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Roughly 150 people are known to be impacted by a GNAO1 related neurodevelopmental disorder.

Most patients have been diagnosed in the past year or two.

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Roughly 150 people are known to be impacted by a GNAO1 related neurodevelopmental disorder.

Most patients have been diagnosed in the past year or two.

What We Do

The Bow Foundation supports GNAO1 families by raising awareness, enhancing research, and fostering community.

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ABOUT GNAO1

To date about 100 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.

STORIES

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Read stories from some of the roughly 100 people impacted by a GNAO1 disorder.

News

Latest from the Bow Foundation and GNAO1 News

Bow Foundation featured on KMOX Radio

Bow Foundation featured on KMOX Radio

Stephen Bell, Bow Foundation co-founder and board member, recently joined KMOX radio to discuss GNAO1, the work being done by the foundation, and recap the GNAO1 medical clinic and conference.

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2018 Year In Review

2018 Year In Review

Since launching in 2017, the Bow Foundation has raised more than $250,000 to fund GNAO1 research, raise awareness, and support families.

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DONATE

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Your donation will help fund GNAO1 medical research and change lives. No amount is too small.