President of Blount’s Disease Strong Foundation
Angela is a mother to four children and an advocate for Blount’s Disease. Her advocacy efforts led the State of Kansas to approve a State Proclamation for Blount’s Disease Awareness Day. She also contributes as a writer for The Mighty website in honor of her daughter and special needs son. When her daughter was diagnosed at 18 months, old she felt alone with little support. Research lacks on this condition and Angela took action to make sure other parents across the world don’t have to face these challenges alone.
Board Member of Blount’s Disease Strong Foundation
At 18 months old Anneliese was diagnosed with Blount’s Disease. She has had multiple operations and is a big advocate for others. On her free time she enjoys making custom made awareness keychains and care packages for other children. She has shared her story in person at the State Capitol and spoke at local universities with future Doctors.