Real people Real stories.

Montel Williams story

When the neurologist said those words -"You Have MS" it hit me like a brick.I thought the diagnosis was a death sentence. I learned that I had been having MS episodes off and on for more than 20 years, but like so many, I was in denial about my illness. I started The Montel Williams MS Foundation. Every dollar raised goes to research dedicated toward a cure for MS. Research shows that early diagnosis and treatment prevents the progression of MS.
The world needs to know the warning signs of MS and the treatment options available. The world needs to understand that many more people have MS than current data indicates. The world needs to mobilize against MS and knock it out for good.I believe to the depth of my soul that all of these goals can be achieved. It will take courage and commitment, but these are qualities we can help each other find in ourselves. I know we can build a future of hope and health, and together we're going to win. To read the full story of Montel's story you can visit The Montel Williams MS Foundation.

Bobby Welker's Story

Bob was diagnosed with Primary Progressive Multiple Sclerosis in January 2007. He had been having symptoms for five years before his diagnosis. He is a fighter and continues to live his life to the fullest. Since he was diagnosed he has participated in the Utah MS walk held every April. He walks the whole 5 KM with the help of his friends and family. The doctors told him that completely this race is like a marathon for him. He is an awesome example to everyone around him.

Clay Walker's MS Story

Clay Walker was the high school football star in Beaumont, Texas. Clay's diagnosis with relapsing-remitting multiple sclerosis (RRMS) came at a pivotal time in his life. In 1996, at the age of 26, he recently had finished his fourth album, his career in country music was exploding, and his oldest daughter had just been born. The last thing he expected was the tingling, numbness on his right side, and facial spasms that hit while he was on tour. After a battery of tests, he was diagnosed with RRMS. He worried how it would affect his career. In characteristic fashion, Clay prayed about it and then set his mind to doing everything he could to overcome the obstacles MS set before him. Clay has kept touring and recording steadily since he was diagnosed. He is well-known for his high-energy concerts and performance style. Knowing that others with MS have not been so lucky led him to the decision to form the Band Against MS Foundation, a not-for-profit organization dedicated to making information about living with MS available and providing funding for research. Being diagnosed with MS hasn't been easy," said Clay. "I choose to view it as a 'bump in the road' rather than a detour, because I have been blessed to still be able to do the things I love." You can visit Clay Walker's Band Against MS for more information.