In the early days of Chris’ diagnosis I was very black and white. The leg had to go. It was easy for me to say, it wasn’t my leg, my life. But for me it was simple. If the leg as it was stayed, infested with a tumour taking over, damaging bones, nerves, muscles, trying […]
I wasn’t there when Chris was told by our GP he had a tumour. He went to the appointment by himself. If I’m honest I don’t think at that point either of us believed that it would ever be anything really serious. Really life changing. I was at work. He rang me. It was the […]
I didn’t know how I would react when I first saw him. I knew, rightly or wrongly, that my reaction weighed heavily on him. My initial response would reflect his. As I’d left him, I had been overwhelmed with the realisation of what was about to happen knowing how much he didn’t want it to. […]
When we found out about Chris’ diagnosis, it was my kids, especially Lily, I thought of first. I knew that regardless of anything else that was going on, I needed to keep things as normal as possible for them. To make sure I was there for bedtime and that they were at home as much […]
It was daunting when we first found out that Chris’ treatment would take at least 12 months. Just think about what you can fit into a year, 365 days, what you can plan for, what you can look forward to. As the New Year bells rang signalling the start of 2016 there wasn’t the usual […]