My husband and I are the parents of two amazing kids. Our son, now 18, has an FASD and he was not officially diagnosed until 3 1/2 years ago. There were very few resources for our son and very few professionals who even knew about FASD. Not only are my husband and I parent advocates for our son, but we started our podcast and website to give other families HOPE and to share the journeys to those in the FASD community. The time is NOW to start talking and start the change to increase awareness, resources and support for those who live with FASD (and their families and loved ones). Let’s use our voices for change and to listen to what is being said by those in the FASD community!