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Manitoba ME/CFS Support Group Inc
Manitoba ME/CFS Support Group Inc
World ME Awareness Day May 12, 2005
May 12th 2025
Certain People Myth
Doctor Myth
Mental Health Myth
Long Covid Myth
Exercise Myth 2025
Tired Myth 2025
Home
About ME/CFS
About Myalgic Encephalomyelitis
Symptoms
Diagnosis/Treatment - Physicians
ME Toolbox
Manitoba Resources
Patient & Caregiver Resources
Severe ME Resources
Physician Resources
Awareness
Aug 8
Healthcare Provider Guides
Books & Films
ME Advocates
Patient Blogs
Links
About Us
Contact
Our Goals & The Mission
Support Group Information
Please Donate
Manitoba ME/CFS Store
Support Group Feedback
Please Donate
Manitoba ME/CFS Support Group Inc
Manitoba ME/CFS Support Group Inc
World ME Awareness Day May 12, 2005
May 12th 2025
Certain People Myth
Doctor Myth
Mental Health Myth
Long Covid Myth
Exercise Myth 2025
Tired Myth 2025
Home
About ME/CFS
About Myalgic Encephalomyelitis
Symptoms
Diagnosis/Treatment - Physicians
ME Toolbox
Manitoba Resources
Patient & Caregiver Resources
Severe ME Resources
Physician Resources
Awareness
Aug 8
Healthcare Provider Guides
Books & Films
ME Advocates
Patient Blogs
Links
About Us
Contact
Our Goals & The Mission
Support Group Information
Please Donate
Manitoba ME/CFS Store
Support Group Feedback
Please Donate
Folder: World ME Awareness Day May 12, 2005
Back
May 12th 2025
Certain People Myth
Doctor Myth
Mental Health Myth
Long Covid Myth
Exercise Myth 2025
Tired Myth 2025
Home
Folder: About ME/CFS
Back
About Myalgic Encephalomyelitis
Symptoms
Diagnosis/Treatment - Physicians
Folder: ME Toolbox
Back
Manitoba Resources
Patient & Caregiver Resources
Severe ME Resources
Physician Resources
Folder: Awareness
Back
Aug 8
Healthcare Provider Guides
Books & Films
ME Advocates
Patient Blogs
Links
Folder: About Us
Back
Contact
Our Goals & The Mission
Support Group Information
Please Donate
Manitoba ME/CFS Store
Support Group Feedback
Please Donate

mbmecfs@gmail.com

This site is for information purposes only, and is not a substitute for the advice of a qualified healthcare professional. See full disclaimer here. Unfortunately, most health professionals do not yet understand the complexities of ME/CFS, and therefore it is important for patients to educate themselves about the illness so that they can advocate better on their behalf. We urge caution and strongly advise individuals with ME/CFS to choose health professionals with some understanding of or willingness to learn about ME/CFS.

We acknowledge that we have the privilege to live and gather on the Treaty 1 territory, traditional territory of the Anishinaabeg, Cree, Oji-Cree, Dakota, and Dene Peoples, and on the National Homeland of the Red River Métis.

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