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Welcome to CureGRIN's Count Me IN Campaign Kickoff!
Thank you for being a GRI Champion. We are so excited you are participating in our Count Me IN campaign.
The momentum and knowledge our GRI Community is building is truly remarkable and leaves us even more hopeful that we will find treatments or cures that will have a meaningful impact on the lives of people living with GRI.
But nothing will happen without funding. This is where we can all play an active role in our kids’ future. Now, more than ever, WE NEED YOUR HELP to push forward our research efforts that were developed with input from parents, researchers and clinicians.
This year, CureGRIN brought together a team of families, researchers and clinicians to develop our research roadmap for the next three years. This document identified 10 essential questions that we need to answer in order to find cures and treatments for GRI Disorders (GRIN, GRIA and GRIK).
These are critical questions, including:
- Is a cure possible at any age?
- Can we deliver gene therapies in a way that will correct enough brain cells?
- What are the best drugs for GRI Disorders and their symptoms?
We can’t answer these questions without you.
We need your help to raise funds for hiring the scientists and doctors that can help us answer these questions. Our goal is to award $1 Million in funding to researchers in early 2022. So far, we are just 38% towards achieving that goal.
We are grateful for your support in raising funds from family, friends and other contacts. The support you raise is crucial for funding CureGRIN’s research roadmap.
Our recommended goal for a GRIN Champion Family is $2,500. But we know each family’s situation is different, so you can increase or decrease your goal during registration. Even families that raise $500 or $1,000 bring us closer to finding a cure.
Once registered, you will see a button where you can set up your personalized Count Me In page and you will also receive an email with instructions on how to personalize your Count Me IN page with your special GRI’s picture and story.
“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
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
Thank You for signing up to be a GRI Champion!
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