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When
Gloria Moss’ daughter, Laura, collapsed and died at a swimming gala
seven years ago, there were no signs she had a heart problem.
Yet, like Laura, more than 400 young and seemingly healthy people
die from sudden adult cardiac death syndrome (SADS) every year.
And an estimated 700,000 people in the UK suffer from arrhythmias
or disturbances in the heart’s natural pumping rhythms.
“Laura
would have been 20 this year if she’d lived.
There was no history in our family of heart problems,” says
Gloria, 44, from Weymouth, Dorset, who works with the campaigning charity
CRY (Cardiac Risk in the Young) to help raise awareness of the problem. “All my kids are sporty but Laura was an extremely gifted
swimmer who’d been picked to represent Great Britain,” adds Gloria.
On
November 28 1997, Gloria took Laura to her school swimming gala, when
tragedy struck. “She was
laughing and joking with her friends as I sat in the seats upstairs.
She got into the pool and the next minute I saw them dragging her
out of the water. I ran to
the poolside and someone said she was fitting.
As soon as I saw her, I could see she was dying – she’d stopped
breathing, so I tried to give her mouth-to-mouth resuscitation.
All her friends were watching – it was horrific.
Laura was rushed to hospital by ambulance, but there was nothing
they could do. The consultant
came out and said Laura had died. I
couldn’t believe it. She
was a happy, healthy child and the next minute she was gone.
Gloria
and husband Alan somehow managed to get through the days that followed.
The autopsy didn’t find anything physically wrong with Laura that
could have caused her death. It was only in the weeks afterwards that Gloria got in touch
with CRY and the charity paid for Gloria, Alan and their other children,
Ryan, 17 and Kate, 15 to have cardiac tests at St George’s Hospital,
London. “They said the mist
likely cause of Laura’s death was a disturbance in the heart’s normal
rhythm, known as long QT syndrome,” says Gloria.
(In 2002 new genetic tests confirmed the presence of a gene in the
family for long QT syndrome). Long
QT can be successfully treated with an implantable automatic
defibrillator, which ‘shocks’ he heart into a normal rhythm.
Gloria’s biggest regret is that Laura wasn’t properly tested.
“there’s a chance that if a screening programme had existed it
would have been picked up and she’d still be alive.
I’d like to see all children and young adults who are active in
sports tested, so that other parents don’t experience what we went
through – seeing their child die in front of them.”
Thanks
to CRY and individual appeals, the Government is taking action to prevent
such deaths in the future. A
group under the National Clinical Director for Heart Disease, Dr Roger
Boyle, will advise on best practice
Find out more
about Long QT Syndrome
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