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 [...]
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 [...]
“Great scientific progress, efficacious therapies, and elegantly written guidelines don’t always end up helping the people they were intended to serve. This is a sobering fact, and in many ways, [...]
Since its establishment seven years ago, the Family Heart Foundation has studied the 1998 World Health Organization (WHO) Report on Familial Hypercholesterolemia (FH). The 11 recommendations within the document guide [...]
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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.
