Hello MS World,
I am so happy to have found this forum. I feel like no one else around me really understands what I've been through the past two months. I ran a 5k on November 10th, 2012 and a few days later starting having severe spasms on the left side of my body. After weeks of no relief my GP requested that an MRI of my brain be done.
There was no question about it....it was definitely MS. Then it all made sense....the numbness and tingling, the inability to focus at work, the excruciating headaches. I just turned 26 at the end of November and all of this has been very overwhelming for me. I go back to my neurologist later this week to decide on a treatment. She has recommended Copaxone but I'm not very comfortable with the thought of giving myself injections. Ahhh...overwhelmed.
** 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. **
I am so happy to have found this forum. I feel like no one else around me really understands what I've been through the past two months. I ran a 5k on November 10th, 2012 and a few days later starting having severe spasms on the left side of my body. After weeks of no relief my GP requested that an MRI of my brain be done.
There was no question about it....it was definitely MS. Then it all made sense....the numbness and tingling, the inability to focus at work, the excruciating headaches. I just turned 26 at the end of November and all of this has been very overwhelming for me. I go back to my neurologist later this week to decide on a treatment. She has recommended Copaxone but I'm not very comfortable with the thought of giving myself injections. Ahhh...overwhelmed.
** 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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