What is the impact of early diagnosis and appropriate treatment on disease management and longevity for individuals with familial hypercholesterolemia (FH) over the course of 45 years?
I answered this and many other questions in this research letter titled “Life by the Numbers: Living with Familial … Read More →
The FH Foundation started 2021 off with an impactful Listening Session with the Food and Drug Administration (FDA) Center for Drug Evaluation and Research Division of Diabetes, Lipid Disorders, and Obesity (DDLO) on Homozygous Familial Hypercholesterolemia (HoFH) on January 4. Kate Robinson and … Read More →
Blog Post from My Journey with Familial Hypercholesterolemia and Heart Disease
Disclaimer: This entry is meant to give you some ideas about what to do if you’re bored during the pandemic (or when you can’t leave the house much). Always listen to the medical officials’ recommendations about … Read More →
Blog Post from My Journey with Familial Hypercholesterolemia and Heart Disease
You will learn fast that when it comes to FH you very often don’t take just one medication. You take several. You don’t follow up with just one test. You follow up with multiple tests (blood tests, imaging, … Read More →
When the FH Foundation asked me to write Avery’s story for Rare Disease Day, I felt an immense amount of pressure to get it just “right.” It’s such an important story and I know with this fast-paced world, getting people to stop scrolling and read past the title would be difficult. What does … Read More →
Tom knew, for as long as he could remember, that almost everyone in his family had very high cholesterol. Both of Tom’s uncles had multiple heart surgeries and strokes before the age of 50. That was normal for his family.
When Tom had a heart attack at the age of 29, he and his wife Rachelle were … Read More →
Blog Post from My Journey with Familial Hypercholesterolemia and Heart Disease
Happy New Year to all and here’s to much health, first. Here’s to everything else, second!
If you have read my blog before and if you are an FH patient yourself, you already heard me say this and you already know … Read More →
The FH Foundation is a true partnership of individuals and families impacted by FH, and the healthcare professionals who diagnose and treat FH. Together, we are raising awareness of FH, driving improved diagnosis, making sure individuals know their treatment options and opportunities for clinical … Read More →
We are excited to see much more coverage of familial hypercholesterolemia (FH) in the news and social media. Recently, Grey Genetics featured Fran Emmolo Gamella on their podcast Patient Stories. Fran shared how she only understood her diagnosis of FH after a heart attack at 31. Unfortunately, it’s … Read More →
Looking back, it was a sunny day in July that would change my family’s lives forever. My Dad had just returned to the house after going for a walk. His face appeared pale, and he could not seem to catch his breath. He had slight chest pains and mild back pains. My mom thought it would be … Read More →
