I have been in the background for a while now. I just wanted to say that this site is great. The best thing is that you know that your not alone. I was dx in May of 2012. RRM, will start Copaxone very soon. I believe that I have had MS for 19 years now. That is a long time to be without a dx. Drs kept saying that it was only my nerves.
What I did was found a new Dr. and was dx in three visits after testing. So I learned to listen to your body, it knows when somthing isn't right.
I am a 55 year old wife and mother of 2 grown daughters, 2stepdaughters,Grandmother of 9 and a great grandmother of 3. I love to read a good book , crochet and fish. I am really glad that I can talk to people who understand. Thanks for listening
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large
blocks of print. **
What I did was found a new Dr. and was dx in three visits after testing. So I learned to listen to your body, it knows when somthing isn't right.
I am a 55 year old wife and mother of 2 grown daughters, 2stepdaughters,Grandmother of 9 and a great grandmother of 3. I love to read a good book , crochet and fish. I am really glad that I can talk to people who understand. Thanks for listening
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large
blocks of print. **
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