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FH can't wait to be diagnosed. We need your help.
Hello,
 
Join us to help children like Aubree.

Aubree is six years old. Every two weeks, Aubree’s parents drive her hundreds of miles to the University of Kansas Medical Center so that she can undergo a procedure to remove heart-damaging cholesterol from her blood.

Aubree was diagnosed when she was just two and a half. She was lucky. Some people aren’t diagnosed until after they have had heart surgery -- or worse.

FH can’t wait. Every single day that a person with familial hypercholesterolemia delays treatment increases their risk of heart disease.
The FH Foundation is committed to finding everyone with FH so that they can be diagnosed and receive the treatment they need to save their lives. But we can’t do it alone….

Your support makes our work possible. Help us find the 90% of undiagnosed patients in the United States and give families a chance at a full life for generations to come.

During this giving season, please make a tax-deductible donation in honor of Aubree and her family. Together we can change the future of families with FH through the early diagnosis and treatment of this life-threatening, yet manageable genetic disorder.

Your support saves lives.
Thank you!
Katherine Wilemon
Founder and CEO