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	<title>Comments on: Information is Power, So I am Going to Get Me Some!</title>
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	<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/</link>
	<description>Learning to Balance Chronic Health with a Chronic Love of Life</description>
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		<title>By: chiropractor chicago</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-1283</link>
		<dc:creator>chiropractor chicago</dc:creator>
		<pubDate>Sat, 20 Mar 2010 08:15:03 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-1283</guid>
		<description>Hi fibrohaven we&#039;ll wait for your next post.Btw  can Fibromyalgia mimic the symptoms of other diseases?  &lt;a href=&quot;http://www.eastbankchiropractic.com/&quot; rel=&quot;nofollow&quot;&gt;chicago chiropractor&lt;/a&gt;</description>
		<content:encoded><![CDATA[<p>Hi fibrohaven we&#8217;ll wait for your next post.Btw  can Fibromyalgia mimic the symptoms of other diseases?  <a href="http://www.eastbankchiropractic.com/" rel="nofollow">chicago chiropractor</a></p>
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		<title>By: Follow up on Dr. Whitcomb &#38; NRCT &#171; Fibromyalgia Haven</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-726</link>
		<dc:creator>Follow up on Dr. Whitcomb &#38; NRCT &#171; Fibromyalgia Haven</dc:creator>
		<pubDate>Tue, 04 Aug 2009 04:46:08 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-726</guid>
		<description>[...] intended to write this follow-up post on my experience with Dr. Whitcomb and his Neurologic Relief Centers Technique last Monday, but have been sidelined by a bad flare-up. Yes, I do attribute my flare to the [...]</description>
		<content:encoded><![CDATA[<p>[...] intended to write this follow-up post on my experience with Dr. Whitcomb and his Neurologic Relief Centers Technique last Monday, but have been sidelined by a bad flare-up. Yes, I do attribute my flare to the [...]</p>
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		<title>By: fibrohaven</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-/#comment-725</link>
		<dc:creator>fibrohaven</dc:creator>
		<pubDate>Sun, 02 Aug 2009 21:49:24 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-725</guid>
		<description>Hi Curtis,

I have a lot to say about Whitcomb and his technique - blog post coming. I haven&#039;t written it yet because I have been in a flare since the workshop. My first instinct was to not be tested, and I wish I had followed it.

I should have my post up Monday or Tuesday. My review will be fair, despite my personal reaction to the technique.

Yesterday I spoke with the practitioner who invited me to the workshop, and he has decided not to implement Whitcomb&#039;s technique. I have to say I think he is making a wise choice. I will elaborate in my post.</description>
		<content:encoded><![CDATA[<p>Hi Curtis,</p>
<p>I have a lot to say about Whitcomb and his technique &#8211; blog post coming. I haven&#8217;t written it yet because I have been in a flare since the workshop. My first instinct was to not be tested, and I wish I had followed it.</p>
<p>I should have my post up Monday or Tuesday. My review will be fair, despite my personal reaction to the technique.</p>
<p>Yesterday I spoke with the practitioner who invited me to the workshop, and he has decided not to implement Whitcomb&#8217;s technique. I have to say I think he is making a wise choice. I will elaborate in my post.</p>
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		<title>By: Curtis</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-724</link>
		<dc:creator>Curtis</dc:creator>
		<pubDate>Sun, 02 Aug 2009 06:45:14 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-724</guid>
		<description>So, did you get the test done at the seminar?  What was your take on it?

Curtis</description>
		<content:encoded><![CDATA[<p>So, did you get the test done at the seminar?  What was your take on it?</p>
<p>Curtis</p>
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		<title>By: Kelly</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-723</link>
		<dc:creator>Kelly</dc:creator>
		<pubDate>Tue, 28 Jul 2009 16:35:18 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-723</guid>
		<description>Jeanne,
Wow, even PhD&#039;s get sick! (joking)
Feeling a bit weary of professionals treating patients like we are all idiots. That&#039;s all.
I have Rheumatoid Arthritis. I keep saying what we need are RA dr&#039;s who have RA. Hahaha.

I have RA in my cervical spine. It does refer pain to arms and hands. This theory is fascinating.</description>
		<content:encoded><![CDATA[<p>Jeanne,<br />
Wow, even PhD&#8217;s get sick! (joking)<br />
Feeling a bit weary of professionals treating patients like we are all idiots. That&#8217;s all.<br />
I have Rheumatoid Arthritis. I keep saying what we need are RA dr&#8217;s who have RA. Hahaha.</p>
<p>I have RA in my cervical spine. It does refer pain to arms and hands. This theory is fascinating.</p>
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		<title>By: Jeanne</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-722</link>
		<dc:creator>Jeanne</dc:creator>
		<pubDate>Tue, 28 Jul 2009 06:24:47 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-722</guid>
		<description>Thanks for your post.  I developed FM after spinal fusion at the c5-c6 and c6-c7 levels.  But also had SEVERE menengitis years before and nearly died from it.  You&#039;ve got me thinking now wondering how all that menengial scar tissue could contribute to nerve tension.

