<?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>Sickle Cell Cure Foundation&#187; Living with SCD</title>
	<atom:link href="http://sicklecellcurefoundation.org/category/living-with-sickle-cell-disease/feed" rel="self" type="application/rss+xml" />
	<link>http://sicklecellcurefoundation.org</link>
	<description>a nonprofit corporation working to cure sickle cell disease</description>
	<lastBuildDate>Tue, 03 Apr 2012 23:19:40 +0000</lastBuildDate>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=3.3.2</generator>
		<item>
		<title>Living with Sickle Cell Disease (SCD)</title>
		<link>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/living-with-sickle-cell-disease-scd</link>
		<comments>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/living-with-sickle-cell-disease-scd#comments</comments>
		<pubDate>Sun, 25 Oct 2009 00:38:13 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Living with SCD]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.ecoonamoly.com/?p=59</guid>
		<description><![CDATA[For thousands of Americans, living with sickle cell disease means a lifetime of painful episodes, blood transfusions and frequent trips to the hospital. These treatments can often cause complications that are just as bad or worse than the effects of the disease itself. Sickle cell disease (SCD) is an inherited genetic disorder that affects red [...]]]></description>
		<wfw:commentRss>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/living-with-sickle-cell-disease-scd/feed</wfw:commentRss>
		<slash:comments>3</slash:comments>
		</item>
		<item>
		<title>J.R. Perry III and his son Jameel</title>
		<link>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/j-r-perry-iii-and-his-son-jameel</link>
		<comments>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/j-r-perry-iii-and-his-son-jameel#comments</comments>
		<pubDate>Sat, 24 Oct 2009 00:39:21 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[j.r. perry III]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.ecoonamoly.com/?p=61</guid>
		<description><![CDATA[Jameel was born in 1999, and within 2 hours of his birth his father J.R. knew that his son would suffer from sickle cell disease. J.R. has devoted the rest of his life to raising awareness of SCD and the need for a cure. A musician, song-writer, promoter, and talk show host, J.R. Perry has [...]]]></description>
		<wfw:commentRss>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/j-r-perry-iii-and-his-son-jameel/feed</wfw:commentRss>
		<slash:comments>16</slash:comments>
		</item>
		<item>
		<title>National Sickle Cell Month</title>
		<link>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/national-sickle-cell-month</link>
		<comments>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/national-sickle-cell-month#comments</comments>
		<pubDate>Fri, 04 Sep 2009 23:05:36 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[clinical trials]]></category>
		<category><![CDATA[non-profit]]></category>
		<category><![CDATA[sickle cell cure foundation]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>
		<category><![CDATA[sickle cell disease cure]]></category>
		<category><![CDATA[united states patent]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.org/?p=743</guid>
		<description><![CDATA[The Sickle Cell Cure Foundation, Inc. (SCCF) has made significant progress in recent months, including a U.S. patent issued 14 April 2009, and further laboratory discoveries showing that less DREPAC is needed than previously believed to reverse sickle cell! To keep this progress going, we need your help! It is our goal to have clinical [...]]]></description>
		<wfw:commentRss>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/national-sickle-cell-month/feed</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
		<item>
		<title>Alicia and Dominick Bibbs</title>
		<link>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/alicia-and-dominick-bibbs</link>
		<comments>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/alicia-and-dominick-bibbs#comments</comments>
		<pubDate>Sat, 08 Aug 2009 23:44:03 +0000</pubDate>
		<dc:creator>broylesr</dc:creator>
				<category><![CDATA[Living with SCD]]></category>
		<category><![CDATA[News]]></category>
		<category><![CDATA[Sickle Cell Disease]]></category>

		<guid isPermaLink="false">http://sicklecellcurefoundation.ecoonamoly.com/?p=220</guid>
		<description><![CDATA[Alicia Bibbs, an SCCF founder &#38; research student, is pictured with her brother Dominick who suffers from sickle cell disease and recently recovered from surgery to have his spleen and gall bladder removed.]]></description>
		<wfw:commentRss>http://sicklecellcurefoundation.org/living-with-sickle-cell-disease/alicia-and-dominick-bibbs/feed</wfw:commentRss>
		<slash:comments>7</slash:comments>
		</item>
	</channel>
</rss>

