Researchers at the National Acoustic Laboratories (NAL) have found a treatment for a hearing problem affecting about 18,000 children that can be installed on a home computer.
The condition, Spatial Processing Disorder (SPD), makes it diffi
Researchers at the National Acoustic Laboratories (NAL) have found a treatment for a hearing problem affecting about 18,000 children that can be installed on a home computer.
The condition, Spatial Processing Disorder (SPD), makes it diffi
The Better Hearing Institute is drawing attention to the importance of hearing checks as an integral part of the Attention Deficit Hyperactivity Disorder (ADHD) diagnosis process. BHI also is encouraging appropriate treatment by a hearing h
About 1.1 million young people under the age of 18 in the United States have hearing loss, and only 16 percent of them use hearing aids. Studies show that children with even mild hearing loss, when left unaddressed, are at risk for learning and other social, emotional, behavioral, and self-image problems.
Hearing aids are the instrument of choice for the majority of the 26 million Americans with hearing loss, but for those who are deaf or severely hard of hearing, cochlear implants may be a better option. Both hearing aids and cochlear impla
Gallaudet University in Washington D.C. is accepting applications for the 3rd cohort of students for The Infants, Toddlers and their Families Interdisciplinary Graduate Certificate Program. The new cohort will begin in May 2013 with 3 days
To learn more, please visit Gallaudet’s Facebook page, https://www.facebook.com/GallaudetITFProgram or contact them at ITF@gallaudet.edu for more information.
The World Health Organization and UNICEF
recently published a new paper, Early Childhood Development and
Disability: A Discussion Paper (September 2012). The paper provides an
overview of disability in early childhood and underscores the need
to strengthen and scale up early childhood development initiatives, in
order to ensure that children with disabilities can participate
meaningfully in their homes, schools and communities. It is meant to
encourage international discussion, planning and action on issues
related to disability, early childhood development, and early
intervention. For free access to a pdf version of the discussion paper, click on the read more link!
Until recently, speech and language disorders
have been viewed as complex disorders produced by multiple-gene
interaction. Participant samples selected for genetics studies consisted
of affected children, their siblings, and, in some cases, the parents or even a multigenerational set of relatives; most samples represented many different families.
Audiology Online presents a Live Webinar: Quality in the Clinic: Design, Implementation and Measurement of the Patient Experience, scheduled for Wednesday, October 10, 2012 at 10:00 am MDT.
Course Abstract
As the delivery of health care e
CEUs/Hours Offered: AAA/0.1 Intermediate; ACAud/1.0; AHIP/1.0; ASHA/0.1 Intermediate, Professional; BAA/1.0; CAA/1.0; CASLPA/1.0; Calif. HADB/1.0 Hearing Aid Related; IHS/1.0
Limited seating is available for this interactive live webinar, so sign up now by following this link.
The sensory cells of the inner ear have tiny hairs called
stereocilia that play a critical part in hearing. It has long been known that
these stereocilia move sideways back and forth in a wave-like motion when
stimulated by a sound wave. After having designed a microscope to observe these
movements, a research team in Sweden has discovered that the hairs not only
move sideways but also change in length.
The discovery, which was made in collaboration with
scientists at Baylor College of Medicine in Texas, USA provides new fundamental
knowledge about the mechanisms of hearing. It is presented in the online
scientific journal Nature Communications.
The October edition of Probes and Tips is now available: OAE Hearing Screening in Home Settings. This edition includes such items as:
Researchers at the University of Cincinnati have found a new genetic mutation they believe may be responsible for deafness and hearing loss associated with Usher syndrome type 1. Follow this link to learn more about these findings, which were published in the Sept. 30 advance online edition of the journal Nature Genetics. This could help researchers develop new therapeutic targets for those at risk for this syndrome.