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These inspirational stories are personal accounts of the experiences of patients, carers or fundraisers - they all have a story to tell about their experience with a blood cancer.
When Carrie began experiencing neck pain and flu-like symptoms at the beginning of 2018, she took herself to the GP. However, over the next few months as Carrie’s symptoms worsened, she was repeatedly told that she simply had a virus. Eventually, Carrie’s symptoms were recognised, and she was diagnosed with chronic myeloid leukaemia (CML).
When 8-year-old Isabella began complaining of pain in her legs and back, her mother Paola took her to see the GP. However, it wasn’t until over a month later that doctors finally discovered Isabella’s symptoms, including four broken vertebrae, were due to acute lymphoblastic leukaemia. Here, Paola recounts her daughter’s story.
When Jo began experiencing shortness of breath and heavy menstrual bleeding, she put the symptoms down to a number of different causes, including general fitness and fibroids. So, it came as a shock when, in November 2016, she was diagnosed with acute lymphoblastic leukaemia (ALL).
A family history of myeloproliferative neoplasms (MPNs) meant that Lucy already knew the signs and symptoms of blood cancer. However, it took four years for Lucy to get her diagnosis of essential thrombocythaemia (ET).
Helen Swambo was receiving treatment for lupus and having two-weekly blood tests when she was told her blood count was abnormal. However, Helen’s results were not followed up on, and it was only when she began experiencing bruising that she pushed for further tests, resulting in her diagnosis of acute myeloid leukaemia (AML). Six years on and in remission, Helen shares her story.
Geoffrey was diagnosed with chronic lymphocytic leukaemia (CLL) completely out of the blue after a routine NHS health check flagged up an abnormal blood test. Read his story here.
When Christopher began experiencing symptoms, he already had an inkling that he may have a blood cancer. However, receiving his diagnosis of chronic lymphocytic leukaemia was still a shock. Here, he recounts his experiences.
Melissa’s only symptom before diagnosis was tiredness, something she attributed to working too hard. So, it came as a shock to Melissa when she was diagnosed with chronic myeloid leukaemia. Here, she talks about her diagnosis and her life since.
Meena had been feeling fatigued for a few months when she decided to visit her GP. However, when the GP called and told her they suspected leukaemia, Meena was shocked. Here, Meena talks about her diagnosis, along with the campaign she has set up to find herself a stem cell transplant match.
20-year-old Nathan Hall had just turned 15 when he decided to see his GP about fatigue. What followed was a diagnosis of acute myeloid leukaemia (AML). Here, Nathan talks about diagnosis, relapse and his life after leukaemia.
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