ABL+ Foundation supports individuals with ultra-rare hypolipidemia diseases

Patient Stories

In 1965, the term “rare diseases” was almost unheard of in the United States. Born that year, Paul was diagnosed with Abetalipoproteinemia (ABL), a rare genetic disorder.

“I lead the life I want to live! If you take anything away from my story please realize that ABL, and the other illnesses the ABL+ Foundation is concerned with, are all treatable with proper diet and vitamins.”

Paul’s journey led to the creation of the ABL+ Foundation in 2019.