We support patients and families

living with ME and FM

Our society works to help ME and FM patients in British Columbia improve their health and quality of life by providing information about these illnesses, and guidance on how to seek and obtain support, appropriate medical help and treatments. We also focus on informing health care professionals, educators and students about ME and FM, as well as raising awareness among, and seeking the support of, government and the general public. 

*Myalgic Encephalomyelitis is also referred to as ME/CFS, Chronic Fatigue Syndrome or SEID

The ME|FM Society of BC is a charity, run by patients, carers and their families, formed to help and support patients with Myalgic  Encephalomyelitis * (ME) and/or  Fibromyalgia  (FM). 

COVID-19 (Coronavirus disease)
Canadian, BC and other resources
Myalgic Encephalomyelitis


Myalgic Encephalomyelitis is complex, chronic neuroinflammatory illness, which impacts systems throughout the body.

Learn more



Fibromyalgia (FM) is a chronic, complex illness characterised by widespread musculoskelatal pain accompanied by fatigue, sleep, memory and other issues.

Learn more


Join our society as a member and/or volunteer with one of our active teams.

Learn more

Looking for an ME or FM friendly doctor? 

Can you recommend a doctor or health care professional?

Read more about our newly launched website:  HealthFinder4ME

We had a great 2019 AGM followed by an excellent presentation by Dr. Nacul, Medical Director, BC Women's Hospital Complex Chronic Diseases Program : 
Has ME/CFS research helped clinicians and patients?
Can we do better?

Meet the Medical Director of the CCDP

Read our 2-part interview with Dr. Luis Nacul, Medical Director of BC Women's Hospital Complex Chronic Diseases Program (CCDP), by ME patient and former ER nurse, Howard Searle.

Part 1

Part 2



After much planning and testing by our support groups teams, we have officially launched our online support forum, where you can share thoughts, ideas, concerns, ask questions, or receive better information and support regarding your experiences with ME/CFS and/or FM. Find the forum under the SUPPORT tab or click below:

From our volunteer forum
Join the Discussion
The category is members only, sign up to join in

Jennifer Brea is about to marry the love of her life when she’s struck down by a fever that leaves her bedridden. When doctors tell her “it’s all in her head,” she turns her camera on herself and her community as she looks for answers and fights for a cure.

"riveting......equal parts medical mystery, science lesson, political advocacy primer and even a love story."

                         The San Francisco Chronicle

   Jennifer Brea's award winning feature documentary

"Unrest" available on

Also available on iTunes, Vimeo and Google Play

What happens when you have a disease doctor's can't diagnose​

Jennifer Brea is a US-based speaker, activist and co-founder of #MEACTION and Sundance award-winning filmmaker of "UNREST". She also has ME. 

"In this poignant talk, Brea describes the obstacles she's encountered in seeking treatment for her condition, whose root causes and physical effects we don't fully understand, as well as her mission to document through film the lives of patients that medicine struggles to treat." [YouTube]

Featured News and Events

Mailing Address

PO BOX 46879 STN D

Vancouver, BC   V6J 5M4


T: 604-878-7707 or
BC Toll-free: 1-888-353-6322

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