Patient stories
Find out about the impact our work has on patients.
“Cancer research is the reason I am here” – Sonia’s breast cancer story
Sonia Bhandal was just 14 when she lost her mum to secondary breast cancer. Then at the age of 28, she found a malignant lump in her own breast. Shortly afterwards she discovered that she carries the BRCA2 gene mutation, putting her at an increased risk of developing various cancers. Today, exactly 29 years since scientists at The Institute of Cancer Research, London, identified the BRCA2 gene, Sonia, now 36, shares her story.
“Hearing the words ‘you have cancer’ blew me away, but I was determined to beat it” – Natasha’s story
When Natasha, 51, was told she had stage 2 DCIS breast cancer in November 2018, she became the third woman in her family to receive such a diagnosis. Now nearly six years on and cancer free, Natasha shares her story.
"I feel incredibly lucky to be here 12 years on from my diagnosis" – Natalie’s ovarian cancer story
Natalie Pearce, 52, was diagnosed with stage 3c ovarian cancer in November 2012. She subsequently discovered she carries the BRCA1 gene mutation, putting her at a higher risk of developing various cancers. Following surgery and treatment, Natalie has been cancer free since April 2013.
“We hope that continued research will bring about kinder treatments for children in the future” – Jesse’s story
Jesse was two years old when he was diagnosed with B-cell acute lymphoblastic leukaemia, a type of blood and bone marrow cancer, in November 2023. Now, a year since his diagnosis and thankfully in remission, Jesse’s mum, Polly, shares their story to mark World Children’s Day.
"I was hoping for 12-18 months… here I am 14 years later" – Sue’s ovarian cancer story
Sue Vincent was diagnosed with ovarian cancer in 2007 when she was 54. In 2010 she discovered it had spread and was inoperable. She was told she had just months to live, until a new targeted treatment changed everything. Sue lives with her husband Pete in Solihull, Birmingham – between them they have four daughters and five grandchildren, with another on the way next year.
“I’m glad to be working on something that makes a difference to people’s lives” – Jessica's cancer research career journey
Dr Jessica May Hislop joined The Institute of Cancer Research as a Bioinformatician in the Houlston Lab in the Genetics and Epidemiology division. Together with her colleagues, she is working towards understanding how mutations in our DNA lead to cancer. But her career almost took an entirely different direction.
"I'm just so grateful for research" – Shelley's story
Shelley Harding is a familiar face at the Terry Fox UK runs. A Canadian, who moved to London 23 years ago, she sells official event T-shirts to raise vital funds for The Institute of Cancer Research. This year she attended Terry Fox Runs in Battersea Park, Hampshire and will be at Wrexham this weekend. Last month she was invited to a special Terry Fox reception at Canada House in London, where Fred Fox spoke about his brother.
“Becoming a cancer patient has given me extra perspective” – Paul’s story
Professor Paul Workman is Harrap Professor of Pharmacology and Therapeutics at The Institute of Cancer Research. He has worked in the field of cancer research for more than 50 years and was the ICR’s Chief Executive and President from 2014 to 2021. During his leadership, he oversaw many of our scientific successes – including the development of smarter and kinder forms of radiotherapy. Now, after being diagnosed with prostate cancer himself in 2022, he reflects on his experience as both a leading cancer scientist and now a cancer patient.
“Every child diagnosed with brain cancer should have a chance at life” – Alison’s story
Alison and Brian set up the Doing It For Daniel Foundation in memory of their son, Daniel, who was diagnosed with an aggressive brain tumour at the age of 16 and passed away seven months later. Here, Alison shares their story and explains why the ICR’s research into a cure for Daniel’s cancer is so important.
“I’m running for Terry Fox to improve the lives of people with cancer” – Brian’s story
Terry Fox is a Canadian hero. He lost his leg to osteogenic sarcoma, a rare bone cancer, but in 1980 began a ‘Marathon of Hope’ – running 3,339 miles over 143 days to raise awareness and money for cancer research. His dream to run across Canada was cut short after his cancer spread to his lungs and he died aged 22.
