TRIPLE GIVING TUESDAY OMF CANADA LAUNCHES

Every donation today through December 3 will be tripled! Today is the first day of Triple Giving Tuesday fundraising campaign, and I’m excited to announce that we have secured matching gifts up to $200 000 through the generosity of several supporters. Thanks to these individuals, when you donate to OMFCA any day of the week today […]

University of Victoria Hosts Educational Seminar on ME/CFS

We’d like to say a special thanks today to Lauren Grubisich for helping to raise awareness of ME/CFS in Canada! Lauren is a Director at Large of The University of Victoria Society for Students with a Disability which recently partnered with the ME|FM Society of BC and The UVic Equity and Human Rights Office to […]

Opera Singer Jacqueline Ko Becomes OMF Canada Ambassador

Join us to welcome Jacqueline and help raise awareness. We are excited to welcome Canadian opera singer, producer and disability advocate Jacqueline Ko as our new OMF Canada Ambassador! Despite her struggle with ME/CFS, which left her bedbound for years, Jacqueline has received multiple awards for her singing, and critical acclaim for her roles in […]

Individual Community Symposium Talks Now Available on OMF YouTube Channel

The individual talks from the OMF-sponsored Third Annual Community Symposium on the Molecular Basis of ME/CFS at Stanford University are now available as individual talks in a full playlist on OMF’s YouTube channel. Check out the speakers you are interested in hearing from, the panel discussions where they answer questions from our worldwide audience, or watch the […]

Linda Tannenbaum & Llewellyn King Interviewed on Joe Madison

OMF CA Founder & President Linda Tannenbaum and activist, reporter, and OMF CA friend Llewellyn King were interviewed on Joe Madison – “The Black Eagle” SiriusXM talk show on Urban View Channel 126! Watch it now:  https://www.youtube.com/watch?v=C20MwiYfSGg  In the interview, Linda and Llewellyn discuss the devastating impact of ME/CFS and the urgent need for increased […]

An Exciting Week for Advancing ME/CFS Research  

I’m pleased to share with the OMF Canada community that the OMF-sponsored Stanford ME/CFS Working Group and Third Annual Community Symposium on the Molecular Basis of ME/CFS once again is helping to advance urgently needed research on this disease. During the three days prior to the Community Symposium, 60 scientists from all over the world, […]

NEW GUIDELINES FOR DIAGNOSING AND TREATING ME/CFS

A resource for clinicians and patients. The U.S. ME/CFS Clinician Coalition, a group of U.S. ME/CFS experts, has authored a handout on the basics of diagnosis and management of ME/CFS. This handout is being made available on our website for the medical community to help them better understand how to recognize ME/CFS and how to […]

INTRODUCING OPEN MEDICINE FOUNDATION CANADA

WE ARE HERE. Open Medicine Foundation is growing our efforts to bring desperately needed resources and world-class research to the fight against ME/CFS! Please join us as we expand our outreach, advocacy and fundraising across Canada in support of groundbreaking research to end ME/CFS and related chronic complex diseases. Open Medicine Foundation Canada (OMF Canada) […]

Canada invests $1.4M in Biomedical Research

Government of Canada invests $1.4M in biomedical research to improve the quality of life of people living with myalgic encephalomyelitis From: Canadian Institutes of Health Research News release August 22, 2019 – Montréal, Québec – Canadian Institutes of Health Research It is estimated that more than 580,000 Canadians live with myalgic encephalomyelitis (ME), formerly known as […]