Colin Beech Foundation
OUR
MISSION
The Colin Beech Foundation was started in honor of our son Colin, who had his life altered as a result of a ruptured AVM (arteriovenous malformation) in his brain during October of 2020. Our foundation’s goal is to further the research and education for those affected by AVM’s. Colin’s foundation donates to local hospitals, rehabilitations centers, and charities that assist people and families suffering from this rare disease. It is our goal to give back to the many organizations that played a part in Colin’s recovery, as we hope to see future advances in patient treatment and care, as well as increased support networks for families.
Charities we Donate to
WHAT IS AN AVM
An arteriovenous malformation is a rare condition where an abnormal and fragile connection of arteries and veins form in the brain or spine. Many cases are congenital and silently form prior to birth. They have a detection rate of 1/100,000 each year in the US. Typically, patients present between the ages of 20 and 60 years of age. Although they can occur at any age, Colin’s AVM ruptured the night before his ninth birthday.
CHECK OUT OUR STORY ON NBC NEWS
Events
Colin Golf Invitational Fore AVM Research
Learn about the upcoming event on Saturday August 10, 2024 and see pictures from last year’s invitational