It’s been a year since I got diagnosed with MS, it’s crazy to think a year ago I got told that I would have MS for the rest of my life. But more importantly It boggles my mind to think just how ill I was this time last year.
Summer last year I had trouble walking in a straight line. I had slurred speech that was hard to understand, and incredibly uncomfortable pins and needles in my right hand, and in my feet. Having lived a year with MS I’ve done so much in this year considering and so much more planned coming up,. Having been on Tysabri nearly a year too, I’m 1000 times better at having the treatment then I was at the start, I still have them days but to reflec on this past year. A lot of stuff has changed, But at the moment I feel strong.