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	<title>Comments on: new user</title>
	<link>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/</link>
	<description></description>
	<pubDate>Fri, 05 Dec 2008 10:14:26 +0000</pubDate>
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		<title>By: Neva Marjory</title>
		<link>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-131</link>
		<author>Neva Marjory</author>
		<pubDate>Mon, 04 Aug 2003 06:50:29 +0000</pubDate>
		<guid>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-131</guid>
		<description>My email addy is mytcelt@...&#60;br
keep it somewhat private....members here and another group only.&#60;br</description>
		<content:encoded><![CDATA[<p>My email addy is <a href="mailto:mytcelt@...&lt;br">mytcelt@&#8230;&lt;br</a><br />
keep it somewhat private&#8230;.members here and another group only.&lt;br</p>
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		<title>By: Neva Marjory</title>
		<link>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-130</link>
		<author>Neva Marjory</author>
		<pubDate>Sun, 03 Aug 2003 05:14:58 +0000</pubDate>
		<guid>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-130</guid>
		<description>I'm IDDM for 16 years and belong to a list of
 pumpers, If you'd like to visit it, it's
 at:&#60;br
 page for your area about 'pump friendly doctors and
 such. You might want to join the mail list, but if
 you're not allowed too much email, you should go for
 'browseror web only' to receive email. This way you don't
 get several hundred emails in a week. The IP list is
 3,000 members strong.&#60;br
 the three pump makers and you can go to their
 websites and get information packs sent to you. Getting a
 pump is like buying a new car almost. It depends on
 your lifestyle and what you want from the pump. Some
 are waterproof, some aren't. Some look nicer than
 others and some have features while others
 &lt;!--more--&gt;
 don't.&#60;br
 book called "Pumping Insulin" by John Walsh and Ruth
 Roberts. This is the 'pumper's Bible' and is a decent
 reference to have.&#60;br
 and wouldn't go back to shots for anything. They'll
 have to pry my pump from my cold, dead
 hand...&#38;lt;G&#38;gt;&#60;br</description>
		<content:encoded><![CDATA[<p>I&#8217;m IDDM for 16 years and belong to a list of<br />
 pumpers, If you&#8217;d like to visit it, it&#8217;s<br />
 at:&lt;br<br />
 page for your area about &#8216;pump friendly doctors and<br />
 such. You might want to join the mail list, but if<br />
 you&#8217;re not allowed too much email, you should go for<br />
 &#8216;browseror web only&#8217; to receive email. This way you don&#8217;t<br />
 get several hundred emails in a week. The IP list is<br />
 3,000 members strong.&lt;br<br />
 the three pump makers and you can go to their<br />
 websites and get information packs sent to you. Getting a<br />
 pump is like buying a new car almost. It depends on<br />
 your lifestyle and what you want from the pump. Some<br />
 are waterproof, some aren&#8217;t. Some look nicer than<br />
 others and some have features while others<br />
 <!--more--><br />
 don&#8217;t.&lt;br<br />
 book called &#8220;Pumping Insulin&#8221; by John Walsh and Ruth<br />
 Roberts. This is the &#8216;pumper&#8217;s Bible&#8217; and is a decent<br />
 reference to have.&lt;br<br />
 and wouldn&#8217;t go back to shots for anything. They&#8217;ll<br />
 have to pry my pump from my cold, dead<br />
 hand&#8230;&amp;lt;G&amp;gt;&lt;br</p>
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	<item>
		<title>By: Neva Marjory</title>
		<link>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-129</link>
		<author>Neva Marjory</author>
		<pubDate>Sat, 02 Aug 2003 03:39:27 +0000</pubDate>
		<guid>http://www.diabetes-symptoms.pocket-book.com/2003/08/01/new-user/#comment-129</guid>
		<description>hi melissa.... I got diagnosed the summer before
 last (im 19 now) and last summer i went on the insulin
 pump. i LOVE it. some of the reasons i got to go on it
 so quickly were 1) i was at a hospital that had a
 very intesive program geared towards putting kids ont
 he pump (getting diagnosed as a 17 year old, i was
 able to go to a childrens hospital still, which tends
 to be a bit better since theyre more used to dealing
 with type 1 diabetics), and 2) i got myself under
 control as soon as i could. I had to really work at it,
 learning all about carb counting and whatnot... i had to
 almost immediately take charge of my disease and
 aggressively work to keep myself in check with my blood
 sugars. they usually wait at least a year before putting
 someone on the pump, though, so dont think its soemthing
 &lt;!--more--&gt;
 that will come around tomorrow... it takes a lot of
 hard work. One other thing... i was on 2 shots at
 first too, but right before getting put on the pump
 they had to change me to 3 shots a day (because of my
 insurance company, they wouldnt pay for it unless i was on
 3 shots a day for some reason... you know how those
 people can be).&#60;br
 whatnot.... i havent had too much of a problem yet. if you
 are really concerned about it, you can opt for a site
 like the sillouette, as this is more easily detached
 from and doesnt leave any tubing on you when you
 detatch from it. It can be kinda a pain in the neck, but
 the ability for freedom ALONE is enough for me to
 deal with the minor inconveniences (like not having
 low blood sugars in the middle of class!!) If you
 have any other questions about the pump or getting
 over the initial shock of diabetes or ANYTHING, please
 dont hesitate to email me, my email is
 emily.slater@... ... i know at least somewhat how you must feel...
 iw as there not too long ago. well, i hope i hear
 from you soon!!&#60;br</description>
		<content:encoded><![CDATA[<p>hi melissa&#8230;. I got diagnosed the summer before<br />
 last (im 19 now) and last summer i went on the insulin<br />
 pump. i LOVE it. some of the reasons i got to go on it<br />
 so quickly were 1) i was at a hospital that had a<br />
 very intesive program geared towards putting kids ont<br />
 he pump (getting diagnosed as a 17 year old, i was<br />
 able to go to a childrens hospital still, which tends<br />
 to be a bit better since theyre more used to dealing<br />
 with type 1 diabetics), and 2) i got myself under<br />
 control as soon as i could. I had to really work at it,<br />
 learning all about carb counting and whatnot&#8230; i had to<br />
 almost immediately take charge of my disease and<br />
 aggressively work to keep myself in check with my blood<br />
 sugars. they usually wait at least a year before putting<br />
 someone on the pump, though, so dont think its soemthing<br />
 <!--more--><br />
 that will come around tomorrow&#8230; it takes a lot of<br />
 hard work. One other thing&#8230; i was on 2 shots at<br />
 first too, but right before getting put on the pump<br />
 they had to change me to 3 shots a day (because of my<br />
 insurance company, they wouldnt pay for it unless i was on<br />
 3 shots a day for some reason&#8230; you know how those<br />
 people can be).&lt;br<br />
 whatnot&#8230;. i havent had too much of a problem yet. if you<br />
 are really concerned about it, you can opt for a site<br />
 like the sillouette, as this is more easily detached<br />
 from and doesnt leave any tubing on you when you<br />
 detatch from it. It can be kinda a pain in the neck, but<br />
 the ability for freedom ALONE is enough for me to<br />
 deal with the minor inconveniences (like not having<br />
 low blood sugars in the middle of class!!) If you<br />
 have any other questions about the pump or getting<br />
 over the initial shock of diabetes or ANYTHING, please<br />
 dont hesitate to email me, my email is<br />
 <a href="mailto:emily.slater@...">emily.slater@&#8230;</a> &#8230; i know at least somewhat how you must feel&#8230;<br />
 iw as there not too long ago. well, i hope i hear<br />
 from you soon!!&lt;br</p>
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