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	<title>Salman Namah &#187; thalassemia</title>
	<atom:link href="http://blog.skdev.net/tag/thalassemia/feed/" rel="self" type="application/rss+xml" />
	<link>http://blog.skdev.net</link>
	<description>Random enough to be declared weird.</description>
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		<title>Pakistan to require premarital blood screening</title>
		<link>http://blog.skdev.net/2009/02/12/pakistan-to-require-premarital-blood-screening/</link>
		<comments>http://blog.skdev.net/2009/02/12/pakistan-to-require-premarital-blood-screening/#comments</comments>
		<pubDate>Thu, 12 Feb 2009 05:52:48 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[I like..]]></category>
		<category><![CDATA[Personal]]></category>
		<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[blood tests]]></category>
		<category><![CDATA[disease]]></category>
		<category><![CDATA[good news]]></category>
		<category><![CDATA[law]]></category>
		<category><![CDATA[news]]></category>
		<category><![CDATA[pakistan]]></category>
		<category><![CDATA[thalassemia]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=585</guid>
		<description><![CDATA[The National Assembly of Pakistan is planning to introduce a bill that would require premarital blood screening in an effort to control the spread of diseases such as HIV/AIDS, thalassemia and hepatitis. The bill also will include a provision that would require the collection of the medical history of all Pakistanis deported from other countries.


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			<content:encoded><![CDATA[<p><i>* Draft of law suggests Rs 50,000-100,000 fine, 6 month-one year jail for violators</i><br />
By Afnan Khan</p>
<p>LAHORE: The National Assembly may soon introduce legislation regarding pre-marital blood screening to control the spread of HIV/AIDS, Thalassemia, Hepatitis and other diseases that are transmitted through genetic abnormalities; blood transmission; and sexual relations, sources within the National Assembly said on Tuesday.</p>
<p>They said the government would impose stern punishment to enforce the law, which would be binding on every Pakistani couple. The punishments would range from a fine of Rs 50,000 to Rs 100,000; six months to a year’s imprisonment; or both. Parliament is also planning on adding a provision to the law to collect the medical history of all Pakistanis deported from foreign countries, especially the Middle East, upon their arrival at airports. The sources said this was necessary as many people are deported from Middle Eastern countries after being found positive for HIV, hepatitis C, etc. Such people rarely inform the government or their families of these conditions to escape stigma and can thus spread the infections, they added.</p>
<p>The parliamentary sources said the law would be implemented through the thousands of basic health units (BHUs) functioning throughout the country. They said the officials working in these BHUs to keep a check on people violating the law.</p>
<p>The Standing Committee for Health in the National Assembly is due to meet today (Wednesday) to discuss the final timetable for placement of the bill before parliament and conduct a final debate on its pros and cons. According to committee Chairman Yasmeen Rehman, they would also discuss the issue of spurious drugs; shortage of life-saving medicine; and the high prices of medicines being sold by multinational companies.</p>
<p>She told Daily Times the committee had already drawn up the outline and major clauses of pre-marital blood screening law. She said passage of this law would ensure the safety of future generations from several deadly diseases.</p>
<p>Source: <a href="http://www.dailytimes.com.pk/default.asp?page=2009\02\11\story_11-2-2009_pg7_11">Daily Times</a></p>


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		</item>
		<item>
		<title>Fatimid Foundation&#8217;s Blood Donor Form</title>
		<link>http://blog.skdev.net/2009/01/22/blood-donor-form/</link>
		<comments>http://blog.skdev.net/2009/01/22/blood-donor-form/#comments</comments>
		<pubDate>Thu, 22 Jan 2009 20:22:12 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[blood camp]]></category>
		<category><![CDATA[confusions]]></category>
		<category><![CDATA[donations]]></category>
		<category><![CDATA[fatimid]]></category>
		<category><![CDATA[permission]]></category>
		<category><![CDATA[thalassemia]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=415</guid>
		<description><![CDATA[Few days ago when I asked one of my friends why he didn&#8217;t come to our blood camp he said because he (and his friends) don&#8217;t trust Fatimid. He told me that Fatimid Foundation arranges a blood camp at their university regularly. He and all his friends used to donate there. But at one occasion [...]


