A family's harrowing experience with multiple heart attacks has led to a crucial health warning, uncovering a dangerous genetic condition that could have gone unnoticed.
After suffering three heart attacks in just four years, the family was left reeling—until medical tests revealed a hidden genetic disorder affecting their cholesterol levels. The condition, known as familial hypercholesterolemia (FH), causes dangerously high cholesterol from birth, significantly increasing the risk of heart disease.
A Shocking Discovery
The nightmare began when the father, in his 40s, suffered a sudden heart attack. Just months later, his brother also collapsed. Then, tragically, their father—previously thought to be healthy—died from a heart attack at 68.
Doctors later confirmed all three cases were linked to FH, an inherited condition affecting roughly 1 in 250 people in the UK. Shockingly, 90% of those with FH remain undiagnosed.
Life-Saving Checks
The family's ordeal highlights the importance of early testing. "If we'd known about this sooner, we could have taken preventative measures," said one family member. "Now, all our relatives are being screened."
The NHS now recommends cholesterol checks for anyone with a family history of early heart disease. Simple blood tests can detect FH, allowing for life-saving treatments like statins.
Warning Signs to Watch For
- Family history of heart attacks under age 60
- High cholesterol despite a healthy lifestyle
- Yellowish cholesterol deposits around eyes or tendons
Experts urge anyone with these risk factors to seek immediate medical advice. "Early detection can add decades to someone's life," said a leading cardiologist.
