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From Advocacy to Action
The information below was initially distributed on October 10, 2025. Today is a significant day. After months of work and 1,045 of you courageously sharing your experiences, we're releasing the BC ME/CFS, Fibromyalgia, Lyme & Long COVID Survey results. The numbers are both shocking and deeply validating. You Are Not Alone. You Are Not Imagining This. 93% of you had negative healthcare experiences. Read that again. This isn't a few "difficult" patients. This isn't an isolate

ME|FM Society of BC
Mar 23 min read


When crisis becomes opportunity
The information below was initially distributed on August 14, 2025. Recent MSP billing compliance changes are set to disrupt care for thousands of patients with ME/CFS, Fibromyalgia, and Long COVID—many of whom were already struggling in a broken healthcare system. With no transition plan in place, approximately 5,000 people face immediate loss of the limited care they had. For a community where 98.5% already have no access to specialized care, this isn't just a service disru

ME|FM Society of BC
Mar 24 min read


Transforming Healthcare for ME, Long-COVID, and Fibromyalgia
Professional Education & Clinical Practice Tools Policy Brief - Community Edition

ME|FM Society of BC
Jan 163 min read
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