Kay Montgomery - Blog

Kay Montgomery was diagnosed with terminal Pancreatic Cancer – Stage 4 – during a routine ultrasound for gall stones on 21 June 2025. Having been a gardening journalist and magazine editor for decades, Kay’s instinct is to regard this event as just another project upon which to report.

This blog offers observations on entering the strange new world of hospitals and cancer. It aims to be a light-hearted view of a very serious issue. And may it update all the many friends, colleagues and acquaintances – who are genuinely concerned for my wellbeing – on the progression and status of the journey.

Update: Kay sadly passed away on Thursday the 24th July 2025.

Sunday 22 June 2025 – Zoning Out

My bed in the hospital became my sanctuary.

Nurses came and went. I zoned out in a blur of  drips delivering nutrients, antibiotics, antacids and painkillers.  Having struggled with fatigue for so many weeks, my body just imploded.

As a news junkie… I watch every aspect of war, politics, volcanoes, floods and earthquakes. I had lost all interest in the outside world. I just lay in my bed as a fatigued vegetable.

“This report is NOT good”, noted Jane, my wildly intelligent… best friend. She appeared at visitors time on Saturday… with a “WTF” expression. Old friends are marvellous. No explaining required. Just … how are you and what is this new journey you are on? Jane threw in a dose of protectiveness. Every nurse was cross questioned on what they were doing and which drips were being administered … and why?

After Jane left, I was collected for a CT scan on Saturday afternoon at 16h00. It was surreal to be collected in a wheelchair. But beyond cheerful chipper conversation with the attendant moving me around in a wheelchair, my brain had become a ‘nothing box’.

I smiled as I remembered conversations with my engineer husband… who said that my brain was like a spagetti of sparky, action neurons, whereas he lived in a world where his brain was located in a ‘nothing box’ for most of the time.  Suddenly, I understood what a ‘nothing box’ felt like…

On Sunday morning, I was wheeled to an MRI scan.

“You will be in the MIR machine for 20-25 minutes”, explained the team. It seemed closer to 40 minutes. I was brought out to sit on a couch. Then, I was then sent back in again for 5 minutes.

“Wow!”, I thought. “There must be an awful lot to see”.

Crunch time took place at 12h30 on Sunday. A intense, passionate, concerned and focussed surgeon appeared at my bedside.

Aa a jounalist… I just let him talk and listened. He was philosophical. He talked about his mum – who had died of brain cancer. He advised that I should do life my way. I should compile a bucket list. If I wanted to go skydiving. Now was the time.

Skydiving?! Phew! No thanks. I get apaling travel sickness and vertigo. The only times I’ve been on luxury yachts and helicopters, I disgraced myself badly by bringing up all over the passengers. Not going down that road again…. I thought.

No. I would go home to my cottage, husband and dog… and plant seeds and bulbs.

He explained that I shouldn’t be pushed into painful operations unless I wished to be there. The subject matter was too high level for my foggy brain. The high level cancer debates flew past my mind. I knew he was explaining important stuff debated by cancer scholars. But I was out of my depth.  I just hadn’t done the preliminary research needed for engaging an interview with a top surgeon. I also wasn’t too sure what all the vocabulary – lingo meant. I am a good listener. I just listened.

He with me for an hour.  But the bottom line was clear.

You have Terminal Pancreatic Cancer – Stage 4. It has metastisized into your liver. You have three months to live.

 

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