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Mia's Memorial

28/8/2018

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Tuesday was the most beautiful day and one we will hold onto forever. Thank you to everyone who came to remember and celebrate Mia. For those who wanted to be with us but could not, we wanted to share some of the moments from our day with you.

A very special thank you to our dear friend Andrew Flakelar who put together the film that played at the end of Mia's service (you can watch the video below).

Thank you to everyone for their kind messages, words and cards.

The sublime smell of roses lingers through out our entire house and our front door has never looked so spectacular.

With love & tears, Hamish, Peta, Toby, Jasper & our bright shining star Mia.
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Photo: Andrew Flakelar
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Our Mia playlist
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    Stories of our love, heartache and friendship. Written by a mother.

    ​Our family is dedicated to raising awareness for Batten Disease. Batten Disease is a rare degenerative genetic disease that affects otherwise healthy children who can sing, dance and bounce. From a young age affected kids start to lose their ability to walk, talk, see and smile. There is no cure for children affected and it will eventually take their lives. Awareness and research into this rare disease is imperative to find a cure.

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