Each one of us is our own scientist specializing in what&#039;s best for us.  I have a Ph.D. in Immunology and damned that it really hasn&#039;t helped a bit in dealing with FM.  What helps most is just listening to my body and using whatever therapy is most applicable at any given time.

The most disappointing thing to me is how much research is being done on pain and how little successful new medicine development comes from it.</description>
		<content:encoded><![CDATA[<p>Thanks for your post.  I developed FM after spinal fusion at the c5-c6 and c6-c7 levels.  But also had SEVERE menengitis years before and nearly died from it.  You&#8217;ve got me thinking now wondering how all that menengial scar tissue could contribute to nerve tension.</p>
<p>Each one of us is our own scientist specializing in what&#8217;s best for us.  I have a Ph.D. in Immunology and damned that it really hasn&#8217;t helped a bit in dealing with FM.  What helps most is just listening to my body and using whatever therapy is most applicable at any given time.</p>
<p>The most disappointing thing to me is how much research is being done on pain and how little successful new medicine development comes from it.</p>
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		<title>By: fibrohaven</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-721</link>
		<dc:creator>fibrohaven</dc:creator>
		<pubDate>Thu, 23 Jul 2009 23:05:57 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-721</guid>
		<description>Scientific attitude is great. Like I said before, we are all like a bunch of scientists trying to figure this whole FM conundrum out.

I am glad you ordered the book. I hope you will be able to attend our follow up meetings in September. The plan is to discuss it as a group, formulate all sorts of questions, and then invite Dr. Sarkozi back to discuss them. It should be very interesting!</description>
		<content:encoded><![CDATA[<p>Scientific attitude is great. Like I said before, we are all like a bunch of scientists trying to figure this whole FM conundrum out.</p>
<p>I am glad you ordered the book. I hope you will be able to attend our follow up meetings in September. The plan is to discuss it as a group, formulate all sorts of questions, and then invite Dr. Sarkozi back to discuss them. It should be very interesting!</p>
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		<title>By: Kathy</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-717</link>
		<dc:creator>Kathy</dc:creator>
		<pubDate>Thu, 23 Jul 2009 19:42:07 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-717</guid>
		<description>&quot;Sales pitch&quot; was perhaps a poor choice of words. I wish I could have been there too.

Thank you for the offer...but the book is (or should be) already on it&#039;s way. I was hoping it would arrive before I left, but I imagine I&#039;ll be tearing through it when I get back.

I have a background that encourages healthy skepticism...but that doesn&#039;t mean I always use it. When I&#039;m hurting, I want it fixed. But I guess my point is that to me, skepticism isn&#039;t the opposite of an open mind.

Maybe skepticism is a poor choice of word, also. Okay, how about a scientific attitude? http://wiki.answers.com/Q/What_is_the_scientific_attitude_and_what_attitudes_and_characteristics_define_a_good_scientist</description>
		<content:encoded><![CDATA[<p>&#8220;Sales pitch&#8221; was perhaps a poor choice of words. I wish I could have been there too.</p>
<p>Thank you for the offer&#8230;but the book is (or should be) already on it&#8217;s way. I was hoping it would arrive before I left, but I imagine I&#8217;ll be tearing through it when I get back.</p>
<p>I have a background that encourages healthy skepticism&#8230;but that doesn&#8217;t mean I always use it. When I&#8217;m hurting, I want it fixed. But I guess my point is that to me, skepticism isn&#8217;t the opposite of an open mind.</p>
<p>Maybe skepticism is a poor choice of word, also. Okay, how about a scientific attitude? <a href="http://wiki.answers.com/Q/What_is_the_scientific_attitude_and_what_attitudes_and_characteristics_define_a_good_scientist" rel="nofollow">http://wiki.answers.com/Q/What_is_the_scientific_attitude_and_what_attitudes_and_characteristics_define_a_good_scientist</a></p>
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		<title>By: fibrohaven</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-720</link>
		<dc:creator>fibrohaven</dc:creator>
		<pubDate>Thu, 23 Jul 2009 18:45:29 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-720</guid>
		<description>Except that it wasn&#039;t a sales pitch Kathy. I wish you had been able to attend the meeting so you could have seen for yourself.

Dr. Sarkozi&#039;s presentation was based on many years of patient treatment, research, and advocacy for Fibromyalgia patients. It was impossible to take all the information he has spent years accumulating, and everything he has written in his book, and fit it into a one hour presentation. Impossible!

Unfortunately there were many things he had to summarize, briefly detail, and refer us to his book for more information. Yes he was looking to sale copies of his book, but that speaks nothing to his commitment to and passionate advocacy for FM patients. He wrote the book FOR US, to HELP US because he believed it to be the best format to reach the largest audience. Should he not promote it? Should he not encourage each of us to buy a copy?

It is okay to be skeptical, but skepticism is best served if you first have as many facts as you can - not just one person&#039;s opinion (and a opinion that she admitted herself was skewed). It was not a perfect presentation. My head is spinning with all the information he shared. It was a lot to absorb. At points I felt his presentation was tailored to his peers, not his patients, and I told him so. I am worried I may have the same experience with his book.