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			<content:encoded><![CDATA[<p><a href='#donorformfullsize'><img style="margin-right:10px;" src="http://blog.skdev.net/wp-content/uploads/2009/01/blood-donors-card-form-150x150.jpg" width="124" height="124" align="left" /></a>Few days ago when I asked one of my friends why he didn&#8217;t come to our blood camp he said because he (and his friends) don&#8217;t trust Fatimid.</p>
<p>He told me that Fatimid Foundation arranges a blood camp at their university regularly. He and all his friends used to donate there. But at one occasion one of the colleagues sister was sick and needed blood so they visited Fatimid showed there donation receipts and asked for a bag of blood. But Fatimid Foundation refused and said they can&#8217;t give them blood.</p>
<p>Well so long story short they don&#8217;t trust Fatimid and they cannot donate blood for Fatimid Foundation.</p>
<p>I was a little busy at that time so I couldn&#8217;t respond but I did say that they have to fulfill their patients requirement and they have stopped new patient registrations just because they were not getting enough blood for patients then how will they give blood to others? It&#8217;s not a <del datetime="2009-01-22T20:25:34+00:00">blood camp</del> blood bank after all.</p>
<p>Anyways I found this written on Fatimid Foundation&#8217;s Blood Donor form which they require you to fill and SIGN before you donate at any of there camp, even it&#8217;s a road-side camp, it says &#8220;DONOR&#8217;S CONSENT &#8211; I want to donate blood voluntarily for the patients of Fatimid Foundation, &amp; will not be entitled to claim any exchange for my donation.&#8221;</p>
<p><a name='donorformfullsize'><center><img src="http://blog.skdev.net/wp-content/uploads/2009/01/blood-donors-card-form.jpg" alt="image" align="center" /></a></p>


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		</item>
		<item>
		<title>Thank you Blood Donors :)</title>
		<link>http://blog.skdev.net/2009/01/22/thank-you-blood-donors/</link>
		<comments>http://blog.skdev.net/2009/01/22/thank-you-blood-donors/#comments</comments>
		<pubDate>Thu, 22 Jan 2009 18:19:59 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Personal]]></category>
		<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[blood donors]]></category>
		<category><![CDATA[camp]]></category>
		<category><![CDATA[thalassemia]]></category>
		<category><![CDATA[thanks]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=412</guid>
		<description><![CDATA[To all friends of F.A.i.T.h (Fight Against Thalassemia) Foundation: We&#8217;d like to thank everyone &#8211; donors, volunteers, recruiters &#8211; who helped with our blood drive. Unfortunately, we fell 51 pints short of our goal of 100 pints. However, the 49 pints of blood we did collect will help patients who need them. Although we didn&#8217;t [...]


