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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.
Kirsty put her symptoms down to both her age and the stresses of a busy job. However, when she suddenly collapsed and was rushed to A&E, tests confirmed she had chronic lymphocytic leukaemia (CLL).
Dharmesh had no symptoms before his diagnosis of chronic myeloid leukaemia (CML), with the condition instead being picked up in a routine blood test. Here, he talks about his road to diagnosis and how he’s doing now.
In 1999, Richard was diagnosed with hairy cell leukaemia, a rare but chronic form of leukaemia. Since then, he has been in remission a number of times after bouts of treatment, and here he discusses what his life has been like over the 20 years since diagnosis.
Last year, WWE (World Wrestling Entertainment) superstar Roman Reigns announced he was taking time out to receive treatment for chronic myeloid leukaemia (CML). We sat down with Reigns for an exclusive interview on his diagnosis, treatment and his newfound position as an advocate for blood cancer patients.
Julie Lewin is a longstanding volunteer for Leukaemia Care. She began volunteering for the charity after she was diagnosed with acute myeloid leukaemia in 1997 at the age of 27. Here, she recounts her diagnosis and treatment, and shares how she’s doing now.
Bernadette Davies put her symptoms down to the flu and working nights. However, she had all the typical symptoms of leukaemia, and was diagnosed with acute myeloid leukaemia in 2005. Here, she talks about her experiences of treatment and life after cancer.
Sophie had only recently given birth to her first child when she began to feel unwell. After a number of trips to her GP, she never would have guessed that her symptoms were due to leukaemia. Here, she gives an honest account of her diagnosis, treatment, and life after leukaemia.
Sarah was eventually diagnosed with acute myeloid leukaemia (AML) after unknowingly displaying symptoms for over two months. The half a year that followed proved to be a difficult journey. However, one-year post-transplant, Sarah hopes to be on the road to recovery.
When Garry began experiencing pain in his chest, doctors believed he was having heart problems. So, when the diagnosis of chronic lymphocytic leukaemia (CLL) came the next day, Garry was shocked. Here he talks about his experience of living with CLL, and why it’s important not to bottle your feelings up.
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).
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