WAAY TV highlights Montgomery family’s journey to a diagnosis

Through the childhood genetic disorders program, HudsonAlpha researchers are finding answers for children in Alabama like Violet Monson.

The Monson family spoke with Double Helix Dash media sponsor WAAY TV about their journey to a diagnosis.

“We were able to get accommodations and supports for her, and we were able to get her mission device. Now she communicates with her eyes,” said Mandy Monson.

Watch the full story from WAAY TV.