Network 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.

Network 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 NETWORK

The network is made up of organisations and individuals that represent FH patient groups within their specific European country.

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Latest News

FH Europe creates a Scientific and Public Health Advisory Committee

FH Europe creates a Scientific and Public Health Advisory Committee

Mar 29, 2021

It is our pleasure to share an important achievement for our Network. FH Europe created its Scientific and Public Health Advisory Committee. The committee consists of 16 international experts and will be chaired by FH Europe trustees Sam Gidding and Marius Geanta. It...

Choose to challenge – women’s heart health

Choose to challenge – women’s heart health

Mar 8, 2021

FH Europe is supporting International Women’s Day 2021. Each year, on the 8th of March, International Women's Day is celebrated to recognise the achievements of women while calling for greater gender equality. This year’s theme for International Women’s Day is “Choose...

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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