Call from man whose threesiblings died of heart issues
A Londonderry man, who is genetically at risk from heart disease and lost two brothers and a sister to heart attacks and strokes whilst they were still in their 30s and 40s, says his life span has been “immeasurably increased due to early detection and effective treatment.”
Charles Logue has witnessed at first hand the devastating effect of Familial Hypercholesterolaemia (FH), which he was diagnosed with almost 50 years ago.
“I was diagnosed as having FH in the 1960s. One Sister and two Brothers of mine were diagnosed at the same time but have since died in their 30’s and 40’s from heart attacks/strokes,” he said.
“I now take a daily tablet for my cholesterol and attend the Lipid Clinic at Altnagelvin Hospital once a year to have my cholesterol checked and the treatment adjusted to keep it under control. The modern treatments are easy to take and very effective in lowering my cholesterol to a normal level,” he added.
“All my wider family members have been checked for the condition including my own children. Because of family testing, the condition can be detected and treated earlier and this means that the younger members and future generations of our family should not suffer from devastating heart disease the way my own brothers and sister did. The condition can be treated very effectively if caught early.
“I would definitely encourage anyone invited for FH family testing to have the test done. Without doubt my life span has been immeasurably increased due to early detection and effective treatment,” said Mr Logue.
FH Lead in the Western Trust, Dr Maurice O’Kane, Consultant Chemical Pathologist /Director for Research and Development said: “Northern Ireland is one of the few countries that have an organised system for identifying people with FH.
“Our aim is to identify everyone with this genetic disorder so that they can get the advice and treatment they need to prevent the early development of cardiovascular disease and premature death.
“Diagnosis of FH is crucial to the patient’s family too. Any child of an FH sufferer has a 50% chance of inheriting the disease. Once one family member is identified as having it, on average another five will be diagnosed as well.
“This regional service will be delivered locally in the Western area and has been developed to actively identify all known cases of FH and offer family follow-up testing to their immediate family members.
“The development of this new service should result in an additional 1,000 people with FH being diagnosed and treated over the first four years of the programme. This should prevent around 170 cardiovascular deaths.”
Elaine Proctor, Familial Hypercholesterolaemia Specialist Nurse with the Western Trust said: “In Northern Ireland only 25 per cent of people who have FH have already been identified.
“This means that 75 per cent are currently undiagnosed. The early detection of the family cholesterol gene empowers patients and their families. It gives them an informed choice to positively influence their life outcomes. This significantly reduces the risk of them developing early cardiovascular disease.
“Research has shown that treatment of FH with cholesterol-lowering drugs is very effective in reducing the risk of heart disease.”
Andrew Dougal, Chief Executive of Northern Ireland Chest, Heart & Stroke, said: “NICHS is delighted that this service is being launched. We have been pressing for this development for some time and have contributed over £35,000 to enable the family follow-up testing service to be set up. This money from our supporters will mean that people with FH can be identified and treated as quickly as possible. Hundreds of lives with be improved and many lives saved across Northern Ireland as a result of their generosity.”