Hello to everyone,

A quick intro, I'm almost 52 and have been diagnosed with Myasthenia Gravis in 2008 at a mild state "Ocular" in left eye drooping and thitching in both eyes, in April of this year I was hospitalized for 8 weeks due to a severe SPIKE! couldn't breath, eat/ swallow, keep my head up nor my arms and barely speak...I'm now on a cocktail of pills and weekly Plex as an out patient...my purpose of joining this Forum is to share my symptoms and try to make things better by sharing individuals experiences with meds and therapies...

Hoping to hear from you all

Hello and welcome to the NeuroTalk Support Groups.

I just wanted to leave you the link to the
Myasthenia Gravis Forum

I'm sure you'll find support and information here.
Take care.

Hello and welcome, happy to see you have come to be with us, it a great place to be. We have a great number and caring fellow members here, where you have find a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways.

Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene