Sorry this blog is a bit sombre, and very long. I’ll try and be cheerier next time. But I’ve been inspired to write an account of this by someone on Twitter who, herself, is going through a painful time – they’ll know who they are if they read this.
Two and a half years ago, my dad died with Oesophageal cancer. From the point of finding out until the end, was a short ten weeks. From around two months before this diagnosis he had been having problems keeping food down, occasionally being sick, which was something he never did. At first it was thought it could simply be a hiatus hernia problem. That was until he had an endoscopy.
I took both my parents to the hospital in the car that morning, dropped dad off and drove mum back to my house for coffee and to wait. We never for one moment even considered anything other than a simple problem that could easily be put right.
Four years previous to this, my dad had suffered a stroke. He wasn’t paralysed in anyway by it, but it did affect his thinking. He resorted to being slightly more child-like, and to begin with it was quite nice. He was like a little boy, almost excited by the world again, much more open and less guarded than he normally was. The only real problem it left him with was an inability to read. He attended speech therapy, and it did help a bit, but he could never again just sit down and relax with a newspaper. Numbers, surprisingly, he was fine with, just not words.
This joie de vivre soon wore off however, only to be replaced by depression; threatening to commit suicide by almost any means. Then on my visits he began to talk about mum behind her back. He would say the most awful things about her. And it was difficult, because I knew this wasn’t really ‘him’. I didn’t want to upset her, by telling her what he was saying. But I also didn’t want him to feel alone by not having anyone else to talk to. I’m an only child, so the burden fell squarely on my shoulders to be in the middle. It was a very difficult time and mum was doing whatever she could for him. Of course it was only natural it would get her down, but she’s very stoic and resilient. And she also knew there was no one else to take care of him. So she got on with it and never complained.
Anyway, back to that fateful day in July. We arrived at the hospital to pick him up and a nurse asked them into a little side room. Mum asked if I wanted to come too, but I said, no it’s okay I’ll just wait. Like her, I thought it was just a formality, signing forms and getting info. On the way out my mum said she wished I had come in. Then she told me what they had said. To say it was like a thunderbolt would be a huge under exaggeration.
On the way out of the hospital, I’ll never forget my dad putting his hand on my shoulder and shaking his head saying: ‘She said cancer. That’s it then.’ And my mum, being discouraging and dismissive, as you would, saying: ‘You can’t say that. You don’t know.’
However, it was the case and things never improved, they only deteriorated. And the fact that he’d had a stroke seemed to make him even more fractious and unreasonable. He wanted into hospital, he wanted out of hospital, he wanted back in. And each time meant hours in A&E before he was admitted, going through the same old form filling, questions and tests. At one point he came out and was re-admitted during the course of a shift. He even ended up in the same bed. The nurses must have thought they had entered a time warp when they came back on duty. Of course this was making things worse and worse for my mum, who had even more to endure now. One day she called saying: ‘guess where I’ve been since six this morning.’ And I knew he was back in. Then, when things got even worse for him at home, she would eat in the kitchen and not in front of him because he’d say things like: ‘You’re lucky you can eat a sandwich.’
However, one day sitting in A&E again, a doctor came to speak to us. If ever there was someone meant for a job it is this woman. She is truly the most caring doctor you could find. She is in charge of the cancer unit, a lovely (if you can use that word to describe it) ward that has a very calming and relaxed atmosphere about it. The rooms are individual and large with everything you could need, should you be patient, family or friend.
The saddest, most poignant day was the one when the doctor came in and sat in front of my dad. I was in one chair and mum in the other. She asked what he would feel if he knew he didn’t have much longer left. I don’t think he really understood as he shrugged with half a smile and gave a lift of his hands saying; well he was seventy now … My mum reminded him he’d just had a birthday, so seventy one. But he carried on, telling the doctor that he just wanted out, and made the actions of a runner off the blocks. She reassured him that he would get home for the weekend after getting some blood. Which he did. This would be his last days at home.
Luckily my daughter, who lives down south, was coming up home that weekend for a friend’s wedding, so got to spend some time with her papa before leaving again. We took photos and he got to see her all dressed up. To him, there was never anyone like her. As he left home to go back to hospital that Monday morning, mum told me he looked around him at the living room, shook his head and said: ‘I won’t be back here.’
That last week saw mum and I spend a lot of time up at the hospital with him in his room. Family members visited; they knew it would be the last time. He drifted in and out of consciousness. My son came up and dad seemed to know he was there, which was nice. Before he left, my mum said to give his papa a kiss. It was the last time.
What I forgot to mention was that during this last week, my husband was working down in London, so I slept alone and with the telephone by my bed. Around 4am on Saturday 23rd September it rang. I knew. We had made arrangements. I live out of the town, so mum would try and get a taxi for speed. If not I’d pick her up, which is what happened. I had clothes ready to jump into. I asked my son if he wanted to come with me, but he said, no. I reassured him that it was fine, his decision, but I had to ask. The road was quiet and I will admit I did go through red lights, and break speed limits. There were more important things to see to.
We made it in time and sat with him for over an hour until the end, holding his hand. It was the first time I had gone through anything like that, but it was in no way scary or frightening. It just seemed the most natural thing in the world and was very peaceful.
Naturally there were tears and I had phone calls to make as we waited for the nurses to wash and change him, before we got to say our final farewells, but I think a strength you don’t know you have takes over and sees you through.
My mum and I often said afterwards, if anyone had ever told us we would be able to arrange a funeral on our own we would have scoffed and laughed it off. Not us, we couldn’t do that. But yet we did. We had the hymns: The Day Thou Gavest Lord Hath Ended, and Abide With Me, which my dad liked. He also loved the music of Matt Monro and as we left the Chapel of Rest, Softly As I Leave You played. His request had always been that he be cremated. So that’s what was arranged. 
His ashes are buried at a place he loved and a Magnolia planted with bulbs all around. Today, in spring, the flowers are up and the bush is in bud. It’s coming alive after the long winter sleep. And yes, I do still cry at Coldplays, ‘Fix You’ especially the line – when you lose something you can’t replace, as I heard it while dad was in hospital. It all seemed so appropriate and true. But, what I’ve come to understand is this; while you do lose something you can’t replace, the one thing you can never lose are the memories of that person. It is those which will be with you, alive, and inside for ever. And they are the strength that will keep you going.