Member Organisations

The European FH Patient Network actively working together to secure early identification and diagnosis of FH patients to prevent early cardiovascular disease.

Countries

The European FH Patient Network actively work together to secure early identification and diagnosis of FH patients to prevent early cardiovascular disease.

Member Organisations

Countries

who we are

FH Europe consists of multiple FH patient groups across Europe. By sharing information & best practice we aim to secure early identification and diagnosis.

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about fh

Familial Hypercholesterolaemia (FH) is an inherited genetic condition that leads to levels of cholesterol that are much higher than that of the general population.

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Our members

Our members are made up of organisations and individuals that represent FH patient groups within their specific European country.

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Latest News

The latest FH Europe eFlash

The latest FH Europe eFlash

The latest e-Flash from FH Europe celebrates what is happening around Europe to mark international FH Awareness Day on 24 September. A key element for many member organisations is helping to ‘find FH’ by means of organising cholesterol testing in shopping centres and…

FH Europe Website is Launched

FH Europe Website is Launched

Since its inception in 2015, the FH Europe network has grown to include 22 member organisations in 21 countries, all sharing the goal of identifying as many people as possible who have familial hypercholesterolaemia (FH) and ensuring they receive early and appropriate…

FH Europe is registered as a charity; Charity number 1170731, registered in England and Wales.

FH Europe is registered as a charity; Charity number 1170731, registered in England and Wales.

FH Europe is supported by an educational grant from Amgen Limited, Sanofi, Akcea Therapeutics Inc. and Amryt