Introducing OMF’s Social Shareables Web Portal! New tool to help educate your personal communities As part of #TripleGivingTuesday, we are pleased to announce that we have developed a new tool to help you educate your personal communities about ME/CFS and
#TripleGivingTuesday Research Feature New OMF funded study: Deep proteome and metabolome profiling From the desk of Alain Moreau, PhD Director of the ME/CFS Collaborative Research Center at CHU Sainte-Justine/Université de Montréal During this first week of #TripleGivingTuesday, I am honored
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
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