Hey there,

New member here from Quebec, Canada.

After years of tests (the healthcare system is slow here) I was finally diagnosed with ocular Myasthenia Gravis this past spring, which became the generalized form this fall and I suffered my first myasthenic crisis shortly after in November.

I wasn't given much information on the disease, so looking forward to reading/hearing others experiences with this disease / coping methods etc.

Very thankful to have found this community!

If you have any advice please feel free to share!