Leukaemia Foundation

Leukaemia Foundation 🩸 We stand with Australia to help everyone impacted by any blood cancer - with care 💙 Your blood is a remarkable thing. We’re funding research to find a cure.

We stand with Australia to help cure and conquer every blood cancer – with care. It keeps you alive by giving your body what it needs, taking away what it doesn’t and fighting off infection. But more than 110,000 people in Australia are living with the devastating impact of blood cancer and it’s one of the biggest causes of cancer death. It’s a cancer of your blood and immune systems, preventing t

hem from doing what they need to keep you alive and healthy. Blood cancer develops in the places of your body where blood is made, but its exact cause is unknown. A range of things affect someone’s chance of surviving blood cancer and, it can be incurable. There are many different types of blood cancer and together they are among the most prevalent and deadly cancers in Australia today. The most common types of blood cancer are called lymphoma, leukaemia and myeloma. When you support us, you support the blood cancer community. We’re driving equitable access to better diagnostics and treatments and, we’re helping people already impacted by blood cancer through emotional support, transport services and providing a home-away-from-home when families have to relocate to access life-saving treatment. Learn more: www.leukaemia.org.au

Join us on:
INSTAGRAM
https://www.instagram.com/leukaemia_foundation

TWITTER
https://twitter.com/LeukaemiaAus

CHECK OUT OUR AMAZING FUNDRAISING CAMPAIGNS
Worlds Greatest Shave
https://facebook.com/LeukaemiaFoundationWorldsGreatestShave

Light the Night
https://facebook.com/LeukaemiaFoundationLightTheNight

U.G.L.Y. Bartender
https://facebook.com/uglybartenderoftheyear

25/08/2026

"Every day I'm a brave girl, receiving treatment for leukaemia."

🥹 Wilston State School rallied around their friend and fellow student, Alia, who shaved her head ahead of her next treatment for blood cancer 🩸

"I see so many kids each week when I go to hospital, going through very tough things like me.

"I'll lose my hair soon, so I might as well do it for a good cause and with the encouragement from my friends and family.

"Let's raise awareness and funds together so that the treatments keep getting better and better."

Alia's school smashed their previous record, raising almost $50,000 to support Australians impacted by blood cancer - just like her 🩵

Thank you to the incredible Wilston community for your support for Alia and the thousands of schoolchildren across Australia fighting blood cancer 👩‍🦲💪

🤝 Exciting news! The Leukaemia Foundation will proudly join forces with COUCH - Cairns.On a shared path forward, the mer...
21/08/2026

🤝 Exciting news! The Leukaemia Foundation will proudly join forces with COUCH - Cairns.

On a shared path forward, the merger is a transformative and sustainable move to improve care for those impacted by cancer in Far North Queensland.

COUCH Chair, Prof Scott Davis, said this major advancement will combine the incredible community-led foundation of COUCH with the national scale of the Leukaemia Foundation.

“The focus of both our organisations is the provision of compassionate, evidence-based, wraparound care for people affected by cancer, with a shared commitment to strengthening and expanding support for people living in regional and rural communities.

“We’re deeply grateful to the families, donors and supporters whose compassion and generosity have built COUCH into what it is today.

“Together with the Leukaemia Foundation, we’re even better positioned to respond to the growing and changing needs of our community, delivering more coordinated, accessible and high-quality support.”

Leukaemia Foundation CEO, Chris Tanti, said the merger will help bridge the health divide between Australians living in metropolitan and regional areas.

"For people facing cancer in North Queensland, having access to support close to home can make an enormous difference.

“Together, we’ll build on the exceptional work already taking place in the region while preserving the local connections that make these services so valuable to the community."

As the founding family of COUCH, the Woodwards see this merger as a positive and deeply meaningful step forward.

🏡 The COUCH Hub will continue operating under its existing name, and donors and supporters can direct funds to COUCH - funds raised locally will remain in the region to directly support people in North Queensland 💙

Prof Davis said that by combining the heart of their local community with national strength and expertise, this partnership marks a new chapter for COUCH.

“This integration is about strengthening the care and support available to local people, ensuring more individuals and families can access the practical, emotional and wellbeing services they need throughout every stage of their cancer experience."

📲 For more information, visit the Leukaemia Foundation's website 👇
https://www.leukaemia.org.au/news/couch-cancer-hub-nq-to-merge-with-leukaemia-foundation/

📸 Leukemia Foundation GM of Corporate Affairs, Susie Howard, COUCH Chair, Prof Scott Davis, Co-Founder of COUCH, Pip Woodward.

"The only thought I had was like… and this might sound quite abrupt, but “Am I dying?”🎂 Kiera noticed something was wron...
20/08/2026

"The only thought I had was like… and this might sound quite abrupt, but “Am I dying?”

🎂 Kiera noticed something was wrong a week before her 16th birthday.

“I was really tired, really pale. Mum said I looked ghostly. I went to get bloods and then an ultrasound to see if my heavy periods were causing anaemia."

👩‍⚕️ After the GP visit, Kiera was rushed to the Women's and Children's Hospital emergency ward in Adelaide.

