Dr. Peter Donald Kaplan MD

The mucous membranes in the airways of people with cystic fibrosis produce mucus that is thick and viscous, more solid than is produced by healthy people, which leads to all sorts of problems in the patient.As anyone with CF knows, the reason the mucus thickens is because the proteins that form the...

Breathe in and breathe out. Isn't it one of the simplest things to do in life? But when you see your loved ones, especially your children, wheezing, it can really make you anxious and stressed. One of the most traumatizing diseases that can leave one struggling for something as basic as oxygen is...

When a person has a debilitating disease, dealing with that reality is enough to bear.But, when there is a drug out there to limit the debilitation of that disease, and governmental decision-makers don’t provide patients with it, the fight about injustice becomes overbearing.The denial for your...

Because cystic fibrosis affects nearly the entire body, all too many people with this genetic disorder think about their symptoms and outlook then fall into a pit of despair. Not everyone. And certainly not Mae Johnson, a 14 year old girl from Adelaide, Australia.In fact, this enterprising teenager...

The human respiratory tract starts at the nose and mouth and continues down to the lungs. The air that we breathe in through our nose and mouth passes down the trachea and into the lungs through a series of branched tubes called the bronchi. For a healthy breathing to happen effectively, these tubes...

Cystic fibrosis (CF) is an inherited disease that is caused by a defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The CFTR protein is responsible for controlling the transportation of salt in and out of cells. Any mutations in the CFTR gene can cause an imbalance in the...