100 years of life post transplant -- Kerrin Litchfield competing in tennis at the World Transplant Games
Patient Stories
100 Years of Life Post Transplant: Meet the Transplant Games Champions Who Refuse to Sit Still

100 years of life What does 100 years of life look like after a bone marrow transplant? It looks like Lisa, Jonathon, and Kerrin — three extraordinary Australians who’ve not only survived bone marrow transplants, but have gone on to…

August 15, 2025
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Jenny Nixon, who has learned how to deal with post transplant fatigue, pictured atop a hill in South Africa, standing under a metal arched structure with the words "This is Living" on it. She is looking at the camera, and there is a spectacular vista of land and sea behind her.
Patient Stories
Rolling with the Punches: Jenny’s Journey through Two Bone Marrow Transplants and Beyond

Jenny Nixon is no slouch. She’s a mother to two sets of twins, who she raised as a single mum from when they were six and three years old, and is a proud grandmother to four. She runs her own…

July 25, 2025
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Young Poppy who had a BMT for Diamond-Blackfan Anaemia. She is pictured ready for school
Patient Stories
Diamond-Blackfan Anaemia, and Poppy’s fight for life.

Poppy Pickett has had more than a lifetime’s worth of medical poking and prodding, with transfusion after transfusion, endless visits to hospitals and specialists, and months in isolation. And she’s only five years old.  Poppy was diagnosed with Diamond-Blackfan Anaemia…

June 26, 2025
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Stem cell transplant patient Serina Dosen, now living with long-term GvHD
Patient Stories
Living with long-term GvHD – Serina’s story

Thursday 7th November 2002 is a day Serina Dosen will never forget. It’s the day she received her new stem cells, and a second chance at life. But it’s also the day she began her “new normal” life, with a…

May 28, 2025
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black and white photo of a person, facing away from the camera, sitting in a wheelchair in a hospital room, used to illustrate the hidden cost of BMT
Patient Stories
Hidden financial cost of BMT

Meagan Clark* is a university lecturer, married, with two kids – all the usual stuff – and considers herself incredibly privileged. But despite her apparent advantages in life, she still struggled with the blows dealt to her and her family…

April 30, 2025
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Latest News Patient Stories
Stacey’s Story: A Mother’s Journey through Andre’s GATA2 Deficiency and Transplant

GATA2. It sounds like something from a SciFi movie, doesn’t it? Perhaps the name of a newly colonised planet, or a space station or something. But no. It’s a protein that regulates gene expression and it plays a key role…

February 10, 2025
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Patient Stories
Living with Multiple Myeloma – Aamu’s story

You don’t expect to have to wear nappies and learn to walk again when you’ve been successfully adulting for decades. And you don’t expect to follow that up with having to watch your 19-year-old learn to walk again either. But…

January 15, 2025
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Katherine Robertson pictured outside her home in 1999 just before she was diagnosed with ALL. Her aunt, Anne Robertson, left a generous gift in will to Arrow the Bone Marrow Transplant Foundation in Katherine's memory.
Latest News Patient Stories Supporter Stories
Anne’s gift in memory of Katherine Robertson

Katherine Robertson, pictured in 1999, not long before her diagnosis with acute lymphocytic leukaemia. Anne Robertson  Anne Robertson was a refined lady, always impeccably presented, with a love for history and family. Anne had a love of the arts enjoying…

November 17, 2024
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Courtney Hughes in her hospital bed holding her nursing degree from Charles Sturt University
Patient Stories
Bedside Nursing Degree for Courtney Hughes!

