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Living with MS I don’t have to give up on my dream shares country star Julie Roberts – learn more on CNN “Human Factor”

May 30, 2014

Accepting my diagnosis of multiple sclerosis was probably the most difficult part of my MS journey. However, it also helped me retake control of my life.
 
For years, I was in denial that I had MS. I thought if I didn't focus on my MS, then maybe it would just go away. It took the Nashville flood in May 2010 for me to "wake up" and decide it was time to take responsibility for what is, and what will be, my life with MS. My Mom, my sister and I lost our home and almost everything we owned in the flood. When we were rescued by boat, we were given another chance at life. I realized then that things can be replaced, but life and good health are invaluable.
 
The stress from the flood brought on a relapse of my MS, which I could no longer ignore. At that point, I decided to accept that MS is part of who I am, and that I needed to learn how to manage it in order to continue living my dreams.
 
Learn more on CNN “Human Factor”

About Multiple Sclerosis

Multiple sclerosis is an unpredictable, often disabling disease of the central nervous system that disrupts the flow of information within the brain, and between the brain and body. Symptoms range from numbness and tingling to blindness and paralysis. The progress, severity and specific symptoms of MS in any one person cannot yet be predicted, but advances in research and treatment are leading to better understanding and moving us closer to a world free of MS. Most people with MS are diagnosed between the ages of 20 and 50, with at least two to three times more women than men being diagnosed with the disease. MS affects more than 2.3 million people worldwide.

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