<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
		>
<channel>
	<title>Comments on: OmniPod Update</title>
	<atom:link href="http://www.diabetesmine.com/2007/05/omnipod_update.html/feed" rel="self" type="application/rss+xml" />
	<link>http://www.diabetesmine.com/2007/05/omnipod_update.html</link>
	<description>A gold mine of straight talk and encouragement for people living with diabetes</description>
	<lastBuildDate>Sun, 12 Feb 2012 21:05:41 +0000</lastBuildDate>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
	<generator>http://wordpress.org/?v=</generator>
<xhtml:meta xmlns:xhtml="http://www.w3.org/1999/xhtml" name="robots" content="noindex" />
	<item>
		<title>By: Jean Haight</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-543800</link>
		<dc:creator>Jean Haight</dc:creator>
		<pubDate>Fri, 28 Oct 2011 23:16:47 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-543800</guid>
		<description>If anyone is ready to start on Medicare we need to work together to get the members of Congress to change the Code Numbers. I know this is a real task. The present Code Numbers are: Pod A 9274 and PDME 0784,which means that they are disposable and Medicare will not cover them. We have to do what people are doing to get anything they want accomplished to get done: write letters,make phone calls,have family members and friends help with these task. If we sit back and wait it’s not going to get done done.

We are not important enough to stimulate action from the Congress,so lets show them how wrong they are. I’ve even been contacting members of the National Media if we can get them interested we have a great ally. I personally believe in the POWER of the PRESS!
If anyone has any other ideas on how to get this accomplished please share them.
Than you,

Jean D Haight</description>
		<content:encoded><![CDATA[<p>If anyone is ready to start on Medicare we need to work together to get the members of Congress to change the Code Numbers. I know this is a real task. The present Code Numbers are: Pod A 9274 and PDME 0784,which means that they are disposable and Medicare will not cover them. We have to do what people are doing to get anything they want accomplished to get done: write letters,make phone calls,have family members and friends help with these task. If we sit back and wait it’s not going to get done done.</p>
<p>We are not important enough to stimulate action from the Congress,so lets show them how wrong they are. I’ve even been contacting members of the National Media if we can get them interested we have a great ally. I personally believe in the POWER of the PRESS!<br />
If anyone has any other ideas on how to get this accomplished please share them.<br />
Than you,</p>
<p>Jean D Haight</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Jean Haight</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-534318</link>
		<dc:creator>Jean Haight</dc:creator>
		<pubDate>Tue, 05 Jul 2011 01:09:48 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-534318</guid>
		<description>I havebeen using the Omni Pod for over 5 years.  I&#039;ve had other pumps before this,this is defintely the best.  The only problem I have with Omni Pod is that I have just started on Medicare and Medicare won&#039;t cover the Omni Pod because of the Code Numbers it has been given.  It literally takes an Act of Congress to get these numbers changed.  I have been working with my Congresspersons Office and the two centers for my State to get the code nubers changed.  The present Code numbers are Pod A 9274 and PDM E 0784. This means that Medicare wont cover the Omni Pod because it is deemed disposable.  If the Congress will change the Code numbers to make the Omni Pod and the PDM durable Medicare will cover it.

