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This is my little buddy William!! He is one of the most amazingly kind hearted kids I’ve ever met. William loves swimming, hanging out, LEGO, his little sister Mia and food. He is my little super hero and I love him. He was also born with the genetic disease, Neurofibromatosis (NF) and its not fair!! Please help me raise some $$ so we can find a cure!

This year his Super Mum Amy has taken on the extra responsibility of being the volunteer race director for Cupids Undie Run on the Gold Coast. We have a team going along to support William and his beautiful family and would love your help. Please donate if you can so we can help find a cure for NF because I believe tumours should never be a person’s normal.

I want to make a difference in the lives of William, other children and families living with the genetic disease, Neurofibromatosis (NF) and am inspired by the work of the Children's Tumour Foundation of Australia.

I am participating in the Cupid’s Undie Run on March 22nd, 2020 and you can help to conquer NF by making a tax deductible donation to my page, through the ‘Donate Now' button.

NF affects 1 in 2,500 births- it is common and yet awareness is lacking. One child is born every 3 days with a condition that causes tumours to form on their nerves, including their brain and spine. It is progressive, unpredictable and there is no cure. Have you heard of NF? Together we can make a difference!

The more people that know about Children's Tumour Foundation of Australia, the greater their impact, so please help improve awareness by sharing my page with your friends and family.

Thank you in advance for your generosity.

Rachael has 15 supporters