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@heogaycanh: Tồi thì làm đéo gì có khái niệm tiếc, luỵ cho đúng kịch bản thôi🔒🩶#ex150 #ex150độkiểng #tamtrang #xh #2001
Fb : Liên Chuppy ✈️🇻🇳🐷
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Ya Nabii 😭🤍 #mimifam #foryou
ME/CFS gets about $13 million a year in federal research funding. For the whole country. Multiple sclerosis, which disables fewer people, gets over $108 million. One peer-reviewed analysis ranked ME/CFS as the most underfunded disease relative to its burden in NIH’s own numbers, at roughly 7% of what that burden would call for. And it’s not just me saying it. A federal report back in 2015 called the funding “remarkably little… given the number of people affected.” To be fair, how you weigh burden against funding depends on which estimates you use, and that per-patient number (about $5 a patient vs $255 for MS) is from 2014. But the underfunding itself really isn’t debated. Whether you call it a moral failure or just neglect, that part is my opinion, not a citation. Not a doctor, and this isn’t medical advice. Sources: NIH RCDC categorical spending, FY2024 Mirin, Dimmock & Jason. Work, 2020. PMID 32568148 Dimmock, Mirin & Jason. J Med Therap, 2016. DOI 10.15761/JMT.1000102 Institute of Medicine, Beyond ME/CFS, 2015. PMID 25668027 NCHS Data Brief 488, 2023 #mecfs #chronicfatigue #myalgicencephalomyelitis #longcovid
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