Event Description
One Love One Heart 5k
All proceeds will go directly to the CdLS Foundation
Kira Czech and I, Hannah Pomfret, are excited to kick off our senior year with the project of organizing this race. We are thrilled to see everyone support IN-PERSON this year.
*CdLS Immediate Family Members register FREE *
CdLS Immediate Family Members inlclude Moms, Dads, Brothers, or Sisters. Immediate family of an individual with CdLS register free but still need to register.
“One love refers to the universal love and respect expressed by all people for all people”.
Event details and schedule
One Love One Heart 5K!!
Piedmont Park, Atlanta, GA
8.6.2022 9:00 AM
Entry Fees:
$25 Pre Registration by July 30, 2022
$30 Late and Race Day Registration
Rain or Shine
When: 9:00 a.m. to 12:00 p.m. Where: Piedmont Park, Atlanta, GA Who:Runner, walkers, wheelchairs, and strollers welcome.
Can't make it? Thats ok! If you still want to support the CdLS Foundation you can visit this website to donate!
PACKET PICK UP & RACE DAY REGISTRATION
Race Day Registration and Packet pick up starting at 8:00 am at Piedmont Park.
Delicious refreshments will be available
Guaranteed short sleeve t-shirts for all pre-registered runners; while supplies last for late and race day registration
Gift Card Awards: Overall male and female, overall masters male and female, top male and female in each age group
PARKING
Stay tuned for parking details closer to the race date.
Information also available at:
www.facebook.com/OneLoveOneHeart5kForCdls
https://sites.google.com/csdecatur.net/oneloveoneheartvirtual5k/home
Cornelia de Lange Syndrome (CdLS) is a genetic disorder present from birth, but not always diagnosed at birth. It causes a range of physical, cognitive and medical challenges and affects both genders equally. CdLS does not discriminate—it’s seen in all races and ethnic backgrounds. The occurrence of CdLS is estimated to be 1 in 10,000 live births.
Through a variety of research programs and activities, the CdLS Foundation plays a major role in advancing clinical and basic scientific knowledge about the syndrome.
The CdLS Foundation is a national non profit organization that supports all people with CdLS as well as their families.
