I met Kaden’s parents, Bridgett and Basil, at the very first HCU Conference in Denver, Colorado back in 2011. That was actually the very first time I’d met any other HCU patients or parents – the beginning of what is now many connections in both the HCU community and the greater rare disease community. The Zaidi family have been great advocates for HCU and I’m thrilled to run a mile for their son, Kaden, in the Miami Half Marathon this upcoming weekend.
Desperate to get information from an experienced professional, we were put in touch with the genetics group at Phoenix Children’s Hospital and it wasn’t until after we met the geneticist and dietitian that we understood the importance of managing this disorder through diet and medical formula.
Ten years ago there wasn’t near the amount of information, resources and most importantly, a community to lean on and share experiences with. These developments have been instrumental to our family over the past ten years. Kaden is remarkable in making good choices and being conscientious as to what he’s eating as well as the importance of getting the protein he needs through medical formula. While he definitely needs a reminder, he understands the nutritional value that comes from his formula and the positive effects of taking his vitamin supplements and betaine. We couldn’t have asked for a stronger and more resilient son!