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I am walking and rolling for Cure SMA!
I started this walk 19 years ago when my daughter Jessica, who had Spinal Muscular Atrophy (SMA), was a year old. SMA is a disease that robs people of their physical strength, significantly impacting an individual’s ability to walk, swallow, or breathe. It affects 1 in 11,000 births in the United States, and 1 in 50 people is a genetic carrier. There is no cure, yet, but there is great reason for hope. And that is why I am fundraising for the Cure SMA Walk-n-Roll!
Research funded by Cure SMA is driving therapies that are changing the course of SMA. Together, we have the power to meet the ever-changing needs of all people with SMA and build a stronger future for generations to come.
We are doing the walk virtually this year so you may join us wherever you are!
Support me by making a gift or registering to walk or roll with me today!
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