I was listening to a speech on MS. The lady with MS was talking about her MS story and she said with another look at a new mri, no new spots it was good news. It started me thinking,did I get a new mri to see if Copaxone is working.
My first was 2011 and not about one to see if I am on the right track.
Next  time I see him is in May and I will ask him. Any comments???
Should I be worried?
Have anyone heard of PBA?



My dr did an MRI at 6 months and than again at 12 months just to make sure that Copaxne was working for me so you may need to ask about that.