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RESOURCES

Sign up for our TAN newsletters to stay in touch with all the latest news and events. Here are some recent newsletters:

March 2025, Issue 23

Jan 2025, Issue 22

Dec 2024, Issue 21

Aug 2024, Issue 20

July 2024, Issue 19

June 2024, Issue 18

Jan 2024, Issue 17

The Angelman Network

NZ Publications

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Download our IAD Postcard 

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Communication

So Much To Say

by Dr. Calculator, Published April 3, 2018

'His philosophy is built upon presuming confidence...'

PURCHASE ONLINE

'I have something to say' by Tracey Campbell, on behalf of ASSERT

DOWNLOAD

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General AS Information 

Angelman Syndrome (Clinics in Developmental Medicine) Paperback - on Amazon 2008, by Bernard Dan 

Raising a child with a rare disorder: A guide for parents and caregivers living in Aotearoa New Zealand. 

DOWNLOAD: This booklet has been created by Rare Disorders New Zealand to help parents and caregivers navigate the path in caring for a child with a rare disorder in New Zealand

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Health

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Health Passport

Health and Disability Commisioner

DOWNLOAD

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NZ General Resources

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Welfare Guardianship Guide

2018 Guide for completing the application forms

DOWNLOAD

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YouTube

View The Angelman Network channel here.

You can search 'Angelman Syndrome' on Youtube to find many informative videos made by AS organisations as well as families around the world. These videos cover many topics and relate to different aspects of the condition. Here are some great links:

STAY IN TOUCH ON SOCIAL MEDIA

Social media platforms are used to:

  • Connect families around the world

  • Raise global awareness for Angelman syndrome/all rare conditions

  • Share new research information

  • Encourage open discussion forums for new therapeutics

  • Gather general & specific data and information

  • Advocate for treatments

  • Fundraise effectively

  • Help find participants for trials

          and much more….

See Social Media

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The Angelman Network is a

Registered Charitable Trust based in New Zealand

CC46746.

angelmannetwork@gmail.com

Disclaimer: Links to other Internet sites are for the convenience of all web-users. The Angelman Network is not responsible for the availability or content of these external sites and we do not endorse, warrant or guarantee any products, services or information that may be offered at these sites.

Always contact your own medical practitioner for any medical advice.

Information about Angelman syndrome and genetics in general is a very fast moving area and while the information on this website is regarded as the best at the time of publication, some facts may change later.

©2025 The Angelman Network

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