Open Medicine Foundation

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OMF.png

The Open Medicine Foundation (OMF) is an American non-profit 501(c)(3) organization established in 2012 for the purpose of funding and initiating groundbreaking research into complex chronic diseases. It supports chronic complex 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 Founder/CEO/President 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 chronic complex diseases. The organization also has an extensive patient network as developed through email newsletter subscriptions.

Stuart Murdoch is Ambassador promoting the OMF's work "through videos and messaging on their social media and websites, personal appearances, and face-to-face interactions with their communities and fans."[1] Amy Carlson is an OMF Ambassador also raising awareness and fundraising. As is celebrated international author Karin Alvtegen and opera star Jacqueline Ko.

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

The advisory board is made up of world-renowned researchers:[2]

Board[edit | edit source]

The OMF board comprises:[3]

Research Projects[edit | edit source]

End ME/CFS Project[edit | edit source]

The End ME/CFS Project is the Open Medicine Foundation's main project, and has been running over a number of years. It aims to:

  • find a diagnostic tool for ME/CFS
  • deliver treatments for ME/CFS
  • ultimately find a cure for ME/CFS[4]

The project has run a number of different studies, including the ME/CFS Severely Ill, Big Data Study.

See also
End ME/CFS Project.

ME/CFS Severely Ill, Big Data Study[edit | edit source]

The ME/CFS Severely Ill, Big Data Study was announced in May, 2015. The most severely ill ME/CFS patients were being studied to find a diagnostic biomarker. The project is now complete.[5]

See also
ME/CFS Severely Ill, Big Data Study.
See also
A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Mestinon trial[edit | edit source]

A clinical trial of mestinon was announced in May 2020. Mestinon is an existing drug which may help with post-exertional malaise (PEM).[6] This will be a pilot treatment trial.

See also
Mestinon.

Kynurenine trial[edit | edit source]

A pilot treatment trial of kynurenine was announced in May 2020. Kynurenine is an amino acid naturally present in the body. This trial is linked to the metabolic trap hypothesis devised by Robert Phair after analysis of the data from the ME/CFS Severely Ill, Big Data Study.CFS[7][6]

See also
Kynurenine.
See also
Metabolic trap.

COVID-19 Study[edit | edit source]

This project was announced in May 2020, during the coronavirus pandemic and aims "to track patients with COVID-19 that have been discharged from the ICU, with the expectation that some will develop ME/CFS."

This will involve collecting biological samples from patients, "continuous health tracking" using wearables, and "symptom data collection" over the course of two years.[6]

See also
COVID-19 Study.
See also
Post-COVID-19 illness.

Other projects[edit | edit source]

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

Collaborative centers[edit | edit source]

Stanford University, United States[edit | edit source]

Led by Ron Davis, the Stanford University OMF collaborative center aims to produce a blood-based diagnostic test for ME/CFS.[8]

Harvard, United States[edit | edit source]

Established in 2018, the OMF's Harvard collaborative center involves Harvard University, and the Harvard-affiliated Brigham Women's Hospital (BWH), Massachusetts General Hospital (MGH) and Beth Israel Deaconess Medical Center (BIDMC).[9] It is led by Ronald Tompkins and Wenzhong Xiao.[9]

Uppsala University, Sweden[edit | edit source]

The OMF's Uppsala University collaborative center is led by Jonas Bergquist.[10]

Montréal, Canada[edit | edit source]

The CHU Sainte-Justine/Université de Montréal collaborative center was established in 2020, and is led by Alain Moreau.[11]

Notable research[edit | edit source]

Funding[edit | edit source]

OMF have fund-raised primarily from ME sufferers and community for the research. The National Institutes of Health have rejected almost all funding applications, except for partial refunding of the technology for creating a diagnostic biomarker in ME/CFS.[13][14][15]

In January 2018 Pineapple fund, a philanthropic project by an early bitcoin investor[16], donated $1 million to OMF.[17] The anonymous donor was so touched by the outpouring of appreciation from the worldwide ME community that they increased the donation to $5 million.[17]

In May 2018, OMF received a new $1 million anonymous pledge to escalate Dr. Ronald Davis’s systems biology approach with Robert Phair.[18]

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.[19][20]

Dr. Davis, along with colleagues, have written and signed open letters in reference to research funds and the PACE trial, and taken part in many Millions Missing protests.

