Can you see ME now?

Raise awareness about Myalgic Encephalomyelitis

Part of the ME/CFS week of action and awareness building – will be posting more on the fact that 600,000 Canadians live with this illness and the impact it has on our lives. With no training for Doctors and Nurses, $0 research funding for causes or cures, let alone treatment protocols from Health Canada, or even at local level, we are just some of the #MillionsMissing with ME/CFS.