I was treated at Alfred I. duPont Hospital for Children for a rare, espohageal motility disorder called achalasia. I owe it to Nemours for giving me my life back. For years, I couldn't eat food, and drinking water deemed itself a challenge. I fought for a diagnosis for so long, but after coming to duPont, they took so much time to listen to me, and my mom and I never left feeling concerned or disappointed. Additionally, being at Nemours gave me so many opportunities, including be the 2019 Rare Disease Day Ambassador, where I advocated for rare diseases, including achalasia. Thank you Nemours for everything. Please help me to help kids going through the same experience as me. No one wants to be in the hospital, but Nemours makes it a manageable, positive experience, from start to end.