Our vision is to bring all Canadians with Aniridia together to make sure that everyone gets the best possible care, information, and treatments possible. Ultimately we strive to help find a cure for Aniridia.
I started this foundation because my wife and daughter have Aniridia. My wife actually comes from one of the largest families with the condition in Canada. Rather than accept the status quo of a fragmented treatment system across the country we decided to create this foundation for the benefit of everyone having this condition. Unless things change people will continue to be met with a lack of qualified professional help and they will ultimately suffer the consequences of that fragmented system.
Meet the Team