Why I Walk for Cystic Fibrosis Growing up, I watched my sister, Jennifer Gavilanes, spend countless days in the hospital battling a disease I didn’t fully understand. As a teenager, I often stayed overnight as a visitor—sitting beside her during rounds of nebulizer treatments, chest physiotherapy, and long conversations with specialists. Those early experiences shaped who I am. They’re the reason I pursued a career in healthcare and became a nurse. Jennifer is a two-time double lung transplant recipient. Both times, she was placed on ECMO, and our family lived in fear of losing her. By what can only be described as a miracle, she received the gift of lungs—twice. Her resilience is something I carry with me every day, but so is the reality of this disease and what it has taken from her and so many others. After having children, I underwent genetic testing and learned that I am a carrier of cystic fibrosis. This means my grandchildren could one day be at risk if my children have children with someone who is also a carrier. Knowing this drives my passion to raise awareness and advocate for a cure. Cystic fibrosis is a devastating illness. It shortens lives, disrupts futures, and takes an enormous toll on families. Too many lives have been lost far too soon. I walk not only for my sister, but for every person fighting this disease—and for those who will be diagnosed tomorrow. Please help me fight for a cure. With your support, we can create a future where cystic fibrosis is no longer a life-threatening condition.