Dandy-Walker Alliance
The Dandy-Walker Alliance is the only nonprofit 501(c)(3) organization in the world advocating for people afflicted by Dandy-Walker Syndrome. We are an all-inclusive organization comprised of individuals directly and indirectly affected by Dandy-Walker. We share a collective interest in educational, informational activities and supporting non-partisan research to increase public awareness of the congenital birth defect Dandy-Walker.
The Dandy-Walker Alliance also support all efforts to determine the cause(s), find the cure and to ameliorate the effects of Dandy-Walker. We believe that by making findings available to families affected in an organized and accessible way and by disseminating the direct and indirect outcomes of translational research we can more swiftly move the results from the bench to the bedside in an expeditious manner.
To learn more and get involved, visit dandy-walker.org or email [email protected].
Webinar: A Neurosurgeon's View of Dandy-Walker with Dr. John Myseros, M.D.
Living with Dandy-Walker: Emily Jones, Advocate and Occupational Therapist
Interview: Krystal Lacey, Dandy-Walker Parent and Northeast Coordinator
An Update from Dr. Bill Loudon, MD, PhD, of Bionaut Labs
Interview: Anntonette Dennis, Dandy-Walker Alliance Southern Coordinator
Webinar: Understanding Dandy-Walker Genetics with Dr. Kimberly Aldinger, PhD
Living with Dandy-Walker: Nick Nguyen, Advocate and Soccer Enthusiast
Interview: Paula Muller Runs the New York Half Marathon for the Dandy-Walker Alliance
Webinar: Dr. Bill Loudon, VP of Neuroscience, Bionaut Labs
Happy Thanksgiving!
Safe at Home Tuesdays – Dandy Walker Alliance
Baby Louise Montage
Dandy Walker interview on WCBI news
Eric Cole-Dandy Walker testimony
Ryans Story
Dandy Walker Children