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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.
At the age of 24, Emma’s summer in 2021 took a turn for the worst after suffering from a bad strain of COVID-19. However, when intense headaches, bone pain and breathlessness began to surface after it passed, Emma knew something was wrong. After navigating her way through several misdiagnoses, she was later diagnosed with acute lymphoblastic leukaemia (ALL). Here, she tells her Spot Leukaemia story…
After returning to work from maternity leave, Eilidh-Ann couldn’t shake the fatigue she was experiencing and began finding unexplained bruising. She was whisked off to the hospital, where she received her acute promyelocytic leukaemia (APML) diagnosis in 2018, at the age of 34. Here, she shares her Spot Leukaemia story…
In 2013, at the age of 65, Derek started to experience signs of leukaemia he was unaware of. After a few months, his wife Jacky urged him to visit the GP. Jacky shares her husband’s Spot Leukaemia story here…
In 2018, 51-year-old Elizabeth was diagnosed with chronic lymphocytic leukaemia (CLL) after routine blood tests. Now 55, Elizabeth shares her Spot Leukaemia story here…
Helen was 59 when she was diagnosed with chronic myeloid leukaemia (CML) in 2018, after months of experiencing symptoms such as bruising, fatigue and night sweats. After going back and forth with her GP who seemed to know little about leukaemia and the symptoms, Helen finally received her diagnosis and was able to start treatment. Here, she tells her Spot Leukaemia story…
Jan had been a fit and avid long-distance walker and cyclist. However, whilst on holiday in Spain, she found herself low on energy and breathless. She visited the hospital abroad where she received her acute myeloid leukaemia (AML) diagnosis, alongside pneumonia. Here she shares her Spot Leukaemia story…
Margaret and Gill were both diagnosed with essential thrombocythaemia (ET), a rare blood disorder that causes a high number of blood cells called platelets to form. Despite the rarity, they found friendship in one another through the Leukaemia Care buddy scheme, to find they only live one village across from one another! Margaret and Gill share their stories...
Imagine you were given only three months to live. What would you wish for? You may wish to be able to move your partner and children closer to family, so they have the support they need. We may wish for somebody to talk to, who is able to share advice in these difficult times. This was a reality for David who was given three to six months to live after being diagnosed with acute myeloid leukaemia (AML) at the end of 2021.
Geoff was 56 when he was diagnosed with chronic lymphocytic leukaemia (CLL) after going to the GP for a blood test due to prostate issue concerns. From here, he has been on Watch and Wait for 12 years, and feels that sometimes he is just left to his own devices as he is not on any form of treatment.
At only 28 years old, Alex was a nurse working with haematology when she was diagnosed with acute myeloid leukaemia (AML). As both a patient and a healthcare professional, Alex retells her unique diagnosis experience as someone caught between two worlds.
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