We are a group of parents who connected through VOGM Facebook group to offer VOGM support to one another. We saw a need for accurate information and emotional and financial support for VOGM network of families and especially those new to the diagnosis. We created this non-profit as a way to alleviate some of the pain and helplessness we felt during our journeys.
CEO
Co-founder
VOGM Parent
CIO
Co-founder
VOGM Parent
CFO
COO
VOGM Parent
Professor of Neuroradiology and Radiology
Director of the Pediatric Cerebrovascular Program at Mount Sinai
Pionier of VOGM/AVM treatment
Vein of Galen Malformation Support Network was founded in 1995 by a group of community members who recognized the need for a local organization dedicated to helping homeless individuals. Since then, we have grown into a thriving nonprofit, serving hundreds of individuals each year.
Our team is made up of dedicated professionals who are passionate about making a difference in the lives of those we serve. From case managers to outreach workers, we work together to provide comprehensive support to our clients.
We are proud to partner with a variety of local organizations to provide the best possible support to our clients. From food banks to healthcare providers, our partners help us extend our reach and impact in the community.
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