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<channel>
	<title>calcinosis Archives - Living with Scleroderma</title>
	<atom:link href="https://livingwithscleroderma.com/tag/calcinosis/feed/" rel="self" type="application/rss+xml" />
	<link>https://livingwithscleroderma.com/tag/calcinosis/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Mon, 23 Mar 2026 20:09:49 +0000</lastBuildDate>
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		<title>700-plus</title>
		<link>https://livingwithscleroderma.com/700-plus/</link>
					<comments>https://livingwithscleroderma.com/700-plus/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 24 Mar 2026 12:00:55 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10947</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/03/beth-macdonald-YZZS3XA4hng-unsplash.jpg?fit=700%2C467&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/2026/03/beth-macdonald-YZZS3XA4hng-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/03/beth-macdonald-YZZS3XA4hng-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>I didn&#8217;t realize it at the time, but at the end of December, I wrote my 700th post on this site. I launched Living with Scleroderma on January 3, 2012, and have been posting nearly every week since, with time off for good behavior when on vacation. That&#8217;s a lot of posts. While there always [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/700-plus/">700-plus</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>10</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10947</post-id>	</item>
		<item>
		<title>Hand-off</title>
		<link>https://livingwithscleroderma.com/hand-off/</link>
					<comments>https://livingwithscleroderma.com/hand-off/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 02 Jul 2024 12:00:12 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10005</guid>

					<description><![CDATA[<img width="700" height="525" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/07/IMG_7044.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" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/07/IMG_7044.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/07/IMG_7044.jpg?resize=300%2C225&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>I&#8217;ve been dropping things lately. This is largely due to calcinosis in my thumbs that makes it harder to hold on. My dexterity waxes and wanes, depending on how a particular piece of calcium is working its way out through the skin, and currently some shards are on the move. And so, Sunday night, when [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/hand-off/">Hand-off</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">10005</post-id>	</item>
		<item>
		<title>Routine Exam</title>
		<link>https://livingwithscleroderma.com/routine-exam/</link>
					<comments>https://livingwithscleroderma.com/routine-exam/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 02 Apr 2024 12:00:25 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[Raynaud's]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<category><![CDATA[tooth resorption]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9855</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/mathew-schwartz-8rj4sz9YLCI-unsplash.jpg?fit=700%2C467&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/2024/04/mathew-schwartz-8rj4sz9YLCI-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/mathew-schwartz-8rj4sz9YLCI-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>Monday afternoon found me in my hometown rheumatologist&#8217;s office. I see her twice a year, so that I always have a specialist nearby who knows my history, in case I need help pronto without driving into Boston. She is chair of the rheumatology department for our local health care organization, very thoughtful, compassionate. She also [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/routine-exam/">Routine Exam</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">9855</post-id>	</item>
		<item>
		<title>False Alarm</title>
		<link>https://livingwithscleroderma.com/false-alarm/</link>
					<comments>https://livingwithscleroderma.com/false-alarm/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 26 Mar 2024 12:00:06 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[mammogram]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[mindfulness]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[stress]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9846</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/03/john-cafazza-9z958EEwNaI-unsplash.jpg?fit=700%2C467&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/03/john-cafazza-9z958EEwNaI-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/03/john-cafazza-9z958EEwNaI-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>I had a routine mammogram a couple of weeks ago. Not my favorite &#8220;non-invasive&#8221; test, as any woman knows. As the tech was arranging me for the inevitable squash grip of the mammography mammoth, I asked her why she had chosen this particular technical specialty. Her answer: &#8220;Because it saves lives.&#8221; Fair enough. Fifteen minutes [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/false-alarm/">False Alarm</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">9846</post-id>	</item>
		<item>
		<title>The Pits</title>
		<link>https://livingwithscleroderma.com/the-pits/</link>
					<comments>https://livingwithscleroderma.com/the-pits/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 20 Feb 2024 13:00:24 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9807</guid>

