From $1.15 Billion in Long COVID Funding to ? Emily Taylor on What Happened and What’s Next for ME/CFS
The Long COVID Funding The 2020 COVID-19 Economic Relief bill had been months and months in the making, and while Emily Taylor, the lead advocate for the Solve ME/CFS Initiative (Solve M.E.), had publicly shared nothing, she was keeping a very close eye on the long...
Large Long COVID Study and Major Media Articles Underscore Link to ME/CFS – Plus Countdown for the NIH
Just as a billion dollars plus in funding came available for long COVID research, a large research study closely linked the symptoms found in the disease with those found in chronic fatigue syndrome. Several major media article also linked the two.
Congress Approves Over a Billion Dollars to Study Long-COVID: Implications for ME/CFS
Emily Taylor of Solve ME/CFS Initiative reported that Congress has approved $1.15 billion (yes that’s a billion with a “B”) for the NIH to fund long-COVID research and clinical trials. $100 million will specifically be used for the rapid acceleration...
GET This! NICE Pulls the Plug on Graded Exercise Therapy and CBT as Treatments for ME/CFS
“There is no therapy based on physical activity or exercise that is effective as a treatment or cure for ME/CFS”. NICE Who would have thought? We knew that National Institute for Health and Care Excellence (NICE) – the executive branch in the U. responsible for...
HR 7057 – Historic Effort to Increase Funding for ME/CFS Gains Steam
H.R. 7057 – The Understanding COVID-19 Subsets and ME/CFS Act is back. There’s a reason this is taking so long. It’s the same reason that it’s taken 4 years of work to get to this point. This is not just an attempt to get more money for ME/CFS:...StudyME
Enroll in the OMF’s StudyME project and help bring about a cure for ME/CFS, fibromyalgia, POTS and long COVID.
