Open Medicine Foundation Canada
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Open Medicine Foundation Canada or OMF Canada is a registered charity founded to seek a cure and improve the lives of people with myalgic encephalomyelitis/chronic fatigue syndrome.[1][2]
Aims[edit | edit source]
"To create a world where people with chronic diseases like myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) live full, productive lives."
Services[edit | edit source]
Notable people[edit | edit source]
- Linda Tannenbaum - President, Founder and President of Open Medicine Foundation in the United States
- Kimberly Hicks - Treasurer/Secretary
- Lynn LaMothe - whose daughter has ME
- Nicholas Routhier
- Elizabeth Sanchez - whose daughter has severe ME[2]
Patrons[edit | edit source]
Scientific board[edit | edit source]
Research/Notable studies[edit | edit source]
History[edit | edit source]
Funding[edit | edit source]
Interviews and articles[edit | edit source]
Online presence[edit | edit source]
- Website
- Facebook page
- YouTube channel
- Address: Open Medicine Foundation Canada (OMF Canada), 2987 Baynes Road, Victoria BC V8N 1Y4 Canada
- Telephone: 416-848-0055
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ "Home". Open Medicine Foundation Canada. Retrieved September 1, 2019.
- ↑ 2.0 2.1 "INTRODUCING OPEN MEDICINE FOUNDATION CANADA". Open Medicine Foundation Canada. September 1, 2019. Retrieved September 1, 2019.
