News

Blog posts on current GRI Disorders news and events

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!

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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.

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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.

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Take Action NOW! Help Secure ICD-10 Codes for GRI Disorders!

The U.S. Centers for Disease Control met last month to consider adding ICD-10 codes for GRIN, GRIA, and GRIK Disorders. ICD-10 code applications are considered by U.S. officials and adopted by the World Health Organization. There is now a public comment period through May 17, 2024.

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Get Moving for GRI 2024

We are excited to kickoff our 5th annual virtual physical family challenge to promote healthy lifestyles while raising money to help find therapies and cures for those living with GRI Disorder.

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L-Serine Trial Update

A recently published clinical trial found that a new treatment, L-serine, appeared to have some positive effects in a small group of children with GRIN Disorder.

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2024 GRI Virtual Conference

Join others from around the world at the 2024 GRI Virtual Conference. Learn more about what’s happening in GRIN research and hear the latest developments from clinicians, researchers, and family members.

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How 2023 brought us closer to treatments and cures

Since our founding in 2019, CureGRIN has been working tirelessly alongside researchers, clinicians and industry to accelerate the path to treatments and cures. There are many promising compounds and genetic treatments, but there are barriers in getting those to clinical trial. Adding ICD-10 codes for these nine genes would remove a significant barrier to clinical trials, by helping us to better understand where our patients are located.

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Rare Disease Day

Join us and #lightupforrare on Rare Disease Day, February 29! Light up in solidarity with over 300 million people living with a rare condition and share our colors.

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CureGRIN’s Letter to the CDC Regarding ICD-10 Codes for GRI Disorders

Since our founding in 2019, CureGRIN has been working tirelessly alongside researchers, clinicians and industry to accelerate the path to treatments and cures. There are many promising compounds and genetic treatments, but there are barriers in getting those to clinical trial. Adding ICD-10 codes for these nine genes would remove a significant barrier to clinical trials, by helping us to better understand where our patients are located.

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Get Moving for GRI 2023

We are excited to kickoff our 4th annual virtual physical family challenge to promote healthy lifestyles while raising money to help find therapies and cures for those living with GRI Disorder.

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CureGRIN awards $652,500 in Research Grants

CureGRIN Foundation is excited to announce that we are funding five research projects for a total investment of $652,500. The announcement was made by CureGRIN CEO Keith McArthur last week at GRI Conference 2023 (GRICON).

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Let’s Talk About Money

Today, I want to be transparent with you about how much money we have to spend on treatments and cures, how far that will take us, and exactly why we need your help to go further.

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Count Me In 2022

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.

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2022 GRI Conference

GRI Conference 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.

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2023 GRI Conference

GRI Conference 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.

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Serve as Treasurer on the CureGRIN Board

Do you know our next Treasurer? CureGRIN Foundation is looking for a Treasurer located in the United States to join our Voluntary Board of Directors. This person does not need to be a family member of someone with GRI Disorder but they must be committed to our mission. If you know anyone with finance or accounting experience interested in serving the global GRI community, please nominate them by providing their contact information to heather@curegrin.org by May 3, 2022.

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Get Moving for GRI 2022 VIRTUAL Event

We are excited to kickoff our 3rd annual virtual physical family challenge to promote healthy lifestyles while raising money to help find therapies and cures for those living with GRI Disorder.

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Serve on the CureGRIN Board

Would you like to join us on our mission to improve the lives of people living with GRIN, GRIA and GRIK Disorder? If you are a Parent, Grandparent, Sibling, or Caregiver of a person with GRIN, GRIA or GRIK Disorder please consider applying for the CureGRIN Board of Directors.

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GRI Genes Roundtable – Dec 2021

We brought together researchers and clinicians studying GRI Disorders, GRIN genes, GRIA genes, GRIK genes, NMDA receptors, and other ionotropic receptors (AMPARs, kainate receptors, and delta receptors) to discuss and exchange ideas on GRIN, GRIA, and GRIK variants. There were 43 participants present for the meeting.

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GRI Genes Roundtable – Oct 2021

We brought together researchers and clinicians studying GRI Disorders, GRIN genes, GRIA genes, GRIK genes, NMDA receptors, and other ionotropic receptors (AMPARs, kainate receptors, and delta receptors) to discuss and exchange ideas on GRIN, GRIA, and GRIK variants. There were 43 participants present for the meeting.

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GRI Genes Roundtable – Sept 2021

We brought together researchers and clinicians studying GRI Disorders, GRIN genes, GRIA genes, GRIK genes, NMDA receptors, and other ionotropic receptors (AMPARs, kainate receptors, and delta receptors) to discuss and exchange ideas on GRIN, GRIA, and GRIK variants. There were 43 participants present for the meeting.

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Count Me In 2021

CureGRIN is looking for GRI Families to help us raise $250,000 to fund research for a cure for GRI Disorder.

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GRI Connect

Introducing GRIConnect: Learn and network with GRI families, GRI researchers and GRI clinicians around the globe!

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GRIN Sibling: Sierra

Sierra Wasielewski, Sister to Austin, shares her experience on being a sibling to her brother with GRIN Disorder.

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GRI Genes Roundtable – Jul 2021

We brought together researchers and clinicians studying GRI Disorders, GRIN genes, GRIA genes, GRIK genes, NMDA receptors, and other ionotropic receptors (AMPARs, kainate receptors, and delta receptors) to discuss and exchange ideas on GRIN, GRIA, and GRIK variants. There were 50 participants present for the meeting.

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GRIN Sibling: Abby

Abby Pellitteri, Twin Sister to Owen, shares her experience on being a sibling to her brother with GRIN Disorder.

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CureGRIN Foundation is a nonprofit, tax-exempt organization as defined in section 501(c)(3) of the Internal Revenue Code and, as such, contributions to CureGRIN are tax-deductible. Fund research. Save a life.

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