Chloe-Fest Foundation

The Chloe-Fest Foundation is a non-profit committed to raising awareness for Osteogenesis Imperfecta (OI), which is a rare skeletal condition also known as brittle bone disease. Our founders, Will and Kate, have a daughter, Chloe, who was born with a severe form of this condition. Breakthroughs in research and access to resources are vital for children with disabilities to live a comfortable and functional life. We raise money through community outreach and a yearly event. These funds are donated to OI research as well as resources for families who have children with disabilities.