The FASD Trust exists as a charity to raise awareness of FASD thereby;

• improving the understanding of those with FASD and;
• increasing the support that those with FASD and their families / carers receive, not just from statutory bodies, but from the wider community. 
• preventing others being born with FASD.

 It aims to do this by:

• running support groups
• having a telephone helpline
• holding training seminars 
• providing advice on "best practice" to teachers, medics and  other professionals involved in the care of those with FASD.
• informing local and national decision makers to ensure provision for those with FASD.
• collaborating with others.