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.
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...
“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...
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:...
The #MEAction post (retitled after I calmed down to “#MEAction’s Support Needed On Bill to Increase NIH Funding”), has stirred up a lot. Boy, did it stir up a lot. It was understandable; the post was, after all, composed in quite a state of heat. I...
Health Rising readers have gotten quite a few blogs on the effort to get Congress to dramatically increase NIH funding for ME/CFS (HR 7057) – and here’s one more. As so often happens, something has unexpectedly come up – and time is short. Congress...
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