Network Organisations

The European FH Patient Network actively working to improve Europe-wide awareness, understanding, and access to diagnosis and treatment of inherited lipid conditions, (specifically FH, HoFH, Lp(a), FCS), so that all those impacted receive optimal treatment and support, resulting in longer and healthier lives

Countries

The European FH Patient Network actively working to improve Europe-wide awareness, understanding, and access to diagnosis and treatment of inherited lipid conditions, (specifically FH, HoFH, Lp(a), FCS), so that all those impacted receive optimal treatment and support, resulting in longer and healthier lives

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

Heart Beat News – May 2023

Heart Beat News – May 2023

May 31, 2023

Read the May 2023 edition of FH Europe’s Heart Beat newsletter to stay up to date with the latest news and events: HoFH Patient Ambassadors advocate at the WHF Rare CVDs Forum. EAS Annual Congress follow-up webinars. Biggest patient organization celebrates their 20th...

International HoFH community advocates at the WHF Rare CVDs Forum

International HoFH community advocates at the WHF Rare CVDs Forum

May 19, 2023

An international community of multidisciplinary stakeholders committed to making lives of people with rare cardiovascular diseases “longer and better” came together at the Rare Cardiovascular Diseases Forum (CVDs). FH Europe together with the HoFH community was...

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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