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			<content:encoded><![CDATA[<p>To all friends of F.A.i.T.h (Fight Against Thalassemia) Foundation:</p>
<p>We&#8217;d like to thank everyone &#8211; donors, volunteers, recruiters &#8211; who helped with our blood drive.</p>
<p>Unfortunately, we fell 51 pints short of our goal of 100 pints. However, the 49 pints of blood we did collect will help patients who need them. Although we didn&#8217;t reach our goal, we had 50% of first-time donors, and they usually become regular donors. And we&#8217;re confident that at the next drive, we&#8217;ll not only meet but exceed our drive goal. Please feel free to pass on any comments about the donation process to Salman Mehmood (03323080461).</p>
<p>In the end I am including our donors list here, maybe it will motivate others to donate blood next time <img src='http://blog.skdev.net/wp-includes/images/smilies/icon_smile.gif' alt=':)' class='wp-smiley' /> </p>
<ol>
<li> Saleem Sheikh</li>
<li> Mutee-Ur-Rehman</li>
<li> Abdul Haseeb</li>
<li> Abdul Hameed Kath</li>
<li> Mrs. Sehrish</li>
<li> Mairaj Bostan</li>
<li> Navara Afridi Malik Meer</li>
<li> Rameez Abbas</li>
<li> Muneeb Khaliq</li>
<li> Yasir Aslam</li>
<li> Noman Rafiq</li>
<li> Waqar Ibrahim</li>
<li> Yaseen Munshi</li>
<li> Khurram A. Hameed</li>
<li> Qasim Qarar</li>
<li> Talha Khan</li>
<li> Mustufa Razzak</li>
<li> Roshan Allah Bux</li>
<li> Faizan Manzoor Ahmed</li>
<li> Umar Farooque</li>
<li> M. Sharique</li>
<li> Saad Saleem</li>
<li> Saad Ahmed</li>
<li> Ali Raza Khan</li>
<li> Waqas Saeed</li>
<li> Fawad Afridi</li>
<li> M. Saleem Mohammad</li>
<li> Mohsin Adhi</li>
<li> Ahmed Rafiq</li>
<li> Umar Khan Sikander</li>
<li> Shoaib Hussain</li>
<li> Abid</li>
<li> A. Basit M. Ilyas</li>
<li> Sohail Ahmed</li>
<li> Salik M. Iqbal</li>
<li> Fahad A. Ghafoor</li>
<li> Marjan Khayal Noor</li>
<li> Faheem A. Qadir</li>
<li> M. Ali M. Shafi</li>
<li> Azhar Afridi</li>
<li> Salma A. Sattar</li>
<li> Muzammil Asghar Ali</li>
<li> Abu Bakar</li>
<li> Muhammad Asif Yahya</li>
<li> Muneer Khan Meera Jan</li>
<li> Sagheer M. Hussain</li>
<li> A. Ghani A. Sattar</li>
<li> Muneer Ahmed</li>
<li>Tariq Baig</li>
</ol>
<p>I can&#8217;t forget to mention few people who really wanted to donate blood but doctors refused them because they had donated blood in last 2-3 months.</p>
<ul>
<li>Farman Ahmed</li>
<li>Major Faisal</li>
</ul>
<p>Again, many thanks for helping to boost the blood supply for Thalassemic Patients.</p>
<p>Sincerely,<br />
Salman Mehmood</p>


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		</item>
		<item>
		<title>Pakistan may enforce mandatory Thalassemia, Hepatitis, HIV tests before marriage.</title>
		<link>http://blog.skdev.net/2009/01/03/tests-before-marriage/</link>
		<comments>http://blog.skdev.net/2009/01/03/tests-before-marriage/#comments</comments>
		<pubDate>Sat, 03 Jan 2009 21:05:53 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[disease]]></category>
		<category><![CDATA[express]]></category>
		<category><![CDATA[government]]></category>
		<category><![CDATA[law]]></category>
		<category><![CDATA[news]]></category>
		<category><![CDATA[pakistan]]></category>
		<category><![CDATA[test]]></category>
		<category><![CDATA[thalassemia]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=344</guid>
		<description><![CDATA[Thalassemia, Aids and Hepatitis tests will be mandatory before marriage in Pakistan,
Government has asked for doctors assistance to help in creating bill to pass this law.
We will take National Assembly's vote, PMA will support this bill, Doctor Samreena Hashmi

Karachi: (Report: Tufail Ahmed) Government has decided to make Thalassemia, Aids and Hepatitis tests required before marriage and has asked all relevant departments to prepare the bill to be presented at national assembly. according to our sources to save new born childrens from getting infected by diseases transferred via parents blood government has taken steps to make sure that thalassemia, HIV Aids and Hepatitis tests are done before marriage.


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			<content:encoded><![CDATA[<p><center><a href="http://blog.skdev.net/2009/01/03/tests-before-marriage/"><img border=0 class="aligncenter size-full wp-image-346" title="express news" src="http://blog.skdev.net/wp-content/uploads/2009/01/logo.jpg" alt="express news" width="113" height="82" /></a><br />
<a href="http://blog.skdev.net/2009/01/03/tests-before-marriage/"><img border=0 class="aligncenter size-full wp-image-345" title="tests before marriage" src="http://blog.skdev.net/wp-content/uploads/2009/01/1100548373-1.gif" alt="tests before marriage" width="512" height="705" /></a><br />
<a href="http://express.com.pk/epaper/PoPupwindow.aspx?newsID=1100548373&#038;Issue=NP_KHI&#038;Date=20090102">Original source: Express News</a><br />
</center></p>


