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Pseudomyxoma Survivor Teresa and her son

My 10-year-old son has recently been to pioneer week where he goes to his new secondary school for a week to experience life there. He was asked to write about someone who inspires them. He just told me that he wrote about me and how well I dealt with my operation and chemotherapy afterwards.

He doesn’t talk much about what we went through but when he does he surprises me how much it really affected him. He was only eight. Be brave, everyone, no matter what stage you are at with this dreadful disease.

In case you missed it...

Receiving a diagnosis

Receiving a diagnosis

My original symptom was an ‘irritated‘ bladder — it is difficult to describe but the closest I can come up with it that it felt like it was vibrating all the time. In March 2010, after several months of bladder discomfort and many trips to my GP, I was referred to the genito-urinary clinic at my local University hospital with suspected bladder prolapse. Eventually, this lead to a diagnosis of pseudomyxoma peritonei (PMP).

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Feeling proud