We Need Heroes!
Join us on August 20th for a virtual Walk for Strength!
As you know, our daughter has a rare, currently untreatable, genetic condition called Creatine Transporter Deficiency (CTD.) Our parent group is committed to raising awareness and funding for gene therapy research and drug development. We know schedules are tricky especially during college soccer season. So, anyone who wants to support ‘Al’s Pals’ on August 20th, we’d be incredibly grateful.