In Memory of Caden
Donate to Cure SMA
Every year we run a Do It Yourself Fundraising (DIY) event to support Cure SMA in memory of our son, Caden. Caden passed away in 2016. He is one of the many reasons we light up the sky during Christmas season. His favorite toy was a small music box with flashing lights. He never got to experience Christmas but we know he would have been in awe of the music and lights.
Spinal muscular atrophy (SMA) is a disease that robs people of their physical strength, significantly impacting an individual’s ability to walk, swallow, or breathe. It affects one in 11,000 births in the United States, and one 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 Cure SMA.
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 people with SMA and build a stronger future for generations to come.
Support by making a tax-deductible gift today! Together we are stronger and can make a difference.
Thank you and Happy Holidays,
Caden Michael Rogers