<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
		>
<channel>
	<title>Comments on: How should doctors deliver a diagnosis of Down syndrome?</title>
	<atom:link href="http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/</link>
	<description>Disability News &#124; PatriciaEBauer.com</description>
	<lastBuildDate>Wed, 24 Nov 2010 22:50:59 +0000</lastBuildDate>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=3.3.1</generator>
	<item>
		<title>By: Tracy</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4868</link>
		<dc:creator>Tracy</dc:creator>
		<pubDate>Thu, 08 Oct 2009 16:27:41 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4868</guid>
		<description>I knew as soon as I saw my baby boy that he had Down Syndrome. I am 39 and had a triple screen that was high risk for Down syndrome, so I took it upon myself to educate myself about it.

When the doctors and staff finally mentioned it to me, they weren&#039;t telling me anything I didn&#039;t already know. Nobody said anything inappropriate, but really, who cares if they did? The general medical community, family and friends are not generally educated about Down syndrome. I think they all appreciated the fact I had understood my risk and prepared myself accordingly.

It saddened me that my son will likely have mental delays, and be more likely to have a litany of other maladies, but that didn&#039;t diminish how much I loved him. I wouldn&#039;t have traded him for a million dollars and a baby without DS. He is my son just like he is.</description>
		<content:encoded><![CDATA[<p>I knew as soon as I saw my baby boy that he had Down Syndrome. I am 39 and had a triple screen that was high risk for Down syndrome, so I took it upon myself to educate myself about it.</p>
<p>When the doctors and staff finally mentioned it to me, they weren&#8217;t telling me anything I didn&#8217;t already know. Nobody said anything inappropriate, but really, who cares if they did? The general medical community, family and friends are not generally educated about Down syndrome. I think they all appreciated the fact I had understood my risk and prepared myself accordingly.</p>
<p>It saddened me that my son will likely have mental delays, and be more likely to have a litany of other maladies, but that didn&#8217;t diminish how much I loved him. I wouldn&#8217;t have traded him for a million dollars and a baby without DS. He is my son just like he is.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: jawanda</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4865</link>
		<dc:creator>jawanda</dc:creator>
		<pubDate>Thu, 08 Oct 2009 01:51:40 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4865</guid>
		<description>I think that we can all agree that regardless of when parents receive the diagnosis of Down syndrome, it is difficult.  The challenge for all of us is to work to educate healthcare professionals, the media, and educators about what people with Down syndrome and other intellectual disabilities bring to this world.  These are the people who impact the decision making of parents and the public at-large. We need them to present accurate, up-to-date and UNBIASED information. Hence the Prenatally and Postnatally Diagnosed Conditions Awareness Act, known as the Kennedy Brownback Bill. Now let&#039;s make it happen!</description>
		<content:encoded><![CDATA[<p>I think that we can all agree that regardless of when parents receive the diagnosis of Down syndrome, it is difficult.  The challenge for all of us is to work to educate healthcare professionals, the media, and educators about what people with Down syndrome and other intellectual disabilities bring to this world.  These are the people who impact the decision making of parents and the public at-large. We need them to present accurate, up-to-date and UNBIASED information. Hence the Prenatally and Postnatally Diagnosed Conditions Awareness Act, known as the Kennedy Brownback Bill. Now let&#8217;s make it happen!</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Scott</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4864</link>
		<dc:creator>Scott</dc:creator>
		<pubDate>Wed, 07 Oct 2009 23:52:35 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4864</guid>
		<description>I&#039;d say the upwards of 80% termination rate for those who receive a pre-natal diagnosis of Down syndrome far outweighs any potential positives.

