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HPN Awareness Week   3-9 August 2014

Please join us as we celebrate this special week and raise awareness of life on Home Parenteral Nutrition.

As HPN Awareness Week draws closer, we'll update with our new PNDU logo, YouTube clip, poster, and more.  So drop by again soon.

Welcome to 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, care givers and professionals affected by intestinal failure requiring Intravenous (IV) nutritional support (parenteral nutrition).      

We welcome you to look around the site, join us in forum discussions and help us grow our network to improve the lives of those living on parenteral nutrition 'down under'.

Please take a moment to become a member (at no cost) in order to enter the site and access the information we are collating on parenteral nutrition and other aspects of intestinal failure.

to our free e-newsletter Dripline which is published quarterly.

And if you are an Aussie or Kiwi consumer 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 parenteral nutrition.

Please Note:  This information is kept in strictest confidentiality, 

Whats Nu @ PNDU

Support PNDU

By making a donation to PNDU you are helping to raise awareness of Home Parenteral Nutrition (HPN) for the kids and adults in your community with Intestinal Failure who cannot eat normal food.  Please note donations are in NZ dollars.