Indiana County family working to raise $2.5 million to treat son's neurodegenerative disease
A community is rallying around a 2-year-old boy living with a rare neurodegenerative disease.
Source: wtae.com
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IT'S A WONDERFUL LIFE FESTIVAL KICKS OFF TONIGHT | WDAD AM1450 & 100.3FM
Downtown Indiana is expected to be busy tonight with the first night of the It's A Wonderful Life festival. Activities are scheduled to start this aft...
United States Zander Marshall Jimmy Stewart Museum Downtown Indiana Wonderful Life Philadelphia Street
Source: wdadradio.com
Their son's condition is incurable, so these parents channel resources to help
Their son may never be cured, but these parents aren’t giving up.
Source: thestar.com.my
Their son may never be cured. But these parents aren't giving up
DALLAS — When Will Woleben was a baby, he followed his mom around their McKinney, Texas, home while she cleaned, waving a toy vacuum. As his second birthday approached, he
Source: wenatcheeworld.com
Cure Mito Foundation releases the first-of-its-kind online resource about Leigh syndrome
The Cure Mito Foundation, a parent-led organization dedicated to advancing research and treatments for Leigh syndrome, has launched the first-of-its-kind online resource about Leigh syndrome, the most common type of pediatric mitochondrial disease.
Kasey Woleben Ibrahim Elsharkawi Megan Craig Harvard Medical School Cure Mito Foundation Assistant Professor
Source: news-medical.net
Parents become drug developers to save their children's lives
Maggie Carmichael wasn't developing like other kids. As a toddler, she wasn't walking and had a limited vocabulary for her age.
United States San Francisco El Paso University Of Texas Southwestern Medical Center James Geraghty Craig Benson
Source: news-medical.net