					<description><![CDATA[<img width="768" height="576" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?fit=768%2C576&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?w=2560&amp;ssl=1 2560w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?resize=300%2C225&amp;ssl=1 300w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?resize=1024%2C768&amp;ssl=1 1024w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?resize=768%2C576&amp;ssl=1 768w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?resize=1536%2C1152&amp;ssl=1 1536w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/02/IMG_6818-scaled.jpg?resize=2048%2C1536&amp;ssl=1 2048w" sizes="auto, (max-width: 768px) 100vw, 768px" /><p>Over the weekend, I pulled yet another calcium pit out of the inside joint of my right thumb. It is the third tiny shard that has emerged in the past month-plus. And although I&#8217;m not certain, it feels like another one is surfacing. This makes grasping objects complicated. These tiny charcoal-gray bits of calcium are [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/the-pits/">The Pits</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>6</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">9807</post-id>	</item>
		<item>
		<title>Small Miracles</title>
		<link>https://livingwithscleroderma.com/small-miracles/</link>
					<comments>https://livingwithscleroderma.com/small-miracles/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 31 Oct 2023 12:00:46 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9639</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/victoria-tronina-L0RqBLzQq2c-unsplash.jpg?fit=700%2C467&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/victoria-tronina-L0RqBLzQq2c-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/victoria-tronina-L0RqBLzQq2c-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>For months, at least since March and maybe longer, I&#8217;ve had a charcoal-gray pit of calcium sticking in my left thumb. I have not been able to budge it or tease it out with tweezers. It has been lodged there, staring at me as I change my bandages morning and night. Sometimes it hurts, other [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/small-miracles/">Small Miracles</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">9639</post-id>	</item>
		<item>
		<title>In Stitches</title>
		<link>https://livingwithscleroderma.com/in-stitches/</link>
					<comments>https://livingwithscleroderma.com/in-stitches/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 03 Oct 2023 12:00:41 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Smell]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[body image]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[mindfulness]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9567</guid>

					<description><![CDATA[<img width="469" height="700" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/anne-nygard-8czYAy10nGI-unsplash.jpg?fit=469%2C700&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/anne-nygard-8czYAy10nGI-unsplash.jpg?w=469&amp;ssl=1 469w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/10/anne-nygard-8czYAy10nGI-unsplash.jpg?resize=201%2C300&amp;ssl=1 201w" sizes="auto, (max-width: 469px) 100vw, 469px" /><p>It&#8217;s been five years since I last had calcium deposits removed from the bridge of my nose, the fifth time I&#8217;ve endured this procedure. Usually, I take care of this annoying issue about every three years, but the pandemic put that on hold this time around—which ultimately meant that the calcinosis got worse. Originally, I [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/in-stitches/">In Stitches</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">9567</post-id>	</item>
		<item>
		<title>Step-wise</title>
		<link>https://livingwithscleroderma.com/step-wise/</link>
					<comments>https://livingwithscleroderma.com/step-wise/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 29 Mar 2022 12:00:28 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[feet]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8356</guid>

					<description><![CDATA[<img width="700" height="393" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2022/03/christopher-burns-I95_6sicXdo-unsplash.jpg?fit=700%2C393&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2022/03/christopher-burns-I95_6sicXdo-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2022/03/christopher-burns-I95_6sicXdo-unsplash.jpg?resize=300%2C168&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>I see my podiatrist this week. It&#8217;s a good thing. Every couple of months, he rescues my feet from corns and tiny bits of calcium emerging from the tip of my right big toe. He also trims my toenails, which I can do for myself with a little difficulty, but still need help. Scleroderma has [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/step-wise/">Step-wise</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>5</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">8356</post-id>	</item>
		<item>
		<title>Unnecessary Procedures</title>
		<link>https://livingwithscleroderma.com/unnecessary-procedures/</link>
					<comments>https://livingwithscleroderma.com/unnecessary-procedures/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 23 Jun 2020 12:00:14 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[calcinosis]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[hand surgery]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=7008</guid>

					<description><![CDATA[<img width="700" height="474" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/06/roman-kraft-RtDwtRDvYQg-unsplash.jpg?fit=700%2C474&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/06/roman-kraft-RtDwtRDvYQg-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/06/roman-kraft-RtDwtRDvYQg-unsplash.jpg?resize=300%2C203&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>For well over a year, I&#8217;ve had a piece of grey calcium protruding from the pad of my right thumb. As I wrote back in February, I finally saw my hand surgeon and worked out a plan for him to remove it—the challenge being that it&#8217;s only the tip of a long chain of calcium [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/unnecessary-procedures/">Unnecessary Procedures</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">7008</post-id>	</item>
		<item>
		<title>Thumbkin</title>
		<link>https://livingwithscleroderma.com/thumbkin/</link>
					<comments>https://livingwithscleroderma.com/thumbkin/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 26 May 2020 12:00:52 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
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					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/05/kon-karampelas-jyG-l45vZM-unsplash.jpg?fit=700%2C467&amp;ssl=1" class="webfeedsFeaturedVisual wp-post-image" alt="" style="display: block; margin-bottom: 5px; clear:both;max-width: 100%;" link_thumbnail="" decoding="async" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/05/kon-karampelas-jyG-l45vZM-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2020/05/kon-karampelas-jyG-l45vZM-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>Memorial Day Weekend was low key for me this year. Not only because of the pandemic, although that certainly set the tone. The weather wasn&#8217;t the culprit; it was quite beautiful here for most of the weekend. There was simply nowhere that I felt like going to mark the beginning of what will be a [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/thumbkin/">Thumbkin</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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