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	<title>interstitial lung disease Archives - Living with Scleroderma</title>
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	<description>Reflections on the Messy Complexity of Chronicity</description>
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		<title>Tag, I&#8217;m It</title>
		<link>https://livingwithscleroderma.com/tag-im-it/</link>
					<comments>https://livingwithscleroderma.com/tag-im-it/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 10 Feb 2026 13:00:35 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[interstitial lung disease]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[medication side effects]]></category>
		<category><![CDATA[resilience]]></category>
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					<description><![CDATA[<img width="700" height="525" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/02/IMG_8504.jpg?fit=700%2C525&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" fetchpriority="high" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/02/IMG_8504.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/02/IMG_8504.jpg?resize=300%2C225&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>And so, despite my best efforts, I caught the flu, too. I thought I was being really careful taking care of Al, who quarantined in our home. Wore a mask, brought him meals, the whole bit. He came down with it last Sunday. By mid-week, I was still doing fine, even went to Pilates on [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/tag-im-it/">Tag, I&#8217;m It</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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		<title>Courier Service</title>
		<link>https://livingwithscleroderma.com/courier-service/</link>
					<comments>https://livingwithscleroderma.com/courier-service/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 14 May 2024 12:00:03 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Smell]]></category>
		<category><![CDATA[interstitial lung disease]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[pulmonary function tests]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9928</guid>

					<description><![CDATA[<img width="768" height="589" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/05/Screenshot-2024-05-13-at-4.15.47%E2%80%AFPM.jpg?fit=768%2C589&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" /><p>A few weeks ago, I had a series of pulmonary function tests—a routine, annual procedure, just tracking my lungs&#8217; status. I&#8217;ve been doing these tests at a local hospital for decades, now, so I continue to do the procedure there to keep a comprehensive record. Only one problem: the hospital&#8217;s electronic medical records do not [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/courier-service/">Courier Service</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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			<slash:comments>2</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">9928</post-id>	</item>
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		<title>Fantastic Voyage</title>
		<link>https://livingwithscleroderma.com/fantastic-voyage/</link>
					<comments>https://livingwithscleroderma.com/fantastic-voyage/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 04 Dec 2012 13:00:05 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Taste]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[echocardiogram]]></category>
		<category><![CDATA[interstitial lung disease]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[pulmonary hypertension]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[X-ray]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=1120</guid>

					<description><![CDATA[<p>In 1966, when movies still cost 50 cents and popcorn a quarter, I went with a friend to the Peekskill Paramount movie theatre on a Saturday afternoon to huddle in the crowded balcony with a bunch of other giggly, wise-cracking kids and watch Fantastic Voyage. In what has become a sci-fi classic, a team of [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/fantastic-voyage/">Fantastic Voyage</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>0</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">1120</post-id>	</item>
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