Greenapple,

I don't have an answer for you but I did want to say......

To NeuroTalk

Thank you! Hello to you too.
I am sorry to jump in with a question like that. My insurance is not going to cover all of it. I have to make come up with a plan soon.
No way can I do the co pay and I have searched out all the options.
I know I used to see some who took it every other day, but that was so many yrs ago and I don't know where

Interesting, I've never heard of that idea. What does your neuro say about it? I'm very curious! Shared Solutions was no help at all?

Shared solutions does not provide assistance. Copaxone uses Nord, we don't qualify for their help.
Thanks for the suggestion. Had a quick conversation with my neurologist.
He says there is evidence that a lower dose of Copaxone would be effective and better than none.
Then there are the other options, TY and IVIG, which insurance will cover.
We are going to head off, take a vacation. I have an appointment for when we get back. For now it's going to the mountains. I will need to decide something after that.
It is very sad with only the ABCR and now T really out there.
Many have had some side effects that rule our one or the other.
Thank you all for your welcome and help.
I am going to go have some fun and then decide.