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:

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!

News Headlines

Brand New Purpose-Bu ...

Posted: July 1, 2020
Prader-Willi Syndrome (PWS) is a rare and complex genetic condition affecting roughly one in every 15 to 20,000 births globally each

Interaction Appoints ...

Posted: June 11, 2020
Interaction Disability Services is pleased to announce the appointment of Brett Thompson as its new Chief Executive Officer commencing