Primary Progressive MS is a lonely place! No drugs specifically approved and none on the way. Neurologist prescribed copaxone. Does it help? Can’t be my own double blind test, so who knows? There must be others out there? Would love to find them. Contact me, please
Mark I was on copaxone for 18 months and it didn’t do anything for me. It didn’t make me ill like Avonex did but each MRI showed new growth on my spine and brain. I just started Tysabri and I’m really hoping that it will help me out. Ask your neuro and see if Tysabri might be an option for you?
Fill in your details below or click an icon to log in:
You are commenting using your WordPress.com account. ( Log Out / Change )
You are commenting using your Twitter account. ( Log Out / Change )
You are commenting using your Facebook account. ( Log Out / Change )
You are commenting using your Google+ account. ( Log Out / Change )
Connecting to %s
Notify me of new comments via email.