Our lives changed the day we were told our baby would be born with Cystic Fibrosis. Within hours of our test results, we met with our incredible pulmonologist who let us know our baby would be one of the lucky ones. Their genetic mutation of CF is one that a miracle drug works really well on. By taking the drug daily, our child should not have to experience most of the daunting symptoms that patients before him have dealt with, and would be able to live a long healthy life. Our son, Thomas was born with lung complications not related to CF, so it is so crucial that these drugs continue to do their job and that we continue to see advancements that will work for ALL cystic fibrosis genetic mutations. We are so extremely blessed that because of all the fundraising, contributions from CF patients, families, friends, and hard work and research doctors, scientists, and pharmaceutical companies have done that we are where we are today. There is still no cure for CF, and our goal is to see one in Tommy’s lifetime. Please help us in our fight to eradicate this disease and have some fun along the way!