Irish Daily Mail

We ALL deserve a ‘good death’

It’s a taboo subject. But when a loved one is terminally ill, it’s better to plan a dignified end to a life well lived instead of being left to chance... as these stories reveal

- By CAROLINE SCOTT OWITH The End In Mind: Dying, Death And Wisdom In An Age Of Denial by Kathryn Mannix (William Collins) €21.

PROFESSOR Paul Cosford has been helping save lives for most of his own. But being faced with your own mortality is very different, as he found out.

Cosford is director for health protection at Public Health England, and is the man responsibl­e for the control of infectious diseases, immunisati­on and for developing the emergency medical response to major incidents such as the London terror attacks.

But last summer, looking at an X-ray of his own lung, he learned that he is also a cancer sufferer and that the disease, which has spread to his liver, is incurable.

‘I thought I probably had a year, or maybe less, to live,’ he told the Royal Society of Medicine in February, in a talk about end-of-life care.

Treatment with new, targeted biological therapies — which stimulate the immune system to fight the cancer — has given him a life expectancy of three to four years.

Professor Cosford, 54, a father of four, decided to approach the near future with scientific rigour. ‘I knew I should stay physically active because there is good evidence it prolongs life, even in incurable cancers like mine,’ he said.

‘I wanted to try to maintain a positive mindset and to continue working, while spending more time with people important to me.’

But despite his best efforts, he found himself worrying constantly about his death, and he spent sleepless nights imagining different, horrific scenarios. ‘The mode of death that worried me most was the tumour invading a major vessel, causing unstoppabl­e bleeding into my lungs, drowning in the blood.’

He realised he could only focus on living well now if he faced the fear of dying upfront.

‘I cannot, of course, predict how I might die,’ he said. ‘But I started thinking that I could focus on living well if I knew I would be able to have some control at the time I need it.’ Six months since his diagnosis, he is sure of one thing: we need to be much more open about how we help each other to die well, and what we mean by that.

‘It seems we have created a climate in which the prevalent belief is that pain and death are avoidable and wrong. We know this isn’t true, but it means that when pain is there, when imminent death is faced, we often don’t know how to handle it.’

The end of life was something former British politician, Tessa Jowell, who died recently aged 70, had spoken about after being diagnosed with brain cancer.

‘In the end, what gives a life meaning is not only how it is lived, but how it draws to a close,’ she said in a speech to her peers.

Her daughter, Jess, said Tessa’s peaceful death had been ‘beautiful’, adding: ‘To the last moment, she was the most magnificen­t person and mother we all know and adore.’

Tessa’s daughter-in-law, Ella Mills, revealed that Tessa died in the arms of her husband, David, and grown-up children, Matt and Jess.

Sadly, not everyone dies in a familiar place surrounded by loved ones. People die in emergency rooms and intensive care units, where the machinery of life preservati­on creates a chasm loved ones feel they cannot cross. On wards where staff are focused on cure, sensitive palliative care can be overlooked.

While we are able to openly discuss birth and loss, few of us know what to expect as death approaches: it makes families anxious, and creates fear and uncertaint­y for the dying.

New research suggests we would like to know more about death and dying, but we don’t know whom or what to ask.

A survey of 1,000 bereaved adults found that some of the main worries people have when someone close to them is dying is not knowing the physical and mental changes to expect as death draws near, or how to make loved ones more comfortabl­e.

THE findings have prompted a call for a ‘national conversati­on’ and greater openness between health and care profession­als and families about what to expect.

‘There’s a specific need for more informatio­n and communicat­ion about the physical and mental signs that indicate death is near,’ says one campaigner.

‘This would help to prepare families with different ways they might respond and comfort their loved one. It could also prompt discussion­s about their last wishes and different ways to help them have a good death.’

Doctors and nurses who are trained to heal may unconsciou­sly collude in this fear about the moment of death; working to prolong life, they may not always recognise the need to support their patient to die.

Barry Ward, 85, a retired golf writer, found the experience of the death of his wife, Christine, so traumatic, that three years later he still struggles to talk about it. ‘She was the love of my life,’ he says.

‘From the night we met, we knew it would be forever. Our marriage was filled with love.’

In April 2014, Christine, a care home administra­tor, then 68, was diagnosed with a brain tumour which was treated successful­ly with chemothera­py. But shortly afterwards, she developed a rare gut infection which caused internal bleeding and was admitted to intensive care on Christmas Day.

‘On January 12, 2015, a young doctor took me to one side and told me there was nothing more they could do for her,’ says Barry.

‘But the following day, amazingly, she began to show signs of recovery. The day after that, her heart rate and blood pressure were better and she was no longer at death’s door. On January 15 she was better still, and on the 16th, she was sitting up in bed smiling, and talking about physiother­apy. Can you imagine my relief and joy?’

In fact, Christine was dying, but had been given a new drug which had slowed her internal bleeding.

However, Barry wasn’t aware that the improvemen­t would be only temporary. He spent January 17 at Christine’s bedside making plans for their 41st wedding anniversar­y.

At about 7pm, he drove home and had just sat down when the phone rang. ‘I was told to come back quickly: I found her unconsciou­s, ghostly white and with her mouth agape.’

At 2am on January 18, Christine died. ‘The shock, when she’d been so well hours before, was appalling, and it has affected my ability to grieve,’ says Barry.

‘I wasn’t prepared for the end, and I don’t think she was either. I would have liked the chance to say goodbye.’

A report by the Irish Hospice Foundation discovered the chances of dying at home or in hospital are dictated by where you live in Ireland.

Researcher­s found 18% of people in Dublin die at home compared to 34% in Donegal, despite a national survey showing that 74% of Irish people want to die at in their own house.

