Meet Caroline Wallendal
Life as a teenager is challenging and complicated for anyone. Add on top of that a life-threatening and changing illness like Cystic Fibrosis, and it is clear that every day brings its own unique experiences. Caroline Wallendal has not let her illness slow her down, in fact, she has used her experiences to strengthen her in all her achievements.
Even if I may look like a normal 16-year-old girl, there’s a lot more to me that most people don’t usually see. When I was just three months old, I was diagnosed with cystic fibrosis (CF). CF is defined as a genetic disorder mainly affecting the lungs and digestive system, but most definitions can’t describe the impact that it can take on one’s life. When I was younger, I did get sick and have some days that I felt like I just had to stay in bed, but I have been fortunate that I don’t have long stays in the hospital as often as some patients do. Even though I didn’t get super sick too often, I still had many challenges and I wouldn’t consider myself as having a “normal” childhood. I always had to take extra precautions in school and I couldn’t participate in all activities like everybody else because of my health.