The American Bar Association (ABA) has selected William “Billy” Edwards as the 2025 winner of the Paul G. Hearne Award for Disability Rights. A member of the FASD United Board […]

Earlier this month, FASD United released its National Education Survey. This year, a small group of educators and FASD advocates worked to enhance the portion of the survey focused on […]

The Policy Forum originally scheduled for November 26th has been rescheduled for Wednesday, December 3rd at 2:00 PM ET to accommodate for Thanksgiving travel. November provided opportunities to meet with Members of Congress and […]

Family physicians are much more than medical service providers. In fact, “they often get to know families better than nearly anyone else outside of the family,” according to Corban Wehr of […]

Rebecca Tillou is on the move again.  A runner since middle school, an FASD self-advocate starting with her diagnosis at age 34, and the founder of Move FASD, Rebecca is […]

National FASD Impact Week is coming up this September 15-17 in Washington, DC.  Join advocates, clinicians, researchers, and professionals from around the country.  Here are 5 ways that YOU can […]

Dr. Petrenko is a leading FASD researcher who is developing innovative mobile apps to support people with FASD and their families.  Working with CIFASD for almost 10 years, Christie’s career […]

FASD United is proud to share a collection of video recordings from the 9th International Research Conference on FASD, held in Seattle, Washington in March 2025.  Recordings cover a range […]

FASD United is proud to take part in the AUCD (Association of University Centers on Disabilities) conference in Washington, DC Nov. 3-6 as a member of the planning committee and […]

Major Advocacy Alert:   An agency of the Federal Government (the Government Accountability Office or GAO) wants to hear how your disability affects your health care.  Responses to a short […]