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	<title>Comments on: Few changes&#8230;</title>
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	<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/</link>
	<description>All About Me &#038; My Surroundings!</description>
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		<title>By: Ayesha</title>
		<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/comment-page-1/#comment-46</link>
		<dc:creator>Ayesha</dc:creator>
		<pubDate>Sat, 03 Sep 2005 12:52:48 +0000</pubDate>
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		<description>Hello Joy Angela!

Thanks for visiting my blog and sharing your problem with me, I have sent an email to you, I hope you have got it..

Take Cares, Bye!</description>
		<content:encoded><![CDATA[<p>Hello Joy Angela!</p>
<p>Thanks for visiting my blog and sharing your problem with me, I have sent an email to you, I hope you have got it..</p>
<p>Take Cares, Bye!</p>
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		<title>By: Joy Angela H. Gepes</title>
		<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/comment-page-1/#comment-43</link>
		<dc:creator>Joy Angela H. Gepes</dc:creator>
		<pubDate>Fri, 02 Sep 2005 08:57:21 +0000</pubDate>
		<guid isPermaLink="false">http://ayesha.thalassemia.com.pk/?p=29#comment-43</guid>
		<description>It is very reassuring to note some people are trying to share info about thalasemia. My 2 and 1/2 yr. old child was diagnosed just last week to have thalasemia. I feel devastated knowing about it, more so when I know it to be a congenital disease. I am a 44 year old mother of 4 from Philippines. This girl is my youngest. I really would like to seek help on how to manage this, if no cure at all, as treatment in the Philippines may not be that popular. I filed my leave of absence from the office just to give time and dedeication to my child with thalasemia.</description>
		<content:encoded><![CDATA[<p>It is very reassuring to note some people are trying to share info about thalasemia. My 2 and 1/2 yr. old child was diagnosed just last week to have thalasemia. I feel devastated knowing about it, more so when I know it to be a congenital disease. I am a 44 year old mother of 4 from Philippines. This girl is my youngest. I really would like to seek help on how to manage this, if no cure at all, as treatment in the Philippines may not be that popular. I filed my leave of absence from the office just to give time and dedeication to my child with thalasemia.</p>
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		<title>By: Ayesha</title>
		<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/comment-page-1/#comment-33</link>
		<dc:creator>Ayesha</dc:creator>
		<pubDate>Tue, 23 Aug 2005 23:23:03 +0000</pubDate>
		<guid isPermaLink="false">http://ayesha.thalassemia.com.pk/?p=29#comment-33</guid>
		<description>Thanks Teeth Maestro &amp; Humaira

Teeth Maestro: Brother me and Salman are trying to help more and more, we are trying to acknowledge as many people as we can, so don&#039;t be formal asking anything, well, there is no substitutes, but as you said &amp; as I know.. Many doctors are doing research and the latest I know is about Italy, they have found this therapy called &quot;stem cell transplantation&quot;, A friend of mine has taken his son to Italy for this therapy and till now we have got the news that the kid is 101% Alright (MashaAllah) and his RBC (Red Blood Cells) are increasing!!, That’s a great news for Thalassemics : ), I haven’t heard any other news or about substitutes

Thanks once again Teeth Maestro &amp; Humaira : )</description>
		<content:encoded><![CDATA[<p>Thanks Teeth Maestro &amp; Humaira</p>
<p>Teeth Maestro: Brother me and Salman are trying to help more and more, we are trying to acknowledge as many people as we can, so don&#8217;t be formal asking anything, well, there is no substitutes, but as you said &amp; as I know.. Many doctors are doing research and the latest I know is about Italy, they have found this therapy called &#8220;stem cell transplantation&#8221;, A friend of mine has taken his son to Italy for this therapy and till now we have got the news that the kid is 101% Alright (MashaAllah) and his RBC (Red Blood Cells) are increasing!!, That’s a great news for Thalassemics : ), I haven’t heard any other news or about substitutes</p>
<p>Thanks once again Teeth Maestro &amp; Humaira : )</p>
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		<title>By: Humaira</title>
		<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/comment-page-1/#comment-32</link>
		<dc:creator>Humaira</dc:creator>
		<pubDate>Tue, 23 Aug 2005 12:23:02 +0000</pubDate>
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		<description>Salam

The changes are really good. 

 I do appreciate you n ur brother for working for such a great cause.</description>
		<content:encoded><![CDATA[<p>Salam</p>
<p>The changes are really good. </p>
<p> I do appreciate you n ur brother for working for such a great cause.</p>
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		<title>By: Teeth Maestro</title>
		<link>http://www.ayesha.thalassemia.com.pk/2005/08/21/few-changes/comment-page-1/#comment-31</link>
		<dc:creator>Teeth Maestro</dc:creator>
		<pubDate>Mon, 22 Aug 2005 20:40:36 +0000</pubDate>
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		<description>Can I ask you one thing.  What is the present development status in making Blood subsitutes - A few days ago I blogged about Euro Blood subsitutes.  they are still in research but is that a solution to Thalasemia, call me a little ignorant on the subject of thalasemia since I am a dentist!</description>
		<content:encoded><![CDATA[<p>Can I ask you one thing.  What is the present development status in making Blood subsitutes &#8211; A few days ago I blogged about Euro Blood subsitutes.  they are still in research but is that a solution to Thalasemia, call me a little ignorant on the subject of thalasemia since I am a dentist!</p>
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