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	<title>We Cue! &#187; Mary-Beth Robie</title>
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	<link>http://wecue.net</link>
	<description>Discussion on how to live, learn, and work using Cued Speech</description>
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		<title>Connections Within the Family</title>
		<link>http://wecue.net/2008/06/connections-within-the-family/</link>
		<comments>http://wecue.net/2008/06/connections-within-the-family/#comments</comments>
		<pubDate>Sun, 22 Jun 2008 17:55:38 +0000</pubDate>
		<dc:creator>Mary-Beth Robie</dc:creator>
				<category><![CDATA[About Cued Speech]]></category>
		<category><![CDATA[Adults]]></category>
		<category><![CDATA[Personal Stories]]></category>

		<guid isPermaLink="false">http://wecue.net/?p=30</guid>
		<description><![CDATA[To come from a family where each of my immediate family members learned how to cue is something I consider a blessing. I even put my life on the line by trying to teach the family cat how to expressively cue to me. I would take her paw and try to move it around her [...]]]></description>
			<content:encoded><![CDATA[<p class="MsoNormal">To come from a family where each of my immediate family members learned how to cue is something I consider a blessing.<span> </span>I even put my life on the line by trying to teach the family cat how to expressively cue to me. I would take her paw and try to move it around her chin/mouth area with the only possible handshape which was handshape 5.<span> </span>I have a scar on my right cheek to prove it.</p>
<p class="MsoNormal">Mom and Dad learned how to cue almost immediately after the diagnosis of my profound bilateral hearing loss. All three sisters learned the system the same way I did which was visually.<span> </span>Mom has told me there is a picture of my younger sister cueing in the playroom when she was 18 months old.<span> </span></p>
<p class="MsoNormal">My speech was basically unintelligible for the first few years of my life. <span> </span>Luckily, all family members were able to cue read so they could understand me. While it is a task for most parents to learn the communication mode they choose for their deaf/hoh child, I consider it extremely important for families to make sure the other siblings or family members who live in the same household (if any) learn the modality too.</p>
<p class="MsoNormal">Inclusion is important for every person in the household whether it be the hearing person trying to understand the deaf/hoh person or vice versa.<span> </span>One way hearing people build their vocabulary and literacy level on a daily basis is by picking up information through what is heard verbally.<span> </span>Some deaf/hoh individuals acquire their language visually; so every word they see is equally important.<span> </span>Now, I grew up with times where I felt frustrated because two people were having a conversation and I didnâ€™t understand everything that was said so I would ask the two parties to repeat.<span> </span>They would respond with â€œOh, it was nothing importantâ€, or they would summarize the conversation from 10 sentences into one sentence.<span> </span>I would rather have had them repeat all 10 sentences to me because even the little details matter in building language.</p>
<p class="MsoNormal">Making an effort to understand every word the deaf/hoh individual communicates will most likely secure the relationships between them and family members.<span> </span>It may be a frustrating process at first while trying to learn how to cue read.<span> </span>In the long run, it should pay off. After all, the deaf/hoh individual wants to fit in with the family and be able to express all of his/her feelings knowing they will be understood to the full extent.</p>
<p class="MsoNormal">In conclusion, it is beneficial if all immediate family members learn the modality chosen for the deaf/hoh individual.<span> </span>It will bring the family closer together.<span> </span>While it is not easy to cue or lipread every word said, it is important to try to include all family members whether they are hearing or deaf/hoh.<span> </span>Every word counts.</p>
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		<title>Giving Back: Ten Years Later</title>
		<link>http://wecue.net/2008/05/giving-back-ten-years-later/</link>
		<comments>http://wecue.net/2008/05/giving-back-ten-years-later/#comments</comments>
		<pubDate>Thu, 29 May 2008 12:07:43 +0000</pubDate>
		<dc:creator>Mary-Beth Robie</dc:creator>
				<category><![CDATA[About Cued Speech]]></category>
		<category><![CDATA[Adults]]></category>

		<guid isPermaLink="false">http://wecue.net/?p=21</guid>
		<description><![CDATA[Ten years ago, I was asked to meet a family with a daughter who had been diagnosed with a profound bilateral hearing loss. This was a first for me. By no means did I know what the role of a deaf model meant. After all, I grew up in a rural town 20 miles north [...]]]></description>
			<content:encoded><![CDATA[<p class="MsoNormal">Ten years ago, I was asked to meet a family with a daughter who had been diagnosed with a profound bilateral hearing loss.<span> </span>This was a first for me.<span> </span>By no means did I know what the role of a deaf model meant.<span> </span>After all, I grew up in a rural town 20 miles north of Burlington, Vermont.<span> </span>At the time and throughout most of my elementary and high school education, I was the only deaf child in the state of Vermont who used Cued Speech.</p>
<p class="MsoNormal">I vividly remember being high strung over meeting the parents.<span> </span>It doesnâ€™t help I have a shy personality when I first meet people. I found it mind boggling when asked about my deafness, my cochlear implant, and how I function on a daily basis. Rather than out of curiosity, those two adults wanted information from me as a deaf person.<span> </span>Thoughts swarmed through my mind as I wondered what I should say and what I shouldnâ€™t say because I knew every answer I give them would most likely affect their future decisions for their deaf first born.</p>
<p class="MsoNormal">Fast-forward ten years later, I have reached the point in life where I am content with who I am as a deaf adult.<span> </span>Between then and now, I went through a period where I discovered my deaf identity and the pride I carry as a deaf person.<span> </span>Giving back to the Northern Vermont community I was born and raised in for 18 years is something I have yearned to do.<span> </span>I was granted the rare window of opportunity to meet with this family again along with another family who has a deaf son. I had never been more enthusiastic.</p>
<p class="MsoNormal">My former Teacher of the Deaf who also works with these students emailed a list of questions they wanted to ask me.<span> </span>During the long 16-hour car ride from Chicago to Vermont I discussed these questions with my boyfriend, Aaron, who is also an adult deaf cuer.<span> </span>I continuously learn something new about myself when under pressure to think about growing up as a deaf cuer.<span> </span>For instance, I realized how much time my transliterator dedicated to serving me along with the countless hours my parents put in advocating for my rights and needs.<span> </span></p>
<p class="MsoNormal">We spent an hour listening to the kids interview us and we answered by cueing back in brief sentences since time was limited.<span> </span>After that session was finished, we sat down with the parents and let them ask us questions and we responded the best we could.<span> </span>There really isnâ€™t one answer that will satisfy all parents because each individual has different experiences and needs.</p>
<p class="MsoNormal">The Cued Speech community is indeed a very small one. Each time I am able to share my story and offer some input, I leave knowing I helped at least one person.<span> </span>It is a gratifying feeling and allows me to continue my journey advocating Cued Speech with increased perseverance.<span> </span></p>
<p class="MsoNormal">I look forward to the next ten years.</p>
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