Locked-in syndrome: rare survivor Richard Marsh recounts his ordeal
When Richard Marsh had a stroke doctors wanted to switch off his
life-support – but he could hear every word but could not tell them he
was alive. Now 95% recovered, he recounts his story.
By Amelia Hill - The Guardian (UK) - August 7, 2012
Richard & Lili Marsh |
Two days after regaining consciousness from a massive stroke, Richard
Marsh watched helplessly from his hospital bed as doctors asked his
wife, Lili, whether they should turn off his life support machine.
Marsh,
a former police officer and teacher, had strong views on that
suggestion. The 60-year-old didn't want to die. He wanted the ventilator
to stay on. He was determined to walk out of the intensive care unit
and he wanted everyone to know it.
But Marsh couldn't tell anyone
that. The medics believed he was in a persistent vegetative state,
devoid of mental consciousness or physical feeling.
Nothing could have been further from the truth. Marsh was aware, alert and fully able to feel every touch to his body.
"I
had full cognitive and physical awareness," he said. "But an almost
complete paralysis of nearly all the voluntary muscles in my body."
The
first sign that Marsh was recovering was with twitching in his fingers
which spread through his hand and arm. He describes the feeling of
accomplishment at being able to scratch his own nose again. But it's
still a mystery as to why he recovered when the vast majority of
locked-in syndrome victims do not.
"They don't know why I
recovered because they don't know why I had locked-in in the first place
or what really to do about it. Lots of the doctors and medical experts I
saw didn't even know what locked-in was. If they did know anything, it
was usually because they'd had a paragraph about it during their medical
training. No one really knew anything."
Marsh has never spoken
publicly about his experience before. But in an exclusive interview with
the Guardian, he gave a rare and detailed insight into what it is like
to be "locked in".
"All I could do when I woke up in ICU was blink
my eyes," he remembered. "I was on life support with a breathing
machine, with tubes and wires on every part of my body, and a breathing
tube down my throat. I was in a severe locked in-state for some time.
Things looked pretty dire.
"My brain protected me – it didn't let
me grasp the seriousness of the situation. It's weird but I can remember
never feeling scared. I knew my cognitive abilities were 100%. I could
think and hear and listen to people but couldn't speak or move. The
doctors would just stand at the foot of the bed and just talk like I
wasn't in the room. I just wanted to holler: 'Hey people, I'm still
here!' But there was no way to let anyone know."
Locked-in syndrome
affects around 1% of people who have as stroke. It is a condition for
which there is no treatment or cure, and it is extremely rare for
patients to recover any significant motor functions. About 90% die
within four months of its onset.
Marsh had his stroke on 20 May
2009. Astonishingly, four months and nine days later, he walked out of
his long-term care facility. Today, he has recovered 95% of his
functionality; he goes to the gym every day, cooks meals for his family
and last month, he bought a bicycle, which he rides around Napa Valley, California, where he lives.
But he still weeps when he remembers watching his wife tell the doctors that they couldn't turn off his life support machine.
"The
doctors had just finished telling Lili that I had a 2% chance of
survival and if I should survive I would be a vegetable," he said. "I
could hear the conversation and in my mind I was screaming 'No!'"
Locked-in syndrome is less unknown than it once was. The success of the 2007 film, The Diving Bell and the Butterfly,
the autobiography of the former editor of French Elle magazine editor,
Jean-Dominique Bauby, brought awareness of the condition to the general
public for the first time.
Then in June, Tony Nicklinson challenged the law on assisted dying
in England and Wales at the High Court as part of his battle to allow a
doctor to end a life he said was "miserable, demeaning and
undignified".
Judgment was reserved until the Autumn.
Marsh,
however, did something almost unheard of: he recovered. On the third day
after his stroke, a doctor peered down at him and uttered the
longed-for words: "You know, I think he might still be there. Let's
see."
The moment that doctor discovered Marsh could communicate
through blinking was one of profound relief for Marsh and his family –
although his prognosis remained critical.
"You're at the mercy of
other people to care for your every need and that's incredibly
frustrating, but I never lost my alertness," he said. "I was completely
aware of everything going on around me and to me right from the very
start, unless when they had me medicated," he said.
"During the
day, I was really lucky: I never spent a single day when my wife or one
of my kids wasn't there. But once they left, it was lonely – not in the
way of missing people but the loneliness of knowing there's no one there
who really understands how to communicate with you."
The only way
for Marsh to sleep, was to be medicated. That, however, only lasted four
hours, after which there had to be a three-hour pause before the next
dose could be administered.
In
questions submitted by Guardian readers to Marsh ahead of this
interview one asked about his experience of his hospital care while the
staff did not think he was conscious. Marsh said: "The staff who
work at night were the newest and least skilled, and I was totally at
their mercy. I felt very vulnerable. I did get injured a couple of times
with rough handling and that always happened at night. I knew I wasn't
in the best of care and I just counted the minutes until I would get
more medicine and just sleep.
In response to another question, about the right-to-die debate, Marsh
said he has no opinion. All he will say is: "I understand the despair
and how a person would reach that point." But he is co-writing a book
that he hopes will inspire hope and provide information to victims of
locked-in syndrome and their families.
"When they first told my
family that I was probably locked-in, they tried to find information on
the internet – but there wasn't any. One of my goals now is to change
that … to be able to reach out to families who find themselves in the
same situation that mine were in so they can help their loved ones.
"Time goes by so slow ... It just drags by. I don't know how to describe it. It's almost like it stands still.
"It's a terrible, terrible place to be but there's always hope," he added. "You've got to have hope."
•
This article was amended on 10 August 2012. The original said that Tony
Nicklinson had failed in his High court bid to change the law on
assisted dying in England and Wales. This has been corrected.
(Tony Nicklinson has failed in his High court bid to change the law on euthanasia and assisted suicide in England and Wales.)
3 comments:
I read the book and saw the movie the Diving Bell and the Butterfly.
A story of immense courage and an example of what wonderful things one can do even in the worst of circumstances.
We should never put people to death...
I think one lesson here should be for medical personnel to always treat their patients like fully aware and functioning human beings. They should be doing that regardless, but in the hospital it's easy to rush and become calloused to the needs of others.
now according to a new research, people who are paralyzed may be able to communicate with each other.
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