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Read conversations, start a discussion, and connect with others about myasthenia gravis.

T cell treatment for ocular myasthenia gravis

Are there any new treatments available.?...

Helpful MG questions

Hi all! I am organising a webinar for people with MG with a leading MG specialist and want to make sure we...

Have You Attended an In-Person Myasthenia Gravis Event or Conference?

Have you attended an in-person Myasthenia gravis event or conference? If not, do you have an interest in it?...

Ocular MG- Botox

My neuro opthamologist suggested botox shots for ptosis and maybe double vision, as well. Has anyone tried this? What was your result?...

Myasthenia gravis and herpes

Hi! I have had hvs2 for 41 years. I'm asymptomatic and take antiviral meds. I've recently met a great guy and we've...

Birth victim of M.G.

Dr. Melvin Greer Shands teaching hospital told parents at age 2 that I like mhave MG first and time Mom saw me...

Ocular to Generalized Myasthenia Gravis

Commonly, the first symptoms of Myasthenia gravis experienced, and possibly the only MG symptoms for years, are double vision or drooping of...

PLEX or IVIG Complications?

Have you had complications or issues arise during or after a PLEX (plasma exchange/plasmapheresis) or IVIG (intravenous immunoglobulin injection) treatment? https://myasthenia-gravis.com/treatment...

Does anyone else in your immediate family have MG?

After a five-year struggle, I was finally diagnosed in 2018 as Seronagative. My journey through a long list of unexplained symptoms help...

Lack of medical support

I live on Cape Cod Mass. and was diagnosed with MG in 2021. I went to a Neurologist and was given the...

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