Valorie: Cockayne Syndrome

Valorie: Cockayne Syndrome

Jace was seven years old when he was diagnosed with Cockayne syndrome type one, which is a very rare genetic condition, and is fatal. His mother, Valorie, became his champion and has started a non-profit organization called Team Jace to help other families walking the...
Angie: Stromme Syndrome

Angie: Stromme Syndrome

During her first prenatal ultrasound, Angie was told that her daughter wasn’t developing properly. She was encouraged to terminate her pregnancy after testing revealed nothing.  Now 12 years later, Ruby has blessed Angie’s life and has inspired others with her...
Erika: Microcephaly

Erika: Microcephaly

Erika was given a very grim diagnosis when she was six months pregnant.  Her daughter, Erilyn was diagnosed with microcephaly.  She was very pressured to abort Erilyn.  Now eight years later, Erika is grateful she chose life and can see that Erilyn is a blessing and...

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