Meet Our Patients

Your generosity powers compassionate care and creates healthier futures for children. See what your support means to our patients and families.
Photo of Emma

Emma, age 14

Emma is a busy teen who loves hanging out with friends, playing sports, listening to music and making people laugh. Right before eighth grade Children’s National experts diagnosed her with Crohn’s disease. Compassionate care helps Emma tolerate and even enjoy her monthly treatments that help her get back to all the things that make her smile!

Photo of Jackson

Jackson, age 18

Jackson plays varsity football and grew up playing basketball, ice hockey, baseball and lacrosse. He began having seizures at age 9 and lost the ability to talk, walk and eat on his own. Neurologists and speech and physical therapists at Children's National helped Jackson recover from his rare illness and keep chasing his athletic dreams.

Photo of Kendric

Kendric, age 12

Kendric loves going to school, writing and playing video games. He is most passionate about genetics and aspires to help others to live healthier lives. Kendric was born with sickle cell disease. He found expert care and innovative research at Children’s National where he is the first person in the country to start a commercially approved gene therapy for pediatric treatment.

Photo of Mariana

Mariana, age 6

Mariana loves painting, running and riding her bike. Soon after she was born, the SkyBear helicopter brought her to Children’s National when she couldn’t breathe. Expert care gave her and her family comfort and a new start. Now, she looks forward to the Kids Dash each year to receive her medal from a superhero.

Photo of Mills

Mills, age 13

Mills enjoys painting landscapes, listening to rock music and playing with Chuck, their German Shepherd. They were born with half a heart and had two surgeries at Children’s National soon after birth. Today, Mills is healthy and grateful to their care team for giving them a new start.

Photo of Reese

Reese, age 15

Reese is always on the move, from doing yoga to playing soccer. Her care team at Children’s National empowered her to understand her heart rate fluctuations with Postural Orthostatic Tachycardia Syndrome (POTS) and learn how to cope. With this support, Reese stays active and listens to her body.

Go Mobile

Manage and share your Move for the Kids experience on the go with our newly-updated mobile app. This FREE app lets you fundraise and connect with others through social media and email, update your web pages and check your fundraising progress—all from the palm of your hand. Download the app to your iPhone or Android today!

Download fundraising app on iTunes