Beneficiary

Head and Neck Cancer Australia

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Raised

$26,349.41

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$1,726
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$1,355
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$1,324
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$1,193
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$1,088
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$38

Fundraising For

Funds raised this Dry July will help improve access to vital information and support for people affected by Head and Neck Cancer

About Us

Head and Neck Cancer Australia is the only national charity dedicated to providing education, support, and advocacy for people affected by Head and Neck Cancer. Founded in 2016 by a team of expert Head and Neck Cancer clinicians, HANCA was established to address the unique challenges faced by people diagnosed with these complex cancers. By working collaboratively with patients, carers, and healthcare professionals, HANCA’s mission is to raise awareness, improve access to vital information, and reduce the burden of this life-altering disease.

A key HANCA initiative is the Head and Neck Cancer Knowledge Base, a free, online directory of up-to-date information to empower people affected by Head and Neck Cancer to self-manage their care and navigate the health system. The Head and Neck Cancer Knowledge Base will also complement the newly launched Head and Neck Cancer Helpline, ensuring that patients, carers and family members and the healthcare professionals who care for them across Australia have access to the information and support they need.

With over 40 types and sub-types of Head and Neck Cancer, treatment can profoundly impact basic abilities such as speaking, eating, breathing, and swallowing. While survival rates exceed 70%, the long-term effects of Head and Neck Cancer can be devastating.

Despite these complexities, no comprehensive Head and Neck Cancer directories exist in Australia or internationally. As HANCA continues to grow, the Head and Neck Cancer Knowledge Base will be an essential tool to help improve patient engagement and care, thereby improving cancer outcomes.

Latest Updates


Head and Neck Cancer Australia will expand trusted support for patients nationwide

During Dry July 2026 you helped Head and Neck Cancer Australia (HANCA) raise an amazing $26,349 which will provide trusted information and support to people affected by Head and Neck Cancer across Australia.

The funds will support the continued growth of HANCA’s free online Knowledge Base, helping patients, families and carers access accurate, up-to-date information and practical resources throughout every stage of their cancer journey. Your support will help more people access specialist information, no matter where they live.

"The funding Head and Neck Cancer Australia receive from the Dry July Foundation enables the ongoing review and development of our online Head and Neck Cancer Knowledge Base.

Access to our comprehensive library of free, evidence-based resources on HANCA’s website provides patients, carers, and loved ones with reliable information about Head and Neck Cancer as they navigate their cancer journey and manage long-term impacts after treatment.

By engaging, educating, and empowering people affected by Head and Neck Cancer, HANCA and our Head and Neck Cancer Knowledge Base is helping to build a community of support, regardless of where people live."

Nadia Rosin, CEO, Head and Neck Cancer Australia

Spreading Awareness and Going Dry for a Cause: Brenton's Story

After being diagnosed with oral cancer in 2020, Brenton knows first-hand how important early detection can be.

“My dentist noticed a small white spot and advised me to have it looked at. This early intervention was crucial in the cancer not spreading, however, I still required several surgeries and missed months of work. As of February 2026, I am now 5 years clear and no longer considered 'at risk' and I am hoping to spread awareness so others can avoid going through the same.” 

Brenton gave up alcohol for the month of March to support people affected by Head and Neck Cancer. 

"Not drinking for the month was a nice break and thankfully my friends really got behind me and didn't pressure me to join them which was a big help! The daily workouts combined with the not drinking and good eating habits lead to a 6kg weight loss in March and another 10kg since!"

Brenton originally set out to raise $1,500 but more than doubled his goal, reaching $3,050 for Head and Neck Cancer Australia!


Lora's Story

Lora, a young mother from Melbourne who was diagnosed with oral cancer and had three quarters of her tongue removed.

In early 2017, Lora Winter noticed a persistent ulcer on her tongue. Initially dismissing it as stress-related, she sought medical advice at her husband’s insistence. What followed was a shocking diagnosis: Stage 4 Tongue Squamous Cell Carcinoma.

Lora underwent 14-hour surgery, losing two-thirds of her tongue, part of her jaw, and requiring reconstructive procedures using tissue from her arm and thigh. She faced months of radiation, speech therapy, and a long recovery process of learning to communicate, eat, and navigate her new normal.

“I never imagined something as small as an ulcer could change my life forever. Simple things like eating, speaking, and even kissing my kids goodnight became enormous challenges.”

Lora highlights the critical need for accessible, specialist information for patients and caregivers: "It was a light in the dark for me knowing that this small but amazing charity was out there providing information to those who need and want it. Head and Neck Cancer can’t be hidden away, it’s visible and I really appreciate that HANCA sees us, hears us and has created resource access that makes us feel we have been seen and heard. For many of us, before finding HANCA’s website, we weren’t sure we wanted to be seen and heard, we wanted to hide in the shadows so it’s wonderful to have HANCA in our lives."

How HANCA Supported Lora:

At diagnosis / during treatment: Access for Lora and her family to the location of HNC Multidisciplinary teams, easy to search directory about her type of HNC linked to further information on treatment options and oral cancer patient stories.

Survivorship: Access to specialist services e.g. lymphoedema therapist, speech pathologist, soft food recipe books. Connection to patient/carer support groups.

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