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News
Childhood Apraxia of Speech Cases on the Rise
Speech pathologists at Nationwide Childrens Hospital report an increasing number of patients diagnosed with childhood apraxia of speech, a motor speech disorder in which children have difficulty saying basic sounds and words.
Specialty
Velopharyngeal Dysfunction Program
The Velopharyngeal Dysfunction (VPD) Program at Nationwide Children’s Hospital provides coordinated interdisciplinary diagnostic and treatment services for patients with speech disorders resulting from velopharyngeal dysfunction. It is the only program of its kind in central Ohio.
Blog
Stuttering: Will My Child Outgrow It?
Stuttering is common when children are learning to talk. As a parent, this can be a stressful time full of questions. It’s difficult to know what is normal and what isn’t.
Blog
Speech Disorders in Children
If you’ve ever wondered if your child’s early speech development is on track, you are not alone. It can be difficult to know what is typical for a child’s age and when to be concerned.
Article
Outpatient Adolescent Neurologic Rehabilitation
We provide specialized neurological and adaptive training and rehabilitation for adolescents. Our expert team treats patients with acquired neurologic diagnoses and congenital neuromuscular diagnoses.
Provider
Jennifer L Haney
Jennifer Haney, MA, CCC-SLP, BCS-S, is Speech Pathology Program Manager at Nationwide Children's Hospital.
News
Two Brothers Born With Forms of Cleft Lip and Palate Raises Awareness of Condition and Risk Factors
Carter and Mason Osborne have a lot in common. Not only are they brothers who love to laugh, they also share one unique characteristic; they were born with forms of cleft lip and palate.
Meet Our Team
Our nationally recognized team offers children and their families comprehensive care.
Blog
From Speech and Hearing to School Readiness: Supporting Early Learning
As your child begins Kindergarten, you’ll need to prepare him or her for the many tests that lie ahead over the years. The Ohio Department of Education recommends that ALL children entering Kindergarten have a developmental screening.
Condition
22q Deletion Syndrome
22q11.2 deletion syndrome, also known as DiGeorge Syndrome, is a condition where there is a small amount of genetic material missing (a microdeletion) on the long arm (the q arm) of chromosome 22. 22q has the potential to impact every system in the body and can lead to a range of health issues.