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	<title>Comments on: If you have Hashimotos, you may want to become aware of this rare associated condition</title>
	<atom:link href="http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/</link>
	<description>Thyroid Treatment Scandal and Hypothyroid Mistreatment</description>
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		<title>By: Carol</title>
		<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/comment-page-1/#comment-147737</link>
		<dc:creator>Carol</dc:creator>
		<pubDate>Mon, 30 Jan 2012 16:21:47 +0000</pubDate>
		<guid isPermaLink="false">http://www.stopthethyroidmadness.com/?p=5591#comment-147737</guid>
		<description>Prednisone certainly is not something to take long-term.  I think that should be emphasized.</description>
		<content:encoded><![CDATA[<p>Prednisone certainly is not something to take long-term.  I think that should be emphasized.</p>
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		<title>By: Jill House DC</title>
		<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/comment-page-1/#comment-105692</link>
		<dc:creator>Jill House DC</dc:creator>
		<pubDate>Wed, 26 Oct 2011 03:02:53 +0000</pubDate>
		<guid isPermaLink="false">http://www.stopthethyroidmadness.com/?p=5591#comment-105692</guid>
		<description>Gluten allergy has been linked to many autoimmune diseases. Get off gluten and in some dairy too and see how you feel. Also iodine deficiency causes tpo antibodies</description>
		<content:encoded><![CDATA[<p>Gluten allergy has been linked to many autoimmune diseases. Get off gluten and in some dairy too and see how you feel. Also iodine deficiency causes tpo antibodies</p>
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		<title>By: Jill</title>
		<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/comment-page-1/#comment-56798</link>
		<dc:creator>Jill</dc:creator>
		<pubDate>Thu, 15 Jul 2010 16:56:27 +0000</pubDate>
		<guid isPermaLink="false">http://www.stopthethyroidmadness.com/?p=5591#comment-56798</guid>
		<description>I read this the day you posted it and thought it sounded like me. At my neurologist appointment this morning, without my ever mentioning it, my doctor told me he thought I probably have this condition. I&#039;m so glad I had read about it here first so I knew what he was talking about, and I&#039;m even happier that after several years and numerous doctors someone has finally hazarded a guess as to what might be wrong with me. Thank you for the information.</description>
		<content:encoded><![CDATA[<p>I read this the day you posted it and thought it sounded like me. At my neurologist appointment this morning, without my ever mentioning it, my doctor told me he thought I probably have this condition. I&#8217;m so glad I had read about it here first so I knew what he was talking about, and I&#8217;m even happier that after several years and numerous doctors someone has finally hazarded a guess as to what might be wrong with me. Thank you for the information.</p>
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		<title>By: Judy</title>
		<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/comment-page-1/#comment-56340</link>
		<dc:creator>Judy</dc:creator>
		<pubDate>Fri, 02 Jul 2010 20:46:56 +0000</pubDate>
		<guid isPermaLink="false">http://www.stopthethyroidmadness.com/?p=5591#comment-56340</guid>
		<description>I have had grave concerns for my mother, who has been treated for years for Parkinson&#039;s and who is now essentially paralyzed, not even able to swallow or move more than her hands, and barely able to speak.  Basically, she has had most of the symptoms you list here, and EACH ONE gets treated as a separate condition or symptom, often resulting in a potentially problematic medication &quot;cocktail.&quot;

Recently, when I had gone too long without following up with my endo and needed a dose increase on my levothyroxine, I started having real problems walking, barely able to shuffle my feet, SO MUCH like my Mom&#039;s Parkinson&#039;s symptoms. Within days of increasing my dosage, the symptoms went away, as did the edema in my lower legs.  This prompted me to try to find out if the same could be a treatable part of my Mom&#039;s problems.

To my shock and dismay, she has never been thoroughly evaluated for thyroid deficits beyond a cursory check to see if her T-4 was WNL, nor for antibodies!  She did NOT show high A-B levels when I finally begged her neurologist to at least look into it, but did show somewhat low T-3. (antithyroglobulin not checked) 

What kills me is how many hypothyroid symptoms do overlap with serious neurological disorders and nobody seems to really be looking at that component, which is generally so very treatable.

