Olive's Chance
Our almost 2 year old girl Olive, was born in 2012 with a rare skin condition called Giant Congenital Melanocytic Nevus. It affects 1 in 50
Nationwide
We are raising money to take Olive and our family to the next conference in Australia in Jan 2015 (please see my profile for more info).
This conference will be invaluable to us, in the way of information, support and great first step to becoming an officially recognised support foundation in NZ.
Latest update
Update for 01/04/2014 1 April 2014
Olive's Chance is going exceptionally well! Thank you all so much. We have some exciting things coming soon, so keep your eyes peeled! In the meantime, please continue to share our page...thank you!
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