Thank You to Everyone for Pounding with us for 10 Years!
We had over 800 people register for this year's race. We look forward to seeing everyone in 2020.
If you prefer to send a check:
Please make your check payable to the Peter Hopkins Foundation:
Peter Hopkins Foundation
955 Stovall Boulevard, Atlanta, Georgia 30319
For any additional information, please email us at: firstname.lastname@example.org
About Pound the Pavement for Peter:
Pound the Pavement for Peter is a Family 5K Fun Run that was started in 2009 in honor of Peter Hopkins, who, suffering from a Peroxisomal Disorder (PBD), lived his life with many disabilities, and eventually lost his life at age 3. This event is held to raise awareness and funds to help families and children with disabilities and debilitating diseases.
In October of 2010, Peter lost his four-year battle with a peroxisomal disorder. During his short time on earth, he touched the lives of every person he came in contact with and will be remembered by all for his beautiful smile and his joyful presence. Children and families struggling with the reality of disabilities and medical fragilities hold a special place in all of our hearts. We are honored to see his life continue to make a difference for families with children with this disease as well as other disabilities through this race.
Last year, more than 500 people participated in this lively 5K family fun run around Capital City Club - Brookhaven. We were all overjoyed funds that the event raised and by the support that the community has shown for this worthy cause. This year’s event is sure to attract a similar crowd and is guaranteed to be an inspiring fun filled morning.
Pound the Pavement for Peter Beneficiaries
Based upon the success of this race in past years, we are overjoyed to announce that we will continue to sharing the proceeds this year to fund 3 critical aspects to realizing the potential and hope for these families – Research, Medical Care and Inclusion in Education. We cannot think of a better way to honor Peter’s memory and other children like Peter than these charities who will enhance the lives of children and families living with severe disabilities.
The specific charities we will support this year are the Global Foundation for Peroxisomal Disorders, The Adaptive Learning Center, and Children’s Healthcare of Atlanta .
The Global Foundation for Peroxisomal Disorders (GFPD) was started by parents of children with Peroxisomal Disorders (PBDs) with the mission to assist families in enhancing the lives of children and to support research for the disease that took Peter’s life. With this money, we are finding a Fellowship Position within National Center for Advanced Translating Sciences (NCATS) at the National Institutes of Health (NIH) to focus on this rare disease that took Peter’s life along with so many other children. This fellowship is working to screen drugs and treatment therapies for enhancing the lives and eventually curing Peroxisomal Disorders for these children. Learn more at www.gfpd.org.
The Adaptive Learning Center is the only organization in Georgia that fully integrates children with special needs into typical preschools – with individualized support from special education teachers – they give children with disabilities the opportunity to be educated alongside their peers. The ALC utilizes a holistic approach to assisting infants and children with developmental disabilities and their families. Last year, they were able to impact the lives of over 500 individuals through partnership with several preschools in the Atlanta area. Learn more at www.alckids.org.
Children’s Healthcare of Atlanta is an amazing organization that is critical to children in Atlanta and the Southeast. The Medically Complex Care Program will be housed at the new Center for Advanced Pediatrics at CHOA, and will be vital to the lives of children with disabilities and diseases. The money raised will go to fund their most pressing needs in helping support these children and families
These are exceptional charities whose missions are to help children like Peter to realize their potential in life, as well as enhance and ease the journey for the child and the family.
Many other children around the world, like Peter, have been severely affected by this disease as well as numerous other disabilities. Research and support for children and families with these disabilities and fragilities is highly underfunded, and they all deserve an opportunity to realize their potential in this world.
2019 Race Planning Committee:
Sumner Bradshaw, Kate Burke, Kathryn Calhoun, Kate Castellaw, Laura Crim, Angela Cunningham, Liza Davidson, Sarah Dozier, Laura Fletcher, Carla Geiger, Kelley Gilbert, Emi Gragnani, Anne Park Hopkins, Jennifer Kellett, Elizabeth Lesley, Margaret Lesley, Katherine Lynch, Molly Lynch, Heather Miller, Stacey Noell, Toney Peer, Lauren Petcho, Meghan Peters, Britt Prevost, Shannon Reynolds, Charles Schoen, Seale Lindsay, Morgan Smith, Lisa Stivers, Maureen Thomas, Julie Tourre, Martin Yoder
Race Founders (Peter’s Pals):
Courtney Amos, Allison Barker, Laura Crim, Liza Davidson, Emi Gragnani, Margaret Lesley, Elizabeth Lesley, Molly Lynch, Elizabeth Newton, Britt Prevost, Anne Park Hopkins