About GBS/CIDP Foundation of Canada

GBS/CIDP Foundation of Canada, a national patient organization, has been supporting patients and families since 2003 through the generosity of private donors and sponsors. Your gift of donation has allowed us to grow, support, educate, connect, and invest in research, in Canada.

Now more than ever, we continue to need your support to help those afflicted with Guillain-Barré Syndrome (GBS), Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), and variants such as, Multifocal Motor Neuropathy (MMN). With your gift of donation, you will provide:

Patient support services, such as peer support and support group meetings

Educational events including conferences and online webinars  

Canadian patient literature

Patient stories, videos and articles

Advocacy

Canadian research

Website content

Above program activities provided in both official languages

Thank you for helping us, help others

Our Mission

To engage in advocacy, including treatment access, (at the federal, provincial and grassroots levels) to improve the quality of life for individuals and families affected by GBS, CIDP, or variants such as MMN.

Our Vision 

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.