TVR_106-3
TVR_106-3
TVR_106-3
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young children with hearing loss may not be receiving the early intervention<br />
or other services they need in a timely manner that will enable them to<br />
enter preschool and school ready to succeed.<br />
As emphasized by this letter, the importance of providing effective early<br />
intervention services to DHH children is the focus of increased emphasis, and<br />
there is widespread agreement that the families of DHH infants and young<br />
children should have access to appropriate educational services in whatever<br />
mode of communication the family chooses (OSERS, 2006). However, this is<br />
impossible in many parts of the country because of serious shortages and<br />
inadequate geographical distribution of:<br />
• educational programs that use the most up-to-date methods for teaching<br />
language in the mode of communication selected by the family,<br />
• health care and education professionals who are trained and knowledgeable<br />
about current methods for effectively educating children with hearing<br />
loss,<br />
• adequate in-service training programs for individuals already in the field<br />
of deaf education and preservice programs for individuals entering the<br />
field and<br />
• information, public awareness and family support programs for helping<br />
families make informed decisions about the educational options for<br />
DHH children.<br />
The shortages noted above have occurred in part because of the success of<br />
universal newborn hearing screening. The fact that the average age of identification<br />
had gone from 30 months to three months during the past ten years<br />
means that there are many more DHH infants and toddlers to be served.<br />
Twenty years ago, most of these children were not identified until they were<br />
too old to qualify for birth-to-three programs. As shown in Figure 2, federally<br />
funded Part C programs that serve children ages birth to three have historically<br />
served between 1.2 and 2.3 percent of this population. Newborn hearing<br />
screening programs are adding another three children per thousand, which<br />
equates to a 17% increase in the average number of infants and toddlers<br />
served during the last 15 years. Such an increase is difficult for a program to<br />
accommodate when it is already seriously underfunded (Limb, McManus, &<br />
Fox, 2006).<br />
Another factor contributing to these shortages is that in most parts of the<br />
country, early intervention systems for DHH children were developed at a<br />
time when the majority of DHH children were not identified until two to five<br />
years of age, and digital hearing aids and cochlear implants were not available;<br />
thus, the nature of services provided was very different. Very few Part<br />
C early intervention providers have the specialized training necessary to<br />
provide state-of-the-art services to DHH infants and toddlers (Marge &<br />
Finishing the EHDI Revolution 241