Family of sudden death syndrome
victim campaign in schools
Pictured
centre, holding a cuddly toy kangaroo with his friend Oilver Kenton.
A
couple who lost their son to a form of sudden death syndrome want to raise
awareness of the tragic disorder.
Gill
and Robert Wood were devastated when their son James died from SADS
(Sudden Arrhythmai Death Syndrome) – similar to cot death in infants –
in September 2002.
James,
who was a fit and active boy, had just turned 15 when he collapsed and
died at the family’s home in Great Amwell.
The
popular and friendly youngster was a pupil at Haileybury
public school near Hoddesdon, and was a member of the 1st
Broxbourne Scouts.
This
week, James’s mother Gill spoke out about the family’s loss and how a
charity had greatly helped them to deal with their grief.
It
is the vital work of this charity CRY (Cardiac Risk in Young People) which
Gill and Robert are hoping to promote.
“James
died suddenly at home and it took many months of further investigation to
try to determine the cause of death, said Gill.
“He
was a very fit, healthy boy with his whole life ahead of him.
The
coroner came to the conclusion that James died of SADS, which is similar
to cot death.”
Gill
added: “The charity CRY has given our family immense support, both in
the form of counselling and explaining what may have happened to James.
“ We want to back the charity in the hope that we can stop this
happening to another family”
On
Tuesday, Gill and Robert organised for a CRY representative to visit
youngsters at Broxbourne Primary School where James’s
younger brother is a pupil.
The School held a special assembly, at which the children met
cuddly mascot toys QT Kanga and CRY Teddy- which will be travelling the
globe to raise money for CRY-as they were told about SADS.
Later
in the day, James’s older brother Christopher,14 took the toys into
Haileybury for another talk on the charity.
“Before
James died, nobody could really tell us what was wrong with him” added
Gill.
“At
one point, doctors thought he had vertigo because he kept having dizzy
spells.
“I’m
not pointing the finger of blame at anyone-it was nobody’s fault.
But at the time, there was a lack of knowledge about SADS on all
sides. “If James had seen a
cardiologist, his problems may have been spotted.
“The
charity promotes the use of cardio screenings for youngsters who could be
at risk of SADS and we fully back this.
“We want more youngsters-particularly those who take part in
sports-to be screened.”
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