<?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/"
	xmlns:media="http://search.yahoo.com/mrss/"
		>
<channel>
	<title>Comments on: Positives not negatives</title>
	<atom:link href="http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/feed/" rel="self" type="application/rss+xml" />
	<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/</link>
	<description>Family with a twist</description>
	<lastBuildDate>Mon, 19 Oct 2009 16:56:57 +0000</lastBuildDate>
	<generator>http://wordpress.com/</generator>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
		<item>
		<title>By: Here we go again &#171; Terrible Palsy</title>
		<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-5332</link>
		<dc:creator>Here we go again &#171; Terrible Palsy</dc:creator>
		<pubDate>Fri, 29 Jun 2007 01:43:08 +0000</pubDate>
		<guid isPermaLink="false">http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-5332</guid>
		<description>[...] negatives when it comes to speaking about people with disabilities. I have ranted about this before here. Actually, I&#8217;ve ranted about it quite a lot of times before. Like [...]</description>
		<content:encoded><![CDATA[<p>[...] negatives when it comes to speaking about people with disabilities. I have ranted about this before here. Actually, I&#8217;ve ranted about it quite a lot of times before. Like [...]</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Karen</title>
		<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-469</link>
		<dc:creator>Karen</dc:creator>
		<pubDate>Sat, 13 Jan 2007 01:30:18 +0000</pubDate>
		<guid isPermaLink="false">http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-469</guid>
		<description>Ok, I have three deaf and hard of hearing kids.  Where&#039;s my trophy? 

:)</description>
		<content:encoded><![CDATA[<p>Ok, I have three deaf and hard of hearing kids.  Where&#8217;s my trophy? </p>
<p> <img src='http://s.wordpress.com/wp-includes/images/smilies/icon_smile.gif' alt=':)' class='wp-smiley' /> </p>
]]></content:encoded>
	</item>
	<item>
		<title>By: The Life and Times of Emma</title>
		<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-450</link>
		<dc:creator>The Life and Times of Emma</dc:creator>
		<pubDate>Thu, 11 Jan 2007 19:06:56 +0000</pubDate>
		<guid isPermaLink="false">http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-450</guid>
		<description>[...] Positives not Negatives, Jacqui from Terrible Palsy shares her frustrations at the point scoring people with disabilities [...]</description>
		<content:encoded><![CDATA[<p>[...] Positives not Negatives, Jacqui from Terrible Palsy shares her frustrations at the point scoring people with disabilities [...]</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: terriblepalsy</title>
		<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-47</link>
		<dc:creator>terriblepalsy</dc:creator>
		<pubDate>Tue, 24 Oct 2006 21:42:27 +0000</pubDate>
		<guid isPermaLink="false">http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-47</guid>
		<description>I agree that even the same type of CP has different presentation in different people.  When we started conductive ed, Moo&#039;s teachers would come over to me and remark how particularly tight his legs are and I would be thinking, well isn&#039;t everybody&#039;s.  Apparently not.  ( I think I should have added a touch wood to my post about Moo&#039;s feet as the physio thinks that this could change if he actually gets up on them)

I met a lovely lady called Sass who has quad CP one day at the shopping centre - I was helping her get her groceries to her taxi as she had run out of room on her power chair.  Anyway, she was approached by a woman while I was helping her who basically accused her of taking the woman&#039;s funding for a power chair as she had been on the waiting list for over a year (and Sass&#039;s power chair was brand new and nice and shiny).  It was really one of those &quot;what the?&quot; situations.  This woman could obviously walk where Sass could obviously not and yet, she thought she was more entitled than Sass.

But my main moan at the moment relates to the articles I read every week in the local community paper.  There is article after article by families of children with disabilities saying basically &quot;our life is cr#p&quot; in order to get donations.  To me, by doing this, you are reinforcing negatives stereotypes and saying that the person with a disability&#039;s life is less valued than others.  That the family should be pitied by &quot;normal&quot; people.  I understand the need to try and get money from whatever source you can, but just wish they would do it with positives, not negatives.

And don&#039;t get me started on the family here that basically hi-jacked the government into giving them respite services by saying without it, they would put their child into foster care.  I could go on all day.</description>
		<content:encoded><![CDATA[<p>I agree that even the same type of CP has different presentation in different people.  When we started conductive ed, Moo&#8217;s teachers would come over to me and remark how particularly tight his legs are and I would be thinking, well isn&#8217;t everybody&#8217;s.  Apparently not.  ( I think I should have added a touch wood to my post about Moo&#8217;s feet as the physio thinks that this could change if he actually gets up on them)</p>
<p>I met a lovely lady called Sass who has quad CP one day at the shopping centre &#8211; I was helping her get her groceries to her taxi as she had run out of room on her power chair.  Anyway, she was approached by a woman while I was helping her who basically accused her of taking the woman&#8217;s funding for a power chair as she had been on the waiting list for over a year (and Sass&#8217;s power chair was brand new and nice and shiny).  It was really one of those &#8220;what the?&#8221; situations.  This woman could obviously walk where Sass could obviously not and yet, she thought she was more entitled than Sass.</p>
<p>But my main moan at the moment relates to the articles I read every week in the local community paper.  There is article after article by families of children with disabilities saying basically &#8220;our life is cr#p&#8221; in order to get donations.  To me, by doing this, you are reinforcing negatives stereotypes and saying that the person with a disability&#8217;s life is less valued than others.  That the family should be pitied by &#8220;normal&#8221; people.  I understand the need to try and get money from whatever source you can, but just wish they would do it with positives, not negatives.</p>
<p>And don&#8217;t get me started on the family here that basically hi-jacked the government into giving them respite services by saying without it, they would put their child into foster care.  I could go on all day.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Emma (WheelchairPrincess)</title>
		<link>http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-45</link>
		<dc:creator>Emma (WheelchairPrincess)</dc:creator>
		<pubDate>Tue, 24 Oct 2006 15:27:28 +0000</pubDate>
		<guid isPermaLink="false">http://terriblepalsy.wordpress.com/2006/10/24/positives-not-negatives/#comment-45</guid>
		<description>What you mean the &quot;I&#039;m more disabled then you are&quot; point scoring game?!  Yeah we have people who play that here too and I HATE IT.  Particularly when people who never need to use a wheelchair moan about not getting funding for one &quot;just in case&quot;  I would agree with pretty much everything you said in this post too.  I would also take it one step further and say that no two people with identical CP dx (i.e both me and Moo are dx with Spastic Diplegia CP) can understand what the other goes through because it is different in both of us - e.g i have issue w/ my feet which you&#039;ve said Moo does not.  But I think that might be where you were headed in this entry anyway.</description>
		<content:encoded><![CDATA[<p>What you mean the &#8220;I&#8217;m more disabled then you are&#8221; point scoring game?!  Yeah we have people who play that here too and I HATE IT.  Particularly when people who never need to use a wheelchair moan about not getting funding for one &#8220;just in case&#8221;  I would agree with pretty much everything you said in this post too.  I would also take it one step further and say that no two people with identical CP dx (i.e both me and Moo are dx with Spastic Diplegia CP) can understand what the other goes through because it is different in both of us &#8211; e.g i have issue w/ my feet which you&#8217;ve said Moo does not.  But I think that might be where you were headed in this entry anyway.</p>
]]></content:encoded>
	</item>
</channel>
</rss>
