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A message from Jules Payne, Chair of FH Europe, and CEO of HEART UK “The time has now come for me to step down as Chair of FH Europe, a role I have been so very proud to fulfil these past four years.  I would like to thank all fellow Trustees, past and present in […]

Join us for a community webinar Ever wondered what a #registry was? Curious to find out how FH registry can impact you and your family? #FamilialHypercholesterolemla (FH) is one of the most common and life-threatening inherited conditions. If you have FH, at least someone else in your #family also has FH. Individuals with FH remain vastly under-diagnosed and under-treated and are […]

The highlight on the FH Europe patients’ community’s agenda is the annual meeting. Since the creation of the Network, the leaders of the respective patient organizations have been coming together face to face to share, exchange and to network. In 2020, in collaboration with DIAGNOZA FH and the Czech Society for Atherosclerosis, the gather was […]

A multi-stakeholder collaboration is critical to resolving the burden of FH. Our community is very pleased to partner with national and international stakeholders – from patient organizations to policy makers, societies and medical communities.

Determined to raise awareness about Familial Hypercholesterolemia among medical community, FH Europe partners with MEDizzy, an online international community of young health care professionals.

FH Europe is pleased to partner with the Global Alliance for Patient Access in preparation to the FH Awareness Day, September 24, to amplify the Global Call to Action on FH and support in-country advocacy efforts to implement the document’s public policy recommendations. A guest blog by Jasmine Patel, MPH, Director, Policy and Outreach, Global Alliance for Patient Access