More and more people are being diagnosed with Parkinson’s, and the cost to our communities is staggering.
It took over two years of continual visits to the doctor and a barrage of tests to finally get a diagnosis. I was consumed with crushing fatigue, visual difficulties, loss of smell, difficulty walking, brain fog, struggles with balance and coordination, stomach pain, chronic constipation, stiffness, joint pain, tremors and repeated falls — one resulting in a concussion. I was continually anxious — at times panicky and filled with depression.
I am passionate about doing what I can in my lifetime to make a difference in the lives of those with Parkinson’s and to those at risk. Through support groups and therapy, I have met the most beautiful people who have become my Parkinson’s family. I would be lost without these resources and support. Continual accommodations are needed to function in the world because Parkinson’s easily strips you of your ability to enjoy life.
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