If you have loved ones who are being treated for movement disorders, please look into the possibility of a thyroid connection.  

Personally, I have been treated for years for a laundry list of &quot;conditions&quot; that ALL fall in line with common hypothyroid symptoms.  I was in the military in southern Germany when Chernobyl blew up and was exposed to a large amount of perchlorate later, both very bad for the thyroid.  I have been though that proverbial &quot;slew of tests&quot; and still only got (if anything) about half the T-4 dose I needed until recently.  Lots of Thyroid Madnees going on here!</description>
		<content:encoded><![CDATA[<p>I have had grave concerns for my mother, who has been treated for years for Parkinson&#8217;s and who is now essentially paralyzed, not even able to swallow or move more than her hands, and barely able to speak.  Basically, she has had most of the symptoms you list here, and EACH ONE gets treated as a separate condition or symptom, often resulting in a potentially problematic medication &#8220;cocktail.&#8221;</p>
<p>Recently, when I had gone too long without following up with my endo and needed a dose increase on my levothyroxine, I started having real problems walking, barely able to shuffle my feet, SO MUCH like my Mom&#8217;s Parkinson&#8217;s symptoms. Within days of increasing my dosage, the symptoms went away, as did the edema in my lower legs.  This prompted me to try to find out if the same could be a treatable part of my Mom&#8217;s problems.</p>
<p>To my shock and dismay, she has never been thoroughly evaluated for thyroid deficits beyond a cursory check to see if her T-4 was WNL, nor for antibodies!  She did NOT show high A-B levels when I finally begged her neurologist to at least look into it, but did show somewhat low T-3. (antithyroglobulin not checked) </p>
<p>What kills me is how many hypothyroid symptoms do overlap with serious neurological disorders and nobody seems to really be looking at that component, which is generally so very treatable.</p>
<p>If you have loved ones who are being treated for movement disorders, please look into the possibility of a thyroid connection.  </p>
<p>Personally, I have been treated for years for a laundry list of &#8220;conditions&#8221; that ALL fall in line with common hypothyroid symptoms.  I was in the military in southern Germany when Chernobyl blew up and was exposed to a large amount of perchlorate later, both very bad for the thyroid.  I have been though that proverbial &#8220;slew of tests&#8221; and still only got (if anything) about half the T-4 dose I needed until recently.  Lots of Thyroid Madnees going on here!</p>
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		<title>By: Trudi</title>
		<link>http://www.stopthethyroidmadness.com/2010/06/22/hashimotos-encephalopathy/comment-page-1/#comment-56157</link>
		<dc:creator>Trudi</dc:creator>
		<pubDate>Sat, 26 Jun 2010 06:30:43 +0000</pubDate>
		<guid isPermaLink="false">http://www.stopthethyroidmadness.com/?p=5591#comment-56157</guid>
		<description>OMG! THANK YOU! My 9 yo daughter has been having a LOT of seizures and major cognitive decline recently and the anti-seizure meds are not working. She has hashimoto&#039;s and most of the above symptoms! Now I hope that one of her doctors (endocrine or neuro) will take a look into this! I&#039;m still working on my own personal DO to get my hashi&#039;s properly treated. Funny how myself and 2 young daughters have hashi&#039;s. I wish proper medical care was not so difficult.</description>
		<content:encoded><![CDATA[<p>OMG! THANK YOU! My 9 yo daughter has been having a LOT of seizures and major cognitive decline recently and the anti-seizure meds are not working. She has hashimoto&#8217;s and most of the above symptoms! Now I hope that one of her doctors (endocrine or neuro) will take a look into this! I&#8217;m still working on my own personal DO to get my hashi&#8217;s properly treated. Funny how myself and 2 young daughters have hashi&#8217;s. I wish proper medical care was not so difficult.</p>
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