Childhood Cancer
Friday 4th February is World Cancer Day. Ironically, in 2022, this was the day our world changed literally overnight as we found out that our youngest child had developed childhood cancer. More specifically, our little boy was diagnosed with B-Cell Acute Lymphoblastic Leukaemia (ALL).
He started 2022 with Covid and just didn’t seem to get better. We now know that as he recovered from the virus, he was starting to display the classic symptoms of blood cancer.
His symptoms were extreme fatigue (one day he fell asleep in the garden at preschool in January), unexplained bruising, night sweats, constant infections and fevers, bone and joint pain and shortness of breath. Throughout January 2022 I called NHS111 twice, visited our GP twice, took him to our local urgent care centre once and visited A&E. The A&E visit was the final contact we had with the NHS prior to diagnosis.
The posts in this category are all about how we as a family are dealing with the news, the charities that have helped us, things we have learnt along the way and advice for parents who sadly find themselves following in our footsteps and people encountering childhood cancer such as friends and relatives.
Writing about it has been hugely beneficial to my mental health as it has given me a non-judgemental outlet for my feelings as I have come to terms with my son’s diagnosis. Needless to say, a childhood cancer diagnosis is a huge rollercoaster of emotions for the whole family, there’s so much to come to terms with.
Friday 4th February was World Cancer Day. Ironically, this was the day our world changed literally overnight as we found out that our child has cancer. More specifically, our little boy has B-Cell Acute Lymphoblastic Leukaemia (ALL). This is rare, less than 500 children per year are diagnosed with it however if you are going […]
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