The National ME/FM Action Network has been informing Canadians about ME and/or FM since 1993. Among our accomplishments, we spearheaded the development of diagnostic and treatment protocols for ME and FM, published statistics on ME and FM, wrote a guide on applying for disability and another on educational issues, published a quarterly newsletter, translated key documents into French, brought an international research conference to Canada, supported the development of the Complex Chronic Diseases Program in BC and supported the development of the ICanCME Research Network.
Advocating for treatment access, appropriate medical care and equitable research funding for ME (Myalgic Encephalomyelitis) in Canada
web: www.millionsmissingcanada.ca/
email: MillionsMissingCanada@
| Jeffery Smith | jefferysmithdesign@gmail.com | |
| Scott Simpson | scott77.simpson@gmail.com | |
| Barbara Fifield | brfifield@rogers.com | |
Action CIND is a registered charity and non-profit organization with a vision to advance the recognition, empathy, treatment and support services for Chronic Immunological and Neurological Diseases (CIND) by raising awareness, advancing research, developing education, providing information and support services and collaborating with other organizations in Canada and internationally.
The ME|FM Society of BC is a Canadian charity run by patients, carers and their families, formed to support British Columbians living with Myalgic Encephalomyelitis (ME) and/or Fibromyalgia (FM) through awareness raising, information sharing, education, advocacy, patient oriented research and phone/online support.
Monthly support meetings Sept-June
Events: May 12, Educational workshops
web: https://www.facebook.com/mbmecfs
email: mbmecfs@gmail.com
contact:
| Nicole Choptain | nicolewpg@shaw.ca |
| Bev Friesen | bevfriesen6@mymts.net |
