Birmingham Post

It’s only because of a lucky set of coincidenc­es that I survived Covid

Former children’s laureate Michael Rosen reflects on how he cheated death from Covid after spending 47 days in intensive care and how it has changed his life. The poet and author talks to HANNAH STEPHENSON

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MICHAEL ROSEN looks like a sprightly 74-year-old, wispy curls of grey hair and short beard framing his long friendly face, as he tells me about the exercise regime he has undertaken to get him back to full health after his terrifying­ly close brush with death from Covid.

“I’m doing the plank, the bridge, weights, walking up and down stairs, I have these resistance bands which I get out when I’m watching football with my son – it drives him mad,” says the former children’s laureate who has delighted youngsters over the years with his most famous book, We’re Going On A Bear Hunt.

“If I overdo it one day, I’m pretty smashed the next, which I think is a residue of Covid, so I have to be careful.

“I walked up Muswell Hill [a notoriousl­y long, steep hill in North London, where he lives] recently – it was a big challenge I’d been afraid of.” A year ago, at the start of the pandemic, the award-winning poet, performer and broadcaste­r entered a nightmare that would last months when he was rushed to hospital suffering from coronaviru­s, almost three weeks after first displaying symptoms of breathless­ness.

He was diagnosed online firstly by a paramedic and later by someone on 111, who suspected he was getting over a virus and advised him to take paracetamo­l and ibuprofen. When things didn’t improve, his wife Emma contacted a GP neighbour and friend, who delivered an oxygen saturation probe to their home while she waited on the doorstep. His reading was 58% (normal is anything over 95%). Technicall­y, he should have been unconsciou­s. “Your life hangs by a thread at that moment and it’s only a lucky coincidenc­e that our GP friend was around, and luck that she had the oxygen probe in her bag. At that moment, I had probably a one in 10,000 chance to survive and it was because of that set of coincidenc­es that I did,” he explains candidly. So urgent was his case, that his wife and daughter helped him into the car and drove him to A&E at the Whittingto­n Hospital in London. The consultant said that any later would have been too late. He spent 47 days in intensive care, most of which were in an induced coma. Doctors gave him a 50:50 chance of survival. April and most of May have been wiped from his memory. Complicati­ons included blood clots in his lung passageway­s and his brain, for which he was put on blood thinners.

“I don’t remember any of it. Once they put you under, you are unconsciou­s in every sense of the word. The mysterious bit is that they see you wake up, but I have no memory of that period of being woken up.” His latest book, Many Different Kinds Of Love, is a touching and, at times, surprising­ly amusing reflective collection of poetry and words of his battle with Covid and his recovery.

The blanks in his memory are filled in with the observatio­nal diaries placed at the end of his bed by the nurses and doctors who looked after him, who charted his slow recovery as his breathing gradually improved and he received less support from the ventilator, between bouts of agitation and hallucinat­ions.

His first memories came about 10 days after he’d been moved from intensive care to a ward, even though he had been awake and talking and, at times, lucid, he explains.

“Emma said, ‘You’ve been in intensive care’ and I just thought they’d been looking after me intensivel­y,” he recalls. “I had no idea about this coma thing.”

Initial physio was exhausting, he recalls. So weak was he, that at first he was winched into a wheelchair and wheeled to a window where Emma and the children were waiting.

He slowly started to come round, to engage in the present, and recalls hearing the nurses whispering about somebody having died. He had no idea a pandemic had swept the country.

“I realised death was in the air and was getting a sense that people were dying of this thing, but I hadn’t seen a newspaper.”

He was eventually transferre­d to a rehabilita­tion hospital, where he spent three weeks.

“Standing up was the hardest thing at first,” he recalls. “I just thought I’d never stand up again. I had a powerful sense that I would be in a wheelchair for the rest of my life.”

He says he had a fatalistic attitude to that prospect, a sort of ‘Oh well, I’m a wheelchair person now’ until the physiother­apists and occupation­al therapists worked their magic.

Nearly a year on, he says he’s OK, although he has numbness in his toes, an eye that has gone ‘foggy’ and deafness in his left ear, as a result of the illness.

“They’ve told me the ear won’t change, because my auditory nerve was damaged, and they don’t know about the eye, but I don’t see any improvemen­t in the last three or four months, although I can see some of the letters on my keyboard. “But my general strength keeps improving, so I’m in quite good nick, in that sense.” Life has changed since his Covid experience, he reflects, although he hasn’t sought counsellin­g. He says that writing is his therapy. “It’s affected my mentality, made me more cautious and less certain about everything. I faff about. Having so nearly died, there’s a feeling of uncertaint­y about life in general.” And he’s started to feel angry at the way the pandemic was handled at the beginning. “I have two magnets – one is regret that I’m not the person I was. I haven’t got that energy or assurednes­s. The other thing is anger, because I’m fairly sure that in February and March [last year] senior people in government and scientists were entertaini­ng this idea of herd immunity without vaccinatio­n. “They knew this would entail the deaths of tens of thousands of people and this seems to me frightenin­g. It makes me angry. It was terrible that some people were supporting the idea that culling the old would be quite a good idea. Suddenly we had a league table of people who were less entitled to survive than others.”

For a man who was on death’s door less than a year ago, he’s busier now than he was before the pandemic, doing live streams to schools across the country, and speaking to intensive care nurses about why patient diaries are so important.

Later this year, he’ll be talking to psychiatri­sts about the psychologi­cal effects of Covid. He has also joined the Facebook longCovid group.

He admits that his brush with death has led him to thoughts about the legacy he will leave – but he needn’t worry.

“The messages that Emma received while I was ill were overwhelmi­ng. And when I posted a tweet when I came round, it got 40,000 likes! It’s a bit like having an obituary and messages of appreciati­on when you’re still alive.”

I had probably a one in 10,000 chance to survive Michael Rosen

■ Many Different Kinds Of Love by Michael Rosen is published by Ebury Press, priced £14.99

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 ??  ?? Michael and Sir Chris Hoy with school pupils at a World Book Day event in 2016 – when such things didn’t have to take place over video
Michael and Sir Chris Hoy with school pupils at a World Book Day event in 2016 – when such things didn’t have to take place over video
 ??  ?? Michael Rosen following his close call with coronaviru­s
Michael Rosen following his close call with coronaviru­s
 ??  ?? Michael as he was before the pandemic
Michael as he was before the pandemic

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