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	<title>Sickle Cell Foundation Inc.</title>
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	<link>http://sicklecellfoundation.org</link>
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		<title>New Treatment for Sickle Cell Brings Hope and a Cure to Chicago Area Patients</title>
		<link>http://sicklecellfoundation.org/363/</link>
		<comments>http://sicklecellfoundation.org/363/#comments</comments>
		<pubDate>Tue, 26 Mar 2013 16:50:47 +0000</pubDate>
		<dc:creator>Jill</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sicklecellfoundation.org/?p=363</guid>
		<description><![CDATA[Description Thanks to a third brother, two brothers were cured of sickle cell disease through a relatively uncommon type of stem cell transplant without chemotherapy. New Treatment for Sickle Cell Brings Hope and a Cure to Chicago Area Patients Released: 3/4/2013 5:45 PM EST Source Newsroom: University of Illinois at Chicago more news from this ...]]></description>
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<td><span style="font-size: 1em; line-height: 19px;">Description</span><br />
Thanks to a third brother, two brothers were cured of sickle cell disease through a relatively uncommon type of stem cell transplant without chemotherapy.</p>
<h1><a title="Permalink to article 599907" href="file:///C:/articles/new-treatment-for-sickle-cell-brings-hope-and-a-cure-to-chicago-area-patients">New Treatment for Sickle Cell Brings Hope and a Cure to Chicago Area Patients </a></h1>
<p><strong>Released:</strong> 3/4/2013 5:45 PM EST<br />
<strong>Source Newsroom:</strong> <a href="file:///C:/institutions/newsroom/126/">University of Illinois at Chicago</a></p>
<p><a href="file:///C:/institutions/newsroom/126/">more news from this source</a></p>
<p>Newswise — Two brothers have been cured of their sickle cell disease at the University of Illinois Hospital &amp; Health Sciences System using a relatively uncommon type of stem cell transplant that is performed without chemotherapy.</p>
<p>Their transplants were possible thanks to a third brother who was a match for both, against long odds.</p>
<p>Julius and Desmond Means never imagined life without sickle cell. The brothers, ages 25 and 19, have spent their lives in and out of hospitals, each suffering from different complications of the disease.</p>
<p>Growing up, they tired easily and couldn&#8217;t keep up with their friends. As they grew older, the disease caused bone damage and affected Julius&#8217;s lungs. Desmond&#8217;s organs were also being damaged, and he was jaundiced.</p>
<p>For either young man to receive a transplant, a healthy sibling who is a compatible donor was needed. An acceptable match requires that at least eight of 10 known human leukocyte antigen (H.L.A.) genes be identical between donor and recipient.</p>
<p>Julius and Desmond&#8217;s healthy older brother Clifford, 27, matched 10 of 10 H.L.A. genes with both of them &#8212; an occurrence of &#8220;extremely low&#8221; likelihood, according to Dr. Damiano Rondelli, director of stem-cell transplantation at UI Health. The men&#8217;s mother, Beverly Means, also noted the good fortune.</p>
<p>&#8220;I had won the lottery of health,&#8221; she said.</p>
<p>In preparation for the transplant, Clifford was given medication to increase the number of stems cells released from the bone marrow into the bloodstream. His blood was then processed through a machine that collects white cells, including stem cells. The stem cells were frozen until the transplants.</p>
<p>Last May, Julius received his transplant at UI Hospital. He was given medication to suppress his immune system and one small dose of total body radiation right before the transplant. Then the frozen bags of stem cells were thawed and hung by IV pole for infusion into him.</p>
<p>Then in September, Desmond received his stem cell transplant.</p>
<p>Now several months since the transplants, both Julius and Desmond no longer have sickle cell disease. Their bone marrow is producing healthy red blood cells.</p>
<p>&#8220;Being cured, I feel like we can do anything,&#8221; says Julius, who composed a rap about his transplant while recovering in the hospital. The brothers are pursuing their interests in rap music and dance and plan to attend college.</p>
<p>The chemotherapy-free stem cell transplant is a new procedure and is much better-tolerated by patients with aggressive sickle cell disease, who often have underlying organ damage and other complications.</p>
