Our Board in Action
- ME|FM Society of BC
- Mar 14
- 1 min read
Five years ago today, the world faced the unprecedented upheaval of the COVID-19 pandemic.
We’re honoured to spotlight our board member, Sophie Harrison, who bravely shared her long COVID journey on CTV’s Morning Show. With 88,000+ British Columbians now living with long COVID — many at risk of developing myalgic encephalomyelitis (ME/CFS)** — Sophie’s story is a rallying cry for urgent action.
From gaps in healthcare to the staggering overlap of these debilitating conditions, her advocacy underscores what’s at stake: lives, dignity, and hope.
If you’re battling long COVID, ME/CFS, or fibromyalgia (FM), you’re not alone. 💙 Join our community for support, resources, and collective strength.
To policymakers: It’s time to prioritize care, research, and equity for ALL invisible illnesses.**
(Stat: BC Health, 2024 | ME/CFS risk based on global studies of long COVID progression)
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