ME|FM Society of BC Director, Sophie Harrison, advocates for those with Long COVID. Watch her March 2025 interview on CTV News as she discusses her experiences with this disease, its connection to Myalgic Encephalomyelitis and the lack of adequate knowledge and care.
The ME|FM Society is revamping the My MLA & ME program for the new Legislative session – and you’re invited to be a part of it . People with myalgic encephalomyelitis know too well what it is to live with a misunderstood disease. From gaslighting to lack of awareness, we are practiced at advocating for ourselves in medical settings. But what does it look like to bring those advocacy skills to the political realm? Since 2020, the Society has run its My MLA & ME campaign, supp
