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new to this.
hey there, my name is Jim and I'm new to this outreach thing. I was diagnosed in '08 with M.S., not a really big deal. When I finally came to terms with this disease I was diagnosed with Syringomyelia. I am just looking for people in the same boat as me. Hoping to get answers that I cannot seem to get from my physician. Mainly, what it is I should expect.
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Hello & Welcome
Jim,
:Wave-Hello: Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Here are a great number of dear friends to listen when you are in need of ears. You will find out we are supportive and relaxing place. Click onto the following forum for some assistance: Arnold Chiari Malformation & Syringomyelia: http://neurotalk.psychcentral.com/forum71.html Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
Hello and welcome! I hope you find your answers here. :hug:
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