Two years ago, I knew next to nothing about Cystic Fibrosis other than what I saw in TV/Movies. But then I met the most amazing man, Rick Wilkins. On our second date he told me he had Cystic Fibrosis. He told me what it was and answered any questions I had. He showed me his enzymes, which was just the tip of the iceberg on what pills and treatments I would soon learn about. After that date I went home and scoured the internet for more information. I checked out books from the library. I printed off booklets from the CF Foundation and tried to learn as much as I could. Rick has always been open and answers any questions I have, even if they may seem stupid. CF has slowly become a regular part of my life as Rick worked in to more of my heart. The hospital stays will never be easy, but I am so thankful for the CF Foundation and all they do in finding a cure. I am excited for the day that CF really does stand for Cure Found!
Please donate to this wonderful foundation that does so much for the CF community.