The sound of the Waisman Center’s work to improve cochlear implants
The Waisman Center has been at the forefront of research on cochlear implants and hearing science for more than two decades.
Advancing knowledge of human development, developmental disabilities, and neurodegenerative diseases.
The Waisman Center has been at the forefront of research on cochlear implants and hearing science for more than two decades.
Our understanding of language relies on more than just the spoken word. A myriad of external cues, like nonverbal signals and a person’s characteristics, contribute to how we understand and process language as we speak and communicate with others.
A dedicated University of Wisconsin–Madison clinician, educator, advocate and researcher, Renata Laxova, professor emerita of medical genetics and pediatrics, passed away recently after a brief illness. She was 89.
As a third year graduate student in school psychology at the University of South Carolina, Lindsay McCary, PhD, was looking for a new advisor to help her with her dissertation.
A new study of children with cerebral palsy could help ease the speech and language challenges many of these children face as they get older.
Children diagnosed with autism spectrum disorder, or ASD, often have significant delays with expanding their vocabularies and other language skills compared to typically developing children. Yet, “we know very little about [language] processing in [children with ASD] or the mechanisms underlying it,” says Susan Ellis Weismer, a professor of communication sciences and disorders at UW-Madison …
Jaden Cassidy is three years old and a whirlwind of energy. He bursts into the exam room, jumps on the exam table, flings off his jacket and cowboys boots and whirls around with a beaming smile, expecting—and getting—an enthusiastic round of applause. Jaden’s vibrant nature masks the difficult journey he and his family and friends …
Denise Ney, professor of nutritional sciences, is a rare disease hero. We all know that, but now it’s official. Ney is one of 30 Rare Disease Heroes named by the Office of Orphan Products Development at FDA. This is part of the agency’s sixth international Rare Disease Day. This is an opportunity to reflect on what has been accomplished for rare diseases, while looking forward to the work that has yet to be done.
“Don’t give up, my love, or I’ll give up with you, because I only live to see the fulfillment of this dream: that you may continue to live. Yours is a life sentence, not a death sentence.”
Tad and Matt Martin recently ate what they had never been able to eat before: hamburgers, hot dogs, ice cream and grilled cheese sandwiches, with real cheese and regular bread.