Both of the neuros I've seen felt I've had MS for quite some time judging by the scarring on my mri. My symptoms were more severe this time then they were in the past. After being on the ivsm, i still have significant balance, numbness and fatigue issues. They both suggested Tysabri would be the most beneficial for me, but my insurance felt otherwise being the specialists that they are LOL! Copaxone gave me nasty migraines so neuro two decided to try again. This time i am learning to look into other options if they won't approve it!
I was placed om Tysabri as my first drug,
he was unwilling to consider anything else and my s/s were minimal which
i won't outline, I believe its the neuro's choice,
just my input
Can I ask why you want to go with Tysabri right away? I am curious as my flares seem to be pretty frequent so I am wondering why did your doctor want to use this as a first line treatment? So far, my only significant disability is in my vision and a mild right foot drop.
I will definitely check into assistance programs. Even if the insurance approves it this time around, our copay is still pretty high. Thank you!
Chris
there are excellent patient assistance programs for all of the drugs. Your insurance may have turned down the Tysabri request at first because they normally want you to try something different, first. It is seen as a second line therapy after the first ones don't work. Now that you can't do copaxone, your insurance should revisit the request and hopefully approve it. I went from copaxone to Tysabri without doing the interferons.
good luck,
Lulu
you might call Tysabri and speak to their financial department; depending on your finances, they have excellent discounts and sometimes free drugs.......
explain that your insurance won't cover it, they may have suggestions.
Tysabri is easy and I think a good choice but that's my opinion because I am on it!