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

Cure Lowe Foundation

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