This November the American Heart Association held their annual conference in Chicago. Over 10,000 clinicians and researchers in attendance. Sessions focused on the latest insights and below we’ve listed [...]
The American Heart Association’s (AHA) 2024 Scientific Session was held in Chicago in November. This is one of the premier scientific meetings of the year with over 10,000 clinicians [...]
93% of primary care conference attendees did not know their own lipoprotein(a) level In October, the Family Heart Foundation team attended a medical conference, comprised of mostly primary [...]
A Governor’s Proclamation is a document making a declaration on behalf of the entire state. They can help influence policy discussions, public awareness, and provide opportunities to engage your community [...]
Every year we dedicate a Sunday to our fathers and father-figures. They guide us through life’s toughest moments, teach us how to stand on our own two feet, and give [...]
Chloe’s family has made advocacy a family tradition. Her father, Scott, and her brother, Luke, are Family Heart Foundation Ambassadors, and her sister Hannah will be training to be an [...]
New research from the Family Heart Foundation shows access to PCSK9 inhibitors (PCSK9i) has slightly improved, but there are still major barriers to these lifesaving drugs. What [...]
Access to Prescribed PCSK9 Inhibitors Remains a Significant Barrier Leaving Patients at Risk for Heart Attacks and Strokes Family Heart Foundation Research Shows Insurance Coverage is an [...]
The Family Heart Foundation wouldn’t be where it is today without the help of our Family Heart community. The key to raising awareness is by getting the message out, [...]
The Family Heart Foundation’s Back and Forth with the United States Preventive Services Task Force Since 2011 the American Academy of Pediatrics (AAP) and the National Institutes of [...]
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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.
