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
Researchers in both fibromyalgia (FM) and chronic fatigue syndrome (ME/CFS) are doing deeper dives into the genetics of these illnesses than have ever been done before and they’re coming up with some surprises. Travis Craddock of the Institute for Neuroimmune...
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
Allyn Archer
Atlanta, United States
Former occupation: Architect, Professor of Architecture
$2,768,291
StudyME
Enroll in the OMF’s StudyME project and help bring about a cure for ME/CFS, fibromyalgia, POTS and long COVID.
