As a lifeling brain disorder, we need insurance companies to cover meds and therapies to help people (especially children) with FASD. Early behavior supports are critical. We also need more professionals who understand the condition and can actually help patients. Frequently doctors and tgerapists have geard of FASD but have no experience, which results in a lifetime of trial and error. There are experts and valuable data and this should become part of a standard curriculum for US providers. More funding needs to be appropriated to find better therapies and support for independent living.