An Important letter to Canadian Patients concerning SCIg (SubQ) treatments 

– updated June 18, 2019

Original letter dated May 14, 2019

About Us

Our Vision, Our Future.

Every person affected by GBS, CIDP, or variants such as MMN, will have access to early and accurate diagnosis, expert interdisciplinary treatment and support, and through continued research, a cure will be developed for GBS.


GBS/CIDP Foundation of Canada is a registered Canadian charity founded in 2003. Our foundation continues its long history of connecting patients and their families with caring and dedicated volunteers who have been affected by GBSCIDP, and variants, such as MMN. It is our hope that no patient or family will have to go through any of these disorders alone.

Along with this patient-to-patient support, the foundation has proudly established a National Medical Advisory Board of 18 Neurologists trained in the diagnosis and treatment of our disorders.

We are committed to building relationships with experts in rehabilitation and support disciplines who understand the challenges facing our patients during and after recovery. Our latest goal is to create a council of professionals that will help guide and educate patients on best practices in their disciplines.

We support Canadian research that will improve the diagnosis, treatment, and rehabilitation of patients affected by GBSCIDP, and variants. Our ultimate goal is to help pave the way to a cure. We proudly support IGOS and the Canadian contribution to the International GBS Outcome Study.

Calgary Walk and Roll
May 26, 2019

Edmonton N.E.R.D. Run

 Sunday June 9, 2019 9:00-12:00

Rundle Park, 2909 113 Ave NW

Click Here => Walk with Us, Create a Team or Make a Donation

For more info visit

Montreal Walk and Roll

Saturday, June 15, 2019

Vieux Port Park – starting at Montreal Science Center

Click Here => Walk with Us, Create a Team or Make a Donation

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