"A doctor said the worst-case scenario was either I had leukaemia or aplastic anaemia. I didn't know what aplastic anaemia was, so I was hoping it was that..."

🎙️ In the latest episode of our Talking Blood Cancer podcast, Kiera talks about her journey after being diagnosed with severe aplastic anaemia at just 15 years old.

"It felt like a movie scene... like, this isn't real. I was reading a book where the main character had blood cancer. And so I thought, have I just jinxed myself?"

"For the first six months, I was off school. I couldn’t go out with my friends. I lost a really close friend because she didn’t keep in contact, and I was too sick.

📞 "My best friend called me every day to check on me and stayed on the phone for hours. If I didn’t have that support, I just wouldn’t have made it through."

While Kiera isn't grateful for her sickness, she does credit her cancer journey for giving her perspective.

"You don’t have to have a smile on your face when you’re going through treatment. You’re strong for existing. Just being here and going through it is enough."

🎧 Listen to this episode now on Spotify, Apple Podcasts, Amazon Music, or on our website.

"I was on a regular walk with my brother through Kings Park when I really realised I had a problem. I had to stop for a ...
18/08/2026

"I was on a regular walk with my brother through Kings Park when I really realised I had a problem. I had to stop for a rest every 10 minutes, feeling out of breath."

That walk in 2014 was the beginning of Mireille’s journey with non-Hodgkin lymphoma 🩸

🗣️ "I visited my GP, who organised blood tests. He had arranged for me to go to Royal Perth Hospital and said they were waiting for me."

"I had a visit from a doctor I hadn’t met before, who pulled the curtain of my cubicle and asked if I was Mireille.

"He said, ‘You have stage four non-Hodgkin's lymphoma. Someone will come and talk to you shortly!' Then walked off!

"To say I was stunned is putting it mildly."

Mireille soon underwent six rounds of R-CHOP chemotherapy and went into remission.

"I just thought I had too much to do to let this get the better of me. Grandchildren to watch grow up!"

🚶‍♀️An avid walker, Mireille joined a gym a year after her diagnosis to train for the Camino Trail. In August that year, she walked 117km in six days with her daughter, Nadia.

That same year, she began fundraising for the Leukaemia Foundation.

A chance meeting at her cocktail fundraising event led to Mireille joining the committee of Gidgestock Music Festival, where she helped establish the Kookaburra Boutique - a second-hand store at the festival raising money for people impacted by blood cancer.

“It was the best decision I could’ve made! Festivalgoers would call by the Boutique to purchase, donate and share their stories of personal or family survival.

"They feel that purchasing and donating is a way they can give back and support a great cause."

Over the years, the grassroots festival has raised more than $50,000 for our blood cancer community.

And at the heart of it all is Mireille - turning her own experience with lymphoma into a way to give back, bring people together and support others affected by blood cancer 🩵

13/08/2026

⏱️ 60 seconds with one of our healthcare experts.

👋 Meet Carly, one of our incredible Supportive Care Navigators based at our Clem Jones-Sunland Blood Cancer Centre in Brisbane (Meanjin)

📞 Picking up the phone on the other end of our 1800 support line, Carly speaks with patients and their families when they're at a difficult time in their diagnosis, treatment journey, or life after cancer 🩵

Our team of healthcare experts understands that living with cancer can bring many challenges for the person diagnosed and for their loved ones.

For specialised blood cancer care and information, check out our website or call 1800 620 420 💙

10/08/2026

Has s*x or romance changed for you since the cancer diagnosis? 💕

🗣️“There's no special diet or food that can cure cancer.”Eleanor Quinn, one of our Supportive Care Case Managers and an ...
07/08/2026

🗣️“There's no special diet or food that can cure cancer.”

Eleanor Quinn, one of our Supportive Care Case Managers and an accredited dietitian, says nutrition is paramount in supporting a patient's wellbeing through a cancer diagnosis and treatment.

“Treatment or cancer-specific side effects may make it hard to eat a balanced diet. They may have a reduced appetite, feel full more quickly, or feel nauseous.

"But a balanced diet can help manage symptoms, support the immune system, reduce treatment side effects, combat fatigue, and support the body’s ability to heal.

"Generally speaking, the best thing to do is try to eat a variety of foods from all five food groups.

1️⃣ Breads, cereals, rice, pasta and noodles.
2️⃣ Meat, fish, poultry, eggs and nuts.
3️⃣ Milk, yoghurt, cheese or alternatives (like soy milk with added calcium).
4️⃣ Vegetables and legumes (like chickpeas and kidney beans).
5️⃣ Fruit.

“Foods to avoid are processed meats like salami, ham, bacon, frankfurts and canned meat, and you should limit consumption of burnt or charred meat.

“While cancer can make cooking difficult, quick and easy meals can still provide a balanced diet.

🥫 “Utilise convenience food items like baked beans, canned fish, microwave rice, canned or packet soups, eggs and pre-cut vegetables.

“Don’t feel pressure to eat a ‘traditional meal’. If you feel like milk and cereal, or a grilled cheese sandwich for dinner, go for it!

“If you prefer fluids over solid food, have nourishing drinks high in energy and protein. Don’t wait to feel hungry, try to eat every two to three hours and try to avoid skipping meals.

