PNDU is being 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’ve received delivery of our PNDU charity cards and will have instructions on how to purchase them in the next few days, so come back soon.
There are 1 x Christmas card design and 2 x blank card designs (shown here). Packs cost $10 (AUD & NZD) for 10 cards, plus postage. Every pack you purchase will assist PNDU continue our work of supporting Aussie and Kiwi HPNers and their families.
Get involved! Our 2015 video clip and other resources will be available soon, but here are a couple of ways to get involved now:
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.