Path: utzoo!utgpu!news-server.csri.toronto.edu!cs.utexas.edu!usc!snorkelwacker!mintaka!yale!bunker!wtm From: news@brian386.uucp (Brian McCane) Newsgroups: misc.handicap Subject: Waardenburg's Syndrome Message-ID: <13021@bunker.UUCP> Date: 23 Jul 90 20:03:49 GMT Sender: wtm@bunker.UUCP Reply-To: news@brian386.uucp (Brian McCane) Distribution: misc Organization: McCane Consulting Lines: 17 Approved: wtm@bunker.UUCP Fidonet: Silent Talk Conference Index Number: 9395 My wife has a very mild form of Waardenburg's Syndrome. Back in December, we had a baby girl, Lindsey. We recognized the features caused by the Syndrome, (white forelock, bow shaped mouth, and licanthic eyes (we had done a LOT of research before we had her)). Anyway, we took her in for a hearing test and found out that she was in fact deaf (105 loss left, 85 loss right). What I am getting around to asking, is has anyone had a child diagnosed as being deaf at such an early age, (< 6 weeks), and if so, what were you able to do to help her at that age. We have people from Ski-Hi helping US, but it doesn't seem like anything is being done for her. Speech pathologists at the nearest children's hospital say that there is not much that can be done to help her until she is old enough to be trained on how to take hearing tests to better ascertain just how deaf she is. What can I do now??? brian