Hi, we're Brady and Colby Nelson, and we have Spinal Muscular Atrophy. On Saturday, October 6th, our family and friends will be walking, running and rolling to raise money for us and all of our friends with SMA.
SMA is the #1 genetic killer of children under age 2. SMA is a genetic disease that destroys the nerves controlling muscle movement, which affects, crawling, walking, head and neck control, swallowing and eventually breathing. There is no cure or treatment for SMA.
BUT A CURE IS ON THE HORIZON... Every penny we raise goes directly to helping find medicine to help our weak muscles. We are getting very close to finding a treatment or a cure for SMA, but research costs a lot of money. That's why we need your help! Donating through this site is simple, fast and totally secure. It is also the most efficient way to help us raise funds. Remember no contribution is too small, and don't forget to forward this to anyone who you think might want to help too!
TOGETHER WE WILL FIND A CURE!
Visit Brady and Colby's website:
Click here to view a video montage about Brady and Colby's journey with SMA.
THANKS to our offline donors:
Bob Cummins (Cummins Charitable Foundation), Jill & Jerry Stanfill, Amanda & Matt Lunnon, Nathan Smith, Jack & Earline Lierly, Barbara Gage, Jim & Jo Ronsick, Debra & Jeff Harding, Doris Fox, Jerry & Demie Adams, Chad & Nikki McCutchen, Heather & Carter Likes, Dale & Vicki Barnett, Barbara & Dan Sipes, Lyle & Eileen Hall, Michael Farris, MaryLynn & Randall Hallett, Virginia Churchill, Dale & Helen Maahs, Gordon & Dorothy Kent, Vi Siefkes & Wes Lowell, Kristen & Jack Levine, Mike & Evon May, Michael Collins, Brent Wakefield, The Dionisio Family, Gary & Rogene Isaacson, David & Cheryl Goehring, Dallen & Lavona Buss, Dwayne & Betty Lewis, Alice Adams, Lee & Janet Anderberry, Jeremy & Adrienne Widick, Art Althouse, Harm & Jaye Harms