Terry continues to inspire people in Canada and beyond to raise money for cancer research, and in the UK the Terry Fox Association proudly supports The Institute of Cancer Research.
Brian Whitman is a Canadian currently serving with NATO at its Allied Maritime Command at the Northwood base in north-west London.
“We still want more time – that’s the role of research” - Yvonne's story
Yvonne Diaz, 55, was diagnosed with stage 4 ALK-positive lung cancer in August 2021. She works in Communications and lives in Holland Park, London with her husband and twin sons, aged 17.
“Being involved in a clinical trial saved my life” – Tony’s story
Tony McHale, a screenwriter, was invited to take part in the IMPACT study in 2012, an international clinical trial offering regular screening for men at increased risk of prostate cancer. Around 18 months later, he was diagnosed with the disease at the age of 61. After undergoing intense radiotherapy treatment, he has remained cancer-free ever since.
“I’m lucky to have been given a second chance” – Michael’s story
Michael Parry was diagnosed with pancreatic cancer at the age of 59. Fortunately, his disease was detected early – and after surgery and chemotherapy, he is now planning for the years ahead with his family. Here he tells his story and explains why more research into hard-to-treat cancers is so vital.
From cancer diagnosis to London Marathon mission – Harry’s story
As a fit and healthy former firefighter, Harry Hall didn’t think there was anything to worry about when he developed a lump in his neck. But after his wife persuaded him to go to the doctors, tests diagnosed Harry with tongue cancer. Here, Harry explains why he wants to raise funds to support our vital research by running the London Marathon.
“I’ve been given a second chance” – Mark’s story
Mark was diagnosed with kidney cancer in April 2021. After surgery to remove the tumour and affected kidney, he was initially told there was no evidence that the disease had spread. However, a biopsy of the tumour showed it was an aggressive type of cancer, prone to returning.
“I survived cancer as a child and now I’m working to defeat it” – Andrew’s story
Andrew Wicks, a PhD student at The Institute of Cancer Research, knows firsthand what it’s like to face cancer. Diagnosed with acute lymphoblastic leukaemia (ALL) at the age of 12, he went through years of treatment before getting the all-clear. Now, wanting to help others with cancer, he is carrying out research in our Breast Cancer Research Division. Here, he shares his story.
“We need to stop other children from having to go through this” - Tommy’s story
Tommy Edwards was just four years old when his parents noticed symptoms suggesting something wasn’t right. Tests revealed he had acute lymphoblastic leukaemia (ALL). Following nearly three years of treatment, Tommy is now looking towards the future. His parents, Chris and Jo Edwards, have set up a charity to fund research into ALL. In this blog, Chris explains how groundbreaking work by scientists at The Institute of Cancer Research is giving them hope for the future.
“My experience has highlighted to me just how vital cancer research is” - Erin’s story
Erin Kennedy MBE is a British Paralympic coxswain. In 2022, at the age of 29, she was diagnosed with triple negative breast cancer, and was successfully treated. She later found she has a mutation in her BRCA1 gene which means she has a higher risk of her cancer returning. In the summer of 2023, she supported our Finish Cancer campaign. Here she tells her story.
“We’re all working towards a future where children don’t die from cancer” – Hannah's story
Hannah Tarplee was four years old when her parents noticed a lump in her tummy which turned out to be a cancerous tumour. Despite intensive treatment, it became untreatable, and Hannah died just seven months after the lump was discovered. The Little Princess Trust, which was set up in her memory, funds our research, as one of our valued family charity partners. Her mum, Wendy Tarplee-Morris, explains how Hannah’s legacy is now giving hair and hope to thousands of children and young people.
“Immunotherapy is a game-changer” – Glenys’ story
Glenys Gregory recently became a grandmother, but at one point, she’d wondered if she would live to see him born. In January 2020, Glenys was diagnosed with advanced lung cancer after nursing her mother through the same disease. Due to the coronavirus pandemic, she went straight onto immunotherapy and a scan in summer 2023 revealed that she had no evidence of disease. Here she tells her story.
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