Without a Ribbon Inc

Without a Ribbon Inc “Without a Ribbon” fighting for support of those diagnosed with Rare Cancer in Australia.
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Established in the 2014 Financial Year, “Without a Ribbon” is a small rare cancer fund raising foundation established to assist those who are so small in numbers that they are not allocated a Ribbon through existing Cancer related Councils throughout the world.

“Without a Ribbon” management and Board will be established with the assistance of volunteers who do not suffer from ACC and who have vi

ewed feedback provided by rare cancer sufferers. Those who have been diagnosed with ACC, also referred to as ADCC, remain, for the greater time, unsupported by the majority of Cancer Charities. From the feedback by those diagnosed with rare cancer, the main support required appears to be:
- Support available when first diagnosed. Support links to online communities with your rare cancer, information regarding worldwide treatment options;
- Face to Face support with others who are going through the same journey within Australia to source information about treatment options and specialists available locally;

If you need to reach us, please reach out through a private message here on Facebook, through email to [email protected] or through mail to PO Box 121 ALLORA QLD 4362

We are here to ensure, that no one fights alone.

10/08/2026

Here’s an extended interview with our fearless President Desiree Fraser.

09/08/2026

Why “Warrior” with a capital R? 💙 It represents the strength of Australians living with rare cancer and the community that stands beside them.

No one facing rare cancer should have to face it alone. 🎗️

08/08/2026

A rare cancer diagnosis can change everything in a moment. 🎗️

Without a Ribbon links Australians facing rare cancers with those who truly understand their struggles.

Spread this video — it might help someone in need of support right now. 💛

withoutaribbon.org

07/08/2026

Did you know that everyone involved with Without a Ribbon is a volunteer? 💛

Our board members, peer supporters, and the behind-the-scenes team all dedicate their time because they truly believe in our mission.

Since we rely on volunteers, every donation goes straight to our initiatives — expanding peer support communities, creating reliable resources for Australians dealing with rare cancers, and assisting more individuals in realizing they don’t have to confront their diagnosis by themselves.

We take immense pride in what our volunteers achieve.

If you want to support an organization where every dollar is maximized by volunteers, we would be extremely thankful for your help. 🎗️

No Australian facing a rare cancer should have to do it alone.

withoutaribbon.org

06/08/2026

What would you do if diagnosed? Rare Cancers can be complex!

06/08/2026

What do you think of when you hear of a rare cancer?

06/08/2026

Why does Mel walk for WaR? 💛

As a rare cancer survivor, Mel knows how powerful it is to connect with people who truly understand the journey.

This year, she’s taking part in the Beach 2 Beach Run/Walk on 23 August to raise awareness for rare cancers and support the WaRriors, partners, carers and loved ones affected by them.

Join us in person or virtually. Every step taken and every dollar raised helps Without a Ribbon continue providing vital peer-to-peer support—so no one facing rare cancer feels alone or without hope.

👟 Walk or run for WaR
💛 Support rare cancer WaRriors
🔗 Register or donate to Mel: https://beach2beach26.grassrootz.com/without-a-ribbon-incorporated/melissa-jarrold

⚠️ 𝐌𝐚𝐧𝐲 𝐩𝐚𝐫𝐞𝐧𝐭𝐬 𝐝𝐨𝐧’𝐭 𝐫𝐞𝐚𝐥𝐢𝐬𝐞 𝐭𝐡𝐚𝐭 𝐩𝐞𝐫𝐬𝐢𝐬𝐭𝐞𝐧𝐭 𝐡𝐞𝐚𝐝𝐚𝐜𝐡𝐞𝐬, 𝐛𝐚𝐥𝐚𝐧𝐜𝐞 𝐩𝐫𝐨𝐛𝐥𝐞𝐦𝐬, 𝐨𝐫 𝐮𝐧𝐞𝐱𝐩𝐥𝐚𝐢𝐧𝐞𝐝 𝐯𝐨𝐦𝐢𝐭𝐢𝐧𝐠 𝐜𝐨𝐮𝐥𝐝 𝐛𝐞 𝐰𝐚𝐫𝐧𝐢𝐧𝐠 𝐬𝐢𝐠𝐧...
31/07/2026

