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

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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 : Spring ’19

FH Europe E-Flash : Spring ’19

Apr 20, 2019

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...

One voice in Europe on FH

One voice in Europe on FH

Apr 9, 2019

The European Atherosclerosis Society FH Studies Collaboration and FH Europe announce partnership We are delighted to announce to a new collaboration between Familial Hypercholesterolaemia (FH) patient representative network, FH Europe, and the FH investigators from...

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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