I am working on it with my Congress Person,a newscaster on the local NBC network,and the Insulet Corporation to get the code numbers changed to make the Omni Pod a durable item.  It seems to be progressing and I&#039;m hoping that in the not to distant future it will be given the code numbers  so that it can be covered by Medicarw.</description>
		<content:encoded><![CDATA[<p>I havebeen using the Omni Pod for over 5 years.  I&#8217;ve had other pumps before this,this is defintely the best.  The only problem I have with Omni Pod is that I have just started on Medicare and Medicare won&#8217;t cover the Omni Pod because of the Code Numbers it has been given.  It literally takes an Act of Congress to get these numbers changed.  I have been working with my Congresspersons Office and the two centers for my State to get the code nubers changed.  The present Code numbers are Pod A 9274 and PDM E 0784. This means that Medicare wont cover the Omni Pod because it is deemed disposable.  If the Congress will change the Code numbers to make the Omni Pod and the PDM durable Medicare will cover it.</p>
<p>I am working on it with my Congress Person,a newscaster on the local NBC network,and the Insulet Corporation to get the code numbers changed to make the Omni Pod a durable item.  It seems to be progressing and I&#8217;m hoping that in the not to distant future it will be given the code numbers  so that it can be covered by Medicarw.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: CB</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-528022</link>
		<dc:creator>CB</dc:creator>
		<pubDate>Sun, 23 Jan 2011 03:00:57 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-528022</guid>
		<description>It took me 20 years to become a &#039;pumper&#039; &amp; omnipod was the one. Diagnosed at age 5 &amp; a Type 1 for 35 years, I was excited by their offering. Unfortunately, I&#039;m very disappointed in their customer service &amp; considering moving to a different pump.</description>
		<content:encoded><![CDATA[<p>It took me 20 years to become a &#8216;pumper&#8217; &amp; omnipod was the one. Diagnosed at age 5 &amp; a Type 1 for 35 years, I was excited by their offering. Unfortunately, I&#8217;m very disappointed in their customer service &amp; considering moving to a different pump.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Laine</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-434769</link>
		<dc:creator>Laine</dc:creator>
		<pubDate>Mon, 30 Nov 2009 17:41:40 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-434769</guid>
		<description>I wish that I was on the Omni Pod so bad but I am only 11 so my parents made sure that I had to get the Animas with tubing. They think that getting the Omni Pod wounld be bad because I preticipate in a lot of sports and such as soccer. And they said that I need to wait till the Omni Pod gets a lot smaller then how big that it already is. Hope that maybe when I get older that I can start to use the Omni Pod which would I think that would make my life a lot better.</description>
		<content:encoded><![CDATA[<p>I wish that I was on the Omni Pod so bad but I am only 11 so my parents made sure that I had to get the Animas with tubing. They think that getting the Omni Pod wounld be bad because I preticipate in a lot of sports and such as soccer. And they said that I need to wait till the Omni Pod gets a lot smaller then how big that it already is. Hope that maybe when I get older that I can start to use the Omni Pod which would I think that would make my life a lot better.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Daniel</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-386924</link>
		<dc:creator>Daniel</dc:creator>
		<pubDate>Wed, 30 Sep 2009 06:49:47 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-386924</guid>
		<description>OK, so I am not sure if this is the site to ask a question on, there seems to be some pretty strong opinions on here on all sides.  I am a clinical social worker with 15 plus years in a Hospital setting and to my surprise continue to remain lost on this aspect of my own care. 

I am a 47 yr old male on insulin for 10 yr now.  I was the last in my family to be diagnosed and now the only brittle one of the bunch.  I have maybe 15 living family members within 2-3 generations currently diabetic and countless that died from complications.  Diet, drugs, exercise, and shots have really done nothing to truly control my sugars and the side effects are now at a point of showing their unhealthy heads.  I have begun discussion with my PCP about finding an Endo in the Phoenix, AZ area (I moved here about a yr ago), but he is reluctant to give up control.  Oh well, he does not have it anyway.  

My questions tend to be based on is a pump something I should now consider?  

My sugars have always spiked 2 hours after eating no matter what I eat, the insulin I take or anything else we can figure out. For example, I was at 97 this AM and had 2 eggs a small sausage patty and coffee ( took 10 units of novolog).  3 hours later I checked my sugars and was at 179. 

I currently take 65 Units of Lantus nightly and between 10-28 units of Novolog with each meal.  My scale starts at 10 units and runs 1 unit for every 10 points above target.  My PCP is wanting me to take more insulin even to the point of causing crashes (I think this is very unsafe).

Would a pump be programmable (and would the OP be a good pump to start with) enough to see these spikes and adjust for them?  I do not mind the 6-8 BSs a day if they work, I do that many tests now.  However, if I end up doing Insulin before a meal and then 2 hours later that could end up as many a 7 shots a day (3 before meals, 3 after meals and 1 at night).  That would get real old real quick.  

