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New group to tackle problem of sudden death syndrome

Sunderland Echo (City) - 17th March 2004 (Courtesy of the Sunderland Echo)

By Ben Garside.  

 

Dad welcomes pledge to help

A Father left devastated by the loss of his son to a form of Sudden Adult Death Syndrome, today welcomed Government moves to help prevent more deaths from the condition.

Health Minister Melanie Johnson announced plans to set up an advisory group to help tackle sudden heart deaths in the young and improve services for people with irregular heartbeats and similar conditions.

The sudden death of 22-year-old Levon Morland, of West Rainton, two years ago, led family and friends to push for more action to be taken against conditions such as the Wolfe Parkinson White syndrome  which claimed his life.

Dad Jeff, a trade union official, has been the driving force behind the Levon Morland Memorial Fund for CRY (Cardiac Risk in the Young), raising more than £40,000 in 20 months.

Jeff, who is also Northern Labour Party chairman, said “The initial private member’s bill put forward was quite narrow, only proposing screenings for those with a family history of the condition, but this is a good step forward to try and get more screenings to other groups, such as those involved in sport or demanding work.

“This condition kills a reported eight people every week, but I believe it’s actually more than that because they are often put down as natural causes.

“Most could have been treated in some way and are curable with pacemakers, drugs or even just lifestyle changes.”

Dari Taylor, MP for Stockton South who used to be a Sunderland councillor and presented the Cardiac Risk in the Young (Screening) Bill said, “We know from research and experience that we can prevent these deaths-but now we need to put that knowledge to work.

“Far too many cases are slipping through the net undiagnosed, misdiagnosed, or diagnosed but not treated.

“This announcement will help prevent such deaths and I am delighted that the Government has taken this terrible condition seriously.”

The new advisory group, headed by National Clinical Director for Heart Disease Dr Roger Boyle, will help raise awareness of the conditions and advise the Health Department on future policy.

It could also lead to a new National Service Framework Chapter setting out advice for doctors on standards and models of care for such conditions.

Voluntary and professional bodies including CRY and the British Cardiac Society will be invited to join.  Patients and families of patients will also have a strong voice in the work.

 

 

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