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WHAT WE DO

The Angelman Network is New Zealand's only organization focused on providing current information about Angelman Syndrome. We share resources through our website, social media, and newsletters, keeping families connected and supported through advocacy, public awareness, gatherings, and fundraising activities.

The Angelman Network (TAN) is managed by a board of trustees who volunteer their time and expertise. We are proactive members of the Rare Disorders NZ collective and the NZ Carers Alliance. To find out more about what we do, see our 2024 Annual Report here.

Network

We aspire to source and distribute evidence-based information on Angelman Syndrome. We network with affiliated organisations in NZ, local councillors and politicians in NZ, researchers and research teams (NZ and global), professionals and specialists working with people who have AS, and other AS organisations around the world. 

Support & Advocacy

We connect families in New Zealand who are affected by AS. We also support them by collaborating with affiliated organisations in NZ that advocate for rare disorders, for AAC (communication support), access to appropriate medication, an accessible society, inclusion in schools, and the wellbeing of caregivers. 

Resources & Publications

This website is our Primary Resource. It is regularly updated with the most current information on Angelman syndrome.

Families in NZ can contact us for an Information Pack.

A range of other publications, resources, media articles

 and important links, can be found on our Resource page.  

Grants

Due to the small population of NZ, and the rarity of Angelman syndrome, we provide small grants for research on Angelman syndrome and/or research on matters affecting social policy and funding that could benefit our NZ families. We also provide Family Grants to assist families to attend conferences/workshops related to Angelman syndrome. 

OUR AFFILIATES

GLOBAL ANGELMAN REGISTERY

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INTERNATIONAL ANGELMAN DAY

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NZ CARERS

ALLIANCE

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ANGELMAN ACADEMY

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ACCESS ALLIANCE

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RARE

DISORDERS NZ

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​RARE DISEASE

DAY

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TALKLINK
TRUST NZ

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INCLUSIVE EDUCATION ACTION GROUP

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EPILEPSY

NEW ZEALAND

 

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The Angelman Network is an Associate member of the

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Angelman Syndrome Alliance (ASA), is a partnership of organizations from around the world, focused on supporting people with Angelman Syndrome (AS) with a  mission to advance groundbreaking research.

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

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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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