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	<title>
	Comments on: House Calls	</title>
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	<link>https://livingwithscleroderma.com/house-calls/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Tue, 17 Dec 2013 20:59:47 +0000</lastBuildDate>
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		<title>
		By: Pat Bizzell		</title>
		<link>https://livingwithscleroderma.com/house-calls/#comment-1880</link>

		<dc:creator><![CDATA[Pat Bizzell]]></dc:creator>
		<pubDate>Tue, 17 Dec 2013 20:59:47 +0000</pubDate>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=2131#comment-1880</guid>

					<description><![CDATA[Virtual doc vs. face to face doc--hmmm. This reminds me of current discussion in higher education about what is optimistically called &quot;distance learning.&quot; Now as a graduate student in Jewish studies, I have experienced some distance learning (I was in South Korea at the time) and found it to be surprisingly congenial, but I think that was at least in part because I had studied with the professor before and was able to enhance his emails with mental images of his kindly, droll face.

I have never tried to be a virtual professor, but I learned from this experience how much organization is required, and probably a lot more time, at least if the teacher is going to stay in email contact with each student individually, as mine did. But all of my teaching work has been done face to face, and I have to say I prefer it that way. Not every student who has a question is willing to raise a hand, but in person, I can see confusion crossing someone&#039;s face. Then again, a student was weeping in my office just the other day. She could have confided in me over the internet, but then, how would I have handed her a tissue?]]></description>
			<content:encoded><![CDATA[<p>Virtual doc vs. face to face doc&#8211;hmmm. This reminds me of current discussion in higher education about what is optimistically called &#8220;distance learning.&#8221; Now as a graduate student in Jewish studies, I have experienced some distance learning (I was in South Korea at the time) and found it to be surprisingly congenial, but I think that was at least in part because I had studied with the professor before and was able to enhance his emails with mental images of his kindly, droll face.</p>
<p>I have never tried to be a virtual professor, but I learned from this experience how much organization is required, and probably a lot more time, at least if the teacher is going to stay in email contact with each student individually, as mine did. But all of my teaching work has been done face to face, and I have to say I prefer it that way. Not every student who has a question is willing to raise a hand, but in person, I can see confusion crossing someone&#8217;s face. Then again, a student was weeping in my office just the other day. She could have confided in me over the internet, but then, how would I have handed her a tissue?</p>
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		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/house-calls/#comment-1879</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 17 Dec 2013 20:14:03 +0000</pubDate>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=2131#comment-1879</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/house-calls/#comment-1878&quot;&gt;Jesse Evans&lt;/a&gt;.

Thanks, Jesse, for your thoughtful story. There are still doctors who make house calls, but from what I could discover online, you either have to pay a premium to belong to a concierge practice or meet low income criteria for regions that are served by groups like the Visiting Physicians Association. With so much attention to the bottom line in medical services, I think most of us will never have the benefits of home visits that meant so much to our parents when we were kids. Still, I feel very lucky to have a team of doctors whose compassion and willingness to take time with me makes up for the lack of convenience.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/house-calls/#comment-1878">Jesse Evans</a>.</p>
<p>Thanks, Jesse, for your thoughtful story. There are still doctors who make house calls, but from what I could discover online, you either have to pay a premium to belong to a concierge practice or meet low income criteria for regions that are served by groups like the Visiting Physicians Association. With so much attention to the bottom line in medical services, I think most of us will never have the benefits of home visits that meant so much to our parents when we were kids. Still, I feel very lucky to have a team of doctors whose compassion and willingness to take time with me makes up for the lack of convenience.</p>
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		<item>
		<title>
		By: Jesse Evans		</title>
		<link>https://livingwithscleroderma.com/house-calls/#comment-1878</link>

		<dc:creator><![CDATA[Jesse Evans]]></dc:creator>
		<pubDate>Tue, 17 Dec 2013 19:55:57 +0000</pubDate>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=2131#comment-1878</guid>

					<description><![CDATA[Hi Evie,  thanks for the trip down memory lane. My Cousin Gordon (for whom my Son is named), died of polio contracted at the national Boy Scout jamboree in the early 50&#039;s. I remember vividly my Mother&#039;s anxiety whenever one of us got a fever, ever mindful of this family loss. When our doctor, (the only one in town) made house calls, her relief was palpable. My Brother and Sister got mild cases of polio, and my Father&#039;s legs were paralyzed by it the day after I was born.  Back then, even though Doctors actually could do less about disease, somehow they meant more to us for the more human services that only they could provide.
Cheers, Jesse]]></description>
			<content:encoded><![CDATA[<p>Hi Evie,  thanks for the trip down memory lane. My Cousin Gordon (for whom my Son is named), died of polio contracted at the national Boy Scout jamboree in the early 50&#8217;s. I remember vividly my Mother&#8217;s anxiety whenever one of us got a fever, ever mindful of this family loss. When our doctor, (the only one in town) made house calls, her relief was palpable. My Brother and Sister got mild cases of polio, and my Father&#8217;s legs were paralyzed by it the day after I was born.  Back then, even though Doctors actually could do less about disease, somehow they meant more to us for the more human services that only they could provide.<br />
Cheers, Jesse</p>
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