Any suggestions?  Am I nuts or just an extremely out of control diabetic?

Right now My A1C is 9.8 and climbing. 

seeking help and advice in desperation,

Daniel ;-)</description>
		<content:encoded><![CDATA[<p>OK, so I am not sure if this is the site to ask a question on, there seems to be some pretty strong opinions on here on all sides.  I am a clinical social worker with 15 plus years in a Hospital setting and to my surprise continue to remain lost on this aspect of my own care. </p>
<p>I am a 47 yr old male on insulin for 10 yr now.  I was the last in my family to be diagnosed and now the only brittle one of the bunch.  I have maybe 15 living family members within 2-3 generations currently diabetic and countless that died from complications.  Diet, drugs, exercise, and shots have really done nothing to truly control my sugars and the side effects are now at a point of showing their unhealthy heads.  I have begun discussion with my PCP about finding an Endo in the Phoenix, AZ area (I moved here about a yr ago), but he is reluctant to give up control.  Oh well, he does not have it anyway.  </p>
<p>My questions tend to be based on is a pump something I should now consider?  </p>
<p>My sugars have always spiked 2 hours after eating no matter what I eat, the insulin I take or anything else we can figure out. For example, I was at 97 this AM and had 2 eggs a small sausage patty and coffee ( took 10 units of novolog).  3 hours later I checked my sugars and was at 179. </p>
<p>I currently take 65 Units of Lantus nightly and between 10-28 units of Novolog with each meal.  My scale starts at 10 units and runs 1 unit for every 10 points above target.  My PCP is wanting me to take more insulin even to the point of causing crashes (I think this is very unsafe).</p>
<p>Would a pump be programmable (and would the OP be a good pump to start with) enough to see these spikes and adjust for them?  I do not mind the 6-8 BSs a day if they work, I do that many tests now.  However, if I end up doing Insulin before a meal and then 2 hours later that could end up as many a 7 shots a day (3 before meals, 3 after meals and 1 at night).  That would get real old real quick.  </p>
<p>Any suggestions?  Am I nuts or just an extremely out of control diabetic?</p>
<p>Right now My A1C is 9.8 and climbing. </p>
<p>seeking help and advice in desperation,</p>
<p>Daniel <img src='https://www.diabetesmine.com/wp-includes/images/smilies/icon_wink.gif' alt=';-)' class='wp-smiley' /> </p>
]]></content:encoded>
	</item>
	<item>
		<title>By: felix</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-363669</link>
		<dc:creator>felix</dc:creator>
		<pubDate>Fri, 14 Aug 2009 23:33:41 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-363669</guid>
		<description>I have a similar experience to Mike D above. I want to love the omnipod since it is easier to give many small boluses (boli?) with the pod than with the needle. Also, I would rather not have a pager type pump on my belt with a tube if possible.

My issue is that the pod fails a *lot*. Either occlusions or failing while priming. A couple  of nights ago I had 3 pods fail in about an hour. Also, failed pods can interfere with the new pod (I assume the wireless signals get mixed up) which leads to more frustration, usually while high. Calling in the failed pods means you have to go thru a 10 minute phone conversation reciting serial numbers and error codes. (I&#039;m not sure why they assume you are calling in failed pods falsely, it&#039;s not like I can do anything with a bunch of extra pods...) Another issue is that a failed pod means you lose all your insulin which means you end up fighting with your insurance company again...

