Image from iOS

Walk for Strength 2022

Join Cadman’s Creatine Crusaders on August 20th for ACD’s seventh annual Walk for Strength and help us raise awareness for Cerebral Creatine Deficiency Syndromes! We will be meeting at 9:00 AM at Mission Bay (San Diego).

View sponsorship information here.

Cadman was diagnosed with the currently untreatable genetic disorder Creatine Transporter Deficiency (CTD) just before his 2nd birthday. At the time, he wasn't walking or talking yet, and while he has come a long way since then, at six years old, Cadman is still mostly non-verbal and faces many additional long-term challenges with the additional diagnoses that come along with CTD including intellectual disability, autism and epilepsy. We love and adore Cadman exactly the way he is yet we have hope for a better future for him thanks to the research efforts being led by ACD. Initial fundraising efforts have been very successful, and donations continue to be needed moving forward for continuing progress on gene therapy and drug development research. Your support means so much to our family and the entire community of people affected by Cerebral Creatine Deficiency Syndromes!