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

Tribute to Gabriele Hanauer-Mader

Tribute to Gabriele Hanauer-Mader

Sep 3, 2019

It was with great sadness that we learnt on 22nd August of the sudden and unexpected death of Gabriele Hanauer-Mader. For all who knew Gaby as a warm, likeable, energetic woman who dedicated a great deal of her time to promoting the cause and treatment of individuals...

FH Europe E-Flash : July ’19

FH Europe E-Flash : July ’19

Jul 31, 2019

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 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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