So at the moment I am looking for an alternative. Any suggestions?</description>
		<content:encoded><![CDATA[<p>I have a similar experience to Mike D above. I want to love the omnipod since it is easier to give many small boluses (boli?) with the pod than with the needle. Also, I would rather not have a pager type pump on my belt with a tube if possible.</p>
<p>My issue is that the pod fails a *lot*. Either occlusions or failing while priming. A couple  of nights ago I had 3 pods fail in about an hour. Also, failed pods can interfere with the new pod (I assume the wireless signals get mixed up) which leads to more frustration, usually while high. Calling in the failed pods means you have to go thru a 10 minute phone conversation reciting serial numbers and error codes. (I&#8217;m not sure why they assume you are calling in failed pods falsely, it&#8217;s not like I can do anything with a bunch of extra pods&#8230;) Another issue is that a failed pod means you lose all your insulin which means you end up fighting with your insurance company again&#8230;</p>
<p>So at the moment I am looking for an alternative. Any suggestions?</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Mike D</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-339604</link>
		<dc:creator>Mike D</dc:creator>
		<pubDate>Tue, 02 Jun 2009 15:09:09 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-339604</guid>
		<description>To address only the most recent comments (as I know insulet has made many progressions since the first years) I have been using the pod for 10 months and have had a very frustrating experience.  I should first say that it IS a great product / idea and for all those concerned over the weight /feel of the pod or placement please do not worry.  I am a very active person (road bike, lift, train for marathons and trail hike on almost a daily basis) and I place the pod on the side of my buttox / hip.  You would be surprised how much it is not a hindrance to being comfortable, does not pull there, is not visible, an barely has a bulge even with tighter jeans (I am a guy girls you may have more of a bulge) or dress pants.  Also, even when on a mountain for multiple nights or running where it bounces etc. the thing stays put and does not come off easy.

The majoy thing for me however, and one that I have been working with insulet with and am praying they come up with a solution, as I have tried everything they have recommended, is that the failure rate is extremely high.  I was told by my doctor that it doesn&#039;t work as well for some people than others, but I had no idea it would be this bad.  I have been tracking my failures in a spreadsheet in an extremely detailed manner in order to best facilitate finding a solution and on average when there is an occlussion, it occurs upon the first bolus.  Sometimes it will happen later, which is even more frustrating because usually my blood sugar will sky rocket due to lack of insulin flow well before the buzzer goes off, which by the way continues to ring until you can get to your meter and push the &#039;ok&#039; button.  To give a detail over the results, I have tracked my progress since the 1st of the year which has been 151 days as of today.  Theoretically this would require 53 pods (1 per 3 days).  Over this time period I have experienced 39 pod failures, 34 of which were due to occlussion.  As an approximation, I figure I &#039;should have&#039; used 51 pods, however 34 were switched out due to occlussions resulting in a total failure rate of 40% (34 failed / 85 total).  I know that my results are not representative of the typical experience, but just want people to know how bad a case can get.  Is there anyone reading that has experienced such difficulty?  I do want to emphasize to any considering the product however that when I get past a couple hours with no occlussions, this thing works awesome, and you may not encounter such occlussion issues.</description>
		<content:encoded><![CDATA[<p>To address only the most recent comments (as I know insulet has made many progressions since the first years) I have been using the pod for 10 months and have had a very frustrating experience.  I should first say that it IS a great product / idea and for all those concerned over the weight /feel of the pod or placement please do not worry.  I am a very active person (road bike, lift, train for marathons and trail hike on almost a daily basis) and I place the pod on the side of my buttox / hip.  You would be surprised how much it is not a hindrance to being comfortable, does not pull there, is not visible, an barely has a bulge even with tighter jeans (I am a guy girls you may have more of a bulge) or dress pants.  Also, even when on a mountain for multiple nights or running where it bounces etc. the thing stays put and does not come off easy.</p>
<p>The majoy thing for me however, and one that I have been working with insulet with and am praying they come up with a solution, as I have tried everything they have recommended, is that the failure rate is extremely high.  I was told by my doctor that it doesn&#8217;t work as well for some people than others, but I had no idea it would be this bad.  I have been tracking my failures in a spreadsheet in an extremely detailed manner in order to best facilitate finding a solution and on average when there is an occlussion, it occurs upon the first bolus.  Sometimes it will happen later, which is even more frustrating because usually my blood sugar will sky rocket due to lack of insulin flow well before the buzzer goes off, which by the way continues to ring until you can get to your meter and push the &#8216;ok&#8217; button.  To give a detail over the results, I have tracked my progress since the 1st of the year which has been 151 days as of today.  Theoretically this would require 53 pods (1 per 3 days).  Over this time period I have experienced 39 pod failures, 34 of which were due to occlussion.  As an approximation, I figure I &#8216;should have&#8217; used 51 pods, however 34 were switched out due to occlussions resulting in a total failure rate of 40% (34 failed / 85 total).  I know that my results are not representative of the typical experience, but just want people to know how bad a case can get.  Is there anyone reading that has experienced such difficulty?  I do want to emphasize to any considering the product however that when I get past a couple hours with no occlussions, this thing works awesome, and you may not encounter such occlussion issues.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Mike D</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-339599</link>
		<dc:creator>Mike D</dc:creator>
		<pubDate>Tue, 02 Jun 2009 15:06:18 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-339599</guid>
		<description>To address only the most recent comments (as I know insulet has made many progressions since the first years) I have been using the pod for 10 months and have had a very frustrating experience.  I should first say that it IS a great product / idea and for all those concerned over the weight /feel of the pod or placement please do not worry.  I am a very active person (road bike, lift, train for marathons and trail hike on almost a daily basis) and I place the pod on the side of my buttox / hip.  You would be surprised how much it is not a hindrance to being comfortable, does not pull there, is not visible, an barely has a bulge even with tighter jeans (I am a guy girls you may have more of a bulge) or dress pants.  Also, even when on a mountain for multiple nights or running where it bounces etc. the thing stays put and does not come off easy.

