She's one of our 148,893 reasons to give.

Meet Carter, an energetic kindergartner and social butterfly who loves all things cars, racing videogames, and playing with his twin brother, Calvin. His parents had no idea they each carried the gene for a rare muscular dystrophy when their twins were born. All they knew was that Carter was not doing as well as his brother. LAMA2-related muscular dystrophy causes muscle weakness and progressive atrophy, which explained Carter’s low muscle tone and difficulties eating. Today, he zooms around in a power chair. Read Carter’s story to learn how he and his family overcome the challenges of a rare disease. 

Born with sickle cell disease, Nate endured painful crises and frequent hospital visits. But with the dedicated care team at Connecticut Children’s by his side, he learned to overcome his challenges. Now 13, he’s an A student, a talented performer, and excited for a bright future—all thanks to supporters like you who make expert pediatric care possible. Your support helps to transform the lives of kids like Nate. Discover how Nate’s amazing spirit continues to inspire everyone he meets.