Loading....
It's time to fight for treatments and cures.
Join us October 1st to kick off our 6th annual Count Me IN campaign!
In just five years, CureGRIN has turbocharged the pursuit of treatments and cures for GRIN, GRIA, GRIK and GRID Disorders. We have even bigger plans to achieve our goal of treatments and cures by the end of this decade. But we need your help!
CureGRIN is recruiting 50 - 100 family fundraisers who will each try to raise between $1,000 and $20,000 from friends and family during this October’s Count Me In Campaign.
As parents of kids with a rare disease, we know how busy life can get. That is why we are 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’re also providing a detailed fundraising guide on everything from how to set up a fundraising page to the psychology of getting over the fear of asking for donations. You will also be able to engage in 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.
Our recommended goal for a GRI Champion Family is $2,500 but you can increase or decrease your goal during registration. Your support is vital and all gifts bring us closer to finding a cure.
Members of the CureGRIN team will be reaching out to GRI families over the next few weeks to assist and answer any questions you may have. We hope we can count on you to say, “Count Me IN”!
“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, GRIN3A, GRIA1, GRIA2, GRIA3, GRIA4, GRIK2, GRIK5 and GRID1 genes. We are a 501(c)(3) charity registered in the United States, but our focus is global.
CureGRIN Foundation
4845 Pearl East Circle, Ste 118 | Boulder, CO 80301
EIN# 83-465-8977 Get in touch! Email info@curegrin.org
CureGRIN Foundation
4845 Pearl East Circle, Ste 118 | Boulder, CO 80301
EIN# 83-465-8977 Get in touch! Email info@curegrin.org
CureGRIN Foundation
4845 Pearl East Circle, Ste 118 | Boulder, CO 80301
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
4845 Pearl East Circle, Ste 118 | Boulder, CO 80301
EIN# 83-465-8977 Get in touch! Email info@curegrin.org