Hi Pepe,
I looked through your old posts but didn't see anything that mentioned when you were dx'd with MG. What tests were used to give you the dx?
I know one neuro mentioned pernicious anemia as a possible alternate dx for my MG once, so I would be curious if I were you too.
Talk to you soon.
Quote:
Originally Posted by Pepe
I have not posted in a while but I do keep up with you all. I am very confused. I was just told that I have pernicious anemia. The symptoms are all very similar to MG, down to difficulty swallowing. Now, of course, I'm wondering if I really have MG. I have not been able to speak to my Neurologist yet. Has anyone had any experience with this? Thanks for any help!  |