• Join the Movement

    Before we can really influence politicians around the world to recognise the unfairness of allowing FH to continue to be underdiagnosed and untreated we need your help.

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  • Welcome

    FH is a shockingly common family genetic disorder that occurs in at least 1 in 300 individuals worldwide.

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  • The Mission

    Our mission is to create a global communication centre where people of all ages, race, creed and gender can find and discover anything they might want to know about FH.

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Welcome to the International FH Foundation

Raising awareness of Familial Hypercholesterolaemia

FH (familial hypercholesterolaemia) today is going undiagnosed and 200,000 people are dying every year from a family inherited disorder that is easily diagnosed and treatable.

With an enhanced understanding and resolve, astute and committed clinicians, along with well-informed patients, and forward thinking politicians have the power to lower the huge financial and human costs of abandoning patients with FH

The International FH Foundation's mission is to create a global alliance and partnership centre where people of all races, creeds, age and gender can come to find and discover anything they might want to know about FH; to make that information universally accessible and useful to patients and their families, to physicians, nurses and dietitians, corporate, government and communication leaders.

Our Aim

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With an enhanced understanding and resolve, astute and committed clinicians, along with well-informed patients, and forward thinking politicians, we jointly have the power to lower the huge financial and human costs of abandoning patients with FH.

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