“If you can’t consume a wide variety of foods for a few days or weeks, don’t beat yourself up. Please don’t feel alone, and make sure you ask your treating team for help.

“And ask a member of your treating team to refer you to a dietitian at the hospital, if you'd like professional help. It's free to see a public hospital dietitian."

🎙️ Hear more from Eleanor in the latest episode of our Talking Blood Cancer podcast, or visit our website for more nutrition and diet resources for living with blood cancer.

😻 Steve says his ferocious fur baby Mo has kept him sane since his chronic lymphocytic leukaemia (CLL) diagnosis six yea...
06/08/2026

😻 Steve says his ferocious fur baby Mo has kept him sane since his chronic lymphocytic leukaemia (CLL) diagnosis six years ago.

Adopted on Steve's 45th birthday, it didn't take long for Mo to show his new family who's boss...

🗣️"Mo was a kitten abandoned way too young in a backhoe bucket. His carer thought he'd die but soon realised he was a 'rascal' and would be fine.

"I learned what a rascal was... fingers and toes are for biting, and the rest of the time he climbs on me so he can ride on my shoulder.

"Mo has attitude. He tells me when it's feed time, when it's play time and when it's time for cuddles - and I must obey.

"He's bitten my brother-in-law and put him in hospital, and I can measure my platelet count by how profusely I bleed after our games."

But it's this attitude that gives Steve a reprieve from his treatment.

"He’s eight years old now, and I’m six years into my cancer journey on my second line of treatment for CLL.

"Every day I go to take my Zanubrutinib, Mo hears the tablets and has decided I'm giving myself a treat, so he has to have one too. Out comes the packet of Greenies and both of us have our 'medicine'.

"Mo doesn't distinguish whether I'm sick or not. But when I'm with Mo responding to his moods and wants, it's easy to forget about the challenges, the fatigue, the infections, the time in clinic.

"He seems to be bonded to me, and while he considers himself superior, he's also dependent on me.

"We have a strange relationship. It’s reassuring knowing that this little creature wants to be with me."

S*x, romance and intimacy all changed for Daniela when she was diagnosed with smoldering myeloma (SM) in 2008.🗣️ "My the...
05/08/2026

S*x, romance and intimacy all changed for Daniela when she was diagnosed with smoldering myeloma (SM) in 2008.

🗣️ "My then-husband didn’t know how to handle the situation, and frankly, I couldn’t blame him.

"It put a tremendous amount of strain and pressure on our marriage. We only got married the year before... our life changed overnight, and so did our romantic life."

Daniela was placed on ‘watch and wait’, and while she wouldn't require treatment for another 13 years, the stress and uncertainty impacted her relationship.

"I felt like I was going through it alone, even though he tried to be as supportive as he could. I guess neither of us wanted to face reality.

"Over time, our relationship eroded. Intimacy was never the same, and s*x felt like an obligation."

💔 Ultimately, they divorced in 2018. When Daniela met her new partner Brad, she tried a new approach – keeping her relationship separate from her cancer.

But that changed when Daniela began treatment in 2021 and had a stem cell transplant, and Brad was called on to be an active caregiver.

"Our s*x life was non-existent at the time. I knew he couldn’t bear to be around me. He'd lift me out of bed in the morning, place me on the couch, and return me to bed at night.

👩‍🦽 "I was bound to a wheelchair for five weeks. This was the most difficult period of my life."

As Daniela started to recover, so did their relationship and intimacy. Reflecting on her experience, she says that while you're allowed to make mistakes, communication is vital.

"It’s crucial that both partners and patients keep a strong positive mindset and know that sometimes it’s okay to not know what you’re doing.

"I wish I'd been more open at the beginning to involve myself in groups and organisations that offer positivity.

"This awful disease is what you want it to be. I know it’s changed my life for the better. I now see life differently."

04/08/2026

"I've watched two of my dearest friends fight the toughest battles against leukaemia, and their courage inspires me every day."

🏃‍♂️ Eman is taking on her first City2Surf this weekend to raise life-changing funds for our blood cancer community.

"I'm certainly not a runner, but I'm one to get behind a good cause. We're helping fund research, provide practical support for patients and families, and give hope to people facing blood cancer.

"My loved ones have been given a second chance at life thanks to the generosity of complete strangers who became stem cell donors.

"It reminds me that one small act from you can completely change someone else's future.

"Please consider registering with Stem Cell Donors Australia as thousands of Australians are waiting for a donor match right now to save their lives.

"I know how hard it can be to find a match for people from diverse ethnic backgrounds, which is why it's so important for young people to join the stem cell donor registry.

"My run this weekend is dedicated to my friends and everyone facing similar battles, while helping the Leukaemia Foundation continue its incredible work supporting patients and their families."

Address

213-217 Street Pauls Tce
Brisbane City, QLD
4006

Opening Hours

Monday 8:30am - 5pm
Tuesday 8:30am - 5pm
Wednesday 8:30am - 5pm
Thursday 8:30am - 5pm
Friday 8:30am - 5pm

Alerts

Be the first to know and let us send you an email when Leukaemia Foundation posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share