Hello folks
My MS is unfortunately quite symptomatic with fatigue, optical neuritis, leg pains, balance issues, urinary, bowel, swallowing, dizziness etc…
My MS treatment history is as follows:
Started on Rebif (Did nothing for me), then was a part of the Campath - Alemtuzumab trial and had this infused over 2 years, next was daily Copaxone injections and finally Tecfidera.
Hoping this is the one for me…
I have a question please: Does anyone else here have any experience of the Campath trial and subsequently ended up on Tecfidera? I would be very interested to know if you experienced any difficulties getting your Neuro to prescribe the treatment. I know mine was initially apprehensive due to not knowing the effects of it after being on Campath…
But my attitude is to throw everything and the kitchen sink at this damn disease in the hope of slowing it down and keeping myself able bodied for longer…