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	<title>Sjogren&#039;s syndrome Archives - Living with Scleroderma</title>
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	<link>https://livingwithscleroderma.com/tag/sjogrens-syndrome/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
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		<title>It&#8217;s Never Simple</title>
		<link>https://livingwithscleroderma.com/its-never-simple/</link>
					<comments>https://livingwithscleroderma.com/its-never-simple/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 17 Mar 2026 12:00:56 +0000</pubDate>
				<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10941</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/03/david-travis-aVvZJC0ynBQ-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/david-travis-aVvZJC0ynBQ-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2026/03/david-travis-aVvZJC0ynBQ-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>A few weeks ago, I ordered new glasses. It&#8217;s been a few years since I&#8217;ve updated my prescription, mainly because I&#8217;ve had so much trouble with dry eyes from Sjogrens that it&#8217;s very challenging to get an accurate eye exam. My eyesight is often blurred due to lack of tears, and when I put in [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/its-never-simple/">It&#8217;s Never Simple</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">10941</post-id>	</item>
		<item>
		<title>Drips and Drops</title>
		<link>https://livingwithscleroderma.com/drips-and-drops/</link>
					<comments>https://livingwithscleroderma.com/drips-and-drops/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 14 Oct 2025 12:00:32 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[how to stay warm]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10729</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/10/iuliia-naumova-f1EglwXLUSc-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/2025/10/iuliia-naumova-f1EglwXLUSc-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/10/iuliia-naumova-f1EglwXLUSc-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>It&#8217;s been raining here for about the past 24 hours, much needed after a long dry spell. According to our official state website that tracks such matters, we are in a &#8220;significant drought.&#8221; You can tell that we haven&#8217;t had enough rain this summer because the fall foliage is muted. Trees need moisture to flame out. [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/drips-and-drops/">Drips and Drops</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">10729</post-id>	</item>
		<item>
		<title>Out of Focus</title>
		<link>https://livingwithscleroderma.com/out-of-focus/</link>
					<comments>https://livingwithscleroderma.com/out-of-focus/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 07 Oct 2025 12:00:24 +0000</pubDate>
				<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[dry eyes]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10720</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/10/jr-korpa-C4nVDgRHGWU-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/2025/10/jr-korpa-C4nVDgRHGWU-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/10/jr-korpa-C4nVDgRHGWU-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="(max-width: 700px) 100vw, 700px" /><p>My eyes have been giving me a hard time, of late. Extremely dry from Sjögrens, they are not happy. No matter what kind of eye drops I use, they burn and itch. When I read, I see a shadow around the letters. My vision is often blurred, especially by day&#8217;s end. Bright sunlight is intolerable. [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/out-of-focus/">Out of Focus</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">10720</post-id>	</item>
		<item>
		<title>Sew-sew</title>
		<link>https://livingwithscleroderma.com/sew-sew/</link>
					<comments>https://livingwithscleroderma.com/sew-sew/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 08 Jul 2025 12:00:43 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[hands]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10537</guid>

					<description><![CDATA[<img width="700" height="525" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/07/IMG_8228.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" loading="lazy" srcset="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/07/IMG_8228.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/07/IMG_8228.jpg?resize=300%2C225&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>I&#8217;ve had some sewing projects in mind for months—in particular, a dress that I sewed up last summer in a test fabric that I liked so much, I&#8217;ve been wearing it on hot days. It would look lovely and feel great in a very soft purple cotton blend that I&#8217;ve had in my fabric stash [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/sew-sew/">Sew-sew</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">10537</post-id>	</item>
		<item>
		<title>No Easy Fix</title>
		<link>https://livingwithscleroderma.com/no-easy-fix/</link>
					<comments>https://livingwithscleroderma.com/no-easy-fix/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 25 Feb 2025 13:00:09 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[adaptive tools]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[finger ulcers]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<category><![CDATA[stress]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10332</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/getty-images-DFKlg_AuEGE-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/2025/02/getty-images-DFKlg_AuEGE-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/getty-images-DFKlg_AuEGE-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>So, here&#8217;s what I learned at my optometrist last week, with a thanks to all who expressed concern and good wishes: My blurry vision is due to the fact that my eyes simply don&#8217;t make enough tears, the result of Sjögren&#8217;s Syndrome that I&#8217;ve had for decades. The relief I&#8217;ve gotten from using EvoTears, which [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/no-easy-fix/">No Easy Fix</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
]]></description>
		
