Lowe Syndrome Association

About Us

Founded over 40 years ago, we are on a mission to improve the lives of individuals living with Lowe syndrome and their families through fostering communication, providing education and supporting research. This rare disease, like many, does not have any meaningful treatment to improve or elongate life. We are determined to change that for our children in the Cincinnati area and beyond. Headquartered in Anderson Township, the LSA serves families worldwide.