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Manitoba ME/CFS Support Group Inc
Manitoba ME/CFS Support Group Inc
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Manitoba ME/CFS Support Group Inc
Manitoba ME/CFS Support Group Inc
Home
About ME/CFS
About Myalgic Encephalomyelitis
Symptoms
Diagnosis/Treatment - Physicians
ME Toolbox
Manitoba Resources
Patient & Caregiver Resources
Severe ME Resources
Physician Resources
Healthcare Provider Guides
Awareness
May 12th
Aug 8
Books & Films
ME Advocates
Patient Blogs
News & Our Blog
Links
MB ME Blog * Coming Soon
News* Coming Soon
About Us
Contact
Our Goals & The Mission
Support Group Information
FAQs* Coming Soon
Please Donate
Please Donate
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
Healthcare Provider Guides
Folder: Awareness
Back
May 12th
Aug 8
Books & Films
ME Advocates
Patient Blogs
Folder: News & Our Blog
Back
Links
MB ME Blog * Coming Soon
News* Coming Soon
Folder: About Us
Back
Contact
Our Goals & The Mission
Support Group Information
FAQs* Coming Soon
Please Donate
Please Donate


40 And Fighting

A girl called Naomi

A Life Hidden

Amy's Chapter

Anil Van Der Zee

Byshi art and words

CFS Graphics

Chronically Craptastic

Corner Stone for Thoughts

Creating With Chronic Fatigue

Fragmented ME

Frozen in Amber

Jessica Taylor-Bearman

Journey Through the Fog

Kirstie Sivapalan

Life of Pippa

ME and my island

ME, myself and chronic illness

ME/CFS Skeptic

Not Just Tired

Phoenix Rising

Puffins and Penguins

Sakara Dee

Sleepy Bookworm

Smiling Clare

Stonebird

Super Pooped

The Low Side

This Thing They Call Recovery

Valerie Eliot Smith

Virology Blog

Whitney Dafoe’s Blog

Zonked Club

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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