Many people die without them or their family knowing the end is coming.

Death is often seen as a failure of treatment, and this can mean missing out on preparatio­ns for a good death.

Debbie Riordan’s parents, Wendy, 76, a hairdresse­r and Rodger, 78, a pharmaceut­ical salesman, died in 2015 within four months of each other.

Wendy had undergone successful chemothera­py for bowel cancer when she developed an infection, and Rodger died from lymphoma, 18 months after he was diagnosed.

‘Mum had terrible sickness, so it was quite upsetting, but we were sure she would make a full recovery,’ says Debbie, a yoga instructor.

‘There were moments when Mum would say: “I’ve never felt this ill; I know I’m not going to make it.”’ Debbie recalls. ‘But

the nursing staff batted her concerns away. So we’d say: “Don’t worry Mum, it’s just a bad day.”

‘But over a period of two weeks, she got worse and worse.’

The medical team must have known she was dying, says Debbie, ‘yet no one ever said: “She really is poorly; now is the time to say what you need to say.”’

By chance, Debbie had heard palliative care consultant and author Kathryn Mannix talking on radio about the signs that someone is dying: ‘I could see Mum was at that point,’ she says. ‘She wasn’t eating, she didn’t want to drink, she was unconsciou­s a lot of the time, and her body was filling up with fluid.

‘We asked the nurses to stop clearing her airways and doing blood tests, but the focus was still on treatment, not how to spend the time she had left.’

DEBBIE feels that as a result of hearing Dr Mannix, she was lucky she was able to have precious last conversati­ons with both her parents. Fortuitous­ly, she was there when her mother died, but missed the moment of her father’s death. She feels it would have been helpful if, instead of ordering more tests, doctors had asked gentle questions such as: ‘How do you think your mum is?’

‘That would have helped us realise sooner what was happening,’ Debbie says. Her dad died early one morning when she and her sister had gone home. ‘If we’d known how close he was to death, we would have stayed.

‘I think doctors and nurses are frightened to initiate a conversati­on about death for fear of upsetting people. But you’ll never have another chance to tell someone how much you love them or say goodbye.’

Dr Mannix, who has spent the past ten years leading a palliative care team, says that when a patient is ‘mortally sick, but saveable, it is absolutely right that everything should be done to treat them’.

She adds: ‘Intensive care medicine buys time so dying is delayed long enough for healing to take place. But intensive care doctors are not always comfortabl­e with difficult conversati­ons and that’s where we come in.

‘I encourage acute care teams to acknowledg­e that while recovery is hoped for, death is possible, and to let us work alongside them.’

Hospital palliative care teams manage physical symptoms such as breathless­ness and pain, but also emotional distress. ‘One of the most important things we bring is candour,’ adds Dr Mannix. ‘We need to ask whether this is the end of the line for this patient and should we be having those difficult conversati­ons about what needs to happen next.’

Not all hospitals have palliative care consultant­s, but all staff should be trained in end-of-life care.

A palliative care consultant might ask: ‘Have the doctors explained things so you understand what’s happening?’ And: ‘What do you fear the most?’

‘The family is often doing everything to avoid the conversati­on going to “the worst place” in case it gets emotionall­y horrible,’ says Dr Mannix.

‘But actually it becomes a lot calmer once you start asking: “If she’s so sick she cannot be saved, what sort of things should we be doing now so we don’t regret anything?”

‘I don’t want them to wish in two weeks’ time, when they are suffering agonising grief, that they’d had that conversati­on at the deathbed.’ Advice on what to expect when death is near is in the top three most viewed pages in 2017, which suggests that as a society we have become so protected from death, we don’t know what normal dying looks like. This finding resonates with Elise Hoadley, a palliative care nurse for 25 years who has spent her entire profession­al life looking after the dying. ‘I have witnessed countless families facing the death of a loved one, not knowing what to expect,’ she says. ‘People think it’s going to involve blood and guts and gore. Yet normal dying is incredibly peaceful and gentle. Most people experience longer and longer periods of unconsciou­sness when they’ll think they’ve been asleep. ‘Breathing becomes shallower, and eventually fades until it finally stops altogether.’ But if people are terrified of the physical unknowns, we’re even more frightened of all the emotions that go with death. ‘Patients sometimes don’t want to talk about their own death because they don’t want to upset their loved ones. And loved ones don’t want to talk to the dying person about it for fear of upsetting them,’ says Elise. ‘If we can facilitate the conversati­on, an element of honesty comes in and everything is less traumatic for the family and patient.’

WHEN your loved one is dying in hospital, you can ask for the palliative care team to be involved. If they are not available, Kathryn Mannix suggests asking the question: Is there someone I can talk to who can explain what is happening?

‘The more patients know, the better they can plan the end,’ agrees Elise Hoadley. ‘A rule of thumb in palliative care is that if a patient gradually declines over months, they will usually have months to live; if it’s weeks, they’ll have weeks, and if you see a decline over a period of days or hours, then death is usually only days or hours away.

‘How wonderful would it be if more people knew that? Because then they could really plan how, and where, they want to die.’

Dr Mannix says deathbed patterns repeat over and over again: ‘The two things people want to say are, “I love you” and, “thank you”. Don’t wait for the last day of someone’s life to say either — say it now.

‘The two biggest regrets people have are not saying, “I’m sorry” and, “I forgive you”. Those are difficult things to express, but deathbeds give you permission to have conversati­ons that don’t happen at any other time.’

 ??  ?? Peaceful end: Tessa Jowell, who died from brain cancer Pictures: ALAMY / ANDREW PARSONS / I-IMAGES
Peaceful end: Tessa Jowell, who died from brain cancer Pictures: ALAMY / ANDREW PARSONS / I-IMAGES

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