GBS/CIDP Foundation of Canada improves the quality of life for individuals and families affected with GBS, CIDP & Variants.
April 27, 2013
This is your chance to learn about all aspects of GBS, CIDP, and variants from initial diagnosis, through treatment and rehabilitation. Meet your medical professionals, ask questions , and get answers. This is your National Conference and we at the Foundation look forward to meeting each of you.
The Canadian Foundation continues to support patients & families, & to be recognized as the Canadian resource for GBS, CIDP, & variants. Until a cure is found, we will increase public awareness by educating both the professional & lay communities, & we will raise funds for the research & treatment of the above mentioned disorders.
- Newsletter Fall/Winter 2012 [PDF]
- Click here to watch our informational videos, now available in French
- Also, click here to browse our many publications, including newsletters and articles.
- Click here to read the Spring 2012 Newsletter.
-President and Regional Director-
Dr. Kenneth Shonk
-Board of Directors-
-Medical Advisory Board-
Steven Baker, MD
Brenda Banwell, MD
Timothy Benstead, MD
Pierre Bourque, MD
Vera Bril, MD
Colin Chalk, MD
Gillian Gibson, MD
Angelika Hahn, MD
Elizabeth Pringle, MD
Zaeem Siddiqi, MD
Jiri Vajsar, MD
|Susan Keast, Ontarioemail@example.com|
|Gail Kammer, Saskatchewanfirstname.lastname@example.org|
|Denis Dupuis, Manitobaemail@example.com|
|Barbara Sherman, Ontariofirstname.lastname@example.org|
|Demetrios Strongolos, Ontarioemail@example.com|
|Sherry Nedjedly, British Columbiafirstname.lastname@example.org|
|Sylvie Daigle, Ontarioemail@example.com|
|Ivan Sheppard, Newfoundlandfirstname.lastname@example.org|
|Howard Huss, Ontarioemail@example.com|