MOAM first met Rosie in 2019, when she was just 7 years old and she quickly stole our hearts with her wonderful spirit.

In early 2020, just before the pandemic closed the world down, we were thankful to send Rosie and her family on a special trip to Queenstown. Those days away became treasured memories, woven with laughter, warmth and precious moments.

Rosie had a complex medical background, including a diagnosis of Bardet-Biedl Syndrome, among other conditions. Yet none of this ever dimmed her ability to love and to be loved deeply by all who knew her.

In July 2021, Rosie grew her angel wings. Though she left this world far too soon, her light continues to shine brightly in our hearts.

Forever remembered, forever loved, forever our Angel Rosie.

In September of 2022, our beautiful MOAM Angel Aisha grew her angel wings, after a battle with brain cancer. Aisha passed peacefully, surrounded by her loving family. In the words of her father, he at the time said, “she has returned to her Lord with a smile.”

In June of 2022, Mates on a Mission had the privilege of sending Aisha, her parents and siblings to Indonesia to visit her grandparents, uncles, aunts and cousins, many of whom Aisha met for the very first time.

These treasured moments, filled with love and togetherness, will remain forever in the hearts of those closest to her.

Aisha’s smile was radiant and her personality unforgettable. She will always be remembered for the joy and light she brought to those around her.

Fly high, beautiful angel Aisha. You will forever be part of the MOAM family.

Spencer was just 13 years old when he sadly lost his battle with Malignant Melanotic Nerve Sheath Tumour. In March 2025, we had the privilege of gifting Spencer and his family a special Sydney staycation, highlighted by a magical helicopter flight over Sydney Harbour. It was a rare moment of light, joy and togetherness in the midst of an incredibly difficult journey.

His mum, Louise, later shared, “You guys allowed us to create the most amazing memories, and we will be eternally grateful for your generosity.”

Spencer will always be remembered as a bright, courageous soul whose strength touched every heart around him. Though his time here was far too short, his memory will forever remain a part of the MOAM family.

Forever our Angel, valiant Spencer.

Angelina was diagnosed as a teenager with Lafora disease, a rare and devastating brain disorder that brings recurrent seizures and gradual loss of function. Through every challenge, Ange faced the world with extraordinary courage, grace and a spark that never dimmed.

Despite the progression of her illness and the absence of a cure, Angelina’s spirit remained radiant. She inspired those around her with her strength, warmth and resilience, leaving an imprint of love that will never fade.

In mid-2025, at just 21 years old, Angelina grew her angel wings. The world lost a beautiful soul, but her light continues to shine in the hearts of all who knew and loved her.

Ange – forever our MOAM Angel.

George was a bright and beautiful little boy whose smile lit up every room he entered. Bursting with energy and charisma, he was an absolute joy to be around.

After bravely undergoing a chemotherapy trial at Randwick Children’s Hospital for Stage 4 Glioma, George experienced some precious months of improved health. During this time, he was able to create cherished memories with his mum, dad and extended family on a special getaway to the Blue Mountains.

Heartbreakingly, not long after their time away together, George grew his angel wings and reunited with his little brother Alfie in heaven. You will always be remembered, and you will always be missed, little guy.

Harvey was heartbreakingly diagnosed with inoperable DIPG, a rare and aggressive childhood brain cancer, in December 2024. When his family was introduced to Mates on a Mission, his mum had one simple wish – time. Time away with her children and partner. Time to just be a family.

So we made it happen.

Harvey and his family were gifted a two day Sydney sightseeing escape, highlighted by a private behind the scenes tour at SEA LIFE Sydney Aquarium. The kids were completely in awe. It was a weekend filled with wonder, laughter and memories that will be cherished forever.

Beautiful little Harvey passed away later that year, leaving his family and the entire MOAM community heartbroken. He will always be their angel, watching over them, and forever a part of the MOAM family.

Steven was a bright, intelligent and beautiful young boy, facing an illness that no child should ever have to endure.

Diagnosed with a high grade glioma, Steven and his family suddenly found themselves navigating a journey no family is ever prepared for.

When Steven was referred to Mates on a Mission, we knew we had to move quickly. With his 12th birthday approaching, our team raced against the clock to create something special for him, a chance to step away from hospital appointments and simply be a kid surrounded by his mates.

Thanks to the incredible generosity of our supporters, we were able to organise a memorable birthday celebration for Steven and his school friends in Dubbo, filled with laughter, bowling, fun and moments of pure joy. For a little while, the focus wasn’t on illness or treatment. It was on friendship, smiles and celebrating a beautiful young boy turning 12.

These are the moments that matter most.

Sadly our little mate lost his fight and returned to God in April 2026. He was a little man but he had HUGE faith.

Our thoughts and prayers remain with his beautiful parents today, and always, and we pray Steven forever rests in peace in the loving arms of Jesus.

Vir was a bright & bubbly young boy, with a beautiful spirit, who was bravely battling Acute Myeloid Leukemia (AML), an aggressive form of blood cancer.

Vir wagef an incredibly tough battle for three years.

In 2023, he was diagnosed with Acute Lymphoblastic Leukaemia (ALL) and endured 18 months of intensive chemotherapy. Just as his family hoped the hardest days might be behind them, another devastating diagnosis came in February 2025 – Myelodysplastic Syndrome (MDS), a serious bone marrow disorder and precursor to leukaemia.

In April 2025, Vir underwent a bone marrow transplant, with his older brother selflessly stepping forward as his donor.

Disappointingly, in January 2026, Vir was diagnosed with Acute Myeloid Leukaemia (AML).

It’s was both remarkable and inspirational that after years of relentless treatment, Vir continued to face this battle with extraordinary courage, surrounded by the unwavering love and strength of his family.

Vir and his family enjoyef a Sydney staycation and a gastronomic experience at one of Sydney’s finest buffets, which is just what foodie Vir requested.

Vir’s entire experience was kindly donated by a member of our MOAM community, who wishes to remain anonymous, but who, upon hearing about Vir’s story, was very touched and inspired to sponsor this MOAM Moments getaway.

Devastatingly, Vir passed away in June 2026, and his loss was felt deeply within the MOAM community. We hold is family in our prayers and know that Vir’s memory will be eternal.