Triple Giving Tuesday starts today: Announcing our sixth Research Center! From the desk of Linda Tannenbaum Chief Executive Officer, Open Medicine Foundation Open Medicine Foundation (OMF) is pleased to share, on the first day of our Triple Giving Tuesday campaign,
New research publication authored by Team OMF! Breaking news! A new research publication authored by Dr. Ronald Davis, Dr. Wenzhong Xiao, OMF’s CEO & Founder, Linda Tannenbaum, and colleagues has been published in MDPI: “A Comprehensive Examination of Severely Ill
New novel features main character with ME/CFS! Spotlight on author Jean Meltzer, person with ME Author Jean Meltzer has the distinction of being an Emmy-award winning writer who is living with chronic illness and disability. Through her unique experiences, Jean
Calling all artists! Submit your art for a chance to become OMF’s Featured Artist during #TripleGivingTuesday! Are you an artist affected by chronic illness? Submit your artwork for a chance to become OMF’s Featured Artist for this year’s annual Triple
People with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) are urging the National Institute for Health and Care Excellence (NICE) to publish finalized guidelines for ME/CFS that ensure accurate diagnosis, appropriate symptom management, and access to the best support available. However,
Updated clinical guidance for myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS), produced by the US ME/CFS Clinician Coalition, may also help patients who remain ill with Long COVID after even mild cases of COVID-19. An article about the update has been
Join us for a webinar and listening session September 2 to learn more! Together with six other organizations, we have submitted a proposal to the National Center for Health Statistics (NCHS) to add myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) to the
“Reproduced by kind permission of Sean O’ Neill, The Times, News Licensing” Jennie Jacques on living with ME: ‘I am a shadow of my former self physically’ The Vikings actress’ career was thriving until she developed the debilitating condition, one
The story of OMF supporter Martin Den Hollander, a musician living with severe ME/CFS. Despite his health battle, he continues to use his music as a force to help those living with ME/CFS.
The View for ME Project August 2021 In recognition of Severe ME Awareness Day on August 8, 2021, Open Medicine Foundation (OMF) is taking this month to share stories from people living with severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) to
OMF Ambassador Jacqueline Ko celebrates her birthday with a fundraiser for research: Donate before August 1 for the chance to have your gift tripled! In celebration of her 30th birthday, multi-award-winning opera singer and OMF Ambassador Jacqueline Ko, kicked off
OMF is inspired and moved by the creativity and resilience of our community. Throughout 2021, Kristine Oma, dancer, choreographer, and person with ME/CFS, has been creating digital dance performances to benefit ME/CFS research.
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