The Cure Lowe Foundation is a non-profit organization dedicated to accelerating research and development of innovative treatments for Lowe syndrome, a rare genetic disorder affecting 1 in 500,000 individuals worldwide
The Cure Lowe Foundation is a non-profit organization dedicated to accelerating research and development of innovative treatments for Lowe syndrome, a rare genetic disorder affecting 1 in 500,000 individuals worldwide. Our mission is to unite top scientists, industry experts, and patient advocates in a common goal: to cure Lowe syndrome. Founded by parents of a child with Lowe syndrome, we are driven by a fierce determination to rewrite not just our son's future, but the future of all children affected by this devastating disorder. Through our unique hybrid approach combining non-profit agility with biotech expertise, we aim to develop a breakthrough gene therapy for Lowe syndrome within the next four years. Our focus areas include: - Funding cutting-edge research in gene therapy - Fostering collaborations between academia and industry - Raising awareness about Lowe syndrome