Category: Personal Stories

The following stories are from people who have had intimate contact with FASD.  The stories are from birth parents, foster and adoptive parents and people with FASD.  It is critical for health practitioners to read about the personal side of FASD to flesh out the clinical aspect of the condition.  The problem that people with FASD have not being able to link cause and consequence means one thing when it is written on paper but it means something completely different to parents.

Interview with Sonia Berton, rffada President

What more can Australia do to combat FASD?

  1. Acknowledge that FASD exits and to levels uncertain in Australia due to an historical reluctance to openly speak about or deal with FASD – for reasons not researched or fully established. There are plenty of theories and anecdotal stories in relation to our strong desire to ignore FASD in Australia – from the costs to service provision through to an outdated view in the alcohol and other drug sector including researchers and policy development personnel.