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

FH Europe E-Flash : July ’19

FH Europe E-Flash : July ’19

The July edition of the FH Europe e-Flash rounds up the latest news In this edition: FH Europe representatives meet EAS FHSC at the EAS Congress in Maastricht and a link to news from the Congress EU news on endocrine disruptors Rare disease and research updates Do we...

FH Europe E-Flash : Spring ’19

FH Europe E-Flash : Spring ’19

The Spring edition of the FH Europe e-Flash rounds up the latest news Stories include: FH Europe and European Atherosclerosis Society agree closer cooperation to improve treatment and research for FH 87th EAS Congress in Maastricht News about Rare Disease Day 2019...

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, Regeneron, Akcea Therapeutics Inc. and Amryt
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