After my initial diagnosis I felt … shocked and isolated and VERY glad I didn’t have a brain tumor. I was told MS was an autoimmune deficiency that is different for every person. Can you imagine my surprise when I came across this video with another lady describing MY LIFE?

Please leave me comments on how you reacted to your initial diagnosis, and what you think of this video. I was terrified at first because I didn’t know what to expect, and I don’t want you to feel like that – you’re NOT ALONE in this, there are other people who have been where you are and WANT TO TALK ABOUT IT!

So please share.