07/16/2026
Help support our girl Harper, and the The Spina Bifida Association of the Carolinas! From her mom - Jenna Pender Brown:
Every year, this walk reminds us how far Harper has come and why this cause will always be close to our hearts.
Harper was born and will live a lifetime with Spina Bifida. She and her SB friends have faced challenges that most people will never experience. Through multiple surgeries, countless appointments, and more determination than I can put into words, she continues to amaze us every single day. She is strong, kind, funny, and never lets her diagnosis define her.
On September 12th, we’ll be walking together at the Charleston Walk-N-Roll to support families like ours.
If Harper’s story has ever inspired you, or if you’d like to help make a difference for others on this journey, we’d be so grateful for your support. Whether you donate, join her team, or simply share this post, every act of kindness helps.
Thank you for loving Harper, cheering her on, and helping us build a future where everyone with Spina Bifida has the opportunity to thrive.
You can visit the link in our bio or go to https://give.sbaa.org/team/837751.