“I’m not the same person I was” says Corby mum-of-three, as charities urgently campaign for awareness of blood cancer symptoms

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Leukaemia Care and Leukaemia UK’s #SpotLeukaemia campaign, encourages people to ‘channel their inner five-year-old’ by asking themselves the difficult questions that could help spot Leukaemia

A Corby mum who was diagnosed with Leukaemia is supporting two charities who have started a new awareness-raising campaign.

Leila Richardson was diagnosed with chronic myeloid leukaemia (CML) in December 2021; a rare type of blood cancer which progresses slowly, and for which there is no cure.

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Now, she is supporting Leukaemia Care and Leukaemia UK’s new #SpotLeukaemia campaign, highlighting the importance of symptom awareness and early diagnosis.

In late 2020, 44-year-old Leila put her hot flushes and feelings of fatigue down to changing hormones, and the demands of a busy life looking after three teenage children. It wasn’t until her health started to plummet that she pushed for more tests.

By July 2021, Leila’s symptoms had worsened to the extent that she struggled to catch her breath.

Due to Covid-19 restrictions it was extremely difficult for Leila to secure a GP appointment, and after repeated failed attempts to secure a diagnosis, Leila was not given a blood test until December 2021 - over a year since her symptoms began.

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Leila said: “The afternoon after I had taken the test, I received a call from the doctor’s surgery telling me there was a problem with my blood.”

Leila Richardson with daughter MollyLeila Richardson with daughter Molly
Leila Richardson with daughter Molly

Leila was then told to get herself to A&E, where the doctor would explain more.

She said: “Obviously without any other information my brain went into overdrive. I felt very panicky and very on my own.”

Leila’s doctor explained that her white blood cell count was astronomically high - 259,000 when it should have been between 4,500 and 11000 - and they believed Leila had Chronic Myeloid Leukaemia (CML); a type of blood cancer which develops slowly, affecting the myeloid blood cells.

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“Within 15 minutes I was in the CT scanner absolutely sobbing, I couldn’t help it, the tears just came. Then the CT nurse leaned over me and said ‘God only gives us what we can cope with, you’ve got this’ and it helped.”

Leila RichardsonLeila Richardson
Leila Richardson

Due to high risk of infection, Leila was not admitted to hospital at the time, but immediately sent home with the chemotherapy drug Hydroxycarbamide, along with anti-sickness tablets and other medication.

Leila said: “I told my husband and daughter first and then told my sons. There were a few tears and lots of questions, but I have the most supportive family, and I couldn’t have got through without them.”

A bone marrow biopsy was scheduled for just a few days later, and Leila continued on a variety of chemotherapy drugs and fortunately her white blood cell count began to decrease.

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Due to the ‘chronic’ nature of Leila’s illness, she will likely continue on medication for the rest of her life, and now approaches life ‘one day at a time’.

Leila is supporting Leukaemia Care and Leukaemia UK’s new #SpotLeukaemia campaign, highlighting the importance of symptom awareness and early diagnosisLeila is supporting Leukaemia Care and Leukaemia UK’s new #SpotLeukaemia campaign, highlighting the importance of symptom awareness and early diagnosis
Leila is supporting Leukaemia Care and Leukaemia UK’s new #SpotLeukaemia campaign, highlighting the importance of symptom awareness and early diagnosis

Leila, now aged 46, said: “I’m not the same person I was 18 months ago and I may never be again. Life has been a rollercoaster, but I’m adapting to my new situation and trying to live the best life I can.”

Leila is now supporting Leukaemia Care and Leukaemia UK, who have joined forces on a new awareness-raising campaign, #SpotLeukaemia, which encourages people to ‘channel their inner five-year-old’ by asking themselves the difficult questions that could help spot Leukaemia.

In a new film released this week, young children are shown asking their grandparents awkward and embarrassing questions such as, “Why is your belly squishy?” or, “Why do you have hair up your nose?”. Shortly after, the same children are shown asking, “Why do you have bruises on your arm?” or, “Why are you always too tired to play?”.

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The film then urges anyone experiencing unusual symptoms to ‘channel your inner five-year-old and ask why’. If the viewer is experiencing fatigue, bruising, unusual bleeding or repeated infections, they are urged to contact their GP and request a blood test.

Leila said: “We all know our own bodies. Better than anyone else. If you feel something's not quite right - tiredness,  bruises, pains you didn't have before - please, please push for a blood test. If I hadn't, I would never have known I was seriously ill. It is so important that you make yourself heard and get it sorted as soon as possible.”

In the UK, 27 people every day are diagnosed with leukaemia, mainly among the over-65s. A lack of awareness of signs and symptoms means people are often diagnosed late, impacting their chances of survival.

Leila in hospitalLeila in hospital
Leila in hospital

Only half of Leukaemia patients live longer than five years after their diagnosis. The most common symptoms experienced by Leukaemia patients are fatigue, repeat infections and bruising or bleeding. Anyone experiencing these symptoms should visit their GP and ask for an urgent blood test.

For more information visit the Spot Leukaemia website.

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