One in 10 people in the United States has a rare disease. Half of those affected by rare diseases are children. There are more than 7,000 rare diseases identified, and many more being discovered as advances are made in the field of genomics. Learn about genetic conditions and hear from people who see only beauty in differences.
While battling a rare condition, a college student is full steam ahead on his dreams.
For a Michigan couple eager to help their son, genetics research is lighting the path ahead.
An energetic 6-year-old is leading the way in treatment for a rare genetic mutation.
Daxton, 2, and Sawyer, 4, battle a rare genetic disease with a team of specialists and the calming power of music.
Genetic testing helps the family of a Michigan boy dig deeper into his unique health challenges.
Genetic testing that pinpointed a rare disorder helped a Michigan couple give their daughter the tools she needs to blossom.
Addison Weith’s genes put her at risk for health troubles. Her family’s vigilance during the pandemic has kept her healthy for the longest stretch ever.
Though they live under the shadow of Huntington's disease, the Shurlow family runs toward a hopeful future.
Kaitlyn Seykora baffled medical professionals all her life. Just last month, a geneticist provided a diagnosis—one so rare, not much is known about it.
Katriona VanDoorne has battled cystic fibrosis since birth. New medicine and genetic discoveries finally allow her to breathe easy and look toward better tomorrows.
Pompe disease had no treatment when doctors diagnosed Tasha Veinbergs. Treatment arrived and her future brightened.
Born with a bone disorder that leaves her vulnerable to fractures, 9-year-old Addilyn won’t let life slow her down.
