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<channel>
	<title>COVID-19 Archives - Living with Scleroderma</title>
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	<link>https://livingwithscleroderma.com/tag/covid-19/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Mon, 10 Nov 2025 18:52:56 +0000</lastBuildDate>
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		<title>Why Me?</title>
		<link>https://livingwithscleroderma.com/why-me/</link>
					<comments>https://livingwithscleroderma.com/why-me/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 11 Nov 2025 13:00:58 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Hearing]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[body-mind balance]]></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=10787</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/11/engin-akyurt-wJaMWPU_VYY-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/2025/11/engin-akyurt-wJaMWPU_VYY-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/11/engin-akyurt-wJaMWPU_VYY-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>For all of the bad things that happened during the COVID pandemic, the one good thing that happened for me was reconnecting with old friends over Zoom. Five years ago, when we were hunkered down, I looked up friends from my teens and twenties and caught up online. Some of us have continued those conversations, [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/why-me/">Why Me?</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">10787</post-id>	</item>
		<item>
		<title>Covid Redux</title>
		<link>https://livingwithscleroderma.com/covid-redux/</link>
					<comments>https://livingwithscleroderma.com/covid-redux/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 07 Jan 2025 13:00:57 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[vaccines]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10267</guid>

					<description><![CDATA[<img width="700" height="484" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/01/evgeni-tcherkasski-JrxP-ua6_cw-unsplash.jpg?fit=700%2C484&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/2025/01/evgeni-tcherkasski-JrxP-ua6_cw-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/01/evgeni-tcherkasski-JrxP-ua6_cw-unsplash.jpg?resize=300%2C207&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>Just in time for 2025, last week Al came down with Covid. He was feeling off Tuesday afternoon and worse by Wednesday evening. What began as a winter head cold deepened into a rough cough, so on Friday he went to urgent care to rule out pneumonia. His lung X-ray was clear, but a Covid [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/covid-redux/">Covid Redux</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">10267</post-id>	</item>
		<item>
		<title>Be Prepared</title>
		<link>https://livingwithscleroderma.com/be-prepared/</link>
					<comments>https://livingwithscleroderma.com/be-prepared/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 03 Sep 2024 12:00:59 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10108</guid>

					<description><![CDATA[<img width="718" height="726" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/09/GS-to-DC-1969-not-really-a-cig.png?fit=718%2C726&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/2024/09/GS-to-DC-1969-not-really-a-cig.png?w=718&amp;ssl=1 718w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/09/GS-to-DC-1969-not-really-a-cig.png?resize=297%2C300&amp;ssl=1 297w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/09/GS-to-DC-1969-not-really-a-cig.png?resize=100%2C100&amp;ssl=1 100w" sizes="(max-width: 718px) 100vw, 718px" /><p>Many years ago, I was a Girl Scout. That&#8217;s 15-year-old me in the middle, with the long pigtails and sunglasses, on a troop trip to D.C. in 1969. (And no, the Senior scout to my right is not smoking a real cigarette!) All that I vaguely recall about that trip, back in the day when [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/be-prepared/">Be Prepared</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">10108</post-id>	</item>
		<item>
		<title>Spring at Last</title>
		<link>https://livingwithscleroderma.com/spring-at-last/</link>
					<comments>https://livingwithscleroderma.com/spring-at-last/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 30 Apr 2024 12:00:14 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Smell]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[mindfulness]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9904</guid>

					<description><![CDATA[<img width="700" height="525" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/IMG_6908.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" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/IMG_6908.jpeg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/IMG_6908.jpeg?resize=300%2C225&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>On Sunday, I walked outside without a coat for the first time this year. What a blessing, especially after feeling so cooped up 10 days ago with Covid. It&#8217;s been spring on the calendar for more than a month, but this was the first day that really felt springy. As far as I can tell, [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/spring-at-last/">Spring at Last</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">9904</post-id>	</item>
		<item>
		<title>Best Laid Plans Department</title>
		<link>https://livingwithscleroderma.com/best-laid-plans-department/</link>
					<comments>https://livingwithscleroderma.com/best-laid-plans-department/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 23 Apr 2024 12:00:39 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Taste]]></category>
		<category><![CDATA[Touch]]></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[Raynaud's]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9897</guid>

