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"Living with ME/Long-COVID"
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What others are saying about this series
"I feel like this series is a life-line for people with ME or Long-COVID who are faced with healthcare and social support systems that provide so little access to knowledgeable help and meaningful support.
It’s making valuable information and tools available to us from within the safety of our own homes, empowering us to learn how to cope with and manage living with these chronic illnesses.
If I’d had access to this information when I first got sick, I would’ve felt less lost and more supported."
Our "Living with ME/Long-COVID" series delivers
Illness management tools and assistance
The most current care and health management tools and options.
Practical support and friendly community
Overcome feelings of isolation. Share ideas and experiences. Learn about our online support groups.
Fact-based, current and useful information
Stay up-to-date and let us and our expert advisors help you sift through misinformation.
Practical tools and information, sent with heartwarming stories, useful tips, and other content from our community.
Compiled with care and insight by friends and experts who know what it’s like to live with these symptoms.
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.