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		</item>
		<item>
		<title>Thalassemia &#8211; A Documentary</title>
		<link>http://blog.skdev.net/2009/01/01/thalassemia-a-documentary/</link>
		<comments>http://blog.skdev.net/2009/01/01/thalassemia-a-documentary/#comments</comments>
		<pubDate>Thu, 01 Jan 2009 02:27:30 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Personal]]></category>
		<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[book]]></category>
		<category><![CDATA[life]]></category>
		<category><![CDATA[life span]]></category>
		<category><![CDATA[miss-conceptions]]></category>
		<category><![CDATA[thalassemia]]></category>
		<category><![CDATA[video]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=339</guid>
		<description><![CDATA[&#8220;This is an edited version of a documentary I produced last month for a local non-profit foundation called the Omair-Sana Welfare Foundation. They deal in the treatment of Thallassaemia..&#8221; - Originaly Uploaded by Rabia Garib at: http://s.current.com/items/88806118/thallassaemia_a_documentary.htm The description given on that page is obviously wrong, we know thalassemics who have grand childrens. We have [...]


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<blockquote><p>&#8220;This is an edited version of a documentary I produced last month for a local non-profit foundation called the Omair-Sana Welfare Foundation. They deal in the treatment of Thallassaemia..&#8221;</p></blockquote>
<p>- Originaly Uploaded by Rabia Garib at:</p>
<p>http://s.current.com/items/88806118/thallassaemia_a_documentary.htm</p>
<p>The description given on that page is obviously wrong, we know thalassemics who have grand childrens.<br />
We have seen many married thalassemics with kids here in Karachi too.</p>
<p>Even in the book which was published 12-13 years ago it says:</p>
<blockquote><p><strong><em>How long can a person with thalassemic major live?</em></strong><br />
People sometimes don&#8217;t like to ask this question directly, but thalassemics and their parents must often ask themselves.<br />
It is difficult to give a simple reply, because:<br />
* It is very hard to know the answer for thalassemics who are well at present.<br />
* The disease and its implications are changing almost from day to day, because of advances in treatment.</p>
<p>We have all seen that patients with thalassemia are living longer and longer. Today it is reasonable to think that people with thalassemia major, who have been well treated from the beginning, may well live as long as people without thalassemia. Only time will tell whether this prediction is right, or too optimistic.</p>
<p>On the other hand, if we want to be pessimistic, it is true that thalassemics live with more risks than others, because of the amount of medical treatment they need. all medical treatments include some risk. But even so, well-treated thalassemic patient at the present day can have an excellent life-expectancy.</p></blockquote>
<p>Source: http://thalassemia.com.pk/kb/chapter2.html</p>
<p>But it is a good video, so anyways Thanks for the great video :]</p>
<p>-Salman</p>


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		</item>
		<item>
		<title>Thalassemia Video</title>
		<link>http://blog.skdev.net/2008/12/19/thal-vid/</link>
		<comments>http://blog.skdev.net/2008/12/19/thal-vid/#comments</comments>
		<pubDate>Fri, 19 Dec 2008 03:35:50 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Personal]]></category>
		<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[difficult]]></category>
		<category><![CDATA[disease]]></category>
		<category><![CDATA[emotions]]></category>
		<category><![CDATA[thalassemia]]></category>
		<category><![CDATA[videos]]></category>

		<guid isPermaLink="false">http://blog.skdev.net/?p=239</guid>
		<description><![CDATA[Click here to download [312 MB] No related posts found.


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<p style="text-align: center;"><a href="http://arrahman-araheem.net/seyretfiles/localvideos/Social_Responsibilities/kashif%20iqbal%20hospital%20final%20without%20logo.flv">Click here</a> to download [312 MB]</p>


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		</item>
		<item>
		<title>Thalassemia.Com.PK</title>
		<link>http://blog.skdev.net/2007/05/07/thalassemia/</link>
		<comments>http://blog.skdev.net/2007/05/07/thalassemia/#comments</comments>
		<pubDate>Mon, 07 May 2007 16:12:25 +0000</pubDate>
		<dc:creator>Salman</dc:creator>
				<category><![CDATA[Personal]]></category>
		<category><![CDATA[Thalassemia Related]]></category>
		<category><![CDATA[Work Related]]></category>
		<category><![CDATA[design]]></category>
		<category><![CDATA[disease]]></category>
		<category><![CDATA[project]]></category>
		<category><![CDATA[showcase]]></category>
		<category><![CDATA[thalassemia]]></category>

