Sick, exhausted and need support?
Practical help, up-to date information, and friendly community for those living with Long-COVID, ME (myalgic encephalomyelitis), and other post-viral, chronic fatigue and autonomic dysfunction illnesses.
Sign up for our "Living with ME/Long-COVID" series
Get a series of friendly, easy-to-use info sheets, tips, tools and up-to date information developed by experts, patients and caregivers straight to your inbox.
Living with ME/Long-COVID: Tips, tools and information
• Understand your symptoms
• Know your options
• Sift through misinformation
• Practical health and living tips
• Tools to manage your illness
• Help for diagnosis
• Feel understood and supported
• Help talking to doctors, family & friends
Christina Wiebe
"This series is full of tools and information I wish I’d had when I first got sick. I know I would have felt less isolated and may not have gotten as sick as I did. And clear and easy for my foggy brain to absorb."
Our "Living with ME/Long-COVID" series delivers
Illness management tools and assistance
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The most current care and health management tools and options.
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Practical support and friendly community
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Overcome feelings of isolation. Share ideas and experiences. Learn about our online support groups.
Fact-based, current and useful information
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Stay up-to-date and let us and our expert advisors help you sift through misinformation.
PRACTICAL
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Practical tools and information, sent with heartwarming stories, useful tips, and other content from our community.
COMMUNITY
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Compiled with care and insight by friends and experts who know what it’s like to live with these symptoms.
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HOPEFUL
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Symptom management, coping strategies, connection to others, and hope for an improved quality of life.
The ME|FM Society of BC is a not-for-profit organization providing free information and research, support groups, news, tools for better living, and events by and for people with ME (Myalgic Encephalomyelitis), Fibromyalgia (FM), Long-COVID and their comorbidities.