Cystic Fibrosis

My son, Andrew, has cystic fibrosis and has been seeing a decrease in his lung function that his doctor’s don’t understand. He’s a very active kid, either playing outside with his friends, playing Little League, or school sports (flag football and now lacrosse?!). His activity level, and lack of bretahing problems don’t support the lung function test results he’s getting. My wife and I think he’s figured out how to make the “nice loop” for the PFT test and stopping, and his smirk a couple nights ago may confirm that. [Read More]