Working on a cure for cystinosis
The mission of the Cystinosis Research Foundation is to support bench and clinical research that is focused on developing improved treatments and a cure for cystinosis.
Read about the Mission of the Cystinosis Research Foundation »
In February 2003, on the eve of Natalie’s 12th birthday, Natalie made a birthday wish that no child should ever have to make.
Read about the origin of the Cystinosis Research Foundation »
View the current list online.
Our Board of Trustees »
The Scientific Review Board is composed of leading cystinosis scientists, researchers and doctors from around the world.
Learn about the Scientific Review Board »
The Cystinosis Research Foundation’s mission is two-fold and focused: to find better treatments and a cure for cystinosis. Funding quality research studies remains a priority and is an ongoing process. The CRF announces two global calls for research proposals in the spring and fall of each year.
Learn about our research progress »