Stay updated with breaking news from William Lambert. Get real-time updates on events, politics, business, and more. Visit us for reliable news and exclusive interviews.
:strip_exif(true):strip_icc(true):no_upscale(true):quality(65)/d1vhqlrjc8h82r.cloudfront.net/09-21-2021/t_2c5a2edca99f42e98b519f96287e8d8b_name_image.jpg)
Ethan Lambert has an extremely rare disorder, so rare it’s estimated only 300 people worldwide have been diagnosed with it. His parents, William and Kassondra Lambert said Ethan is one of three known cases in Michigan.
IRONTON — A local group has filed to become a 501(c)(3) tax-exempt group seeking to establish a free-standing museum to tell the exploits of World War I ace William Lambert,
Kelly Mulholland is among 10 doctoral students awarded dissertation prizes for 2020 and 2021. Mulholland, shown here being hooded by Louis Rossi, dean of the Graduate College, and her adviser Calvin Keeler, interim dean of the College of Agriculture and Natural Resources, received the Interdisciplinary Research Prize for her work developing tools and techniques to identify bacteria, viruses and fungi found in a chickenâs respiratory tract. Dissertation scholars shine UD doctoral students honored for work in preservation studies, engineering, chemistry, psychology and more The Universi...
How progressive reforms helped level a historic part of black Detroit
Michigan boy diagnosed with rare neurological disorder that only affects 300 people worldwide Updated Apr 29, 2021; Facebook Share PINCKNEY, MI -- There’s no cure and no treatment, but parents Kassondra and William Lambert of Pinckney hope to raise awareness of a rare neurological disorder their son was recently diagnosed with. KIF1A Associated Neurological Disorder, also known as KAND, affects less than 300 people across 20 countries, according to the KIF1A.ORG nonprofit organization. The Lambert’s 3-year-old son Ethan is one of them. KAND is a progressive neurodegenerative disorder tha...