Living with M.S

Hi All My name is David and I'm from Mid Wales. I have had M.S since 1999 first symptoms were double vision had my M.S confirmed by an MRI scan and lumbar puncture had a really bad relapse in 2003 just before I started on Rebif injections, the relapse affected my Right hand side of my body but still managing to work until I was made redundant in 2014. I was on Rebif for just over 10 years with only a few relapses but had to stop Rebif due to liver problems. I am on Tecfidera now no relapse but slowly getting worse waiting for results of last MRI scan and it might be SPMS that I have now and will have to change my medication.