The Game of Death – New Players

Warning: If you want to avoid the topic of death and dark humour read no further.

Covid 19 has made people think and talk about how people should die, with emphasis on not being alone, preferably with family. Covid patients in isolation have been unable to see loved ones.

In reality most of us cannot choose where to die or plan the scenario; victims of murder or major disasters certainly don’t have the luxury of dying in their own beds comforted by family. Awful circumstances such as terrorist attacks find total strangers holding the hand of a dying person, giving their death some dignity. As no one comes back to tell us, we cannot know if the surroundings and company or lack of it make any difference to their own unique internal solo journey. Celebrities often seem to have died ‘peacefully at home with their family present’ but folk lore and family tales seem to indicate that dying people often wait till the very moment loved ones pop out of the room.

Most terminally ill people will probably get the chance to opt for palliative care at home, though it can’t be guaranteed; they may need to go to hospital or a hospice eventually, but Covid has made it even more desirable to stay at home and leave hospital beds free for others. Unless everyone in your family is a medical person, carers will need help along the way or near the end; team work and various bits of equipment are required to make life easy for patient and carers. There is nothing to stop you ordering wheelchairs and all sorts on Amazon and getting next day delivery, but the National Health Service is geared up to lend what you need and the various teams helping you will be busy arranging equipment. The largest item is the hospital bed; you might die in your own home, but probably not in your own bed, however romantic that looks in films. The beds have to be plugged in and do all sorts of things. The bed and other items come with wheels and stiff pedal brakes impossible to put on or off if you are only wearing your slippers!

In the first few months of the lockdown I coped fine by myself with Cyberspouse. District nurses were trying to avoid going in any homes, but they phoned regularly with advice and to arrange some of the medications. They were ready to come out with their protective gear if necessary. Cyberspouse was happy not to have any visits, medical or otherwise, relaxing at home in the exceptionally sunny weather we had.

Later on, family help was more vital than keeping isolated and they took turns to come and stay; it was only in the last ten days that the district nurses came and arranged for Marie Curie nurses to parachute in with four visits a day. A helpful bright yellow book arrived promptly in the post. We were also glad a few times to ring the emergency numbers that had been sitting by the phone for months; night duty district nurses and 111 doctors. Marie Curie were excellent, compassionate and caring ladies and one chap. Visits rapidly increased and they made sure I had a night nurse for what turned out to be the last night, one of the few nights I was going to be by myself. They told me I was going to have wonderful Linda who had been doing the overnighter ‘forever’.

Linda arrived with a huge bag, rather like a mature Mary Poppins. I explained yet again that none of the family lived nearby, but they had all been to visit and my daughter was coming back the next day. It was a busy week in real life with two grandchildren just back in the UK and starting a new school and my daughter’s son starting school! Younger son had just got engaged. Linda was there to make sure Cyberspouse was comfortable, to organise the practicalities and make sure I didn’t miss the moment…

I later got a nice card from Marie Curie and they have rung me a few times to see how I am getting on. They are a charity well worth supporting.

Handy Home Hints

You might think your loved one is past the point of seeing the GP, but it is the GP who has to prescribe the drugs and you will have to go and sign for the ‘just in case’ controlled drugs as well as collecting various ongoing prescriptions.

It is helpful if someone in the family works for the NHS or has a friend in palliative care nursing … my daughter is a physiotherapist and had that very friend to ask for advice. She always made lists of questions and sounded professional on the phone, so we were well prepared.

After the death a doctor has to come and certify the death, either the GP or the on call ( 111 ) doctor at night. After that you must call the funeral director, but you can decide if you want them to come as soon as possible or wait a while.

Afterwards you will have to return all the drugs to a pharmacy, especially the controlled drugs, but unused needles have to be returned to the doctors’ surgery.

Darkly Funny Moments.  

The next day, Thursday, the funeral directors phoned to say they had not had the notification from our GP of the death. The on call night duty doctor had sat at the kitchen table typing into his lap top, saying ‘everything is going straight through to your doctor’s surgery’ but my writer’s mind thought ‘I have no proof he’s even been here, no piece of paper, was he actually a doctor?’ I was slightly reassured that nurse Linda knew him. When my daughter tried phoning our surgery she couldn’t get through and in the end resorted to using her internal NHS email. Luckily the information did end up in the right place.

One thing the district nurses requested unsuccessfully was a hospital bed extension, we had been expecting it for weeks. When a chap with a truck arrived at the door on Thursday morning I thought he was very quick to collect the hospital bed until he said cheerfully ‘I’ve brought the bed extension’. Poor bloke was embarrassed when I apologised that it was too late.

We had not seen much of the palliative care team from the local hospital who originally got us organised. One of the nurses had phoned the previous week saying ‘I’ll touch base with you on Friday.’ Sure enough on Friday the phone rang and she said brightly ‘Just calling to touch base’… so I had to tell her the news.  