The majoy thing for me however, and one that I have been working with insulet with and am praying they come up with a solution, as I have tried everything they have recommended, is that the failure rate is extremely high.  I was told by my doctor that it doesn&#039;t work as well for some people than others, but I had no idea it would be this bad.  I have been tracking my failures in a spreadsheet in an extremely detailed manner in order to best facilitate finding a solution and on average when there is an occlussion, it occurs upon the first bolus.  Sometimes it will happen later, which is even more frustrating because usually my blood sugar will sky rocket due to lack of insulin flow well before the buzzer goes off, which by the way continues to ring until you can get to your meter and push the &#039;ok&#039; button.  To give a detail over the results, I have tracked my progress since the 1st of the year which has been 151 days as of today.  Theoretically this would require 53 pods (1 per 3 days).  Over this time period I have experienced 39 pod failures, 34 of which were due to occlussion.  As an approximation, I figure I &#039;should have&#039; used 51 pods, however 34 were switched out due to occlussions resulting in a total failure rate of 40% (34 failed / 85 total).  I know that my results are not representative of the typical experience, but just want people to know how bad a case can get.  Is there anyone reading that has experienced such difficulty?  I do want to remind anyone considering this product however that once I get the pod attached and past the first 1 or 2 boluses without an occlussion, it works great and you may very well experience just that without the occlussion problems at all.</description>
		<content:encoded><![CDATA[<p>To address only the most recent comments (as I know insulet has made many progressions since the first years) I have been using the pod for 10 months and have had a very frustrating experience.  I should first say that it IS a great product / idea and for all those concerned over the weight /feel of the pod or placement please do not worry.  I am a very active person (road bike, lift, train for marathons and trail hike on almost a daily basis) and I place the pod on the side of my buttox / hip.  You would be surprised how much it is not a hindrance to being comfortable, does not pull there, is not visible, an barely has a bulge even with tighter jeans (I am a guy girls you may have more of a bulge) or dress pants.  Also, even when on a mountain for multiple nights or running where it bounces etc. the thing stays put and does not come off easy.</p>
<p>The majoy thing for me however, and one that I have been working with insulet with and am praying they come up with a solution, as I have tried everything they have recommended, is that the failure rate is extremely high.  I was told by my doctor that it doesn&#8217;t work as well for some people than others, but I had no idea it would be this bad.  I have been tracking my failures in a spreadsheet in an extremely detailed manner in order to best facilitate finding a solution and on average when there is an occlussion, it occurs upon the first bolus.  Sometimes it will happen later, which is even more frustrating because usually my blood sugar will sky rocket due to lack of insulin flow well before the buzzer goes off, which by the way continues to ring until you can get to your meter and push the &#8216;ok&#8217; button.  To give a detail over the results, I have tracked my progress since the 1st of the year which has been 151 days as of today.  Theoretically this would require 53 pods (1 per 3 days).  Over this time period I have experienced 39 pod failures, 34 of which were due to occlussion.  As an approximation, I figure I &#8216;should have&#8217; used 51 pods, however 34 were switched out due to occlussions resulting in a total failure rate of 40% (34 failed / 85 total).  I know that my results are not representative of the typical experience, but just want people to know how bad a case can get.  Is there anyone reading that has experienced such difficulty?  I do want to remind anyone considering this product however that once I get the pod attached and past the first 1 or 2 boluses without an occlussion, it works great and you may very well experience just that without the occlussion problems at all.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Andy</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-334025</link>
		<dc:creator>Andy</dc:creator>
		<pubDate>Wed, 20 May 2009 17:36:50 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-334025</guid>
		<description>I&#039;ve been on the Pod 3 1/2 years and make no significant effort to hind it even though I can easily hide it if I want.  If I was a kid I would carry a Sharpie and let kids sign it like a cast.  If you think the ignorance is bad today you should have seen it in 1955.  BTW for those that care the Pod is way easier to hide than a pump because it goes so many more places and is less than 40%a the size of any other pump.  And that&#039;s not including the bulk of the tubing and catheter for the other pumps.

