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Children's Tumour Foundation of Australia
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I am joining the fight against neurofibromatosis (NF) by fundraising in support of the Children's Tumour Foundation of Australia (CTF).

EVERY 3 DAYS A CHILD IS BORN WITH NF IN AUSTRALIA

NF is a lifelong genetic condition that causes tumours to form around nerves, under the skin and deep in the body.
Progressive and unpredictable, these tumours can lead to physical differences, blindness, deafness, learning difficulties, chronic pain, and scoliosis and in 10% of people living with NF, they can become cancerous.

There is no cure and treatment options are limited.

I have a goal to raise $1000 to support the Children's Tumour Foundation and their vision of a life without limitations for everyone living with NF.

As the only non-clinical service provider, the CTF work to ensure anyone regardless of location, NF type or financial position can access balanced information and personalised support free of charge, while also enabling important connections with community and healthcare professionals.

In addition to helping provide practical support for those impacted (as well as their families), your donation will help fund promising research to improve treatment options, and eventually lead to a cure.

I believe that tumours should never be a child's normal, so please help me reach my goal by making a tax-deductible donation.

Thank you.

MAY IS NEUROFIBROMATOSIS AWARENESS MONTH
Amanda is fundraising for

MAY IS NEUROFIBROMATOSIS AWARENESS MONTH

May is an opportunity to educate the community on the signs and symptoms of NF, advocate to improve health outcomes, and elevate the voices of those living with this devastating condition.

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