Lindsey Pietrzyk grew up with a mysterious heart condition. Now she's part of a growing family with faith in the future.
Born with a bone disorder that leaves her vulnerable to fractures, 9-year-old Addilyn won’t let life slow her down.
Born with a rare and life-threatening immune system disorder, baby Emmett gets a new start with a bone marrow transplant.
Meet baby Owen, the first child in Michigan to benefit from a lightning-fast whole genome sequencing program.
Most babies with trisomy 18 never make it to birth. Those who do typically die shortly thereafter. This toddler is blasting the odds.
The Schneider family faced profound questions about their daughter’s developmental differences. Advances in genetic testing finally revealed answers.
After her brother dies of Duchenne muscular dystrophy, a woman ponders whether to get genetic testing.
Parents of children with rare genetic diseases celebrate their daughters' unique gifts.
Shelby Lentz is competing for the Miss Michigan title. But since her diagnosis, she's now competing in a race against time.
Sally and Greg Brown have shared 33 years of marriage. Now, they share cancer.
A 40-foot mobile mammography unit that showed up at her workplace may have saved Deb Browers' life.
Little Hayden, born with two rare disorders, might be the first of his kind. His parents treasure his uniqueness.
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