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2025 Holiday Gift Guide

Whatever holiday you celebrate, we are here to provide you with the perfect CureGRIN inspired gifts that keep on giving…to the recipient and to our kids!

Count Me In 2024

CureGRIN is looking for GRI Families to help us raise funds for research into treatments and cures, as well as other education and community-building programs provided by CureGRIN Foundation.

Coming Soon: A Guide to Treating / Curing GRI Disorders

Last week, CureGRIN brought together the world’s top experts in GRI Disorder Research for a two-day symposium in Toronto, Canada where we discussed the suitability of every type of treatment for each GRI gene and class of variants. 

Rare Across America with Kat

My name is Kat Reiher, I am the lead Ambassador for CureGRIN, and I wanted to write about Rare Across America!

Early Results from GRI Census

In just one week, nearly 150 families representing 10 genes and 16 countries have completed and submitted the GRI Census.

GRICON25

GRICON25 brings together GRI families, researchers and clinicians, and industry representatives from around the world to educate, collaborate and network for treatments and cures for GRI Disorders.