Pain, trouble sleeping, fatigue, brain fog, sound/light sensitive?
Sick and in pain? Other unexplained symptoms? Can’t seem to “get better”? You may be living with a post-viral or chronic fatigue illness like Long-COVID or ME (myalgic encephalomyelitis). There is no need to suffer alone.
Free email series from a safe, trusted non-profit:
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Pain, exhaustion and not getting better?
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Other symptoms like sleep troubles, dizziness, sensitivities or brain fog?
Find out if you have ME/CFS or Long-COVID, and get help: diagnosis, symptoms, treatments and more.
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If you have some or all of the following symptoms, you may have ME/CFS or Long-COVID:​
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Extreme fatigue
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Worse symptoms after physical, mental, emotional effort (even a day later)
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Poor sleep
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Brain fog
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Light-headedness, dizziness
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Joint and body pain
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Sensitivities (light, smell, sound...)
If you are not sure, find info on symptoms and how to get a diagnosis here.
What others are saying about this series
Christina Wiebe
"I feel like this series is a life-line for people with illnesses such as 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 free "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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Banish 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, treatment options, coping strategies, 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.