But here are the facts I am most taking away from the evening. He knows we are all suffering. He knows we do not get adequate care from our doctors. He believes that our pain is real and that it has a source, and he is trying to start a movement that will change/help all of that. Dr. Sarkozi believes strongly that the movement will succeed best if he takes it directly to the patients, not to his peers.

So, here is someone who cares, and wants to take action to change a medical system that disregards FM patients. Here is someone who believes we can all have a better quality of life.  Here is someone willing to donate his time and travel anywhere in the country to share his work with support groups and patients. Why wouldn&#039;t you want to own his book? Or at the very least be interested enough to borrow my copy when I am done reading it. It is yours if you want it. Just let me know.</description>
		<content:encoded><![CDATA[<p>Except that it wasn&#8217;t a sales pitch Kathy. I wish you had been able to attend the meeting so you could have seen for yourself.</p>
<p>Dr. Sarkozi&#8217;s presentation was based on many years of patient treatment, research, and advocacy for Fibromyalgia patients. It was impossible to take all the information he has spent years accumulating, and everything he has written in his book, and fit it into a one hour presentation. Impossible!</p>
<p>Unfortunately there were many things he had to summarize, briefly detail, and refer us to his book for more information. Yes he was looking to sale copies of his book, but that speaks nothing to his commitment to and passionate advocacy for FM patients. He wrote the book FOR US, to HELP US because he believed it to be the best format to reach the largest audience. Should he not promote it? Should he not encourage each of us to buy a copy?</p>
<p>It is okay to be skeptical, but skepticism is best served if you first have as many facts as you can &#8211; not just one person&#8217;s opinion (and a opinion that she admitted herself was skewed). It was not a perfect presentation. My head is spinning with all the information he shared. It was a lot to absorb. At points I felt his presentation was tailored to his peers, not his patients, and I told him so. I am worried I may have the same experience with his book.</p>
<p>But here are the facts I am most taking away from the evening. He knows we are all suffering. He knows we do not get adequate care from our doctors. He believes that our pain is real and that it has a source, and he is trying to start a movement that will change/help all of that. Dr. Sarkozi believes strongly that the movement will succeed best if he takes it directly to the patients, not to his peers.</p>
<p>So, here is someone who cares, and wants to take action to change a medical system that disregards FM patients. Here is someone who believes we can all have a better quality of life.  Here is someone willing to donate his time and travel anywhere in the country to share his work with support groups and patients. Why wouldn&#8217;t you want to own his book? Or at the very least be interested enough to borrow my copy when I am done reading it. It is yours if you want it. Just let me know.</p>
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		<title>By: Kathy</title>
		<link>http://www.fibrohaven.com/2009/07/22/information-is-power-so-i-am-going-to-get-me-some/comment-page-1/#comment-718</link>
		<dc:creator>Kathy</dc:creator>
		<pubDate>Thu, 23 Jul 2009 18:05:41 +0000</pubDate>
		<guid isPermaLink="false">http://fibrohaven.wordpress.com/?p=1379#comment-718</guid>
		<description>Dr. Whitcomb&#039;s hypothesis sounds a lot like Dr. Holman&#039;s. Dr. Holman is a rheumatologist in Renton (near Seattle) who&#039;s work was highlighted in Fibromyalgia Network Journal (see a brief summary at www.fmnetnews.com/basics-issue.php )

Dr. Holman&#039;s research has been published in the Pain Journal and received accolades. However, both my primary care doctor (whose office was on the same floor of the hospital as Dr. Holman) and my rheumy seriously questioned his conclusions. Every doctor has their opinion!

Keeping an open mind is very important. But skepticism (in the form of suspended judgement) is a valuable tool to use with that open mind. The fact that Dr. Sarkozi&#039;s presentation was a sales pitch without discussion of the findings is a concern. I&#039;m glad he&#039;s willing to come back.

There is an answer, a solution (or many), to fibromyalgia. Thank you for helping us try to find the information, Dani. I really appreciate your herculean efforts!</description>
		<content:encoded><![CDATA[<p>Dr. Whitcomb&#8217;s hypothesis sounds a lot like Dr. Holman&#8217;s. Dr. Holman is a rheumatologist in Renton (near Seattle) who&#8217;s work was highlighted in Fibromyalgia Network Journal (see a brief summary at <a href="http://www.fmnetnews.com/basics-issue.php" rel="nofollow">http://www.fmnetnews.com/basics-issue.php</a> )</p>
<p>Dr. Holman&#8217;s research has been published in the Pain Journal and received accolades. However, both my primary care doctor (whose office was on the same floor of the hospital as Dr. Holman) and my rheumy seriously questioned his conclusions. Every doctor has their opinion!</p>
<p>Keeping an open mind is very important. But skepticism (in the form of suspended judgement) is a valuable tool to use with that open mind. The fact that Dr. Sarkozi&#8217;s presentation was a sales pitch without discussion of the findings is a concern. I&#8217;m glad he&#8217;s willing to come back.</p>
<p>There is an answer, a solution (or many), to fibromyalgia. Thank you for helping us try to find the information, Dani. I really appreciate your herculean efforts!</p>
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