Diverse, Inclusive, Welcoming
Stronger Together – United to Support, Inform and Raise Awareness
Interesting Facts and Numbers
The Myasthenia Gravis Society of Canada’s (MGSC) was founded in 1984 to create a safe space for Canadians affected by myasthenia gravis (MG) to support one another. If you are affected by MG, we invite you to join our diverse, inclusive community.
MG was first documented by an English physician named Thomas Willis in 1672.
MG patients on average see 7 specialists before being diagnosed.
MG affects 32 persons for every 100,000 in Canada.
We Meet Every Wednesday
All are welcome to attend! We are inclusive and welcoming of everyone because MG affects people from all backgrounds.
Every Wednesday
Join Our Weekly Support Group
The online support group meetings we organize are one of the most important facets of MGSC. We would love you to join us!
Help Us, In Your Own Way
The MGSC is run by volunteers and funded by people like you that support our cause. Our mission is an important one, and we appreciate your support however you may offer it.
We Need You
MGSC is a volunteer-based organization. We strive to be diverse and inclusive. MGSC is grateful to all the volunteers that have contributed in the past and would love to add you to our team.
Every Dollar Counts
Your donation helps MGSC carry out its important mission! Without the generous donations from supporters like you we could never spread the word and change so many lives.
Personal Stories
From Personal Pain to Community Strength.
Linda’s Story
I am a retired RN who was diagnosed with MG at the age of 42. I had symptoms as a child. I was forced onto disability at that time. So, I have been living with this for a very long time. There was no internet at that time, so all my information came from a pamphlet.
I was tested for MS. The test came back negative.
Then I saw a new ophthalmologist who thought I might have MG. He wanted me to see a neuro-ophthalmologist on the mainland. I live on Vancouver Island, so the trip to see them and get back takes 16 hours. I was very nervous, and my GP, trying to be optimistic and reduce anxiety, said, “Go see the specialist, but don’t worry; you don’t have it.” Famous last words.
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