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	<title>Comments on: Fraud allegations dog disabled project in Mazar</title>
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	<description>Journalism for public good, supported by the Institute for War &#38; Peace</description>
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		<title>By: Olin</title>
		<link>http://www.iwpr.org.af/fraud-allegations-dog-disabled-project-in-mazar-3#comment-198</link>
		<dc:creator>Olin</dc:creator>
		<pubDate>Fri, 24 Aug 2012 16:11:22 +0000</pubDate>
		<guid isPermaLink="false">http://www.iwpr.org.af/?p=256#comment-198</guid>
		<description>Why are you here? This is from the Bush years, it&#039;s gone yaar.  But people keep serichang, because there were recent posts on the guestbook.Invisible disabilities  it can get lonely.Which is why I love this place and all the blogs and ljs linked because You do that too?! (I did say that at one person&#039;s LJ where she mentioned having to change meds/dosages because of tolerances.) It&#039;s like thinking you&#039;re the only Bollywood fan in the area, and well  the internet has been an enabler (sleep or X-files fanfic?) in my life, so why not help sometimes?Question for those who went to college or are still in college   was there ever a group for students with disabilities?* Because we don&#039;t have one, and you can&#039;t tell who has an invisible disability or is fighting with depression. ( Go away, I have homework to do! Okay, I&#039;ll watch Jhoom Barabar Jhoom. But just this once! Ha ha, Abhi is silly. ) And while I do talk to the student who uses a wheelchair (about her hair, about  normal  stuff, we&#039;ve never had a class together) I don&#039;t feel comfortable asking her about  that.*See my angry yet polite (okay, maybe not POLITE, but no swearing) letter about using  crazy  in a negative way where I point out that queer students have a support group, but us crazies don&#039;t. ex    I know they&#039;re my friends and all, but it does get annoying when I start crying for no reason and everyone asks if I&#039;m okay.   I know, I know. Sometimes just validation is all you need, that you&#039;re not the only one going through some messed up stuff, physically or emotionally. Though I think I&#039;m pretty unique physically   I have the flu. I have no fever. I thought I was sweating horribly Tuesday because of the power of suggestion, but it was merely the fact that it was 80 F in my room. This morning? Freezing, but because the AC works and it&#039;s 60 F! Whoops. I can&#039;t even do the flu normally anymore!And this has been going on   mmm, *most* people don&#039;t do this   since I was 13 and seeing Dr Endo every week because I reacted (negatively) to all the treat the symptom meds rather quickly. And then the skin at 15. The only thing that worked was the pain medication and the OTC cream. Barely. But Dr Derm tried for 3 months until he found the right thing.So while I won&#039;t find my exact medical problems clone online, I can find one person who&#039;s had horrible eczema, one who&#039;s lost xer thyroid, one with chronic pain   undiagnosed or not. And plenty dealing with mood swings. And tons dealing with the internal battle  I don&#039;t want to be an addict, but OH MY GOD I CAN&#039;T BREATHE ow. So  y&#039;all have helped so much. I found this place in November, when I was at home because the pain had shot up worse than usual and well, I wasn&#039;t alone online. Or at home, I had Mikey&#039;s butt on my head. As usual.</description>
		<content:encoded><![CDATA[<p>Why are you here? This is from the Bush years, it&#8217;s gone yaar.  But people keep serichang, because there were recent posts on the guestbook.Invisible disabilities  it can get lonely.Which is why I love this place and all the blogs and ljs linked because You do that too?! (I did say that at one person&#8217;s LJ where she mentioned having to change meds/dosages because of tolerances.) It&#8217;s like thinking you&#8217;re the only Bollywood fan in the area, and well  the internet has been an enabler (sleep or X-files fanfic?) in my life, so why not help sometimes?Question for those who went to college or are still in college   was there ever a group for students with disabilities?* Because we don&#8217;t have one, and you can&#8217;t tell who has an invisible disability or is fighting with depression. ( Go away, I have homework to do! Okay, I&#8217;ll watch Jhoom Barabar Jhoom. But just this once! Ha ha, Abhi is silly. ) And while I do talk to the student who uses a wheelchair (about her hair, about  normal  stuff, we&#8217;ve never had a class together) I don&#8217;t feel comfortable asking her about  that.*See my angry yet polite (okay, maybe not POLITE, but no swearing) letter about using  crazy  in a negative way where I point out that queer students have a support group, but us crazies don&#8217;t. ex    I know they&#8217;re my friends and all, but it does get annoying when I start crying for no reason and everyone asks if I&#8217;m okay.   I know, I know. Sometimes just validation is all you need, that you&#8217;re not the only one going through some messed up stuff, physically or emotionally. Though I think I&#8217;m pretty unique physically   I have the flu. I have no fever. I thought I was sweating horribly Tuesday because of the power of suggestion, but it was merely the fact that it was 80 F in my room. This morning? Freezing, but because the AC works and it&#8217;s 60 F! Whoops. I can&#8217;t even do the flu normally anymore!And this has been going on   mmm, *most* people don&#8217;t do this   since I was 13 and seeing Dr Endo every week because I reacted (negatively) to all the treat the symptom meds rather quickly. And then the skin at 15. The only thing that worked was the pain medication and the OTC cream. Barely. But Dr Derm tried for 3 months until he found the right thing.So while I won&#8217;t find my exact medical problems clone online, I can find one person who&#8217;s had horrible eczema, one who&#8217;s lost xer thyroid, one with chronic pain   undiagnosed or not. And plenty dealing with mood swings. And tons dealing with the internal battle  I don&#8217;t want to be an addict, but OH MY GOD I CAN&#8217;T BREATHE ow. So  y&#8217;all have helped so much. I found this place in November, when I was at home because the pain had shot up worse than usual and well, I wasn&#8217;t alone online. Or at home, I had Mikey&#8217;s butt on my head. As usual.</p>
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