Talks and interviews[edit | edit source]

Community Symposium

Ronald Davis

2019

2018

2017

2016

Ronald Tompkins

2019

Linda Tannenbaum

2019

2018

2017

2016

Christopher Armstrong

2019

Online presence[edit | edit source]

Learn more[edit | edit source]

See also[edit | edit source]

References[edit | edit source]

  1. ↑ "OMF Ambassador - Stuart Murdoch | Open Medicine Foundation". Open Medicine Foundation. Retrieved October 9, 2018.
  2. ↑ "Scientific Advisory Board | Open Medicine Foundation". Open Medicine Foundation. Retrieved October 9, 2018.
  3. ↑ "Foundation Board | Open Medicine Foundation". Open Medicine Foundation. Retrieved October 9, 2018.
  4. ↑ Open Medicine Foundation. "The End ME / CFS Project". Open Medicine Foundation. Retrieved May 1, 2020.
  5. ↑ Davis, R.W.; Wilhelmy, J.; Nemat-Gorgani, M.; Kashi, A.; Esfandyarpour, R. (April 25, 2019). "A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)". Proceedings of the National Academy of Sciences. 116 (21): 10250–10257. doi:10.1073/pnas.1901274116. ISSN 0027-8424. PMID 31036648.
  6. ↑ 6.0 6.1 6.2 Open Medicine Foundation. "#May Momentum 2020". Open Medicine Foundation. Retrieved May 1, 2020.
  7. ↑ Phair, Robert D.; Davis, Ronald W.; Kashi, Alex A. (2019). "The IDO Metabolic Trap Hypothesis for the Etiology of ME/CFS". Diagnostics. 9 (3): 82. doi:10.3390/diagnostics9030082.
  8. ↑ Open Medicine Foundation (December 7, 2017). "Collaborative Research Center at Stanford aims to produce blood-based diagnostic technology for ME / CFS". Open Medicine Foundation. Retrieved April 22, 2020.
  9. ↑ 9.0 9.1 Open Medicine Foundation. "The Harvard ME / CFS Collaboration at the Harvard Affiliated Hospitals". Open Medicine Foundation. Retrieved April 22, 2020.
  10. ↑ Open Medicine Foundation. "ME / CFS Collaborative Research Center at Uppsala University". Open Medicine Foundation. Retrieved April 22, 2020.
  11. ↑ Open Medicine Foundation. "University of Montreal Collaborative Research Center". Open Medicine Foundation. Retrieved April 22, 2020.
  12. ↑ Bynke, Annie; Julin, Per; Gottfries, Carl-Gerhard; Heidecke, Harald; Scheibenbogen, Carmen; Bergquist, Jonas (August 1, 2020). "Autoantibodies to beta-adrenergic and muscarinic cholinergic receptors in Myalgic Encephalomyelitis (ME) patients – A validation study in plasma and cerebrospinal fluid from two Swedish cohorts". Brain, Behavior, & Immunity - Health. 7: 100107. doi:10.1016/j.bbih.2020.100107. ISSN 2666-3546.
  13. ↑ Esfandyarpour, R.; Kashi, A.; Nemat-Gorgani, M.; Wilhelmy, J.; Davis, R.W. (May 21, 2019). "A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)". Proceedings of the National Academy of Sciences. 116 (21): 10250–10257. doi:10.1073/pnas.1901274116. ISSN 0027-8424.
  14. ↑ https://projectreporter.nih.gov/project_info_description.cfm?aid=9577948&icde=40034644
  15. ↑ Janet Dafoe [@janetdafoe] (April 22, 2020). "This is so disingenuous" (Tweet) – via Twitter.
  16. ↑ "Pineapple Fund". Retrieved June 23, 2019.
  17. ↑ 17.0 17.1 "Pineapple Fund increases donation to $5 million | Open Medicine Foundation". Open Medicine Foundation. February 2, 2018. Retrieved October 9, 2018.
  18. ↑ "New $1 million donation for ME/CFS research! | Open Medicine Foundation". Open Medicine Foundation. May 24, 2018. Retrieved October 9, 2018.
  19. ↑ Ryan Prior (Director); Nicole Castillo (Director); Anthony Komaroff; Hillary Johnson; Ron Davis (2015), Forgotten Plague (documentary film)
  20. ↑ #ME Action (December 2015), Forgotten Plague Screening Announcement, Palo Alto, CA, US
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