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The OMF was founded in 2012 by Linda
Tannenbaum after her daughter became ill with ME/CFS in 2006. Tannenbaum has said, "For a long time, the medical world didn’t feel ME/CFS was a real disease," and advocates for increased federal research funding.
156:-based blood test for ME/CFS, studies on the density and deformability of blood cells compared to healthy controls, work on mitochondrial function, and investigation of potential altered metabolism in people with ME/CFS. One project involved a
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Along with the
Bateman Horne Center, the OMF maintains the Medical Education Resource Center, a website to educate doctors on diagnosis and treatment of complex chronic illnesses. OMF maintains a
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Research has included investigations into T-cells and immunological genes, analyses of muscle and other tissues, a study on families of patients, an attempt to develop a
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of 20 severe ME/CFS patients. Plans to fund multicenter trials of treatments have also been announced.
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235:""Our Next National Health Disaster." Boosting Research into Long COVID and Chronic Fatigue"
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The OMF provides funding for seven collaborative research centers, including one center at
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384:"Open Medicine Foundation Commits $ 1.8M to Research ME/CFS at Harvard Hospitals"
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270:"Anonymous Bitcoin Philanthropist Donates $ 5 Million to Medicine Foundation"
296:"'Unrest' Film Sheds Light on Misunderstood Disease Impacting Local Lives"
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93:(OMF) is a US-based charity that funds research into the illnesses
167:(StudyME) to help researcher find participants for their studies.
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In 2018, the OMF received a donation of $ 5 million in
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Linda
Tannenbaum is CEO and president, while geneticist
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Medical and health organizations based in
California
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617:Myalgic encephalomyelitis/chronic fatigue syndrome
484:Myalgic encephalomyelitis/chronic fatigue syndrome
95:myalgic encephalomyelitis/chronic fatigue syndrome
346:"A reboot for chronic fatigue syndrome research"
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627:Scientific organizations established in 2012
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321:"Read about the Ongoing Science at OMF"
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622:Health charities in the United States
179:heads the scientific advisory board.
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319:Simon-Gersuk, Marilyn (2018-05-31).
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199:"Open Medicine Foundation Press Kit"
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103:post-treatment Lyme disease syndrome
432:Archibald, Timothy (16 May 2016).
294:Matthiessen, Connie (2017-10-12).
125:from the anonymous founder of the
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268:Kelly, Jemima (2 February 2018).
16:American nonprofit organization
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596:Whittemore Peterson Institute
39:; 12 years ago
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370:10.1038/d41586-017-08965-0
344:Maxmen, Amy (2018-01-03).
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586:Open Medicine Foundation
413:Open Medicine Foundation
206:Open Medicine Foundation
91:Open Medicine Foundation
56:Agoura Hills, California
20:Open Medicine Foundation
591:Solve ME/CFS Initiative
508:Post-exertional malaise
147:University of Montreal
498:Clinical descriptions
158:whole-genome mapping
538:Society and history
434:"The puzzle solver"
362:2018Natur.553...14M
239:Inside Philanthropy
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438:Stanford Medicine
325:#MEAction Network
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555:Notable patients
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241:. 25 August 2022
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208:. 6 July 2021
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390:. 2018-05-23
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99:fibromyalgia
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52:Headquarters
279:7 September
212:7 September
637:Long COVID
611:Categories
513:2-day CPET
443:2022-09-08
418:2024-01-27
394:2022-09-08
330:2022-09-08
305:2022-09-08
245:2022-09-08
183:References
171:Leadership
154:nanoneedle
133:Activities
107:long COVID
97:(ME/CFS),
503:Treatment
409:"StudyME"
388:Genomeweb
274:U.S. News
177:Ron Davis
141:, one at
63:President
34:Formation
529:DecodeME
522:Research
139:Stanford
545:History
358:Bibcode
143:Harvard
123:Bitcoin
113:History
72:Website
42: (
350:Nature
105:, and
202:(PDF)
281:2022
214:2021
89:The
81:.ngo
79:.omf
44:2012
37:2012
366:doi
354:553
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