					<description><![CDATA[<img width="700" height="705" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/Birthday-flowers.jpg?fit=700%2C705&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/2024/04/Birthday-flowers.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/Birthday-flowers.jpg?resize=298%2C300&amp;ssl=1 298w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/Birthday-flowers.jpg?resize=150%2C150&amp;ssl=1 150w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/04/Birthday-flowers.jpg?resize=100%2C100&amp;ssl=1 100w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>And so, despite my best efforts, I did get Covid last week, after all. In fact, I tested positive on Tuesday afternoon. At first, I thought it was just allergies. All the trees have finally bloomed here, and pollen is in the air. Just to be sure, though, I took a test. When I first [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/best-laid-plans-department/">Best Laid Plans Department</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">9897</post-id>	</item>
		<item>
		<title>And So It Goes</title>
		<link>https://livingwithscleroderma.com/and-so-it-goes/</link>
					<comments>https://livingwithscleroderma.com/and-so-it-goes/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 16 Apr 2024 12:00:16 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9887</guid>

					<description><![CDATA[<p>I was planning to write an upbeat post today, in anticipation of my 70th birthday on Thursday. But life has a way of throwing curve balls. On Sunday, we discovered that Al has Covid. So far, he seems to be doing okay, and we expect a green light for him to start a course of [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/and-so-it-goes/">And So It Goes</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">9887</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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		<post-id xmlns="com-wordpress:feed-additions:1">9567</post-id>	</item>
		<item>
		<title>First in Line</title>
		<link>https://livingwithscleroderma.com/first-in-line/</link>
					<comments>https://livingwithscleroderma.com/first-in-line/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 26 Sep 2023 12:00:52 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[COVID-19]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9559</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/09/tim-mossholder-KZcWygxZ_J4-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/2023/09/tim-mossholder-KZcWygxZ_J4-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/09/tim-mossholder-KZcWygxZ_J4-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>I got my new Covid shot a week ago, as soon as it was available. Glad to have that out of the way. It seems that the wily virus is popping up everywhere, once again disrupting lives, albeit with less serious risks for most, thanks to progress with vaccines and a build-up of natural immunity. [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/first-in-line/">First in Line</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">9559</post-id>	</item>
		<item>
		<title>Moving On</title>
		<link>https://livingwithscleroderma.com/moving-on/</link>
					<comments>https://livingwithscleroderma.com/moving-on/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 23 May 2023 12:00:23 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[anxiety]]></category>
		<category><![CDATA[body-mind balance]]></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=9287</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/05/vera-davidova-cuzH5S-8ZOQ-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/2023/05/vera-davidova-cuzH5S-8ZOQ-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/05/vera-davidova-cuzH5S-8ZOQ-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>The last time I had a doctor&#8217;s appointment, I went without a mask. It was a few days after the Covid public health emergency was lifted in May, and masking in medical settings was no longer required. This felt strange, but liberating. I asked the medical assistant who took my vital signs how it felt [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/moving-on/">Moving On</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">9287</post-id>	</item>
		<item>
		<title>To Mask or Not to Mask</title>
		<link>https://livingwithscleroderma.com/to-mask-or-not-to-mask/</link>
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		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 04 Apr 2023 12:00:51 +0000</pubDate>
				<category><![CDATA[Body]]></category>
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		<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/2023/04/pexels-cottonbro-studio-3951628.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/2023/04/pexels-cottonbro-studio-3951628.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/04/pexels-cottonbro-studio-3951628.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>Ten days out from my trip to Germany, and I&#8217;m feeling fine, thank you. This, despite the fact that I stopped wearing my mask about halfway through the trip, except when on a crowded, stuffy bus or subway. I did not even wear my mask on the eight-hour flight home. I was sitting way in [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/to-mask-or-not-to-mask/">To Mask or Not to Mask</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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