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The mother of a 15-year-old
boy who collapsed and died from an undetected heart condition has praised
MP Richard Taylor for supporting her campaign to get checks she hopes
could save other youngsters made law.
Diane
Tolley is urging people to write to their own MPs asking them to back the
Cardiac Risk in the Young (Screening) Bill.
Mrs
Tolley lost her son, Robert Poysor to Sudden Death Syndrome almost eight
years ago.
In
a letter to Mrs Tolley Doctor Taylor pledged his support telling her he
agreed that screening should be offered to close relatives of children
known to have suffered one of several conditions connected to Sudden Death
Syndrome.
He
said: “If there is anything I can do I certainly will.
The bill will raise the profile of the problem and can do nothing
but good.”
A
post mortem revealed the sporty Bewdley High School pupil had an
undetected heart condition.
It
is known as hypertrophic cardiomyopathy, a thickening of the heart wall
muscle which stops the heart beating properly.
It
is a common cause of Sudden Death Syndrome in children and young adults.
It
is estimated up to eight children die suddenly each week in the UK
If
the bill, which is due to have its second reading in the House of Commons
on March 12, is passed it will mean mandatory screening for children
considered to be at high risk, such as the siblings of victims of Sudden
Death Syndrome, children whose families have a history of heart problems,
and youngsters who have previously shown symptoms, such as fainting.
Since
Robert’s death Mrs Tolley, aged 56, of New Road, Wribbenhall, has given
support to other families in the West Midlands whose children have
suddenly died.
She
said the bill would be the first step towards getting all children
screened through an ECG test, saying: “It is very important MPs support
the bill because it is a step towards a national screening programme.”
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