HADDS Resources

Use these resources for distribution at community and fundraising events or for those recently diagnosed.

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The HADDS Educational Packet is to be used for distribution to those newly diagnosed, healthcare providers and to others interested in learning more about the syndrome.

After receiving a diagnosis, there are many questions and many revolve around understanding the genetics and the test results, so you can determine next steps.  This webinar, hosted by Pilar Magoulas, MS, CGC, provides a brief genetics 101, details the types of genetic tests, how to read the results and answers a few common questions. 

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The HADDS Quick Guide describes the syndrome, highlights the growing community and speaks to the ongoing research, and its long-term impact on our community. Translations in Arabic, English, German,  Italian and Spanish.

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HADDS School Awareness Packet was designed for February's HADDS Awareness Month, but could be used year round. The packet has ideas and a checklist. Click for a video about HADDS for School age children.

This resource will help jumpstart fundraising efforts globally with a packet of ideas, logos and quick stats and facts about HADDS & the Foundation's work. 

Coming Soon in 2021!