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In 2004 I had to go to a scooter to get around. I had lost all control of my legs. To get around the house, my husband had to make our doorways wider. In March 2006 we changed my treatment from Avonex to Tysabri. It started really well but it ran its course and I started going backwards again. I was on Tysabri for 10 years. In 2016 I was changed to Copaxone.
My body is weak now after having MS over 30 years. Hope, determination, belief. Dementia, old age, elderly. Dialysis, renal kidney failure. Hope, determination, belief. Getting rid of a dog. Duke goes with me to the nursing home to visit the residents. The residents love it and Duke loves it.
MS sucks, but it has forced me to be the best me I can be! I used to wonder if I could ever be disabled that way and what it would be like. It turns out I had the perfect assessment test handed to me in the first week of June. But when I disrupt my calm home environment and add in all the constant distractions of life, I am immediately reminded. This is a reassurance to me that I am doing everything .