Parenteral Nutrition Down Under

Welcome to PNDU


The February-April 2015 edition of our newsletter, Dripline, is now out. Click here to see.  

Don't miss out receiving future editions!  If you haven't already, sign up to become a member of PNDU today. 

Let's go travelling!

PNDU's long-awaited updated Travel Information Booklet has recently been released with lots of helpful information for Aussie and Kiwi HPNers, carers and hospitals on how to plan and organise safe travel with HPN.

Download a soft copy of the Booklet here.

If you are an Aussie or Kiwi HPNer or carer and would like a hard copy of the booklet, please email us.  Likewise, if you are an Aussie or Kiwi clinician and would like a hard copy for you or your patient(s), please contact us

A bit about PNDU

Our mission at PNDU is to support, research and inform consumers, carers and providers of Parenteral Nutrition for Intestinal Failure.

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 new 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.

Support PNDU

By making a donation to PNDU you are helping us support kids and adults in your community with Intestinal Failure who cannot survive by simply eating.  You are also helping to raise awareness of the complex life support therapy - Home Parenteral Nutrition (HPN).  Please note donations are in NZ dollars.  Thank you for your generosity.