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	<title>Uncategorized Archives - Living with Scleroderma</title>
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	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Mon, 29 Jun 2026 18:37:52 +0000</lastBuildDate>
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		<title>Back to Reality</title>
		<link>https://livingwithscleroderma.com/back-to-reality/</link>
					<comments>https://livingwithscleroderma.com/back-to-reality/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 30 Jun 2026 12:00:31 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[pulmomnary function test]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=11077</guid>

					<description><![CDATA[<img width="700" height="513" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/06/getty-images-TW8VMRa3ye4-unsplash.jpg?fit=700%2C513&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/2026/06/getty-images-TW8VMRa3ye4-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/06/getty-images-TW8VMRa3ye4-unsplash.jpg?resize=300%2C220&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>As is always the case when I come back from abroad, it all too soon seems like a distant memory. I am trying to retain the clarity and calm I experienced in Japan. But it&#8217;s been a challenging week. Last Thursday I had my regular pulmonary function tests (PFT) at Boston Medical, then saw both [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/back-to-reality/">Back to Reality</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">11077</post-id>	</item>
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		<title>Blue Mind</title>
		<link>https://livingwithscleroderma.com/blue-mind/</link>
					<comments>https://livingwithscleroderma.com/blue-mind/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 25 Mar 2025 12:00:59 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10374</guid>

					<description><![CDATA[<p>Last week, after all the mishegas with my roller-coaster blood pressure was mostly resolved (no, thank goodness, I was not experiencing scleroderma renal crisis, which would be a rare but very serious development at this stage of my disease), Al and I went to Cape Cod for a few days. I had planned this trip [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/blue-mind/">Blue Mind</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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		<post-id xmlns="com-wordpress:feed-additions:1">10374</post-id>	</item>
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		<title>Cooped Up</title>
		<link>https://livingwithscleroderma.com/cooped-up/</link>
					<comments>https://livingwithscleroderma.com/cooped-up/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 11 Feb 2025 13:00:03 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[how to stay warm]]></category>
		<category><![CDATA[infections]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[stress]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10319</guid>

					<description><![CDATA[<img width="700" height="525" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/IMG_7603.jpeg?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" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/IMG_7603.jpeg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/IMG_7603.jpeg?resize=300%2C225&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>It&#8217;s 30 degrees F here today, but the real feel is about 19. It snowed over the weekend, just over four inches of fluffy white stuff, very pretty for a day and now shrinking into icy clumps. It&#8217;s too cold for me to take a walk, and the streets are patched with ice. Ugh. I [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/cooped-up/">Cooped Up</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>4</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10319</post-id>	</item>
		<item>
		<title>Untressing</title>
		<link>https://livingwithscleroderma.com/untressing/</link>
					<comments>https://livingwithscleroderma.com/untressing/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 21 Jul 2020 12:00:21 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[body image]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[mindfulness]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=7057</guid>

					<description><![CDATA[<img width="768" height="512" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/07/ugur-peker-aB35C9W7Gj4-unsplash.jpg?fit=768%2C512&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/07/ugur-peker-aB35C9W7Gj4-unsplash.jpg?w=1000&amp;ssl=1 1000w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/07/ugur-peker-aB35C9W7Gj4-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/07/ugur-peker-aB35C9W7Gj4-unsplash.jpg?resize=768%2C512&amp;ssl=1 768w" sizes="(max-width: 768px) 100vw, 768px" /><p>So, I finally took the plunge and got my hair cut. I had been putting this off for months, even after hair salons reopened under Phase I here in Massachusetts. Indeed, I rescheduled at least twice, because I was just too nervous about the pandemic risks. Then the heat wave hit. It&#8217;s July, it&#8217;s really [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/untressing/">Untressing</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>2</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">7057</post-id>	</item>
		<item>
		<title>Luminous</title>
		<link>https://livingwithscleroderma.com/luminous/</link>
					<comments>https://livingwithscleroderma.com/luminous/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 25 Dec 2018 13:00:31 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[Worcester Art Museum]]></category>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=5736</guid>

					<description><![CDATA[<p>So much tumult this past week, leading up to the holidays. And so, Dear Reader, I offer you this peaceful respite⎯a beautiful stained glass exhibit at the Worcester Art Museum. In the 1890s, when these artworks were created, stained glass windows were designed to uplift the spirit and provide an opportunity for contemplation. We all [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/luminous/">Luminous</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">5736</post-id>	</item>
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