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[INSERT YOUR CHILD'S NAME] Story
[INSERT YOUR CHILD'S STORY BELOW]
Please use this space to tell us a little about your child and the importance of a cure for GRI Disorder.
Suggested word count is 250-450 words.
We are grateful for your support in our journey to a cure.
We’ve got the plan.
In 2021 CureGRIN brought together families, researchers, clinicians and biotech to identify 10 “essential questions” that need to be answered in order to find cures and treatments for GRIN Disorder. Thanks to the passion of our family fundraisers and the generosity of our donors, we’re confident we will be able to provide at least $750,000 in research grants in our first round of funding beginning this May. This first wave of funding will set the pace for GRI research and tackle as many of the 10 essential questions as possible.
Researchers are ready to go. But we still need more funding.
CureGRIN has built a global network of 100+ scientists. These researchers are standing by to help make it happen. But research is expensive. They need our help to get started on the next big phase of research for our GRI community.
There will be many new and exciting opportunities to make advancements towards treatments and cures for the first time. While $750,000 will help us make great strides, we know we’ll need to say “no” to critical research opportunities without more funds to invest.
We need your help to grow the GRI Research Accelerator Fund (GRAF) to at least $1 million so we can say “yes” to the right investment opportunities.
Can we count on your support?
About CureGRIN
CureGRIN is a US-based, global, parent-led 501c (3) foundation committed to finding cures and treatments for people affected with GRI Disorders caused by variants in the GRIN1, GRIN2A, GRIN2B, GRIN2D, GRIA1, GRIA2, GRIA3, GRIA4, and GRIK2 genes.
Where do donations go?
Our plan is to partner with the world’s best researchers to help us answer all 10 questions.
Our goal is to award $1 Million in funding to researchers in early 2022 to help us answer questions such as:
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Is a cure possible at any age?
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Can we deliver gene therapies in a way that will correct enough brain cells?
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What are the best drugs for GRI Disorders and their symptoms?
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How do we prove to regulators that new treatments are working so they can be made available as soon as possible?
All funds raised by April 30, 2022 will be invested in this critical first round of research through the GRI Research Accelerator Fund. The more work we get done through this first round, the faster we’ll get to better treatments and cures.
Thank You to Our Donors!
Mail Checks to: CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134 (please write child's or family name in memo)
EIN# 83-4658977 Need help? Email [email protected]
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-4658977 Need help? Email [email protected]
Thank you for your donation!
Thank You!
Thank you for trusting us with your generous donation. Your gift gives GRI families around the world hope for a better future for their loved ones.
Your support is crucial in driving forward our Research Roadmap --CureGRIN’s three-year plan that focuses on 10 essential research questions that need to be answered in order to find cures and treatments for GRI Disorder.
We will work tirelessly to ensure your gift has the biggest impact to improve the lives of those with GRI Disorder.
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-4658977 Need help? Email [email protected]