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The children and families at our heart

Everything we do is for these families. With their kind permission, they've shared their stories — of fear and hope, and of the support that helped them through.

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Our Inspiration

Our origin story

Dannie's Story

Daniella Logun, known to her family as Dannie, passed away from a brain tumour in 2016. The Daniella Logun Foundation was founded in her memory, and in the hope that no other family would walk this road alone.

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Our children

Meet the families we support

Edward's story

Edward was diagnosed with a Medulloblastoma brain tumour in November 2018, at just 3 years old. His mum Catherine shares their family's journey — from the rawness of diagnosis to the hope of treatment.

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Elliot's story

Elliott was diagnosed with a Dnet brain tumour in the thalamus in 2020 — incidentally, while doctors were looking for complications of birth hypoxia. He also lives with ASD, ADHD, dyspraxia, hypermobility, and a history of absence seizures.

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Olya and Alexander's story

Olya's son Alexander was diagnosed with a brain tumour before his first birthday in 1997. He passed away at 18. Olya shares the years of silence, the isolation no-one acknowledged, and her call for the systemic support bereaved families need.

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Elsie's story

Elsie was diagnosed with a brain tumour four years ago. Her mum Chantal has been her voice through every meeting, every decision, and every fight for the right support.

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Jake's story

Jake's family share the start of their journey — when ordinary illness turned into something far more frightening.

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Jas' Story

A chatterbox, bright, energetic, bubbly and friendly — Jas is as curious as they come, always primed with a question for each minute. His mum M shares their family's journey through diagnosis and the anxiety that came with it.

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Brett's story

Brett was a healthy and happy 8-year-old until November 2019. His mum Jill shares the misdiagnosis, the 10-hour emergency surgery at Alder Hey, and a journey now well into its sixth year.

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Eloise's story

Eloise was diagnosed with an Embryonal Tumour with Multi-layered Rosettes (ETMR) in 2020, five months after her first birthday. Her parents Mel and Pete share the rollercoaster of one of the rarest, most aggressive brain tumours.

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Nally's story

Nally was diagnosed with Leukaemia. His mum Shay shares how the family found their feet in the hardest first year — and what happened when the in-hospital support fell away.

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Stand with our families

Your gift stays local and reaches a family this week.

Every pound supports a child with a brain tumour and the people caring for them — right here in our community.

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