I just signed up . After1/3 of my life with MS, the hard thing is writing in a blog. It is hard to type, so I use a microphone, I'm not even quite sure about where the tools are or how to do this. Pardon the spelling and punctuation errors. AutoCorrect is not my friend.
I'm 69 years old and I was diagnosed when I was 42, they say I could have had my first relapse/episode back when I was 27. When I was diagnosed, there was no medication, no DRTs . I am now on Tecfidera, after being on three previous drugs. MS was fairly quiet the first 10 or 15 years, but has really accelerated in the last five or seven. Getting older and having MS, it is hard to sort out what is what. I think I'm just trying to reach out to a bigger community in a new form.