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After Fifteen

This publication follows my family and our collective experiences of growing up and living with Alison, my sister who was born with Angelman Syndrome. In this publication we answer questions that people frequently ask and address things that people are curious about.

The publication contains personal interviews with family that span from the heartbreak of diagnosis to challenges of daily life to hope for the future. Funny stories add light hearted breaks throughout the publication and serve as a contrast between the challenge of life as a carer for Alison, and the bittersweet memories of joy and happiness that we would not have had without her.

To find out more about Angelman Syndrome please go to: Angelman Syndrome Ireland

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