Well I guess I will jump in and say hi.

I was diagnosed with RRMS one year ago and have been on Rebif since. I have been looking for an answer to my symptoms since I was about 14. I'm 24 have a four year old daughter and two year old son. I also have a very supportive husband and a wonderful family who I would be lost without.

I was also diagnosed with POTS last June, and now they are in the process of trying to diagnose me with some type of myopathy most likely MG.

I get spells where I can't move or talk and can barely breath. As far as MS goes I have ON, cognitive issues, balance problems and left sided weakness. I have been through so many tests in the last two years I want to scream and will be glad when they finally decide they know what's wrong with me. Well besides the fact that I'm just weird But I've known that all along.

I have been on the web md support group for a while know and found this site for the MG support group. I have been on there for a couple weeks now and thought I would join in some conversations here.

I hope everyone is doing good today.

Kristie