CureGRIN Foundation is a parent-run charity dedicated to improving the lives of those with GRI disorder. We work closely with scientists and the medical community to drive research that will lead to treatments cures. Our goal is simple and bold: To find cures and therapies for people living with disorders caused by variants in the GRIN1, GRIN2A, GRIN2B, and GRIN2D genes. These genes contain the code to create NMDA receptors, which are essential for learning and memory. GRIN Disorders are rare genetic conditions with severe life-limiting consequences. Many GRIN patients are non-verbal, unable to walk, and many cannot feed or toilet themselves. They often suffer severe and frequent seizures that are not responsive to medical therapies.