Elara’s story
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Elara’s story

Two year old Elara spent Christmas 2019 in hospital, after being diagnosed with neuroblastoma on 13 December 2019. She had an 11cm mass in her tummy and needed treatment straight away.

“It will be a huge celebration to have Elara at home this Christmas and I am so grateful she’s responding well to treatment. This is our story.”

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Eva's story
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Eva's story

“In February 2016, Eva was diagnosed with Stage 4 neuroblastoma and our life totally changed. She was sadly taken from us in May 2017 aged just seven years old, but her courage, strength and humour were incredible throughout all her treatment.”

Eva’s mum Lauri shares their story.

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Florence's story

“Our beautiful daughter Florence was diagnosed with neuroblastoma in December 2015. On 11 February 2017, Florence passed away peacefully with her family around her. She was two and half years old. “ Florence’s mum Carolyn shares their story.

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Rory's story
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Rory's story

Rory was diagnosed with stage 4s neuroblastoma when she was just two weeks old and was given a 30% chance of survival. In September 2019, Rory was in remission.

“If you look at Rory now, you’d never know she’d been through so much. She is a wild and feisty little girl - our miracle baby. We are so very lucky.” Rory’s mum Emily shares their incredible story.

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Toby's story
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Toby's story

“Our son Toby is ten years old, loves school, football and keeping fit. But nine years ago, we experienced the worst night of our entire life when he was diagnosed with neuroblastoma.”

Margaret, Toby’s mum shares their story.

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Evie's story
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Evie's story

Evie and her twin sister Ella were born three months premature, weighing just over 2lb.

Evie was soon to endure another fight for her life. Shortly before the twins first birthday, aged just ten months, Evie was diagnosed with stage four high risk neuroblastoma. Imogen, Evie’s mum, shares their story.

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Mik's story
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Mik's story

Mik Scarlet, broadcaster, actor, journalist, musician and disability rights expert, is not only a man of many trades, but stands as a ray of hope for children and families affected by neuroblastoma.

Read Mik’s heartwarming story about his life with and after neuroblastoma.

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Renly's story
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Renly's story

“Renly was diagnosed with high-risk neuroblastoma when he was two years old. It was just four short weeks from diagnosis to Renly passing away... but that’s typical of his journey; he arrived too soon and left too soon.”

Renly’s mum Sarah shares their story.

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