<p>UI Health is the first center in the Chicago area to offer this treatment, and one other patient has been successfully transplanted here. The efficacy and safety of the pre-transplant medication regimen are currently being studied at UI Health.</p>
<p>About 30 adults have received chemotherapy-free stem cell transplants for sickle cell disease at the National Institutes of Health in Bethesda, Md. Approximately 85 percent have been cured.</p>
<p>Sickle cell affects as many as 100,000 people in the U.S., predominantly of African ancestry. The disease is an inherited defect that causes the red blood cells to become crescent-shaped. These cells can obstruct small blood vessels, depriving the body&#8217;s tissues of oxygen. The disease can cause extreme pain and damage the lungs, heart, kidneys and liver. Stroke and other complications can be life-threatening.</p>
<p>The University of Illinois Hospital &amp; Health Sciences System provides comprehensive care, education and research to the people of Illinois and beyond. The UI Health System includes a 495-bed tertiary hospital; the University of Illinois at Chicago colleges of Medicine, Dentistry, Pharmacy, Nursing, and Applied Health Sciences, the UIC School of Public Health and UIC’s Jane Addams College of Social Work; 22 outpatient clinics located in Chicago; 12 federally qualified health centers throughout the city; and College of Medicine and affiliated health care facilities in Urbana, Peoria and Rockford.</p>
<p>For more information about the University of Illinois Hospital &amp; Health Sciences System visit <a href="http://www.hospital.uillinois.edu/">www.hospital.uillinois.edu</a>.</p>
<p><a title="Permalink" href="file:///C:/articles/new-treatment-for-sickle-cell-brings-hope-and-a-cure-to-chicago-area-patients"><em>Permalink to this article</em></a></td>
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<li>©2013 Newswise, Inc.</li>
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<p>&nbsp;</p>
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		<title>2012 Crescent Moon Gala Courage Award Winner Meet Angela Holloman!</title>
		<link>http://sicklecellfoundation.org/2012-crescent-moon-gala-courage-award-winner-meet-angela-holloman/</link>
		<comments>http://sicklecellfoundation.org/2012-crescent-moon-gala-courage-award-winner-meet-angela-holloman/#comments</comments>
		<pubDate>Wed, 22 Aug 2012 14:32:55 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sicklecellfoundation.org/?p=319</guid>
		<description><![CDATA[Angela Holloman is the 2012 Courage Award winner for the Annual Crescent Moon Gala. To hold a title such as the Courage Award Winner, Holloman said she was honored. “I felt like I was not alone, other people understood where I was coming from. That one moment vindicates everything I went through,” Holloman said. Holloman ...]]></description>
				<content:encoded><![CDATA[<p>Angela Holloman is the 2012 Courage Award winner for the Annual Crescent Moon Gala. To hold a title such as the Courage Award Winner, Holloman said she was honored. “I felt like I was not alone, other people understood where I was coming from. That one moment vindicates everything I went through,” Holloman said.</p>
<p>Holloman has been living with the sickle cell disease for over 20 years. At the age of 8 Holloman knew that she was different.  “I didn’t understand until I was unable to do the things other children did, I knew then that I was different,” Holloman said.  However, it was not until Holloman was a teenager that she realized the full extent of her illness. “You don’t come to fully understand it or get the full definition of it until you are a teenager,” she said. </p>
<p>Faced with the possibilities of a crippling disease, Holloman believes that sickle cell is just one of life’s burdens. Holloman encourages those who suffer from the life threatening disease to never give up. “No matter what doctors may say, they don’t rule your life, you make your life what you want it to be,” she said.</p>
<p>One of the biggest misconceptions that some people have about sickle cell patients is their constant need for medical treatment. Even though the sickle cell disease and trait vary in the medical field, Holloman makes it clear that the required treatment is the same in both cases. “Doctors don’t believe that those with the sickle cell trait can actually have pain,” she said.</p>
<p>As the 2011 Courage Award winner Holloman encourages this year’s winner to “keep fighting and be encouraging to other people,” said Holloman. </p>
