Watch this space. We aim to launch our new website very soon!
Interested to know what HPN is like in other countries? This presentation was given by 3 HPNers at a 2015 PNDU social gathering, giving HPNer observations about living with HPN and the services received from the PN manufacturers and delivery/support services in 4 countries - Australia, New Zealand, United Kingdom and USA.
PNDU has registered as a not-for-profit incorporated association!
Given our steadily growing numbers and growing activity, the Management Committee determined that it was appropriate and beneficial to move our community into a formal structure. Operating as an incorporated association will provide the organisation with a number of advantages, including importantly, the following:
PNDU Inc’s Objectives and Constitution is on our Documents page.
The Management Committee will continue to work together in the following roles:
We are a group of Australian and New Zealand consumers, parents, carers and professionals affected by Intestinal Failure requiring Intravenous (IV) nutritional support (Home Parenteral Nutrition or HPN).
Please take a moment to become a member in order to enter the site and receive our free e-newsletter Dripline which is published quarterly. Click here for the latest edition of Dripline.
And if you are an Aussie or Kiwi HPNer or carer and would like to take part in our private consumer/carer-only email forum and/or our closed Facebook group, please contact us with a brief history in relation to your Home Parenteral Nutrition.
Please Note: This information is kept in strictest confidentiality.
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