Family on a mission: Child’s rare neuro-genetic disorder inspires a cause
Originally published March 17, 2018 by Delaware State News
It took almost two years for Lillie Larimore to be diagnosed with Angelman syndrome, a rare neuro-genetic disorder that causes developmental delays, lack of speech and seizures. Lillie’s mom and her husband are now determined to foster awareness, in part, by organizing Delaware’s first Angelman Syndrome awareness walk this year to raise funds and help find a cure.
Read the full story from Delaware State News here.
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