InsideSources – The Monster Disease Medical Schools Don’t Mention
Author: Llewellyn King For 10 long years, I’ve been writing and broadcasting about Chronic Fatigue Syndrome, now called Myalgic Encephalomyelitis (ME). Like all chronic
TRIPLE YOUR IMPACT during Triple Giving November | All Donations to OMF are TRIPLED through December 2
Author: Llewellyn King For 10 long years, I’ve been writing and broadcasting about Chronic Fatigue Syndrome, now called Myalgic Encephalomyelitis (ME). Like all chronic
Dans ce #OMFScienceWednesday, nous voulons vous présenter l’un des chercheurs les plus talentueux et les plus dévoués, dont le travail est financé par OMF grâce
On this #OMFScienceWednesday we want to thank one of our Community Symposium sponsors ProHealth.com. ProHealth is a steadfast supporter of OMF’s mission and research. Thank you to founder Rich Carson for
Author: Anthea Rowan Twenty million people suffer from myalgic encephalomyelitis, yet there is still no test for it, nor any approved treatment. We talk to
Dear Friends – We’d like to alert you to an exciting opportunity to help win funding for OMF’s research to end ME/CFS: Chiara Ferragni, a fashion
On this #OMFScienceWednesday we want to introduce you to one of the extremely talented, dedicated researchers whose work OMF funds thanks to your generous support.
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