Open Medicine Foundation: Difference between revisions

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
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(added names to board)
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*[[Wenzhong Xiao]] (computational genomics)
*[[Wenzhong Xiao]] (computational genomics)
*[[David Bell]] (ME/CFS clinician. See [[1985 Lyndonville outbreak|Lyndonville outbreak]])
*[[David Bell]] (ME/CFS clinician. See [[1985 Lyndonville outbreak|Lyndonville outbreak]])
*[[Maureen Hanson]] (cell and molecular biology)
*[[Øystein Fluge]] (oncology)
*[[Olav Mella]] (oncology)


==Board==
==Board==

Revision as of 18:14, May 25, 2017

OMF.png

The Open Medicine Foundation (OMF) is an American non-profit 501(c)(3) organization established in 2012. It funds and initiates groundbreaking research into complex chronic illnesses. It supports neuro-immune disease research with a focus on Chronic Fatigue Syndrome (CFS), Myalgic Encephalomyelitis (ME), Fibromyalgia (FMS), and Chronic Lyme Disease.

The OMF's current project is the End ME/CFS Project.

Many of those involved in OMF, including Executive Director Linda Tannenbaum, either have a neuro-immune disease or have a family member who has a neuro-immune disease.

OMF's strategy is to include highly recognized and accomplished scientists with expertise in body systems linked to neuro-immune diseases. The organization also has an extensive patient network as developed through email newsletter subscriptions.

ME/CFS Scientific Advisory Board[edit | edit source]

The advisory board is made up of world-renowned researchers:[1]


Board[edit | edit source]

The OMF board comprises:[2]

Research Projects[edit | edit source]

The ME/CFS Severely Ill, Big Data Study was announced in May, 2015. The most severely ill ME/CFS patients are being studied to find a diagnostic bio-marker.

In 2016, "Mitochondria Man Gets Money UK Goes Mega Chronic Fatigue Syndrome Research Moves Forward"

Notable research[edit | edit source]

2016, Metabolic features of chronic fatigue syndrome

Advocacy[edit | edit source]

The OMF and the Davis-Dafoe Family held two screenings of Forgotten Plague. Dr. Davis spoke about ME/CFS and research after the screening.[3][4]

Dr. Davis, along with colleagues, have written Open letters in reference to research funds and the PACE trial.

Talks and interviews[edit | edit source]

Ronald Davis

2017

2016

Linda Tannenbaum

2016

Online Presence[edit | edit source]

Learn more[edit | edit source]

See also[edit | edit source]

References[edit | edit source]

  1. Open Medicine Foundation - Scientific Advisory Board
  2. OMF Board
  3. Ryan Prior (Director); Nicole Castillo (Director); Anthony Komaroff; Hillary Johnson; Ron Davis (2015), Forgotten Plague (documentary film)
  4. #ME Action (December 2015), Forgotten Plague Screening Announcement, Palo Alto USA