With that, I have a tremendous amount of respect for those who receive a pre-natal diagnosis and decide to have the baby.</description>
		<content:encoded><![CDATA[<p>I&#8217;d say the upwards of 80% termination rate for those who receive a pre-natal diagnosis of Down syndrome far outweighs any potential positives.</p>
<p>With that, I have a tremendous amount of respect for those who receive a pre-natal diagnosis and decide to have the baby.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Nancy Iannone</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4862</link>
		<dc:creator>Nancy Iannone</dc:creator>
		<pubDate>Wed, 07 Oct 2009 20:20:23 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4862</guid>
		<description>&quot;Don&#039;t get the test in the first place&quot; is truly NOT the answer to the inadequacies of delivering a prenatal diagnosis.  These words touch a nerve with many of us who have struggled over prenatal testing decisions. There are very real and concrete benefits of a prenatal diagnosis to both parents and child (as well as downsides).  Parents in post-diagnosis pregnancy have a LOT to deal with, including emotional turmoil, potential negative comments by doctors and loved ones, and fear and anxiety.  They certainly do not need to be made to feel separated in the Down syndrome community, with their reasons for undergoing invasive testing treated as frivolous.

I am so grateful these doctors took the time to analize this issue and hope it benefits many parents in the future.</description>
		<content:encoded><![CDATA[<p>&#8220;Don&#8217;t get the test in the first place&#8221; is truly NOT the answer to the inadequacies of delivering a prenatal diagnosis.  These words touch a nerve with many of us who have struggled over prenatal testing decisions. There are very real and concrete benefits of a prenatal diagnosis to both parents and child (as well as downsides).  Parents in post-diagnosis pregnancy have a LOT to deal with, including emotional turmoil, potential negative comments by doctors and loved ones, and fear and anxiety.  They certainly do not need to be made to feel separated in the Down syndrome community, with their reasons for undergoing invasive testing treated as frivolous.</p>
<p>I am so grateful these doctors took the time to analize this issue and hope it benefits many parents in the future.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: jawanda</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4860</link>
		<dc:creator>jawanda</dc:creator>
		<pubDate>Wed, 07 Oct 2009 17:47:17 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4860</guid>
		<description>I am just thinking if the best way to avoid a bad experience with a pre-natal diagnosis is to skip it in the first place, then the best way to avoid a bad experience with a post-natal diagnosis would be not to have a baby? That is not really a solution to the issue.

I had a pre-natal diagnosis. The experience was as good as it could have been under the circumstances. My doctor did a fine job - the best thing he did was not pass judgment. He gave me information and comfort and guidance. My doctor, my husband and I made the decision to have the pre-natal diagnosis. The day of my daughter&#039;s birth was one of the happiest days and greatest celebrations ever! My path. Not everyone&#039;s.</description>
		<content:encoded><![CDATA[<p>I am just thinking if the best way to avoid a bad experience with a pre-natal diagnosis is to skip it in the first place, then the best way to avoid a bad experience with a post-natal diagnosis would be not to have a baby? That is not really a solution to the issue.</p>
<p>I had a pre-natal diagnosis. The experience was as good as it could have been under the circumstances. My doctor did a fine job &#8211; the best thing he did was not pass judgment. He gave me information and comfort and guidance. My doctor, my husband and I made the decision to have the pre-natal diagnosis. The day of my daughter&#8217;s birth was one of the happiest days and greatest celebrations ever! My path. Not everyone&#8217;s.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Scott</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4854</link>
		<dc:creator>Scott</dc:creator>
		<pubDate>Tue, 06 Oct 2009 00:22:23 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4854</guid>
		<description>The best way to avoid a bad experience while receiving a pre-natal diagnosis - don&#039;t get the test in the first place.

After the blessed event, I don&#039;t think there is a good way to deliver the news.  

However, it certainly shouldn&#039;t happen when the mom is alone and it shouldn&#039;t be presented as a death sentence.</description>
		<content:encoded><![CDATA[<p>The best way to avoid a bad experience while receiving a pre-natal diagnosis &#8211; don&#8217;t get the test in the first place.</p>
<p>After the blessed event, I don&#8217;t think there is a good way to deliver the news.  </p>
<p>However, it certainly shouldn&#8217;t happen when the mom is alone and it shouldn&#8217;t be presented as a death sentence.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Lance Boldt</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4850</link>
		<dc:creator>Lance Boldt</dc:creator>
		<pubDate>Sat, 03 Oct 2009 19:06:16 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4850</guid>
		<description>About 5 minutes after our son was born, our doctor told us that he suspected Down syndrome. He delivered the news very compassionately. However, he was unprepared to answer any of our questions, but did arrange for a specialist to come in later that day to talk with us. That was very helpful â€“ but it was a frightening wait.

