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IAD Resources

This page shares ideas and resources for International Angelman Day (IAD) that are specific to Aotearoa New Zealand. You are free to use them to help raise national awareness for Angelman syndrome, starting with your own local communities. More can be found at AS Resources, or on the IAD Collective website, here.

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Please note that The Angelman Network (TAN) logo and the IAD logo cannot be used for commercial use, nor can they be changed in any way. (If in doubt, please check with us first) ​

TAN Postcards for IAD

To share with teachers, teacher aides, GPs & nurses, therapists, neighbours, friends, family/whanau in Aotearoa New Zealand. Please contact us if you would like us to post a batch to you. 

 

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Social Media
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PHOTO GALLERY FOR IDEAS

LOGOS

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Contact

Please contact us if you would like to:

  • request a photo-frame with your loved one in these IAD resources

  • discuss a fundraiser for TAN with us

  • organise a local gathring in your region - we can help to fund an event

  • request hi-res files for logos for printing purposes

  • request postcards, flyers, and/or Info-packs to be posted to you

angelmannetwork@gmail.com

021-1382878

STAY IN TOUCH ON SOCIAL MEDIA

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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.

©2026 The Angelman Network

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