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...
2021 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 2021 year in review – Bow Foundation 2021 Year in...
Rare disease charity funds nearly $350,000 in groundbreaking research
Charlottesville, VA – The Bow Foundation today announced a total of nearly $350,000 in grants to fund four projects to advance medical research into GNAO1-related neurodevelopmental disorders, a rare genetic condition with no common name. Collectively, this...
2020 Year in Review
Thank you for your past support of the Bow Foundation. The Foundation was established in 2017 to fund GNAO1 medical research, support families, and raise awareness about this rare disease with no common name. Because of your generosity, we are building a better...
Rare disease charity awards UCSF $100,000 for epilepsy zebrafish study
Rare disease charity awards UCSF $100,000 for epilepsy zebrafish study January 30, 2020 Charlottesville, VA – The Bow Foundation today announced a grant of $100,000 to the University of California, San Francisco to study GNAO1-related neurodevelopmental disorders, a...
Rare disease charity awards $50,000 post-doctoral fellowship to Scripps Research Institute researcher
Rare disease charity awards $50,000 post-doctoral fellowship to Scripps Research Institute researcher Thursday, January 30, 2020 Charlottesville, VA – The Bow Foundation today announced a grant of $50,000 to Dr. Brian Muntean, a researcher in the Martemyanov lab at...
2019 Year in Review
Thank you for your past support of the Bow Foundation. The Foundation was established in 2017 to fund GNAO1 medical research, support families, and raise awareness about this rare disease with no common name. Because of your generosity, we are building a better...
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.
St. Louis Post Dispatch: First Clinic for GNA01 Patients
Three dozen families came here from Argentina, Italy and all over the U.S. this week to help doctors understand the medical challenges caused by a mutation of the GNAO1 gene.