CureGRIN Foundation
GRIA, GRID, GRIK and GRIN
What are GRI Disorders?
GRI Disorders are rare single-gene disorders related to the GRIA, GRIK, GRID and GRIN genes. Many GRI patients are non-verbal, unable to walk, and many cannot feed or toilet themselves. They often experience severe and frequent seizures that are not responsive to medical therapies.
You can help us
find a cure.
CureGRIN is a foundation founded and run by parents who are committed to improving the lives of people living with GRI Disorders.
We need YOUR support! Whether you give $5 or $500, your donation brings us one step closer to finding a cure for GRI Disorders worldwide! Can’t donate right now? Volunteer or Connect with CureGRIN Foundation.
Our personal GRI Disorder stories
GRI Disorders affect many families. Get to know some of the children and people affected by this rare disease.
GRI Disorders Research
Learn more about the ongoing research towards therapies and cures for GRI Disorders.
The rarity of GRI Disorders
An estimated 1,000 people worldwide have been diagnosed with GRI Disorder. There could be more than 100,000 yet to be diagnosed.
