Building a better tomorrow for GNAO1 patients and families
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Building a better tomorrow for GNAO1 patients and families
Most patients have been diagnosed in the past year or two.
400+ people are known to be impacted by a GNAO1 related neurodevelopmental disorder.
What We Do
The Bow Foundation supports GNAO1 families by raising awareness, enhancing research, and fostering community.
ABOUT GNAO1
To date about 400+ people worldwide have been identified as having a mutation on the GNAO1 gene.
RESEARCH
We fund cutting edge research into GNAO1–related neurodevelopmental disorders and similar rare diseases.
COMMUNITY
We facilitate opportunities for families affected by GNAO1 to connect and share their stories.
Who is GNAO1?
DONATE
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Your donation will help fund GNAO1 medical research and change lives. No amount is too small.
News
Latest from the Bow Foundation and GNAO1 News
Bow Foundation Announces $540,000 in Rare Disease Research Grants
Charlottesville, VA – The Bow Foundation is awarding $540,000 in grants to fund six groundbreaking research projects aimed at advancing medical understanding and treatment options for GNAO1-related disorders, a rare neurological genetic condition. This grant program...
Bow Foundation Announces $300,000 in Rare Disease Grants
Charlottesville, VA – The Bow Foundation today announced a total of $300,000 in grants to fund three new projects to advance medical research into GNAO1-related disorders, a rare neurological genetic condition with no common name. The Bow Foundation grant program is...
2022 Year in Review (PDF)
We want to send you a special note of thanks for your continued support of the Bow Foundation and our mission to build a better tomorrow for GNAO1 patients and their families. Click here to view our full 2022 year in review - Bow Foundation 2022 Year in Review
STORIES
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Read stories from some of the roughly 400+ people impacted by a GNAO1 disorder.