We didn&#039;t leave the hospital with a single scrap of paper (this was before the internet) â€“ it took us about a month to locate resources on our own. They did offer to have us talk with a nurse who had a son with DS â€“ but he was in his twenties and we wanted to talk with parents with an infant or toddler â€“ the gap between our baby and a man with Down syndrome seemed to wide to comprehend.

After my first meeting with other parents of children with disabilities (about 6 months later) I saw how we were all struggling with &quot;why&quot;. The next morning I awoke with a story in my head. Here&#039;s a link to it. It helped us and has been well received by others as well.

http://tinyurl.com/secretjourney</description>
		<content:encoded><![CDATA[<p>About 5 minutes after our son was born, our doctor told us that he suspected Down syndrome. He delivered the news very compassionately. However, he was unprepared to answer any of our questions, but did arrange for a specialist to come in later that day to talk with us. That was very helpful â€“ but it was a frightening wait.</p>
<p>We didn&#8217;t leave the hospital with a single scrap of paper (this was before the internet) â€“ it took us about a month to locate resources on our own. They did offer to have us talk with a nurse who had a son with DS â€“ but he was in his twenties and we wanted to talk with parents with an infant or toddler â€“ the gap between our baby and a man with Down syndrome seemed to wide to comprehend.</p>
<p>After my first meeting with other parents of children with disabilities (about 6 months later) I saw how we were all struggling with &#8220;why&#8221;. The next morning I awoke with a story in my head. Here&#8217;s a link to it. It helped us and has been well received by others as well.</p>
<p><a href="http://tinyurl.com/secretjourney" rel="nofollow">http://tinyurl.com/secretjourney</a></p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Diana</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4849</link>
		<dc:creator>Diana</dc:creator>
		<pubDate>Sat, 03 Oct 2009 17:39:48 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4849</guid>
		<description>My recommendation is to try to wait (if possible) until a patient is already scheduled to come to the office, so that they&#039;re not already figuring out it is some kind of unwelcome news. I was called at work &amp; told I needed to come in to discuss my amnio. I am 41, and this is my 3rd baby. Obviously, I knew something was up. This was a Thursday, and I had an appointmet that Monday. I was a few days shy of 17 weeks pregnant, so there was no emergency in letting me know that day. Instead, I wound up immediately driving to my drs&#039; office, which was a 45 minute car ride from my job, in a torrential downpour, by myself, hysterically sobbing all the way. It is no wonder I didn&#039;t get killed in a car accident on the way there. When I got there, my dr said it was bad news, and told me I had time to make a decision. I had already decided I was keeping my baby no matter what, and I expressed that right then &amp; there,  so it would have been nice to hear some of the positives, and given some encouragemnet on raising a baby with Down Syndrome, instead of feeling like I had been given a death sentence. In my doctor&#039;s defense, he didn&#039;t harp on termination, like some doctors do, and when I explained how I felt at my next appointment, his partner apologized profusely and said she was glad I shared how I felt about how I was told, because they wanted to grow as doctors and that included being open to learning a better way to deliver news like this. They both turned out to be sympathetic and supportive my whole pregnancy, up to and including when I had to change to a high-risk OB. They wanted me to make sure I still came to them if I needed anything at all.</description>
