Living with Multiple SclerosisThis section is a place to share stories about Living with Multiple Sclerosis Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download MS and polio I am presently 55 years old. I was diagnosed as having polio at 18 months of age (I was diagnosed after the fact). The polio vaccine was not widely available when I was born (June/53). I was left with a wasted left leg but I was able to become a nurse (RN) and work in hospitals and the community for 15 years. I skiied and played raquetball, allbeit not too gracefully. When I was 35 I got a flu that knocked me on my butt. The drs thought I had post polio/chronic fatique/depression/spinal cancer? I was left with weakness in my good leg, fatigue, poor concentration/slurred speech when I got tired/depression. I was called depressed by my employer’s health provider and received no long term benefits from them but I did qualify for a disability benefit from the Canadian government. I received very little help from my fellow nurses. I must admit that the union now seems to be supporting the nurses now, but it is a bit late for me. I muddled along until I got a sudden numbness on my right cheek about 3 years ago. I had thought perhaps I was having little TIA’s. Saw the dr. and she referred me to another neurologist who figured it was a virus and would go away in a year. Over a year later my doctor and I talked and I paid for a private MRI and the result showed numerous plaques in my brain. I saw a new neurologist and he figured I probably had the MS since I had been 35 and had the attack initially in ‘88. He ordered an MRI of my spine which showed no spinal involvement. While I don’t have a definitive diagnosis, the neurologist feels the areas affected are typical of MS and my gait, numbness etc. are typical of the disease. Just because I have had polio, it doesn’t preclude me from having MS–I’m just ‘lucky’ to have both. I’m finding that my good leg strength is weakening at a more rapid rate and I have a degenerative knee on my ‘good’ leg. So far I am having limited vision changes. Fatigue and depression seem to be recurring problems. I am presently on Amantadine 100 mg daily/twice daily. Anyone else out there have the same luck? Comments
September 2008
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