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	<title>Comments on: Stem Cell Hair Regeneration &#8211; A Cure for Baldness?</title>
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	<link>http://www.belgraviacentre.com/blog/stem-cell-hair-regeneration-a-cure-for-baldness-122/</link>
	<description>Up-to-date information on hair loss and related issues – join the hair loss discussions and interact</description>
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		<title>By: Placenta Stem Cell Therapy</title>
		<link>http://www.belgraviacentre.com/blog/stem-cell-hair-regeneration-a-cure-for-baldness-122/comment-page-1/#comment-17648</link>
		<dc:creator>Placenta Stem Cell Therapy</dc:creator>
		<pubDate>Wed, 01 Sep 2010 12:23:20 +0000</pubDate>
		<guid isPermaLink="false">http://www.belgraviacentre.com/blog/?p=4369#comment-17648</guid>
		<description>I was diagnosed with Hepatitis C in early 1997. Then started Interferon treatments a few months later; with great disappointment my doctor said I could not take it due to various side effects. My liver enzymes at that time were ALT 264 AST 141. So I waited for a new type of medicine.

A lady I got to know told me of a Dr that had been treating her with placenta implants for her lupus and immune deficiency. Her doctors here had given her months to live.

With a bit of despair and not too much belief in this placenta implant thing, I went to see the Dr. At the time I went to see him, Nov. 2001, my ALT was 587 and my AST 318. After my implant, I had blood work done Nov. 2002. My ALT was 152 and AST 89. I waited so long because I was still pessimistic in the implant. So I was a little excited but still pessimistic. I had my second implant Dec. 2002, and then had blood work the end of Jan. 2003 ALT 75 AST 49.

I was almost in full belief until Dec. 2003 my ALT was 47 and AST 42 . My level had not been that low in almost 15 years. Feb. 2003 ALT 34 AST 14 . So now when my levels start creeping up to 100 or so I get another implant. Recently, I had an implant Oct. April 2007 then blood work Nov. September 2007. Blood work came out normal, what a good word to hear when you have Hep C.

I am by all means not saying this is curing my Hepatitis C because it is not. My viral count a year ago was 21 million; I don&#039;t get that checked any more, a little to depressing. Even with the immune system of a Hep C patient, I rarely ever get sick. I have no doubt these implants have extended my life with Hep C. 

.</description>
		<content:encoded><![CDATA[<p>I was diagnosed with Hepatitis C in early 1997. Then started Interferon treatments a few months later; with great disappointment my doctor said I could not take it due to various side effects. My liver enzymes at that time were ALT 264 AST 141. So I waited for a new type of medicine.</p>
<p>A lady I got to know told me of a Dr that had been treating her with placenta implants for her lupus and immune deficiency. Her doctors here had given her months to live.</p>
<p>With a bit of despair and not too much belief in this placenta implant thing, I went to see the Dr. At the time I went to see him, Nov. 2001, my ALT was 587 and my AST 318. After my implant, I had blood work done Nov. 2002. My ALT was 152 and AST 89. I waited so long because I was still pessimistic in the implant. So I was a little excited but still pessimistic. I had my second implant Dec. 2002, and then had blood work the end of Jan. 2003 ALT 75 AST 49.</p>
<p>I was almost in full belief until Dec. 2003 my ALT was 47 and AST 42 . My level had not been that low in almost 15 years. Feb. 2003 ALT 34 AST 14 . So now when my levels start creeping up to 100 or so I get another implant. Recently, I had an implant Oct. April 2007 then blood work Nov. September 2007. Blood work came out normal, what a good word to hear when you have Hep C.</p>
<p>I am by all means not saying this is curing my Hepatitis C because it is not. My viral count a year ago was 21 million; I don&#8217;t get that checked any more, a little to depressing. Even with the immune system of a Hep C patient, I rarely ever get sick. I have no doubt these implants have extended my life with Hep C. </p>
<p>.</p>
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