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	<title>Comments on: Is a Mostly Liquid Diet Really That Bad?</title>
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	<link>http://www.mindlessmommy.com/2009/01/is-a-mostly-liquid-diet-really-that-bad.html</link>
	<description>Autism, ADHD, Anxiety and Siezures</description>
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		<title>By: Jenn</title>
		<link>http://www.mindlessmommy.com/2009/01/is-a-mostly-liquid-diet-really-that-bad.html/comment-page-1#comment-5003</link>
		<dc:creator>Jenn</dc:creator>
		<pubDate>Wed, 07 Jan 2009 02:44:56 +0000</pubDate>
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		<description>Glad to hear he&#039;s getting some good caloric intake - no matter which way!  We went through a hunger strike phase with Nick around the time he was diagnosed PDD-NOS.  At the time we saw the specialist Nick was drinking 2 pediasures a day and eating (maybe) 1 small meal/day.  VERY nervewracking!  Monitoring his food intake practically became an obsession.  It was the 1st thing I asked of any babysitter or at daycare, &quot;how much did he eat today?&quot;

I know you are not doing biomedical intervention, but thought I&#039;d share our anecdotal findings... Our doctor did the blood testing for food allergies and Nick came back positive for gluten, casein and egg.  Once we transitioned Nick to a GFCF diet, he ate.  And ate and ate and ate.  3 regular meals a day.  If we slip up and he gets something &quot;off limits&quot; I notice his appetite wanes for 2-3 days.

As Nick&#039;s expressive language developed, one day Nick made the announcement, &quot;I can&#039;t eat those chicken nuggets, Daddy&quot; as he pointed out the car window at the McDonalds as they passed, &quot;They make my tummy hurt.&quot;  We were floored.  Was he having GI problems due to the gluten and/or casein and he was unable to express verbally to use before?

Just wondering if you&#039;ve considered a trial dietary intervention.

I&#039;ll be praying the pediatric GI doc has some answers for you!</description>
		<content:encoded><![CDATA[<p>Glad to hear he&#8217;s getting some good caloric intake &#8211; no matter which way!  We went through a hunger strike phase with Nick around the time he was diagnosed PDD-NOS.  At the time we saw the specialist Nick was drinking 2 pediasures a day and eating (maybe) 1 small meal/day.  VERY nervewracking!  Monitoring his food intake practically became an obsession.  It was the 1st thing I asked of any babysitter or at daycare, &#8220;how much did he eat today?&#8221;</p>
<p>I know you are not doing biomedical intervention, but thought I&#8217;d share our anecdotal findings&#8230; Our doctor did the blood testing for food allergies and Nick came back positive for gluten, casein and egg.  Once we transitioned Nick to a GFCF diet, he ate.  And ate and ate and ate.  3 regular meals a day.  If we slip up and he gets something &#8220;off limits&#8221; I notice his appetite wanes for 2-3 days.</p>
<p>As Nick&#8217;s expressive language developed, one day Nick made the announcement, &#8220;I can&#8217;t eat those chicken nuggets, Daddy&#8221; as he pointed out the car window at the McDonalds as they passed, &#8220;They make my tummy hurt.&#8221;  We were floored.  Was he having GI problems due to the gluten and/or casein and he was unable to express verbally to use before?</p>
<p>Just wondering if you&#8217;ve considered a trial dietary intervention.</p>
<p>I&#8217;ll be praying the pediatric GI doc has some answers for you!</p>
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