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Setting Summer Boundaries: Navigating Social Expectations with Chronic Illness
Summer's social calendar can feel like a minefield when you're managing chronic illness. Just as you've figured out how to keep your body cool, you're faced with a different kind of heat: social pressure. Family barbecues, outdoor weddings, patio dinners, and weekend festivals all come with the unspoken expectation that summer equals participation. But for people with ME/CFS, Fibromyalgia, or Long COVID, summer social events can trigger serious symptom flares that last for da

ME|FM Society of BC
Aug 6, 20255 min read
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Summer Pacing: Conserving Energy for What Matters Most
Energy conservation isn't just helpful during summer with chronic illness - it's essential. When you're living with ME/CFS, Fibromyalgia, or Long COVID, heat doesn't just make you uncomfortable; it fundamentally changes how much energy you have available for everything else. Introducing Our "Navigating Summer" Toolkit Today marks a significant milestone - the official launch of our comprehensive "Navigating Summer" toolkit. This 42-page resource represents a community minded

ME|FM Society of BC
Jul 16, 20252 min read
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