This is sharing of an amazing experience our family had in caring for our youngest daughter born with Trisomy 18 also known as Edwards Syndrome. It was a venture into the unknown and after being told we were unlikely
to take her home as her disabilty was said to be incompatible with life - there was little we could do but take one day at a time. In New Zealand Trisomy 18 was almost unknown, so as a family we felt there was little else we could do but love our wee
girl and treasure each moment and day we had with her.
I have written this book pictured here on the right in order to relate how her disability impacted on family life and share all that Melissa taught us
ISBN13 softcover: 978-1-4797-9350-1 ISBN13 ebook: 978-1-4797-9351-8
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