ME/CFS scores as a large study cements the link between it and long COVID just after over a billion dollars is slated to go for long COVID research “The findings show that—even in those people who don’t require hospitalization for severe COVID-19—the...
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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