FH affects every race on every continent. Current estimates are that between 14 million – 35 million people have FH world wide. Tragically, 90% of them are unaware that they and their families have a treatable but life-threatening genetic condition! The FH Foundation is a global organization that is working to bring about urgent change. We are joined by committed and capable patient advocacy organizations and leading experts around the world that are committed to raising awareness of FH.
Click the flags to find out what each country is doing to address the barriers to care and to learn about their efforts in bringing FH to the forefront.