyME
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