Champions of the Foundation
Meet Aidan
Aidan’s a young teen with a sparkling spirit and a beautiful smile. But as a newborn, there were many unknowns for his parents who faced significant medical complications with him almost immediately. They knew challenges were ahead as they thought about his future.
The medical reality before them was in stark contrast to their love for a wonderful child with a full head of hair and big brown eyes, whom they adored instantly.
At only four-hours old, Aidan had his first of many choking episodes due to severe GERD. At 9 months old, he was not able to sit up on his own, would not make eye contact, was not babbling, and had seemingly no interest in the world or people around him. He was finally diagnosed with a rare genetic disorder known as Dup15q Syndrome.
Over the next few years, Aidan received many additional diagnoses. With so many overwhelming obstacles before him, he’s still made progress worth celebrating.
Whatever you are going through, know that understanding the cause is probably in the future. We know that your world is being shaken right now, but trust that you will find solid ground to stand on and know that you will become a better person because of the journey. Love and patience will see you through. Robert & Adrienne – Aidan’s parents
Courageous Faces Champion Aidan’s entire life has changed and his world has been greatly enriched and expanded through his parents love and determination to help him reach his greatest potential. Courageous Faces Foundation is there to support them on the way.
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