RRMS
I was diagnosed with RRMS 8 months ago, was a massive runner but started struggling a couple of years ago and just thought it was getting old until I collapsed about 14 months ago and had loads of tests. I struggle walking some days know which is so crap as I loved going out for a run. Get numb arms and feet most days and a lot of pains in my legs when I was diagnosed I fell apart for a few days but knew I had the write mentality to get threw this and with a lot of help from my ms nurse and family I hot on with life but life has changed massively.
Hi I have never like runner but was very active but now I can't really walk on my own I have always rode a bike but can't now because of my balance my social worker wanted me to get electric wheelchair I live in France and the help is really good it would have been funded by the state but I didn't want a electric wheelchair but I had seen a electric off road Trikecycle and managed to see get one last year partly funded it's amazing now I am mobile again and it's wonderful to be outside again getting exercise,I think you need find different ways to live your life it takes longer and not always easy
I go to the gym 3 times a week know instead of running which is perfect for me but anymore and I'd be over doing it.