Reducing the Burden of Familial Hypercholesterolemia Healthcare systems around the world have failed to rescue individuals born with Familial Hypercholesterolemia (FH), even though we have had life-saving therapies [...]
Family Heart Foundation, World Heart Federation, and International Coalition Collaborate to Tackle the Global Burden of Familial Hypercholesterolemiathe Family Heart Foundation and the World Heart Federation announced today a Global [...]
Familial Hypercholesterolemia Global Impact In 1998, the World Health Organization (WHO) and several members of the international FH Community published the WHO Report on Familial Hypercholesterolemia (FH). This prescient document [...]
Global Call to Action on FH Roundtable the Family Heart Foundation is thrilled to continue the Global Call to Action on FH initiative during the 2018 World Congress of Cardiology [...]
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Early diagnosis and treatment can mean years, even decades of life for someone with impacted by familial hypercholesterolemia (FH) and lipoprotein(a), also known as Lp(a).
Yet a majority of people with these inherited disorders haven’t even been diagnosed.
Your gift allows us to continue to engage the research, advocacy, and education that helps individuals with FH, HoFH, or elevated Lp(a) get the vital medical care that they need.