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		<title>Sickle Cell Foundation Newsletter Volume 2</title>
		<link>http://sicklecellfoundation.org/sickle-cell-foundation-newsletter-volume-2/</link>
		<comments>http://sicklecellfoundation.org/sickle-cell-foundation-newsletter-volume-2/#comments</comments>
		<pubDate>Tue, 21 Aug 2012 14:47:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sicklecellfoundation.org/?p=321</guid>
		<description><![CDATA[Download the latest Sickle Cell Foundation Newsletter with all the current updates that include the Courage Award Winner and the Sickle Cell Foundation Poster Child. DOWNLOAD the Sickle Cell Foundation Newsletter]]></description>
				<content:encoded><![CDATA[<p>Download the latest Sickle Cell Foundation Newsletter with all the current updates that include the Courage Award Winner and the Sickle Cell Foundation Poster Child. </p>
<p><a href='http://sicklecellfoundation.org/wp-content/uploads/2012/08/SickleCellFoundation_Newsletter_2012.pdf'>DOWNLOAD the Sickle Cell Foundation Newsletter</a></p>
]]></content:encoded>
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		<title>In-Service</title>
		<link>http://sicklecellfoundation.org/in-service/</link>
		<comments>http://sicklecellfoundation.org/in-service/#comments</comments>
		<pubDate>Mon, 16 Apr 2012 17:21:39 +0000</pubDate>
		<dc:creator>Jill</dc:creator>
				<category><![CDATA[FYI]]></category>

		<guid isPermaLink="false">http://sicklecellfoundation.org/?p=249</guid>
		<description><![CDATA[Sickle Cell Foundation Presents: Information/Education Awareness Discharge Planning Service Delivery To Sickle Cell Patients Information &#38; Referrals Individual/Family Counseling &#160; Capital Regional Medical Center 1st Floor Classroom 2626 Capital Medical Blvd Tallahassee, FL 32308 Tuesday, April 17th 11:00 a.m. to 12:00 noon Presenter:  Phillip Randall, RN Lunch Provided For further information, please contact Velma Stevens, ...]]></description>
				<content:encoded><![CDATA[<h1 align="center">Sickle Cell Foundation</h1>
<p align="center">Presents:</p>
<p align="center">Information/Education Awareness</p>
<ul>
<li>Discharge Planning</li>
<li>Service Delivery To Sickle Cell Patients</li>
<li>Information &amp; Referrals</li>
<li>Individual/Family Counseling</li>
</ul>
<p>&nbsp;</p>
<h2 align="center">Capital Regional Medical Center</h2>
<p align="center">1<sup>st</sup> Floor Classroom</p>
<p align="center">2626 Capital Medical Blvd</p>
<p align="center">Tallahassee, FL 32308</p>
<h2 align="center">Tuesday, April 17<sup>th</sup><br />
11:00 a.m. to 12:00 noon</h2>
<p align="center"><strong>Presenter:  Phillip Randall, RN</strong></p>
<p align="center"><strong>Lunch Provided</strong></p>
<p align="center">For further information, please contact Velma Stevens, MSW at (850) 222-2355</p>
]]></content:encoded>
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		<title>SUPPORT SICKLE CELL FOUNDATION</title>
		<link>http://sicklecellfoundation.org/support-sickle-cell-foundation/</link>
		<comments>http://sicklecellfoundation.org/support-sickle-cell-foundation/#comments</comments>
		<pubDate>Tue, 10 Apr 2012 16:45:42 +0000</pubDate>
		<dc:creator>Jill</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sicklecellfoundation.org/?p=235</guid>
		<description><![CDATA[Ladies and Gentlemen!!  Boys and Girls!! Please Support Us By Purchasing a Meal @ Miller&#8217;s Ale House Restaurant A percentage of the proceeds will be contributed to the Sickle Cell Foundation DATE:  April 10th, 17th, 24th, 2012 TIME:  6 PM &#8211; 8 PM WHERE:  722 Apalachee Pkwy Tallahassee WHY:  In Support of Sickle Cell Foundation, ...]]></description>
				<content:encoded><![CDATA[<p style="text-align: center;">Ladies and Gentlemen!!  Boys and Girls!!</p>
<p style="text-align: center;">Please Support Us By Purchasing a Meal @</p>
<p style="text-align: center;"><strong>Miller&#8217;s Ale House Restaurant</strong></p>
<p style="text-align: center;">A percentage of the proceeds will be contributed to the Sickle Cell Foundation</p>
<p style="text-align: left;"><strong>DATE:</strong>  April 10th, 17th, 24th, 2012</p>
<p style="text-align: left;"><strong>TIME</strong>:  6 PM &#8211; 8 PM</p>
<p style="text-align: left;"><strong>WHERE</strong>:  722 Apalachee Pkwy Tallahassee</p>
<p style="text-align: left;"><strong>WHY</strong>:  In Support of Sickle Cell Foundation, Inc.</p>
<p style="text-align: left;"><em><strong>**</strong>We greatly appreciate the<strong> Buffalo Soldiers </strong>for hosting this great event.</em></p>
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