Events
The GBS/CIDP Foundation of Canada organizes many events throughout the year for patients and their families – both virtually and in person.
Find the Right Event For You or Your Family
Support Groups
Our private support group meetings - both virtual and in-person - provide a safe and supportive space to connect. Hear patient stories, ask questions, gain insights about dealing with your condition, discuss treatment insights, and learn how to make the most out of doctor’s visits, and more.
Awareness Events
The Foundation is committed to raising awareness about our rare conditions. You can help by taking part in our events.
Fundraising Events
In-person events like our Walk and Roll are a fantastic way to raise funds for GBS, CIDP, and MMN. It’s also a great opportunity to connect with others who are facing similar challenges. ! We’d love to see you there!
Educational Events
One of the main goals of our organization is to empower our community through knowledge – often in the form of webinars and online conferences! Join us to learn from doctors and other experts.
National Conference
As a community, we value coming together for learning and connection. To support this, the Foundation hosts the GBS/CIDP National Conference regularly indifferent cities. Stay tuned for details about the 2026 conference in Alberta.
Why join an event?
- Help us raise awareness and fund research towards GBS, CIDP, and MMN
- Get support from others who understand your experiences as a patient or affected family member
- Stay up to date on the latest condition and treatment information from doctors and specialists with our educational webinars
- Become part of a welcoming, empathetic, and supportive community!
Become a Volunteer!
We count on our dedicated and passionate volunteers to help us accomplish our mission. If you’d like to join us, please explore the volunteer opportunities and register to sign up!
Volunteer