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  1. About Us
  2. Our people
  3. Our Committee

Committee

Lucy Jones

Lucy Jones

Lucy Jones is the mother of Sienna and Jamie Hoffmann. Lucy is focused on driving change in survival rates through more research, having tragically lost her daughter Sienna to the illness in 2010. Read more

Posted to: Committee

Published: 1st July, 2019

Updated: 17th October, 2019

Author: Karina May

Related topics:
  • Committee

Rochelle Yates

Rochelle is a mother of two, and Chairman of a global logistics company where she specialises in marketing. Rochelle's career includes vast experience in events and promotions and she has brought this skill to help coordinate numerous fundraising events and activities for Neuroblastoma Australia. Read more

Posted to: Committee

Published: 2nd July, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee

Jane Price

Jane Price holds a Bachelor of Arts and a Bachelor of Laws. She is a small business owner, running her own immigration consultancy business, which she has grown in a few short years into a thriving practice with a couple of employees. Jane is lucky enough to have a “pigeon-pair” of children (aged 11 & 14) and was also privileged to know Sienna Hoffman. Read more

Posted to: Committee

Published: 3rd July, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee

Dr Louise Causer

Louise is a medical epidemiologist and lecturer currently based at The Kirby Institute, UNSW Australia and has worked internationally both in clinical and research settings across a number of fields. Having trained and working in a highly academic setting for the past decade, Louise has direct experience and key insight into the research setting in Australia and internationally. Read more

Posted to: Committee

Published: 4th July, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee

Sarah White

Sarah is a paediatric Occupational Therapist and is passionate about working with children and families. Sarah brings 20 years experience working in private, not for profit and government health roles specifically in childhood disability and mental health. Since her daughter Isabella was diagnosed with Stage 3 Neuroblastoma in 2011, Sarah has been actively involved in creating awareness and fundraising for Neuroblastoma research. Read more

Posted to: Committee

Published: 26th August, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee

Isabella Mannix

Isabella has a background in Marketing and Sales, with twenty years’ experience working in a variety of senior roles within the Financial Services sector and more recently the Health sector. After her daughter Georgia was diagnosed with Stage 1 Neuroblastoma in 2012, Isabella and her family have supported various childrens’ cancer charities – including the Childrens’ Cancer Institute, the Kids Cancer Project, Redkite and Neuroblastoma Australia. Read more

Posted to: Committee

Published: 26th August, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee

Sarah Jones

Passionate about working with children, Sarah is a mum of three with a teaching qualification, who is currently pursuing postgraduate studies in Special Education. Sarah has experience in the not-for-profit sector, having worked for many years at The Starlight Children’s Foundation helping to develop in-hospital entertainment programs for seriously ill children. Sarah has been involved with fundraising for research into Neuroblastoma for over 5 years. Read more

Posted to: Committee

Published: 26th August, 2019

Updated: 24th September, 2019

Author: Karina May

Related topics:
  • Committee
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Showing 10 of 7

Latest

  • Ava's Story #3KM

    A true hero, Ava has pushed through 18 months of treatment with strength beyond her years. She is now participating in a trial with the hope it will keep her cancer free.

  • Nixon sitting in chair

    Nixon's Story #31KM

    Diagnosed with Stage 4 High Risk Neuroblastoma MYCN Amplified at just 16 months old, this amazing little man has endured an intensive treatment regime before getting the all clear in March 2019. Sadly he relapsed just a few month later. He's now taking on treatment for relapsed neuroblastoma.

  • Sophie's Story #9KM

    Little Sophie's family had never heard of neuroblastoma when she was diagnosed in 2019. This little hero is currently undergoing immunotherapy having already endured six rounds of chemo, surgery, stem cells transplants and radiotherapy.

  • Declan banner #8KM

    Declan's Story #8KM

    Declan's battle with neuroblastoma began just before his fourth birthday and tragically ended just before his eighth. Loved and missed by his heartbroken family.

Most read

  • Run2Cure 2020

    Book your Run2Cure tickets by Friday 28 February and save 25% in our Super Earlybird Sale!

  • Accessibility

    Neuroblastoma Australia is committed to providing a website that is accessible to the widest possible audience, regardless of technology or ability. Our website endeavours to conform to level Double-A of the World Wide Web Consortium W3C Web Content Accessibility Guidelines 2.0.

  • Kahlilla smiling with a pink hat

    Kahlilla's Story #14km

    Little Lilla's light continues to shine. Always and forever.

  • Detection, diagnosis & staging

    Most symptoms of neuroblastoma are caused by the growth of the cancer into nearby tissues or organs, or its spread to distant parts of the body such as bones or bone marrow.

  • What is neuroblastoma?

    Neuroblastomas are cancers that start in early nerve cells (called neuroblasts) of the sympathetic nervous system. This means that tumours can be found anywhere along this system; most commonly (about 50%) start in the adrenal glands (above the kidney), or near the spine, chest, neck or pelvis.

  • Indianna and her mum and dad

    Indianna's Story

    Indianna was diagnosed with high-risk neuroblastoma at just 12 months of age. Even while enduring high strength chemotherapy she found the strength to play peak a- boo with the nurses and charm the doctors with her smile and incredible dimples.

  • Maddy dressed up with her mum Monique

    Childhood Cancer Awareness Month

    This September, wear gold and join our #hope campaign to raise awareness of all forms of children's cancer and the toll it takes on the youngest members of our community and their families.

  • Two research grants awarded to the Children's Cancer Institute

    Today we announced funding grants to two ground breaking research projects which we hope will take us a step close to finding a cure for the rare and deadly children’s cancer neuroblastoma.

  • Young Zach in hospital with fluffy grey toy cat

    Zach's Story

    Paolo and Diana Carniel had never heard of neuroblastoma before August 2018 when their son Zach, just five years old at the time, was first diagnosed.

  • Declan banner #8KM

    Declan's Story #8KM

    Declan's battle with neuroblastoma began just before his fourth birthday and tragically ended just before his eighth. Loved and missed by his heartbroken family.

Tag cloud

2little Golf2Cure research Vital research Zach's neuroblastoma story

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Neuroblastoma Australia Level 1, 441 Pacific Highway, Crows Nest, NSW 2065,
+61 (0)406 991 606, [email protected]