		<content:encoded><![CDATA[<p>My recommendation is to try to wait (if possible) until a patient is already scheduled to come to the office, so that they&#8217;re not already figuring out it is some kind of unwelcome news. I was called at work &amp; told I needed to come in to discuss my amnio. I am 41, and this is my 3rd baby. Obviously, I knew something was up. This was a Thursday, and I had an appointmet that Monday. I was a few days shy of 17 weeks pregnant, so there was no emergency in letting me know that day. Instead, I wound up immediately driving to my drs&#8217; office, which was a 45 minute car ride from my job, in a torrential downpour, by myself, hysterically sobbing all the way. It is no wonder I didn&#8217;t get killed in a car accident on the way there. When I got there, my dr said it was bad news, and told me I had time to make a decision. I had already decided I was keeping my baby no matter what, and I expressed that right then &amp; there,  so it would have been nice to hear some of the positives, and given some encouragemnet on raising a baby with Down Syndrome, instead of feeling like I had been given a death sentence. In my doctor&#8217;s defense, he didn&#8217;t harp on termination, like some doctors do, and when I explained how I felt at my next appointment, his partner apologized profusely and said she was glad I shared how I felt about how I was told, because they wanted to grow as doctors and that included being open to learning a better way to deliver news like this. They both turned out to be sympathetic and supportive my whole pregnancy, up to and including when I had to change to a high-risk OB. They wanted me to make sure I still came to them if I needed anything at all.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: sue</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4848</link>
		<dc:creator>sue</dc:creator>
		<pubDate>Sat, 03 Oct 2009 12:45:27 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4848</guid>
		<description>My recommendation for a postnatal dx?  Let me hold my child first.  I was robbed of the first moments of my child&#039;s life because I was not able to hold him before they told me they thought he had Ds.  This is after the prenatal quad screen was &quot;messed up&quot; by the lab, but they assured me there were no soft markers in the ultrasound, plus I&#039;m young.  Anyway, it would have been great to have had time to hold him and love him without the proverbial elephant in the room.  Now when I look at him now, I see the baby, not the dx, but you never get to make a new memory of those first few moments of life back.</description>
		<content:encoded><![CDATA[<p>My recommendation for a postnatal dx?  Let me hold my child first.  I was robbed of the first moments of my child&#8217;s life because I was not able to hold him before they told me they thought he had Ds.  This is after the prenatal quad screen was &#8220;messed up&#8221; by the lab, but they assured me there were no soft markers in the ultrasound, plus I&#8217;m young.  Anyway, it would have been great to have had time to hold him and love him without the proverbial elephant in the room.  Now when I look at him now, I see the baby, not the dx, but you never get to make a new memory of those first few moments of life back.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Heather</title>
		<link>http://www.patriciaebauer.com/2009/10/02/down-syndrome-diagnosis-23265/comment-page-1/#comment-4847</link>
		<dc:creator>Heather</dc:creator>
		<pubDate>Sat, 03 Oct 2009 03:59:53 +0000</pubDate>
		<guid isPermaLink="false">http://www.patriciaebauer.com/?p=23265#comment-4847</guid>
		<description>I applaud this recommendation in particular:  &quot;Women who received the news prenatally said they wished to hear it in person or at a pre-established time by phone.&quot;  What comes over medical professionals and their sense of timing?  Is it that much of a 911 emergency that they MUST hound us out of meetings, classes and simply grocery shopping?  My prenatal test results were delivered unexpectedly by phone in the middle of a busy, stress filled law firm.  Hardly the place to fall apart.  Keeping ones &quot;Game Face&quot; on is expected though near impossible at times like that.</description>
		<content:encoded><![CDATA[<p>I applaud this recommendation in particular:  &#8220;Women who received the news prenatally said they wished to hear it in person or at a pre-established time by phone.&#8221;  What comes over medical professionals and their sense of timing?  Is it that much of a 911 emergency that they MUST hound us out of meetings, classes and simply grocery shopping?  My prenatal test results were delivered unexpectedly by phone in the middle of a busy, stress filled law firm.  Hardly the place to fall apart.  Keeping ones &#8220;Game Face&#8221; on is expected though near impossible at times like that.</p>
]]></content:encoded>
	</item>
</channel>
</rss>

