Myasthenia Gravis Society of Canada is a national non-profit charitable organization which strives to empower people affected by myasthenia gravis through information sharing, peer support and community building. Our weekly support group meetings, newsletter and webinar series aim to inform and foster a community of support and information exchange. In collaboration with this community, we raise awareness of MG with all Canadians.

Vision

Canadians affected by myasthenia gravis (MG) will have the information and support needed to attain optimal health.

Mission

Myasthenia Gravis Society of Canada’s (MGSC) mission is to empower people affected by MG through information sharing, peer support and community building.

Goals

1. Provide information and resources related to myasthenia gravis and its management
   
   • Website with key information and useful external resources
   • Bi-annual newsletter
   • Online webinar series
2. Provide peer support in an equitable, inclusive, and compassionate environment while fostering the exchange of information
   
   • Weekly support group meetings
   • Peer to peer program
3. Increase the public and health care professionals’ awareness of MG