February 2023 – I was knee-deep in nappies and spit up with my four-month-old daughter. I was desperately trying to balance the needs of my newborn baby with the demands of raising a two-year-old toddler. The nights were long and the days wild.
I'd had a routine colonoscopy a month earlier due to some symptoms relating to childbirth (thanks, girls). When I was in the theatre room, the doctors had been lovely – it was clear they thought nothing of my symptoms. Despite being referred by my GP for the procedure, multiple doctors asked me if I was there to "ease my mind?".
I said I was and thought my symptoms just came with postpartum territory. I had my procedure on a Monday and the week passed by without me giving the results a second thought.
That all changed with a phone call from my gastroenterologist on a Sunday afternoon.
"I'm sorry, we found a neuroendocrine tumour," they said.
Watch: Lea's cancer story. Post continues below.
I am an occupational therapist and have worked in a hospital for my entire career, yet had never heard this term before. Words such as "rare" and "shocked" crossed the lips of my specialist.
I was told to make an appointment with my GP to discuss a treatment plan and stay off Google. I only took one piece of her advice.
I started looking for answers as to how this could have happened. Bad luck was the only answer I could find. I felt like my entire world had been turned upside down and all I could do was look at my girls and weep.