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The PWSA of Victoria Web Site is intended to provide information only - not to diagnose or advocate particular treatment options. The Diagnosis and treatment of Prader-Willi Syndrome should be made through a qualified medical professional. Thus, it is strongly urged that patients do not change treatment without first consulting their doctor.
The inclusion of any resource or link in the PWSA of Victoria Web Site does not imply endorsement.
Site design: Helen Anderson
On this Prader-Willi Syndrome Association of Victoria (Australia) website you will find:
- Details on our Association, what we offer and how we can be contacted
- Information for those who have had a recent diagnosis of PWS for your infant or toddler
- General information about PWS across all age groups
- A list of books, publications, and tapes available in our Members Library
- Stories and pictures from some of our members
- Contacts for other Australian PWS Associations
- Links to PWS Associations around the world and other useful organisations
- A link to our community at MC2 (at the top of the page) where you can look at, or post messages to, a forum where parents and others discuss PWS issues. You can also "chat" to others in your situation and find out about events
Prader-Willi
Syndrome Association of Victoria Inc ABN 93 836 682 679
Privacy:
We have no means of identifying you whilst visiting this site. It will be your decision whether to contact us or not.
