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 : May ’18

FH Europe e-Flash : May ’18

May 9, 2018

The May edition of the FH Europe e-Flash rounds up the latest news Stories include: FH Europe members attend a media training workshop. First face-to-face meeting of the new Trustee Board. Results of the ODYSSEY OUTCOMES clinical trial. Lifestyle News from around the...

FH Europe e-Flash : Feb ’18

FH Europe e-Flash : Feb ’18

Feb 26, 2018

The February edition of the FH Europe e-Flash rounds up the latest news Stories include: FH Europe appoints two new Trustees. FH Europe website updates its image. Capacity building opportunity for members of the European Patients’ Forum. Request for patient education...

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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