⚠️ 𝐌𝐚𝐧𝐲 𝐩𝐚𝐫𝐞𝐧𝐭𝐬 𝐝𝐨𝐧’𝐭 𝐫𝐞𝐚𝐥𝐢𝐬𝐞 𝐭𝐡𝐚𝐭 𝐩𝐞𝐫𝐬𝐢𝐬𝐭𝐞𝐧𝐭 𝐡𝐞𝐚𝐝𝐚𝐜𝐡𝐞𝐬, 𝐛𝐚𝐥𝐚𝐧𝐜𝐞 𝐩𝐫𝐨𝐛𝐥𝐞𝐦𝐬, 𝐨𝐫 𝐮𝐧𝐞𝐱𝐩𝐥𝐚𝐢𝐧𝐞𝐝 𝐯𝐨𝐦𝐢𝐭𝐢𝐧𝐠 𝐜𝐨𝐮𝐥𝐝 𝐛𝐞 𝐰𝐚𝐫𝐧𝐢𝐧𝐠 𝐬𝐢𝐠𝐧𝐬 𝐨𝐟 𝐂𝐡𝐢𝐥𝐝𝐡𝐨𝐨𝐝 𝐌𝐞𝐝𝐮𝐥𝐥𝐨𝐛𝐥𝐚𝐬𝐭𝐨𝐦𝐚.

Childhood Medulloblastoma is the most common type of malignant brain tumor found in children. It forms in the cerebellum, which is the part of the brain that controls balance, movement, and coordination. If not treated, it can spread to other parts of the brain and spinal cord.

Symptoms like ongoing morning headaches, nausea, dizziness, trouble walking, changes in vision, seizures, or extreme fatigue should never be overlooked. Although these symptoms can arise from various issues, identifying them early and consulting a doctor can lead to better outcomes.

At Without a Ribbon, we are dedicated to helping individuals and families impacted by rare cancers through education, advocacy, and community support. By increasing awareness, we can encourage earlier diagnoses, enhance access to resources, and provide hope to those dealing with these tough situations.

💜 You can make a difference. Every donation, sponsorship, and volunteer effort helps us continue to support rare cancer patients and their families while raising awareness for conditions that need more attention.

Together, we can offer hope, inspire action, and ensure that no family has to face a rare cancer journey alone.

🚨 𝐍𝐨𝐭 𝐞𝐯𝐞𝐫𝐲 𝐜𝐡𝐢𝐥𝐝𝐡𝐨𝐨𝐝 𝐡𝐞𝐚𝐝𝐚𝐜𝐡𝐞 𝐨𝐫 𝐬𝐞𝐢𝐳𝐮𝐫𝐞 𝐢𝐬 “𝐣𝐮𝐬𝐭 𝐚 𝐩𝐡𝐚𝐬𝐞.” 𝐈𝐧 𝐫𝐚𝐫𝐞 𝐜𝐚𝐬𝐞𝐬, 𝐢𝐭 𝐜𝐨𝐮𝐥𝐝 𝐛𝐞 𝐬𝐨𝐦𝐞𝐭𝐡𝐢𝐧𝐠 𝐟𝐚𝐫 𝐦𝐨𝐫𝐞 𝐬𝐞𝐫𝐢𝐨𝐮𝐬.CNS N...
30/07/2026

