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Real life story

"Three of my brothers died young from heart attacks"

Wendy Cook was diagnosed with familial hypercholesterolaemia after the sudden deaths of three brothers. She explains how statins have given her a future and how she’s helped her family understand the importance of cholesterol tests.

Wendy Cook

After losing her brothers, Wendy Cook discovered she had familial hypercholesterolaemia (FH), a genetic condition that causes high cholesterol from birth and can lead to a heart attack at an early age. She now takes statins and is celebrating a birthday that she thought she might not reach.

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“Philip was the first of my brothers to pass away, and the inquest said he had died of ischaemic heart disease. He was 45. Then three years later we lost my brother Paul to the same condition, and then another brother, Michael, two years after that. That left me, my brother Tony and sister Christine. It all happened so fast I didn’t have time to come to terms with it all.

After Paul died, I contacted my GP and that’s when she first mentioned FH. I was 52 and had never heard of it, but it was clear that heart disease was in the family and my cholesterol was high. I went on statins and my cholesterol came right down. I just take my tablet before I go to bed. The fact that statins can give you a future is amazing. It means my family don’t have to go through all that again.

After Michael died, my GP sent me for genetic testing and the results came back saying I have an altered gene. It’s not one of the main genes already known to be linked to FH but they said in future, with more research, they may be able to link the gene to FH.

It’s my 60th birthday in July. I’m not a party kind of person - I would like to celebrate in a quieter way with my husband Paul and family. I am just glad to get to this age. It’s such an achievement in our family to reach 60.

My nephews and nieces all have their cholesterol tested. I am looking after myself, but I would like the next generation to be really aware and the generation after that. I am definitely hopeful.”

How the BHF is helping FH research

The BHF has been a major funder of FH research, particularly through our support over 30 years for the leading UK expert in FH, former BHF Professor Steve Humphries. Professor Humphries and his team discovered many of the genetic defects which cause FH, leading to a blood test for the faulty genes, so doctors could diagnose or rule out FH. They also showed that genetic testing for family members of a person with FH (a process called cascade testing) helped to spot more people with the condition. Identifying people who have FH and cascade testing of family members is now an NHS priority.

We’ve also helped to fund clinical trials that have demonstrated the ability of statins to reduce the risk of heart attack, heart disease and stroke. Statins have saved the lives of many people, both with and without FH.

Bernadette Williams standing in her kitchen.