The CPRF Impact
The foundation is a federally recognized 501(c)(3) non-profit organization, established with the vision of making meaningful contributions toward research to cure Spinal Muscular Atrophy, and providing support to families with children facing difficult medical challenges.
MEET OUR BOARD
Facts About SMA
- SMA is the number one genetic cause of mortality in infants
- 1 in 40 people are carriers of the gene that causes SMA
- 7.5 million Americans are carriers
- The child of two carriers has a 1 in 4 chance of developing SMA
- SMA affects approximately 1/6,000 – 1/10,000newborns in the US
- Currently there is no definitive cure for SMA
The CPRF Board
The Cole Parker Randall Foundation was established with three primary goals:
- Spread awareness of the number one genetic cause of mortality in infants
- Raise funds to promote a variety of research methods currently underway
- Honor Cole’s life and memory, SMILE
Our board is comprised of dedicated individuals driven by a common purpose to one day find a cure for Spinal Muscular Atrophy.
Dave Randall
Co-Founder / President
Shawna Randall
Co-Founder / Secretary
Cameron James
Treasurer
Casey McQuaid
Board Member
Tommy Bookman
Board Member
Nikki James
Board Member
Iliana Rommel
Board Member
John Stevens
Board Member
Luka Arnerich
Board Member
