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	<title>Comments on: Bald Women Reveal What Life with Alopecia is Like</title>
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	<link>http://www.belgraviacentre.com/blog/bald-women-reveal-what-life-with-alopecia-is-like-164/</link>
	<description>Up-to-date information on hair loss and related issues – join the hair loss discussions and interact</description>
	<pubDate>Tue, 16 Mar 2010 02:19:33 +0000</pubDate>
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		<title>By: Denise Knepp</title>
		<link>http://www.belgraviacentre.com/blog/bald-women-reveal-what-life-with-alopecia-is-like-164/comment-page-1/#comment-7471</link>
		<dc:creator>Denise Knepp</dc:creator>
		<pubDate>Fri, 26 Jun 2009 03:16:23 +0000</pubDate>
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		<description>After so many years of having alopecia, I thought I would randomly do a search for any updates, only to find my exact words to others that are searching for that miracle cure .. If there we're a cure "It would be out there".
I do however find the BGDL interesting.  I've spent more time on this website than any other I've ever found.  If my scheduled permitted and I we're spontaneous enough, I would fly out to Calif.  just for lunch.  I have gone through the "Very Bad Wig Days" and even spending over a $1000.00 to get a special molded fit for human hair.  Only it was my very worst experience since my hair loss from at least 15 yrs. now.  I like many others have many stories but, life goes on only in a more fashionable way now.</description>
		<content:encoded><![CDATA[<p>After so many years of having alopecia, I thought I would randomly do a search for any updates, only to find my exact words to others that are searching for that miracle cure .. If there we&#8217;re a cure &#8220;It would be out there&#8221;.<br />
I do however find the BGDL interesting.  I&#8217;ve spent more time on this website than any other I&#8217;ve ever found.  If my scheduled permitted and I we&#8217;re spontaneous enough, I would fly out to Calif.  just for lunch.  I have gone through the &#8220;Very Bad Wig Days&#8221; and even spending over a $1000.00 to get a special molded fit for human hair.  Only it was my very worst experience since my hair loss from at least 15 yrs. now.  I like many others have many stories but, life goes on only in a more fashionable way now.</p>
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		<title>By: Thea Chassin</title>
		<link>http://www.belgraviacentre.com/blog/bald-women-reveal-what-life-with-alopecia-is-like-164/comment-page-1/#comment-6937</link>
		<dc:creator>Thea Chassin</dc:creator>
		<pubDate>Fri, 29 May 2009 16:33:04 +0000</pubDate>
		<guid isPermaLink="false">http://www.belgraviacentre.com/blog/?p=5338#comment-6937</guid>
		<description>What a beautiful way to inspire other women with alopecia - thank you Pat and Ivonna! - for showing that life with alopecia while a life of adapting, is also as fantastic a life as any.  With role models like yourselves to show the way,  more women will take control of their own lives and realize they can and should put their needs first to  live normal and successful lives. The more the public knows about women like Pat and Ivonna, the more,hopefully, other women will talk openly - and that is the key to better public acceptance. It starts with the women who have aa themselves being able to be open and nonchalant. For women with alopecia, having hair on or off should be seen as the choice of selecting any accessory: whether it be a hat, scarf, earrings or  necklace. She decides how she wants to look and be comfortable. Everyone has can learn to go with the flow.

Thea Chassin, founder and president
Alopecia Universalis since 1996
baldgirlsdolunch.org</description>
		<content:encoded><![CDATA[<p>What a beautiful way to inspire other women with alopecia - thank you Pat and Ivonna! - for showing that life with alopecia while a life of adapting, is also as fantastic a life as any.  With role models like yourselves to show the way,  more women will take control of their own lives and realize they can and should put their needs first to  live normal and successful lives. The more the public knows about women like Pat and Ivonna, the more,hopefully, other women will talk openly - and that is the key to better public acceptance. It starts with the women who have aa themselves being able to be open and nonchalant. For women with alopecia, having hair on or off should be seen as the choice of selecting any accessory: whether it be a hat, scarf, earrings or  necklace. She decides how she wants to look and be comfortable. Everyone has can learn to go with the flow.</p>
<p>Thea Chassin, founder and president<br />
Alopecia Universalis since 1996<br />
baldgirlsdolunch.org</p>
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