In September, the FH Foundation participated in the “New Strategies in Public Health Genomics” conference at the Centers for Disease Control (CDC). Experts and key stakeholders, including advocates, community leaders and clinicians, came together to discuss evidence-based genomic programs … Read More →
FH News & Blog
Original story published on October 8, 2012
Christian Jacobs, 20, was diagnosed with homozygous familial hypercholesterolemia, a rare genetic disease, at age 2. It led his cholesterol levels to be 4 times higher that of a healthy adult.
Like any patient at risk of a heart attack, … Read More →
FDA Advisory Committee Information:
Notices of the upcoming Endocrinologic and Metabolic Drugs Advisory Committee meetings have been made available on the FDA website: https://www.fda.gov/advisorycommittees/default.htm
Date and Time: The meetings will be held on October 17 and 18, 2012, from 8 a.m. … Read More →
Diann Goolsby of Crosby has a mission in life. Goolsby was born with a defective gene that has her living with dangerously high levels of cholesterol.
TENS of thousands of patients who have inherited a dangerously high risk of a heart attack in early life are going undetected, warn cardiologists, who are calling for a new integrated screening system to pick up their condition before it becomes life-threatening.
The condition, called familial … Read More →