		<guid isPermaLink="false">http://skdev.wordpress.com/?p=79</guid>
		<description><![CDATA[Thalassemia, is a genetic blood disorder, and this website is for a Thalassemia Support Group called FAiTh, Fight Aainst Thalassemia. It features all the information a thalassemic and his/her family should know. From recent Thal-Events, to News, and Research Material.. everything is available there for free.. Thalassemia.Com.PK is a pretty static site and since it [...]


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			<content:encoded><![CDATA[<p><a title="Home Page" href="http://blog.skdev.net/wp-content/uploads/2007/05/thal_1.jpg" target="_blank"><img class="alignleft" style="margin-left:6px;margin-right:6px;" src="http://blog.skdev.net/wp-content/uploads/2007/05/thal_1.thumbnail.jpg" border="0" alt="Home Page" width="118" height="128" align="left" /></a> Thalassemia, is a genetic blood disorder, and this <a href="http://www.thalassemia.com.pk" target="_blank">website</a> is for a Thalassemia Support Group called <strong>FAiTh</strong>, <strong>F</strong>ight <strong>A</strong>a<strong>i</strong>nst <strong>Th</strong>alassemia. It features all the information a thalassemic and his/her family should know. From recent Thal-Events, to News, and Research Material.. everything is available there for free..</p>
<p><span id="more-79"></span> <a href="http://www.thalassemia.com.pk" target="_blank">Thalassemia.Com.PK</a> is a pretty static site and since it doesn&#8217;t offer any interaction or useful services it never looks like active, but we are working on a few stuff that will surely make it a handy and useful site for visitors from Pakistan at least.. I really love it&#8217;s design because I created it from top to bottom, it was my first and maybe last creation that is completely mine..! (except for the two images used in the header and few icons) Apart from the design, the complete website is built using PHP and mySql, it has lots of different scripts and alot more are under construction, I work on them in my leisure time.. right now you can find out stuff like research material, ways to support thalassemics and things, articles related to thalassemia and the website. Anyways, I will update this one as soon as we do some work on the website.. click thumbs, view full, the usual yada yada.</p>
<p><a title="Home Page" href="http://blog.skdev.net/wp-content/uploads/2007/05/thal_1.jpg"><img style="border:1px solid #<a href="http://search.twitter.com/search?q=%23000000" rel="nofollow" target="_blank" title="000000 in Twitter">000000</a>;" src="http://blog.skdev.net/wp-content/uploads/2007/05/thal_1.thumbnail.jpg" border="0" alt="Home Page" /></a> <a title="Research Material" href="http://blog.skdev.net/wp-content/uploads/2007/05/thal_2.jpg"><img style="border:1px solid #<a href="http://search.twitter.com/search?q=%23000000" rel="nofollow" target="_blank" title="000000 in Twitter">000000</a>;" src="http://blog.skdev.net/wp-content/uploads/2007/05/thal_2.thumbnail.jpg" border="0" alt="Research Material" /> </a><a title="Support Us Page" href="http://blog.skdev.net/wp-content/uploads/2007/05/thal_3.jpg"><img style="border:1px solid #<a href="http://search.twitter.com/search?q=%23000000" rel="nofollow" target="_blank" title="000000 in Twitter">000000</a>;" src="http://blog.skdev.net/wp-content/uploads/2007/05/thal_3.thumbnail.jpg" border="0" alt="Support Us Page" /> </a><a title="Treatment Page" href="http://blog.skdev.net/wp-content/uploads/2007/05/thal_4.jpg"><img style="border:1px solid #<a href="http://search.twitter.com/search?q=%23000000" rel="nofollow" target="_blank" title="000000 in Twitter">000000</a>;" src="http://blog.skdev.net/wp-content/uploads/2007/05/thal_4.thumbnail.jpg" border="0" alt="Treatment Page" /></a></p>


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