Courtney Hughes’ pathway to her nursing career is not your average one, but then Courtney probably isn’t your average kind of girl. Courtney was leading an active life, busy working as a prison officer doing lots of physically demanding work…

October 4, 2024
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Jordan Lambropoulos recovering after receiving her BMT for Crohn's Disease
Patient Stories
BMT for Crohn’s Disease – The worst and the best time of my life

“My bone marrow transplant was the worst and the best time of my life.” That’s how Jordan Lambropoulos describes her ground-breaking stem cell transplant now that she has another year of living under her belt. Bone marrow or stem cell…

June 20, 2024
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Aplastic aneamia patient and bone marrow transplant recipient Sam Sheehan pictured in hospital. Alongside him is his partner Hannah.
Patient Stories
Aplastic Anaemia

Meet Sam Sheehan, an Aussie living and working in Vietnam with his partner.  Sam, with his ever-positive outlook on life, put a lot of his seemingly innocent health woes down to travel bugs and a difference in health care systems,…

May 29, 2024
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Patient webinars are launching soon at Arrow. This image is the logo for Transplant Talk Live, Arrow's new series of patient webinars. It has the Arrow logo on the right, with the words "Transplant Talk LIVE" on the left.
Patient Stories
Patient Webinars: Transplant Talk LIVE!!

Arrow’s newsletter, “Transplant Talk” is going live. Join us for a series of patient webinars with expert guests covering topics such as returning to work after bone marrow/stem cell transplant, survivorship, dealing with graft v. host disease, and much more….

February 15, 2024
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Allogeneic stem cell transplant recipient Jackie second from left, with her four daughters celebrating her first post BMT mother's day. An allogeneic stem cell transplant saved her life.
Patient Stories
Jackie’s cat saved her life. (Oh, and an allogeneic stem cell transplant.)

A woman with a cat bite walks into a medical centre… No, it’s not the start of a bad joke, but what followed for Jackie was so surreal it felt like it could have been. She had been feeling fatigued…

January 31, 2024
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Hardship can happen to anyone. Arrow really matters: we support people during and after bone marrow transplant. Picture shows holding hands across the table. Coffee cup nearby
Patient Stories
Hardship can happen to anyone

“How are you doing today?” It’s an innocuous question for most of us, something we ask often without really listening to the answer. But hardship can happen to anyone. “I’ll tell you on Tuesday,” was the answer I got when…

December 20, 2023
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Des Kitson talks with Arrow Bone Marrow Transplant Foundation about the role of a positive attitude
Patient Stories
Today of all days. (The role of a positive mindset.)

“Today of all days, Jen.” It had taken quite a bit of to-and-fro to arrange a time to speak with Des. He’s a busy man: playing golf, catching up with friends, enjoying concerts, and back in full time work after…

October 17, 2023
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The team at The Individual Wig standing in front of some wigs displayed on mannequins
Patient Stories
A fresh new look for the Tracey Scone Wig Library

Unless you’ve been through it, you probably don’t really understand the impact losing hair can have on a cancer patient. Losing your hair is a visible sign of illness and can trigger all sorts of unwanted responses from well- meaning…

August 25, 2023
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Blondes have more fun! Woman wearing blonde shoulder-length wig, standing in front of a bookshelf.
Patient Stories
Do blondes have more fun? Clare is about to find out!

Of all the hardships that cancer patients endure, losing their hair is often the thing that people tell us is one of the hardest to take. It’s such a visible manifestation of the treatment they’re going through, and it screams…

July 3, 2023
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Lisa Cuthbertson and her sister holding the Australian flag at the World Transplant Games in Perth 2023
Patient Stories
World Transplant Games in Perth 2023

Making a splash 38-years post bone marrow transplantation Camaraderie, commitment and courage are three words that come to Lisa Cuthbertson’s mind when she talks about the World Transplant Games, recently held in Perth, Western Australia, 15-21 April 2023.   “Camaraderie…

May 26, 2023
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Outside Northern NSW Cancer Institute
Patient Stories
Wigs lift spirits in Lismore

Lismore is doing it tough. First the COVID pandemic, and then the devastating floods just over a year ago now, the effects of which are continuing to be felt throughout the community. During these difficult times, people of Lismore and…

May 16, 2023
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Robyn (Robbie) Canner and her son Scott at a Tour de Cure event
Patient Stories
Robbie Canner: a mother’s undying love

Robyn (Robbie) Canner was a single mum with little support around her when her son Scott was diagnosed with non-Hodgkin lymphoma. “It was a tough time,” Robbie says. “Everything happens so fast with this disease. We got the diagnosis, Scott…

May 12, 2023
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