I'm Kaylee, Carol's daughter! You may or may not know a lot about me, but trust me, I'm worth getting to know! If you're reading this, you know that I have cystic fibrosis. Having cf means that my days are a little different. I don't always feel great and spend more time in hospitals than the average person. I have to do inhaled medications 3 times a day and I take many more meds throughout the day. Often when I go away my medical bag is packed fuller than my backpack! Though for me, it doesn't stop me from doing the things I love. Dancing and having fun with my friends, are just two of the things I love to do. Even though I try not to let it get to me, I still often find myself wondering what my like without cf would be like. Researchers are making progress everyday, so maybe I will be able to experience life without it! You can help by making a donation, even the littlest amount can put us in the right direction towards a cure. I'd also like to thank you for choosing to support cystic fibrosis, it means so much to me.