I have just discovered this forum. My husband has been suggesting that I look for chat rooms for sometime now and I'm glad I finally am. I thought I should stick with the posting though since my coordination makes typing a bit of a challenge and I'm not fast enough for a chat room.
I'm a woman in my 40's and I was diagnosed with RRMS about 15 years ago. My symptoms are numbness/tingling, coordination/balance, fatigue, and other stuff. I walk with a cane and have for many years now. This summer has been a tough one (very hot).
I live in Ontario, Canada. It is me, my very supportive husband, my 2 golden retrievers and my bunny. I have a daughter who is in her 20's and has left home.
I try to stay positive but somedays it is a challenge. I am enjoying reading other people's posts. I think I tend to isolate myself and this is a great way to find poeple I can relate to.
I'm a woman in my 40's and I was diagnosed with RRMS about 15 years ago. My symptoms are numbness/tingling, coordination/balance, fatigue, and other stuff. I walk with a cane and have for many years now. This summer has been a tough one (very hot).
I live in Ontario, Canada. It is me, my very supportive husband, my 2 golden retrievers and my bunny. I have a daughter who is in her 20's and has left home.
I try to stay positive but somedays it is a challenge. I am enjoying reading other people's posts. I think I tend to isolate myself and this is a great way to find poeple I can relate to.
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