<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	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:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Tony Chachere&#039;s Blog &#187; Great Strides</title>
	<atom:link href="http://blog.tonychachere.com/tag/great-strides/feed/" rel="self" type="application/rss+xml" />
	<link>http://blog.tonychachere.com</link>
	<description>Because Tony&#039;s makes everything taste better</description>
	<lastBuildDate>Fri, 02 Dec 2011 16:07:37 +0000</lastBuildDate>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=3.2.1</generator>
		<item>
		<title>Great Strides</title>
		<link>http://blog.tonychachere.com/2010/05/12/great-strides/</link>
		<comments>http://blog.tonychachere.com/2010/05/12/great-strides/#comments</comments>
		<pubDate>Wed, 12 May 2010 18:07:02 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Cystic Fibrosis]]></category>
		<category><![CDATA[Great Strides]]></category>
		<category><![CDATA[Tony Chachere]]></category>

		<guid isPermaLink="false">http://blog.tonychachere.com/?p=636</guid>
		<description><![CDATA[When we signed up to cook for Great Strides for CF, I knew I was doing a good thing. I knew this was an event that would give me warm fuzzies and I could be proud of. I had no idea how touched I would be by the story of one little boy and his struggles each and everyday.]]></description>
			<content:encoded><![CDATA[<p>We decided to cook for the <a href="http://www.cff.org/Chapters/batonrouge/GREATSTRIDES/" target="_blank">Cystic Fibrosis Foundation&#8217;s Great Strides</a> because of Kayla. Kayla has been a member of the <a href="http://www.tonychachere.com/" target="_blank">Tony Chachere&#8217;s</a> family for a few years now as the head of housekeeping. When I  came to work for the company, Kayla and I became fast friends. After a few months of knowing Kayla she shared with me the story of her son, Christopher. Christopher was born July 24, 1989 and fought every day of his 5 months on this earth as the doctors searched for a diagnosis and cure for ailed the precious little boy. It is only after this death that he was diagnosed with CF.</p>
<div id="attachment_639" class="wp-caption aligncenter" style="width: 222px"><a href="http://blog.tonychachere.com/wp-content/uploads/2010/05/Kayla2.jpg"><img class="size-medium wp-image-639" title="Christopher" src="http://blog.tonychachere.com/wp-content/uploads/2010/05/Kayla2-212x300.jpg" alt="" width="212" height="300" /></a><p class="wp-caption-text">Christopher</p></div>
<p style="text-align: center;">
<p style="text-align: left;">While cooking for Great Strides, Kayla and I were able to spend time with a wonderful little boy named Anthony. Anthony is 2 1/2 years old and was diagnosed with CF in infancy. He is a very short boy for 2 1/2 but that is one of the symptoms of CF and his body not being able to digest what he eats without the help of enzymes. He was like any other 2 year old in some ways; full of energy, sweet as can be, and even said &#8220;cheese&#8221; to take a picture with us. According to his grandmother, Denise, Anthony is continually surprising his doctors and they are learning so much about CF from his case.</p>
<div id="attachment_637" class="wp-caption aligncenter" style="width: 310px"><a href="http://blog.tonychachere.com/wp-content/uploads/2010/05/Anthony-in-the-hospital.jpg"><img class="size-medium wp-image-637" title="Anthony in the hospital" src="http://blog.tonychachere.com/wp-content/uploads/2010/05/Anthony-in-the-hospital-300x225.jpg" alt="" width="300" height="225" /></a><p class="wp-caption-text">Anthony</p></div>
<p style="text-align: left;">Christopher, Anthony, and many babies like them have helped with the research on CF and how to treat it. CF is a genetic disorder where thick mucus is found in the lungs and digestive tract. This disease is fatal with a maximum life expectancy of 37.2 years (an improvement over years past). Children and young adults with CF have delayed growth, belly pain from severe constipation, and recurring pneumonia as just a few of the symptoms. their daily life includes inhaled medicines to open their airways, enzymes to help with digestion, and chest percussions and drainage up to 4 times a day. This is not the life you think of for a young child.</p>
<p style="text-align: center;">
<div id="attachment_638" class="wp-caption aligncenter" style="width: 310px"><a href="http://blog.tonychachere.com/wp-content/uploads/2010/05/Anthony.jpg"><img class="size-medium wp-image-638" title="Anthony" src="http://blog.tonychachere.com/wp-content/uploads/2010/05/Anthony-300x199.jpg" alt="" width="300" height="199" /></a><p class="wp-caption-text">Kayla, Anthony and Samantha</p></div>
<p style="text-align: left;">Great Strides is a fundraiser put on by the <a href="http://http://www.cff.org/" target="_blank">Cystic Fibrosis Foundation</a> in an effort to educate and raise money for CF research. The event is a 6.2 mile walk (so that you can feel what CF child&#8217;s every breath is like) followed by children&#8217;s activites, food and festivities. It was a great crowd for a great cause and we hope to be invited back next year.</p>
<p>Samantha Moreau<br />
Sales &amp; Marketing Assistant</p>
<p><a href="http://twitter.com/samanthamoreau" target="_blank">Follow Samantha on Twitter!</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.tonychachere.com/2010/05/12/great-strides/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>

