Tag: supporter stories
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Taking To The Airwaves: Ellen’s brain tumour story
Ellen Yates is guest hosting on local radio to raise awareness of brain tumours.
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Paying it forward
How Pearl and Dean is helping to raise awareness of brain tumour symptoms this summer.
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Family celebrates medication milestone
Alexander, 10, can now have treatment at home and his family can close their crowdfunding page.
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Wishing Diving Duo Tom Daley and Noah Williams, Olympic Games success!
Tom has passionately supported us over many years in our drive to raise awareness and much-needed funds for vital research.
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Double your donation to double your impact: Matthew’s story
Have double the impact in giving people like Matthew a brighter future when you donate via The Big Give between 22 July and 29 July.
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The Glad Game and the Power of Positivity
The Glad Game has been turned into a book, play and film, to help people stay positive during the darkest times.
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Being Benign – Callum Ewing’s story
Callum is a recent broadcast journalism graduate who used his final project to highlight his brain tumour diagnosis. Being Benign is a two part documentary where he interviews his parents, others in the brain tumour community and also a professor who works on childhood brain tumours.
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Spotlight on Supporter Group, Firth’s Fundraisers
Paul set up Supporter Group Firth’s Fundraisers, and with family and friends, has raised over £20,000 since his diagnosis in March last year
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Mental health and growing up after losing a loved one to a brain tumour – Guest post by Ed Ryan
Ed, one of our Young Ambassadors, explains how losing his mum following her brain tumour diagnosis affected his mental health.
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The mental health effects of caring for someone who has a brain tumour – Guest post by Francesca Silverton
Francesca, one of our Young Ambassadors, explains how her mental health was affected after becoming a carer for her boyfriend when he was diagnosed with a brain tumour.
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To our 2024 Machu Picchu team – thank you!
Find out how our 2024 Machu Picchu team got on, and how their fundraising will improve the lives of everyone affected by brain tumours.
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Living with a brain tumour inspired Anna to write Little Nipper to the Rescue
Her children’s book is about the community bus she travelled on daily, having had to surrender her driving licence.
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“Carpe Diem, that motto is important to me. I live in the moment”
Natalie McKenna-Mounty was diagnosed with a glioblastoma in 2020, her tumour returned in June this year, and now she is supporting our new research funding to find better glioblastoma treatments.
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Alastair’s Story: Part One – Crossing a Threshold
In this four-part series, Ali Travis, who was diagnosed with a high-grade glioma at just 32, shares his beautifully written and, somehow, positive experience of coming to terms with his diagnosis.
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Alastair’s Story: Part Two – A robot called Stealth
In his second guest blog post, Ali Travis describes coming to terms with his diagnosis and explaining it to his loved ones.
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Alastair’s Story: Part Three – A Battle We’ll Lose
In the third of a four-part series, Ali Travis, who is living with a high-grade glioma, shares his experience of coming to terms with his diagnosis.
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Alastair’s Story: Part Four – Best Year of my Life
In the last of this four-part series, Ali Travis explains how being diagnosed with cancer taught him that “a good life cut short, is still a good life.”
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“There is nothing more important than saving lives and without research the reality is that lives will be lost.”
Toni O’Callaghan tells us about her son Jay’s glioblastoma diagnosis in 2021 and highlights the importance of funding glioblastoma research.
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Living with a pilocytic astrocytoma – Jerome’s story
Jerome van Leeuwen, age 42, originally from The Netherlands and now living in Fife, Scotland was first diagnosed with a pilocytic astrocytoma brain tumour when he was just two years old, it later returned in his 30s.
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Fundraiser sets out on 20 Walks Challenge – to mark 20 years since his brain tumour diagnosis
Tom, from London, will stride out across the UK this year to raise funds and awareness of brain tumours. His next walk is Kielder Water, Northumberland, this weekend.
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“This should never have been part of Ramona’s life”
Ramona Read was just nine-years-old when she was diagnosed with a low-grade pilocytic astrocytoma in 2021. Her mum, Vicky, shares their story ahead of their appearance on Channel 4’s The Dog House – where families are matched with dogs who hope to find their forever home.
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Amazing in-memory fundraising by the Christian White Memorial Fund
Christian’s family and friends have been tireless in their efforts to raise money for glioblastoma research in his memory
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Navigating the path unknown –James’ story.
James was first diagnosed with a brain tumour after having a seizure in 2018. Since then, he has had two awake craniotomies and a string of treatment types. Here, he shares his story on how he has navigated the uncertainty which came with it all.
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Family share how they are coping with dad’s incurable brain tumour.
A family has shared how they are preparing themselves, including their teenage children, for losing their father after he was diagnosed with an incurable brain tumour.