Guest guest Posted October 26, 2000 Report Share Posted October 26, 2000 I have the opportunity to make some presentations to people from early intervention programs in connection with the beginning of the Newborn Hearing Screening Program in our state (California). My job, as parent coordinator, is to collect resources for parents of children who are identified through the newborn screening. I'm collecting lots of info, from this list, Kay's website, and from some other lists (although none is as good as this, and I refer people here from other lists frequently). My question for all of you has to do with getting this information out to the parents. My contact is through early intervention. What can I tell them that will help? Many of the parents in our area do not speak English, many have no computer access, and within that population, there is a strong bias toward believing whatever the professionals tell them. I would like to excerpt and edit, with identifying info deleted, the recent exchange in response to Lori's post, with all the diverse and heartfelt answers. May I get permission to do that, for the purpose of showing how valuable lists like this can be? Any advice will be gratefully accepted, whether I follow it or not. Judith Quote Link to comment Share on other sites More sharing options...
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