I was diagnosed with MS 2 years ago when I was 56 in 2016. I saw a neurologist once! Apparently he can’t see me as he is only seeing “The newbies” We only have one neurologist in Plymouth! My MS nurse is really not much help as she hasn’t helped me much at all! I went on Steroids for my first relapse which helped me tremendously but the second relapse is worse than the first. I can’t walk very well as it hurts my legs to try. Going out I have to use a wheelchair. I just hate it to be this bad. I wake up every morning thinking I will be able to walk (As I am a positive thinking person) I am never pessimist. my words get all mixed up as well when talking at a normal speed so I have to be very conscious of what I am saying and speak slower
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