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Welcome to CureGRIN's Count Me IN Campaign Kickoff!
Our main focus is on funding research to answer the “10 Essential Questions” outlined in CureGRIN’s Research Roadmap.
We recently asked researchers to submit proposals to answer these questions and we received applications asking for more than $2-million.
Rare disease parents are busy! For 2022, we’re providing more options, training, prizes and support to make fundraising less complicated and more fun. We’re providing more options for you to fundraise however works best for you, whether that’s using our software to build a customized fundraising page for your child, setting up a Facebook campaign, or simply printing out a pledge sheet and collecting cash or checks.
We’ll send you CureGRIN merch for hitting different fundraising targets. You’ll also get entries into a drawing for big prizes including a suite for three nights next March at the Royal Sonesta Cambridge Hotel for GRI Conference 2022.
We’re also providing support on everything from how to set up a fundraising page to the psychology of getting over the fear of asking for donations. We provide a detailed fundraising guide, host a Count Me In discussion group on GRI Connect, and attend office hours where we can help you set up your campaign in real time.
There are at least 1,500 patient families in our GRI community, but fewer than 100 have participated in fundraising campaigns. If you haven’t participated yet, this is your chance to join.
You don’t need to raise a lot to make a big difference in our search for treatments and cures.
If you haven't participated yet, this is your chance to join. Register today!
“The support we have received from the CureGRIN Foundation will enable us to continue to serve patients, clinicians, and basic scientists by supporting the functional analysis of GRIN variants. This work represents a critical step forward in understanding how to best help GRIN patients and will be important as we eventually move forward towards clinical trials. We are deeply appreciative of the efforts of CureGRIN, the generosity of the donors who make this work possible, and we draw inspiration from the resilience of the GRIN patients and their parents and families. ” Stephen Traynelis, PhD and Director of the Center for Functional Evaluation of Rare Variants
About CureGRIN
CureGRIN is a parent-led 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. We are a 501(c)(3) charity registered in the United States, but our focus is global. the United States
Where do donations go?
This year, 92% of CureGRIN’s expenses are earmarked for research and programs, including $900,000 to answer the “10 Essential Questions.” These questions were identified in our Research Roadmap as critical to finding treatments and cures for GRI Disorder.
Questions include:
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-465-8977 Get in touch! Email info@curegrin.org
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-465-8977 Get in touch! Email info@curegrin.org
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-465-8977 Get in touch! Email info@curegrin.org
You will receive an email with instructions on how to set up your team page.
CureGRIN Foundation
P.O. Box 2182
Parker, CO 80134
EIN# 83-465-8977 Get in touch! Email info@curegrin.org