Family overcomes obstacles of living with a rare condition called Au-Kline syndrome.
Genetic testing helps a Michigan mom and dad find answers to their baby's rare condition.
In the quest to treat their 6-year-old boy's rare disease, a California couple finds answers in West Michigan.
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.
Pompe disease had no treatment when doctors diagnosed Tasha Veinbergs. Treatment arrived and her future brightened.
The Schneider family faced profound questions about their daughter’s developmental differences. Advances in genetic testing finally revealed answers.
