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	<title>Scleroderma Foundation Archives - Living with Scleroderma</title>
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	<description>Reflections on the Messy Complexity of Chronicity</description>
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		<title>It&#8217;s Up to Us</title>
		<link>https://livingwithscleroderma.com/its-up-to-us/</link>
					<comments>https://livingwithscleroderma.com/its-up-to-us/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 13 Dec 2016 13:00:23 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[research]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=4251</guid>

					<description><![CDATA[<p>There&#8217;s a lot going on in scleroderma research, particularly regarding efforts to understand the causes of fibrosis—what makes skin get too thick—as well as possible treatments. Just this October, a study published in Arthritis Research &#38; Therapy found that &#8220;two approved treatments for pulmonary arterial hypertension— Tracleer (bosentan) and Opsumit (macitentan)—can block a molecular pathway that promotes [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/its-up-to-us/">It&#8217;s Up to Us</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">4251</post-id>	</item>
		<item>
		<title>Plant a Seed</title>
		<link>https://livingwithscleroderma.com/plant-a-seed/</link>
					<comments>https://livingwithscleroderma.com/plant-a-seed/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 30 Jun 2015 12:00:32 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[Touch]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<category><![CDATA[World Scleroderma Day]]></category>
		<category><![CDATA[World Scleroderma Foundation]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=3388</guid>

					<description><![CDATA[<p>In Australia, the sunflower has become the symbol of scleroderma awareness—because those of us with the disease feel better in the warmth of the sun. I like this idea a lot. Enough, in fact, to consider trying my hand at planting some sunflowers, if not this summer, then next. Yesterday, on June 29, scleroderma associations [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/plant-a-seed/">Plant a Seed</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">3388</post-id>	</item>
		<item>
		<title>Imagine</title>
		<link>https://livingwithscleroderma.com/imagine/</link>
					<comments>https://livingwithscleroderma.com/imagine/#respond</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 07 Apr 2015 12:00:48 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Hearing]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[ALS]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[scleroderma research]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=3238</guid>

					<description><![CDATA[<p>Passover this past weekend was extra special. A few hours before we were scheduled to begin our seder on Friday night, we learned that one of our cousins received the all-clear on her lymphoma, following six months of chemotherapy. There were big hugs all around when she and her family arrived for dinner. A central [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/imagine/">Imagine</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">3238</post-id>	</item>
		<item>
		<title>May I Have Your Attention?</title>
		<link>https://livingwithscleroderma.com/may-i-have-your-attention/</link>
					<comments>https://livingwithscleroderma.com/may-i-have-your-attention/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 19 Aug 2014 12:00:55 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Hearing]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Sight]]></category>
		<category><![CDATA[scleroderma awareness]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=2744</guid>

					<description><![CDATA[<p>If you spend any time on social media, watching TV or reading the newspaper, by now you’ve undoubtedly heard of the extraordinarily successful “Ice Bucket Challenge” that has raised record-breaking donations for ALS research. It goes like this: You pour a bucket of ice water on your head while someone makes a video of your [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/may-i-have-your-attention/">May I Have Your Attention?</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">2744</post-id>	</item>
		<item>
		<title>Ray of Hope</title>
		<link>https://livingwithscleroderma.com/ray-of-hope/</link>
					<comments>https://livingwithscleroderma.com/ray-of-hope/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 07 Jan 2014 13:00:38 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[Hal Dietz]]></category>
		<category><![CDATA[Johns Hopkins University]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[scleroderma research]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=2172</guid>

					<description><![CDATA[<p>Nothing like starting the new year with some good news about scleroderma research. In my email box last week, I found this item in the Scleroderma Research Foundation’s monthly eNewsletter (12-30-13): Researchers Prevent and Reverse Mice Fibrosis in a Mouse Model of Stiff Skin Syndrome; Study Shows Promise for Scleroderma I read on, heart quickening: [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/ray-of-hope/">Ray of Hope</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">2172</post-id>	</item>
		<item>
		<title>Enough, Already</title>
		<link>https://livingwithscleroderma.com/enough-already/</link>
					<comments>https://livingwithscleroderma.com/enough-already/#comments</comments>
		
		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 02 Jul 2013 12:30:04 +0000</pubDate>
				<category><![CDATA[Body]]></category>
		<category><![CDATA[Mind]]></category>
		<category><![CDATA[HR1429]]></category>
		<category><![CDATA[Scleroderma Foundation]]></category>
		<category><![CDATA[scleroderma research]]></category>
		<category><![CDATA[Scleroderma Research Foundation]]></category>
		<category><![CDATA[World Scleroderma Awareness Day]]></category>
		<guid isPermaLink="false">http://www.livingwithscleroderma.com/?p=1736</guid>

					<description><![CDATA[<p>On Monday afternoon, I took Ginger to the vet. This was her semi-annual check-up, time for renewing all her shots. For a nearly 15-year-old Golden, she’s doing great, though getting a bit slow on the up-take, between arthritis, some hearing loss and what I suspect is a touch of senility, as well as the inevitable [&#8230;]</p>
<p>The post <a href="https://livingwithscleroderma.com/enough-already/">Enough, Already</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">1736</post-id>	</item>
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