I had a CAT scan yesterday and they found a thymoma. I'm meeting with a surgeon next week. My neuro said removing the tumor could eliminate my MG. That sure would be a twist on this roller coaster ride I'm on. I was just starting to get used to being myasthinic and just hoping symptoms didn't get worse in the next year. Now, there's more thoughts to process.

I want to thank this forum for giving me a place to vent to knowlegable and understanding people. This process has been hard for me and yet, so far, I've been lucky. Thanks....