Experience the magic of Cromer Golf Club at this exclusive 18-hole charity tournament on Tuesday 27th February 2024 in support of the Children's Tumour Foundation and families impacted by neurofibromatosis (NF).
As a private member’s Club in the Northern Beaches of Sydney, this is a unique opportunity to play a round on one of the best greens in Sydney, providing golfers of all levels a wonderful golfing experience.
What to expect
Playing in teams of four, you can enjoy coffee on arrival, followed by 18-holes and an exquisite two-course lunch with beverages, where guest will learn more about the cause and have the chance to win great prizes.
Everyone who registers to play will receive a free Children's Tumour Foundation branded cap.
We will have a number of additional challenges that you can choose to participate in (even if you aren’t Pro circuit ready) for your chance to win, while also helping raise much needed funds.
WHAT ARE YOU PLAYING FOR?
NF is a genetic condition that causes tumours to form on nerves in the body, including the brain and spine. It can lead to a range of significant health issues, including deafness, blindness, physical differences, bone abnormalities, learning difficulties, chronic pain and even cancer.
It is unpredictable, progressive and there is no cure.
The Children's Tumour Foundation is the only patient advocacy and support services for families impacted by this devastating condition in Australia.
As a parent we all have hopes, dreams and expectations for our children. Sometimes when a child is diagnosed with NF, it can leave parents feeling a sense of grief and loss for what could have been.
Importantly, the impact of NF can reach well beyond the person affected including all extended family and friends.
NF can affect anyone regardless of age, ethnicity or gender, with 50 per cent of cases arising in families with no history of the condition.
We need your help to improve understanding of the signs and symptoms of NF, to share the stories of real people affected by the condition and raise much needed funds.
Every 3 days a child is born with NF in Australia and they will need a lifetime of support.