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A Fife
couple whose 26-year-old son died suddenly two years ago have thrown their
weight behind a campaign to raise awareness of Sudden Adult Death
Syndrome.
Maggie
and Andrew Tait, of Glenrothes are supporting a bid by Fife MEP Catherine
Stihler to have the shocking condition officially recognised by the World
Health Organisation.
Only
then, they say, will it be properly researched and lives could be saved.
The
Tait’s son, Andy, died in February 2001, after collapsing with chest
pains and a racing heart at this Kirkcaldy home.
He had
been a fit young policeman with a promising career ahead of him and
enjoyed playing football and golf and often went running.
His
death was officially recorded as heart failure but his devastated parents
were unable to understand how their apparently healthy, athletic son could
just collapse and die.
“He
had never had any illnesses in his life but we later found out eight young
people die every week in the UK of heart-related problems.” Said Andrew,
a former sergeant with Fife Police’s traffic department.
“These
deaths seem to affect young, athletic people and when we saw how many
people actually died of this we realised there was obviously a problem.”
Andrew
and Maggie found their statistics on a website set up by the organisation
Cardiac Risk in the Young (CRY) and through them they met the families of
other young people who died in similar circumstances to Andy, something
they found helpful.
In
hindsight, they realise there were signs something was wrong with Andy.
Despite his fitness he was often unable to play a full 90 minutes
of football and became breathless easily.
Maggie
hailed the awareness campaign as extremely important and said she hoped it
would prevent deaths in the same way as the cot death campaign had in
babies.
CRY is
raising money to set up mobile screening units across the country,
although there is not one in Fife at the moment and the Tait’s feel it
is important that all young people are given an echocardiogram (ECG).
A
recent screening programme in the Western Isles saw 400 children tested
with heart defects picked up in 15 of them.
Maggie
said, “It costs £34 to test each child, which is nothing.
If every surgery had an ECG machine perhaps it would save lives.”
CRY
put the couple in touch with Catherine Stihler, Labour’s health
spokeswoman in the European parliament, who launched her campaign in
Brussels earlier this week.
“I
am calling on the World Health Organisation to officially recognise and
name sudden death syndrome,” said the MEP.
“Since
cot deaths were officially recognised as Sudden Infant Death Syndrome,
deaths have fallen by 70% in a 10-year period.
“The
death of 26-year-old Andy Tait, a policeman and fit and talented
footballer here in Fife, is a vivid reminder that this syndrome can affect
anyone, even those who seem most healthy in our community.”
Mrs
Stihler said she hoped that sustained pressure from her colleagues across
Europe would help persuade the WHO that his small step could save lives.
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