Welcome

Prader-Willi Syndrome (PWS) is a rare and complex genetic condition which is non-inherited and linked to the deletion or incompleteness of genes of the 15th chromosome.  This chromosome abnormality leads to neurological changes, causing altered growth patterns, cognitive disability and excessive eating patterns.

Interaction has provided best practice PWS services and supports since 1992.  As a person-centred organisation we take a great deal of pride in sharing our knowledge, expertise, services and support to people with Prader-Willi Syndrome and their families.  We offer training and advice for families and/or organisations that are impacted by the issues that those with PWS and their support networks face.

Interaction has recently expanded its high quality level of services and supports – with programs that can be specifically tailored to meet the individual needs of children and adults with Prader-Willi Syndrome.

Please take a look at our PWS introduction video by clicking the first video image.  Other videos include:

• Spencer and his family, who talk about what it’s like when you find out your child has PWS.
• A siblings point of view – Spencer’s siblings talk about their thoughts and feelings.

We hope the information contained within our website is of benefit to you, please contact us today and find out more about how Interaction can help you!