Also in answer to an earlier post.  Yes in the early days Insulet had some Pod failure issues. They have been addressed and the failure rate is now very close to zero.</description>
		<content:encoded><![CDATA[<p>I&#8217;ve been on the Pod 3 1/2 years and make no significant effort to hind it even though I can easily hide it if I want.  If I was a kid I would carry a Sharpie and let kids sign it like a cast.  If you think the ignorance is bad today you should have seen it in 1955.  BTW for those that care the Pod is way easier to hide than a pump because it goes so many more places and is less than 40%a the size of any other pump.  And that&#8217;s not including the bulk of the tubing and catheter for the other pumps.</p>
<p>Also in answer to an earlier post.  Yes in the early days Insulet had some Pod failure issues. They have been addressed and the failure rate is now very close to zero.</p>
]]></content:encoded>
	</item>
	<item>
		<title>By: Jill</title>
		<link>http://www.diabetesmine.com/2007/05/omnipod_update.html/comment-page-1#comment-333240</link>
		<dc:creator>Jill</dc:creator>
		<pubDate>Tue, 19 May 2009 04:18:04 +0000</pubDate>
		<guid isPermaLink="false">http://diabetesmine.dreamhosters.com/2007/05/22/omnipod-update/#comment-333240</guid>
		<description>I have a question for all of you who are concerned about &quot;hiding&quot; the pod;  why would you want to?  In the eight years since my son was diagnosed type 1, I have been absolutely gob-smacked over the ignorance of the general public and diabetes and its issues.  When ever someone comments on his pod (all very politely I might add) he uses it as a teachable moment.  Lots of people have gained a better understanding of this disorder thanks to my wonderful, willing, and (gee...what IS the opposite of vain? ;) ) 15 year old son.  Diabetes is not something anyone needs to be ashamed of.</description>
		<content:encoded><![CDATA[<p>I have a question for all of you who are concerned about &#8220;hiding&#8221; the pod;  why would you want to?  In the eight years since my son was diagnosed type 1, I have been absolutely gob-smacked over the ignorance of the general public and diabetes and its issues.  When ever someone comments on his pod (all very politely I might add) he uses it as a teachable moment.  Lots of people have gained a better understanding of this disorder thanks to my wonderful, willing, and (gee&#8230;what IS the opposite of vain? <img src='https://www.diabetesmine.com/wp-includes/images/smilies/icon_wink.gif' alt=';)' class='wp-smiley' />  ) 15 year old son.  Diabetes is not something anyone needs to be ashamed of.</p>
]]></content:encoded>
	</item>
</channel>
</rss>

