4th Annual SMA 5K – Eat ‘n Run
Hardaway High School
Saturday, March 1, 2014
Help us develop a treatment and cure for Spinal Muscular Atrophy
Visit our story from 2013 to learn a bit more about Caleb, his family, and SMA.
To attend the event OR donate to a specific walker or team, visit our registration and fundraising site!
Event Day Schedule
7:30 – 8:45 a.m. Check-in and Day-of Registration Open
9:00 a.m. Race Begins!
10:00 a.m. Food, Fun, and Prizes
Registration Options
5K (timed)
Mini-K (untimed)
5K (timed-Wheelchair Division)
5K (timed-Stroller Division)
Walk or Run either course
Wheelchairs/Strollers welcome!
Prizes will be awarded to the 5K winner in each age category.
Online Pre-Registration Pricing
Adults (18 & up): $20
Youth (11-17): $20
Child (3-10): $10
2 & Under: Free
Registration price includes event t-shirt and meal!
Register early to save $10 on the registration fee!
T-shirts only guaranteed to pre-registered participants.
Online Registration will close at 11:59 PM. Wednesday, February 26th.
Day-of Registration Pricing
Adults (18 & up): $30
Youth (11-17): $30
Child (3-10): $20
2 & Under: Free
Click here to visit our Facebook page.
Families of SMA is the world’s leader focused on funding SMA research to develop a treatment and cure for the disease. The successful results and progress that the organization has delivered, from basic research to drug discovery to clinical trials, provide real hope for families and patients impacted by the disease. The charity has invested over $55 million in research and has been involved in funding almost two thirds of all the ongoing novel drug programs for SMA.
Families of SMA is a nonprofit 501(c)3 organization, with 31 Chapters and over 110,000 members and supporters throughout the United States. The organization’s work has produced major discoveries, including identification of the underlying cause and a back-up gene for the disease, which provides a clearly defined target for disease altering therapies. The organization is also dedicated to supporting SMA families through networking, information and services and to improving care for all SMA patients.
Click here to learn more about Families of SMA and our programs.
If you have any questions, please contact Kari Merriken at (706) 718-5580 or [email protected]