🚨 𝐍𝐨𝐭 𝐞𝐯𝐞𝐫𝐲 𝐜𝐡𝐢𝐥𝐝𝐡𝐨𝐨𝐝 𝐡𝐞𝐚𝐝𝐚𝐜𝐡𝐞 𝐨𝐫 𝐬𝐞𝐢𝐳𝐮𝐫𝐞 𝐢𝐬 “𝐣𝐮𝐬𝐭 𝐚 𝐩𝐡𝐚𝐬𝐞.” 𝐈𝐧 𝐫𝐚𝐫𝐞 𝐜𝐚𝐬𝐞𝐬, 𝐢𝐭 𝐜𝐨𝐮𝐥𝐝 𝐛𝐞 𝐬𝐨𝐦𝐞𝐭𝐡𝐢𝐧𝐠 𝐟𝐚𝐫 𝐦𝐨𝐫𝐞 𝐬𝐞𝐫𝐢𝐨𝐮𝐬.

CNS Neuroblastoma, NOS is a rare and aggressive tumour that affects the brain or spinal cord, primarily in children and teenagers. By raising awareness, we can help with earlier diagnosis, enhance understanding, and provide hope to families dealing with this uncommon illness.

💜 At Without a Ribbon, we are committed to supporting those impacted by rare cancers through education, advocacy, and community assistance.

Every donation, volunteer effort, and sponsorship enables us to keep making a positive impact.

Discover more and support our cause: https://withoutaribbon.org

⚠️ 𝐌𝐨𝐬𝐭 𝐩𝐞𝐨𝐩𝐥𝐞 𝐡𝐚𝐯𝐞 𝐧𝐞𝐯𝐞𝐫 𝐡𝐞𝐚𝐫𝐝 𝐨𝐟 𝐌𝐞𝐝𝐮𝐥𝐥𝐨𝐞𝐩𝐢𝐭𝐡𝐞𝐥𝐢𝐨𝐦𝐚—𝐛𝐮𝐭 𝐞𝐚𝐫𝐥𝐲 𝐚𝐰𝐚𝐫𝐞𝐧𝐞𝐬𝐬 𝐜𝐨𝐮𝐥𝐝 𝐦𝐚𝐤𝐞 𝐚 𝐝𝐢𝐟𝐟𝐞𝐫𝐞𝐧𝐜𝐞.Medulloepithelioma is ...
29/07/2026

⚠️ 𝐌𝐨𝐬𝐭 𝐩𝐞𝐨𝐩𝐥𝐞 𝐡𝐚𝐯𝐞 𝐧𝐞𝐯𝐞𝐫 𝐡𝐞𝐚𝐫𝐝 𝐨𝐟 𝐌𝐞𝐝𝐮𝐥𝐥𝐨𝐞𝐩𝐢𝐭𝐡𝐞𝐥𝐢𝐨𝐦𝐚—𝐛𝐮𝐭 𝐞𝐚𝐫𝐥𝐲 𝐚𝐰𝐚𝐫𝐞𝐧𝐞𝐬𝐬 𝐜𝐨𝐮𝐥𝐝 𝐦𝐚𝐤𝐞 𝐚 𝐝𝐢𝐟𝐟𝐞𝐫𝐞𝐧𝐜𝐞.

Medulloepithelioma is a rare type of tumor that typically forms in the eyes of young children. Its symptoms can often mimic those of more common eye issues, making early diagnosis difficult—but catching it early can really change the outcome.

Symptoms like blurred vision, eye discomfort, redness, a white reflection in the pupil, or sudden changes in vision should always be taken seriously. Raising awareness about rare childhood cancers is crucial for helping families identify possible warning signs and get medical help sooner.

At Without a Ribbon, we are dedicated to supporting those impacted by rare cancers through education, advocacy, and community assistance. By spreading knowledge and boosting awareness, we can help ensure that fewer families have to face these rare diagnoses on their own.

💜 You can help make a difference. Every donation, sponsorship, and volunteer effort plays a role in supporting individuals and families dealing with rare cancers, while also helping us continue our mission of raising awareness and offering hope.

Together, we can illuminate the path for those affected by rare cancers and provide support to those who need it the most.

Address

PO Box 121
Allora, QLD
4362

Website

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