Because of  Covid we were saved a trip to the registry office; instead I had a nice phone chat to Polly the registrar including Cyberspouse’s no funeral request. After taking most of the details she asked me my occupation. Oh oh, was I going to fail this part? I replied that I had done all sorts of things and she said ‘How would you like to be known in a hundred years?’ Well who in a hundred years would know I didn’t earn a living at it, so of course I replied  ‘A writer!’

https://www.mariecurie.org.uk/help/support/terminal-illness/preparing/what-to-expect

Silly Saturday – Careless Carers

Since the start of the pandemic many people have found themselves being carers for the first time; isolated with granny, uncle’s paid carers not able to visit or caring for Covid survivors in the family. Happily most people seem to have risen to the challenge, but it takes real skill to become a Careless Carer.

Some of you may have become carers without even realising it…

HOW TO RECOGNISE IF YOU ARE A CARER

You are a carer if you are busy gardening and a cup of coffee does not appear at the back door.

You are a carer if you yell DOORBELL! And nobody goes to answer the front door.

Ditto if you yell PHONE! And nobody goes to pick up the landline or the mobile phone left upstairs.

WHAT WILL A NORMAL DAY BE LIKE FOR A CARELESS CARER?

Take water, the wrong tablets and a cup of tea to the special person, who will remind you they always have coffee in the morning. Tell them you will be back in ten minutes to help them shower.

Now it’s time for you to have a quick cuppa ready for a busy day – take your time and check all the social media on your phone, share some Facebook Covid jokes, go in the garden and take a few pictures for Instagram, phone friend to tell them how busy you are… forget to turn shower on to warm up…

It’s important to answer the phone promptly, it could be a medical person to ask how things are and tell you no one can come to visit. Or it could be a friend and now is your chance to be properly careless, have a good chat, maybe they are lonely, fed up or hating working from home, discuss last night’s drama on television. Can you believe the time and you haven’t even got breakfast ready yet… then you remember you left your caree in the shower!

Ask the precious one what they would like for breakfast, even though it’s nearly lunchtime and forget what they said by the time you get in the kitchen.

Forgetting is a key attribute of the Careless Carer and the opportunities are infinite;

Forget to turn on the radio or television

Forget to turn off the radio or television

Forget to open/close curtains, windows, doors.

Forget to bring or put within reach glasses, newspaper, book, TV controls, mobile phone, ipad and the cup of coffee you forgot to make an hour ago.

Good luck.

Friday Flash Fiction – 700 -Two Months To Live

If Sonya had known her ex husband would survive a good deal longer than two months she would never have let him come back. If Sonya had known a pandemic would come along and trap him in isolation with her, two weeks after he moved in, she would never have let him over the front door step.

When he had phoned her early in March and told her he only had two months to live, she was shocked. Sonya hadn’t seen him for years, didn’t even know his second wife had booted him out and kept the house. It seemed a Christian, a human thing to do; she imagined the alternative, the father of her children found in two years time, mummified in his dreadful bedsit. To care for him in his last weeks would bring closure to both the good years and the bad. One of her daughters said she was insane and on no account must she let him anywhere near her home. The other daughter said of course she must help him, he was her father after all and she would soon be back from Thailand to help. The kindly daughter was still in Thailand and the sensible daughter still in New York.

At first he did a few DIY jobs, they Facetimed the girls together and he made a good job of settling his few possessions in the back bedroom and making it homely. He assured her various medical teams and charities were on his case and all she would have to do was a bit of cooking.

Then he got his letter from the Prime Minister telling him he was very vulnerable and must not leave his house. Her house Sonya pointed out to him. The letter reminded him how frail he was and he couldn’t even help wash the dishes. His medical support teams could not visit because of Covid 19 and he no longer qualified for help from the charities as he was no longer homeless.

A new routine was soon established, as if they had always been carer and invalid in the midst of a pandemic. Sonya was heartily grateful for her rescue dog, the perfect excuse to get out of the house for exercise and a chance to have socially distanced chats with neighbours and other dog walkers. Vivienne down the road she had hardly known before, but now she and the dog would pause by the front gate when Vivienne was in the garden and discuss on line shopping. The other woman would complain about her divorced son who had moved back in and Sonya would regale her with the latest domestic dramas.

Her ex husband had his good points, well she vaguely recalled he did in the early years of their marriage, sense of humour, carefree attitude to life. That young man was long gone and his most irritating features were enhanced by illness. The husband who had once been glued to the television with football, war movies and endless crime dramas involving noisy car chases and shootings, now complained about the noise if she listened to Jeremy Vine on the radio and griped that the television was doing his head in if she tried to watch Celebrity Chef.

When he received another letter from the Prime Minister saying he could go out and about on the first of August, he showed a rare spark of life and decided it would be good for him to come out with Sonya and the dog. This was how she found herself today, plodding wearily back down their road, trying to hang on to the dog’s lead and being told to mind the bumps as she pushed his wheelchair. She had not seen Vivienne lately, only to be expected as Vivienne’s daughter and family were staying. A large camper van was parked outside her friend’s house and the door suddenly swung open as they passed, just missing the wheelchair. Two children tumbled down the steps and flew through the garden gate to the front door, yelling to be let in.

