Looking for others who have Congenital Myasthenia Syndrome (CMS). I want to reach out to as many people as I can find I've had symptoms my whole life, but was not properly diagnosed until I was about 25 years old (I just turned 40!). It was a long, difficult journey. I am so grateful to be where I am today
Well, here i am! I'd love to hear from others.

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Look forward to talking to you guys!
Good night