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Dance Marathon is a nationwide movement involving college and high school students at more than 150 schools across the country, all raising money for the Children’s Miracle Network Hospital in their community. These students spend a year learning invaluable leadership and life skills while raising funds and interacting with children’s hospital patients and families. The year culminates with a 12-40 hour long event where the students stay on their feet through dancing, games and entertainment in celebration of the total amount raised that year.

Why stay on your feet for that long? To quote the first Children’s Miracle Network Hospitals Dance Marathon’s mission statement: “We dance for those who can’t.” It is this solidarity to – and connection with – the cause that makes Dance Marathon an event unlike any other.

In 1991, students at one university founded Dance Marathon in the memory of Ryan White, a fellow student. The program now spans the entire country, benefiting hundreds of hospitals and countless kids. Dance Marathons have become a tradition on campus and in the community. Each event is entirely student run and all donate 100% of the funds raised directly to their local Children's Miracle Network Hospital. Last year alone, college dance marathons raised more than $8 million.
Click here to get started now. Bring a new tradition to your school and help children in your area to have a brighter future. Do it for your school. Do it for you. Do it For The Kids!

Miracle Child
Miracle Child

Ayla

Blood Disorder

When Ayla was 3 years old, a minor accident on the playground resulted in severe dark bruises on her legs. When her worried parents took her to the doctor, the test results turned their world upside down.

Ayla was diagnosed with a rare blood disorder called idiopathic thrombocytopenic purpura (ITP), a disease that affects the body’s ability to clot blood and stop bleeding. The disease made Ayla’s body unable to control even the smallest cut or bruise—a frightening scenario for an active toddler. Although 90 percent of childhood ITP cases clear up within a year, Ayla’s did not. Her ITP is chronic, necessitating numerous blood transfusions, frequent hospital visits and even a splenectomy.

A few months after her diagnosis, Ayla’s family moved to Denver, Colo., so she could receive ongoing care at The Children’s Hospital. “At our first appointment, we knew we had found the right place,” said Ayla’s father, Jay.

Now 10, Ayla is mature, empathetic and patient with the challenges of her disease. She plays the piano and violin, and loves to swim and dance.

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