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			<slash:comments>11</slash:comments>
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">10332</post-id>	</item>
		<item>
		<title>All a Blur</title>
		<link>https://livingwithscleroderma.com/all-a-blur/</link>
					<comments>https://livingwithscleroderma.com/all-a-blur/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 18 Feb 2025 13:00:59 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[dry eyes]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=10323</guid>

					<description><![CDATA[<img width="700" height="394" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/nigel-hoare-wG9g114L-7c-unsplash.jpg?fit=700%2C394&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/2025/02/nigel-hoare-wG9g114L-7c-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2025/02/nigel-hoare-wG9g114L-7c-unsplash.jpg?resize=300%2C169&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>It&#8217;s a good thing I&#8217;m seeing my eye doctor this week for my very dry eyes. For several months, I&#8217;ve been struggling with blurred vision, and it is getting worse—to the point where it&#8217;s affecting my ability to read easily and see the computer screen clearly. This could be due to one or a combination [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/all-a-blur/">All a Blur</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">10323</post-id>	</item>
		<item>
		<title>The Eyes Have It</title>
		<link>https://livingwithscleroderma.com/the-eyes-have-it/</link>
					<comments>https://livingwithscleroderma.com/the-eyes-have-it/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 11 Jun 2024 12:00:50 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[body-mind balance]]></category>
		<category><![CDATA[managing chronic disease]]></category>
		<category><![CDATA[resilience]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9969</guid>

					<description><![CDATA[<img width="700" height="467" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/06/ed-leszczynskl-R3ofE-8DyLk-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/2024/06/ed-leszczynskl-R3ofE-8DyLk-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2024/06/ed-leszczynskl-R3ofE-8DyLk-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>Scleroderma is complex enough on its own, but Sjogren&#8217;s Syndrome, which can accompany scleroderma, adds yet another layer of complexity. Sjogren&#8217;s is also an autoimmune disease, which typically presents with dry eyes and dry mouth but can cause other internal organ issues. I&#8217;ve lived with this for decades alongside scleroderma, and I take medication that [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/the-eyes-have-it/">The Eyes Have It</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">9969</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>Routine Exam</title>
		<link>https://livingwithscleroderma.com/routine-exam/</link>
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		<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" loading="lazy" 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="auto, (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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		<post-id xmlns="com-wordpress:feed-additions:1">9855</post-id>	</item>
		<item>
		<title>Dry Spell</title>
		<link>https://livingwithscleroderma.com/dry-spell/</link>
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		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 31 Jan 2023 13:00:09 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Smell]]></category>
		<category><![CDATA[dry eyes]]></category>
		<category><![CDATA[scleral contact lenses]]></category>
		<category><![CDATA[Sjogren's syndrome]]></category>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9016</guid>

					<description><![CDATA[<img width="700" height="466" src="https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/01/petri-heiskanen-vqO_1fUCNxg-unsplash.jpg?fit=700%2C466&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/2023/01/petri-heiskanen-vqO_1fUCNxg-unsplash.jpg?w=700&amp;ssl=1 700w, https://i0.wp.com/livingwithscleroderma.com/wp-content/uploads/2023/01/petri-heiskanen-vqO_1fUCNxg-unsplash.jpg?resize=300%2C200&amp;ssl=1 300w" sizes="auto, (max-width: 700px) 100vw, 700px" /><p>Dealing with dry eyes in a Northeast winter is always a challenge. Even as ours has been milder, so far (knock on wood—or not, given that the planet is warming) there&#8217;s just no escape from dry heat indoors, regardless of source. Some solve this with a humidifier, but I&#8217;ve found them difficult to keep mold-free. [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/dry-spell/">Dry Spell</a> appeared first on <a href="https://livingwithscleroderma.com">Living with Scleroderma</a>.</p>
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