Patient Story: Meet Cam
Cam has been a patient of Dr. Murray’s since he was 8 years old due to a rare disease called; Hereditary Hemorrhagic Telangiectasia (HHT). This is a rare autosomal dominant genetic disorder that affects Cam’s lungs and oxygen levels.
Cam and his family take countless trips to Toronto for treatment and they often look forward to appointments at NEO Kids where they are able to stay closer to home. As a single parent house-hold trips down south is often difficult for the entire family, as school and other activities have to be sacrificed when they are away. Cam and his family love that NEO Kids is local and focuses solely on children’s needs.
Cam is now fifteen and is an avid video game player, skier and tennis player. He enjoys the outdoors and spending time with his friends and family.
“We would love to see NEO Kids grow to allow children with similar situations to stay closer to home for treatment.”