Open Medicine Foundation: Difference between revisions
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The OMF's current project is the [[End ME/CFS Project]]. | The OMF's current project is the [[End ME/CFS Project]]. | ||
Many of those involved in OMF, including Executive Director [http://www. | Many of those involved in OMF, including Executive Director [http://www.omf.ngo/about-us/omf-board/ 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 [ | 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 [https://www.omf.ngo/community/ patient network] as developed through email [https://www.omf.ngo/newsletter-sign-up/ newsletter subscriptions]. | ||
== ME/CFS Scientific Advisory Board == | == ME/CFS Scientific Advisory Board == | ||
The advisory board is made up of world-renowned researchers:<ref>[ | The advisory board is made up of world-renowned researchers:<ref>[https://www.omf.ngo/scientific-advisory-board/ Open Medicine Foundation - Scientific Advisory Board]</ref> | ||
*Dr. [[Ronald Davis]] (Scientific Advisory Board Director, and father of [[Whitney Dafoe]]) | *Dr. [[Ronald Davis]] (Scientific Advisory Board Director, and father of [[Whitney Dafoe]]) | ||
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==Board== | ==Board== | ||
The OMF board comprises:<ref>[ | The OMF board comprises:<ref>[https://www.omf.ngo/about-us/omf-board/ OMF Board]</ref> | ||
*[[Linda Tannenbaum]] (Executive Director) | *[[Linda Tannenbaum]] (Executive Director) | ||
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== Online Presence == | == Online Presence == | ||
*[ | *[https://www.omf.ngo Website] | ||
*[https://www.facebook.com/OpenMedicineFoundation Facebook] | *[https://www.facebook.com/OpenMedicineFoundation Facebook] | ||
*[https://twitter.com/OpenMedF Twitter] | *[https://twitter.com/OpenMedF Twitter] | ||
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== Learn more == | == Learn more == | ||
*[ | *[https://www.omf.ngo/what-is-mecfs/ What is ME/CFS?] | ||
==See also== | ==See also== |
Revision as of 00:25, July 20, 2018
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]
- Dr. Ronald Davis (Scientific Advisory Board Director, and father of Whitney Dafoe)
- Paul Berg (cellular metabolism, Nobel laureate)
- Mario Capecchi (genetics, Nobel laureate)
- Mark Davis (immunology)
- Craig Heller (exercise physiology)
- Andreas Kogelnik (OMI founder)
- Robert Naviaux (virology & cell biology, mitochondrial specialist)
- Baldomero Olivera (neurobiology & pain)
- Ronald Tompkins (trauma & metabolism)
- James Watson (genetics, Nobel laureate)
- Wenzhong Xiao (computational genomics)
- David Bell (ME/CFS clinician. See Lyndonville outbreak)
- Maureen Hanson (cell and molecular biology)
- Øystein Fluge (oncology)
- Olav Mella (oncology)
Board[edit | edit source]
The OMF board comprises:[2]
- Linda Tannenbaum (Executive Director)
- Kimberley Hicks (Treasurer)
- Patti Linsley (Secretary)
- R.P. Channing (MD)
- Deborah Rose (MD)
- H. Kenneth Walker (MD)
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
Funding[edit | edit source]
OMF have fund-raised primarily from ME sufferers and community for the research. NIH have not stepped up to fund the research.
In January 2018 Pineapple fund, a bitcoin investor, donated $1 million to OMF. The anonymous donor was so touched by the outpouring of appreciation from the worldwide ME community that they increased the donation to $5 million.[3]
In May 2018, OMF received a new $1 million anonymous pledge to escalate Dr. Ronald Davis’s systems biology approach with Robert Phair.[4]
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.[5][6]
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
- Q&A on ME/CFS Research with Dr. Ron Davis (Mar 7)
- An Update on ME/CFS Research with Dr. Ronald W. Davis (Feb 21)
- Scientist Ron Davis Tells How We Are "Fast-Tracking" ME/CFS Research (Feb 3)
2016
- Getting Answers to ME/CFS Faster through Collaboration and Openness (Dec 13)
- Short Story of a Family's Struggle with ME/CFS (May 21)
Linda Tannenbaum
2016
- Episode 79 - Linda Tannenbaum (May 8)
Online Presence[edit | edit source]
Learn more[edit | edit source]
See also[edit | edit source]
References[edit | edit source]
- ↑ Open Medicine Foundation - Scientific Advisory Board
- ↑ OMF Board
- ↑ Pineapple Fund
- ↑ New 1 million donation for ME/CFS research
- ↑ Ryan Prior (Director); Nicole Castillo (Director); Anthony Komaroff; Hillary Johnson; Ron Davis (2015), Forgotten Plague (documentary film)
- ↑ #ME Action (December 2015), Forgotten Plague Screening Announcement, Palo Alto USA