I just learned that I probably have MS. The neurologist wants me to start Copaxone once she feels really confident about the diagnosis.
Do you have tips on avoiding Lipoatrophy?
Also, I’m worried about injection rotation because I fear my stomach is unusable due to all my stretch marks, and I won’t have consistent help injecting in my arms and hips (my husband travels for a living and I have no other helpers). What would you do?
Hi there. When you start Copaxone, your neurologist might connect you with Shared Solutions, Copaxone's patient information and financial support program. I believe that they have nurses available who can speak with you about this. They may also offer injection training and can speak with you about your options.
Thank you so much for your reply.
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