FH is a form of hereditary high cholesterol.

In the UK, FH is thought to affect about one in 500 people, which means approximately 120,000 people are thought to be affected.

A doctor confirmed Bryan’s initial suspicion and he was diagnosed with FH.

As it runs in the family, he immediately got his children tested and his worst fears were confirmed: one of his children had FH.

Thankfully, it was caught in time, to Bryan and his wife’s immense relief.

As the dad points out, the longer FH goes untreated, the greater the risk “your arteries firm up”, which leaves you vulnerable to heart disease.

FH – everything you need to know

FH is caused by a gene alteration inherited from a parent, rather than an unhealthy lifestyle.
Symptoms can include:

• Bumps or lumps around your knees, knuckles, or elbows
• Swollen or painful
• Achilles tendon
• Yellowish areas around your eyes
• A whitish gray color in the shape of a half-moon on the outside of your cornea

People with familial hypercholesterolaemia have raised cholesterol from birth, which can lead to the early development of heart problems, such as atherosclerosis and CHD.

There’s a one in two (50 percent) chance that a child or brother or sister of someone with familial hypercholesterolaemia will also have the condition.

It’s worth noting that most people will not get symptoms and you can only find out if you have it by getting a blood test.

And, although FH is one of the most common inherited conditions, high cholesterol levels are generally the result of an unhealthy lifestyle.

“You can lower your cholesterol by eating healthily and getting more exercise. Some people also need to take medicine,” explains the NHS.