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Angeltales

This website is dedicated to all those who share in the life and adventures of a Child who has Angelman Syndrome. Melissa was diagnosed in November 2003, (UPD). We shed many tears in the beginning but now we take each day at a time and overcome all new obstacles in turn. It is not always an easy path we tread, our lives are organised around Hospital appointments and we survive on very little sleep. Our homes are thrown into chaos, we are exhausted by the end of the day, often we cry when we think of the future. But what we have that many don't is the smile of our Angel, the laughter and hugs and the realisation that together we can handle all of the problems that come with a diagnosis of AS. We are truly blessed to have Melissa in our lives and hope you all enjoy this site and have a little laugh as you share her way of looking at life.

Welcome to my website, I hope you enjoy sharing my sightly different way of looking at life, but when you are an Angel anything goes!! Love

Melissa x