I've been on Copaxone since April. I know that I should give it 4-6 months but I feel severly impaired right now and would love to do something about it by trying a harder drug. I am 98% wheelchair-bound, unable to drive, scoot down stairs on butt, climb stairs in sections (meaning I climb a few and rest). There was a 3-month time span that I was able to fold the wheelchair up and put it away. I was walking. Now, I'm scared that while I'm waiting for Copaxone to help, I am damaging myself and letting MS have the chance to do more permanent damage. My neurologist is no help. Please tell me your story! Thank you so much!