 ‘Bloody children, bloody camper vans’ said Sonya’s ex husband in a loud voice, just as Vivienne opened her front door and waved to her friend.

The Game Of Life- Covid 19 Edition

Essays submitted to BBC Radio 4’s PM programme detailing its listeners’ coronavirus experiences are to be archived by the British Library.

https://www.bbc.co.uk/news/entertainment-arts-52487414

The Covid Chronicles were launched in March when presenter Evan Davis asked his audience to write in with personal accounts of life during lockdown. Perhaps this is what I would write, though I have exceeded the suggested 400 words.

The last day life was normal for us was Burns’ Night, 25th January 2020. Friends came round for dinner, my husband cooked. The day before, his birthday outing of choice was a trip to Ikea, our last outing.

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Life hadn’t been completely normal since his cancer diagnosis in autumn 2018, but chemotherapy had gone well and 2019 was filled with what was normal for most of us last year, holiday breaks, long walks, family visits, going out with friends…

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By February this year things had gone off at an unexpected tangent and downhill. Family were flying over, driving down, coming in shifts and helping out with stays in three different hospitals. We were aware of the virus, but the main defence was hand gel; how ridiculous that seems now. The main entrance of Southampton Hospital, where his major operation took place on 2nd March, was like an airport; twenty four hour Costa Coffee, shops, cafes and people, lots of people. The intensive care unit was a quiet little bubble away from all this; you had to phone from the waiting room to be let in, but that was the only restriction.
On two occasions we were called into a little room to talk to a doctor, but after a few days my husband was on a ward. In the background to our little lives hospitals were planning for the virus to get worse, suddenly he was transferred to our local hospital and we were wondering how this Coronavirus was going to pan out. Our physiotherapist daughter had already been organising the NHS and her brothers and now she made sure our house was ready, persuading the ‘social care team’ I would cope fine in my new role as carer. I don’t drive, but I’m fit, we have great local shops, family would continue to come and stay at regular intervals and friends would be dropping in for coffee and jigsaws, what could possibly go wrong? The reluctance to let my husband go suddenly changed to a flurry of Covid 19 bed emptying activity on his ward.

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At home things went as planned, some friends were already voluntarily isolating, but others came round for coffee. Our last family visitors left the evening after Mothering Sunday, by the time they were on their way home, on Monday 23rd March, the Prime Minister was telling everyone to stay home and close everything. We were already confined to home, now everybody would be at home; though I certainly wouldn’t have wished for a world wide pandemic just to feel we were all in the same boat.
My husband soon got The Letter – the most vulnerable people to stay at home for twelve weeks; I was now a shielder as well as a carer. By now we all understood the theory, it was a duty for everyone not to get Covid 19. My humble Covid Challenge, my contribution to the NHS was to keep my husband out of hospital and not get the virus myself as I am his sole carer.

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So here we are in our cosy little bubble, thanks to our kind next door neighbours and the local greengrocers, butcher and Co Op doing home deliveries, I don’t go near any shops. I only venture out for a walk and to our doctors’ little pharmacy; one customer at a time, the staff wear masks and shields. The amazingly fine weather and the garden have given lockdown a holiday feel. As a retired couple with lots of interests we’re used to having relaxing days at home; now every day is a relaxing day at home. Real carers are people who look after severely disabled children or partners or parents with dementia, for year after year. Apart from having to think what to have for dinner and cook every single day, life is easy and there is time for gardening, writing and blogging.

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In the Game of Life, Covid 19 Edition, over 35,000 people have died in the UK.

We have been given another extra turn and got some bonus points; loved ones and friends have been safe so far. Lucky to have a garden, not have to worry about losing a job or trying to home school children. Lucky that what happened to us came just before lockdown.

Have you written a Covid Chronicle or kept a journal?

Friday Flash Fiction – Health Crisis

I looked at the list of unpronounceable names on the drugs list. They actually trusted people to administer these to their loved ones? Trusted wives, sons, nieces, the next door neighbour to hand out the right tablets in the right number at the right time? The hospital expected me to ‘do the meds’ without a key or a trolley?

Four tonight, next two days four twice a day, the following day three twice a day… take one three times a day… what a collection, what a selection of pretty sweets for Brian’s ghastly grandchildren; pity they won’t be visiting. This corona virus; good excuse for his daughter to get out of helping and Young Brian away in Spain, couldn’t get a flight back. Not so resentful of me now they have a free carer for their father. I certainly didn’t sign up for this.

Better get organised. Take with food… must be taken one hour before eating… swallow with one glass of water… box of 32 paracetamol, that’s handy, in great demand at the moment, I’m sure Brian doesn’t need those with all the other stuff. A quarter tablet, how the hell am I meant to cut up that microscopic tablet. See leaflet for possible side effects, take me all night to read this… must seek medical help immediately if you accidentally take more than the prescribed dose. Wouldn’t that be a shame, could happen easily, especially with the size of the writing on those little brown bottles… oh, I thought it said 12 not 2 tablets. Ah… ONE 3 times a day, not 3, 3 times a day? No wonder, that explains it…

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