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	Comments on: False Alarm	</title>
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	<link>https://livingwithscleroderma.com/false-alarm/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Tue, 26 Mar 2024 22:35:05 +0000</lastBuildDate>
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		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/false-alarm/#comment-88387</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 26 Mar 2024 22:35:05 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9846#comment-88387</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/false-alarm/#comment-88385&quot;&gt;Amanda Mullinex&lt;/a&gt;.

Amanda, thank you for sharing what you&#039;re going through. I&#039;m so sorry to hear about your discomfort. Calcinosis is really mysterious, as my rheumatologist told me. Every one of my docs has said the same thing. No one knows what causes it, and there is as of yet no remedy. However, stay away from Dr. Google! Too much scary stuff online, and this disease is unique to each individual. That&#039;s really important to remember! What you see online and what actually happens in your unique case are quite different. 
          
I hope you have a good rheumatologist and other specialists, given your overlapping diagnoses. That&#039;s a lot to manage. If there is a scleroderma support group in your community, that might be worth a visit, to see if it would be a helpful resource as you deal with all of this. I list some reliable online resources on my blog. Also, Johns Hopkins has good information here: https://www.hopkinsscleroderma.org/scleroderma/. Take care, and good luck with your mammogram.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/false-alarm/#comment-88385">Amanda Mullinex</a>.</p>
<p>Amanda, thank you for sharing what you&#8217;re going through. I&#8217;m so sorry to hear about your discomfort. Calcinosis is really mysterious, as my rheumatologist told me. Every one of my docs has said the same thing. No one knows what causes it, and there is as of yet no remedy. However, stay away from Dr. Google! Too much scary stuff online, and this disease is unique to each individual. That&#8217;s really important to remember! What you see online and what actually happens in your unique case are quite different. </p>
<p>I hope you have a good rheumatologist and other specialists, given your overlapping diagnoses. That&#8217;s a lot to manage. If there is a scleroderma support group in your community, that might be worth a visit, to see if it would be a helpful resource as you deal with all of this. I list some reliable online resources on my blog. Also, Johns Hopkins has good information here: <a href="https://www.hopkinsscleroderma.org/scleroderma/" rel="nofollow ugc">https://www.hopkinsscleroderma.org/scleroderma/</a>. Take care, and good luck with your mammogram.</p>
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			</item>
		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/false-alarm/#comment-88386</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 26 Mar 2024 22:26:34 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9846#comment-88386</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/false-alarm/#comment-88384&quot;&gt;Donna C.&lt;/a&gt;.

Thank you, Donna, for your kind words. I&#039;m glad to know that you&#039;ve mostly recovered from your renal crisis. I&#039;m sure that must have been a terrifying experience, and I hope your health continues to strengthen. Feedback like yours is the reason I&#039;ve continued to write this blog all these years. Take care, and be well.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/false-alarm/#comment-88384">Donna C.</a>.</p>
<p>Thank you, Donna, for your kind words. I&#8217;m glad to know that you&#8217;ve mostly recovered from your renal crisis. I&#8217;m sure that must have been a terrifying experience, and I hope your health continues to strengthen. Feedback like yours is the reason I&#8217;ve continued to write this blog all these years. Take care, and be well.</p>
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			</item>
		<item>
		<title>
		By: Amanda Mullinex		</title>
		<link>https://livingwithscleroderma.com/false-alarm/#comment-88385</link>

		<dc:creator><![CDATA[Amanda Mullinex]]></dc:creator>
		<pubDate>Tue, 26 Mar 2024 15:32:20 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9846#comment-88385</guid>

					<description><![CDATA[I am glad it wasn&#039;t cancer. I am 40 and have my first mammogram coming up. I have scleroderma, rheumatoid arthritis and lupus overlap. Lately my body has been breaking out fairly rapidly in lumps under my skin in several areas of my body and what I just recently found out was calcinosis. I was recently just wondering if they were going to show up in my breasts because they are mostly all in fatty areas of my body. Google results are pretty frightening. The ones on my butt are starting to be a little bothersome when I sit. I just want to pretend this is as far as it&#039;ll go but my fear is it&#039;ll advance to the disfiguring images I&#039;ve seen on Google. I hope for both of us, they stay put and don&#039;t grow any further. I thought I had escaped the calcinosis thus far, 5 years in, but it&#039;s just been hiding out. Good luck to youm]]></description>
			<content:encoded><![CDATA[<p>I am glad it wasn&#8217;t cancer. I am 40 and have my first mammogram coming up. I have scleroderma, rheumatoid arthritis and lupus overlap. Lately my body has been breaking out fairly rapidly in lumps under my skin in several areas of my body and what I just recently found out was calcinosis. I was recently just wondering if they were going to show up in my breasts because they are mostly all in fatty areas of my body. Google results are pretty frightening. The ones on my butt are starting to be a little bothersome when I sit. I just want to pretend this is as far as it&#8217;ll go but my fear is it&#8217;ll advance to the disfiguring images I&#8217;ve seen on Google. I hope for both of us, they stay put and don&#8217;t grow any further. I thought I had escaped the calcinosis thus far, 5 years in, but it&#8217;s just been hiding out. Good luck to youm</p>
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			</item>
		<item>
		<title>
		By: Donna C.		</title>
		<link>https://livingwithscleroderma.com/false-alarm/#comment-88384</link>

		<dc:creator><![CDATA[Donna C.]]></dc:creator>
		<pubDate>Tue, 26 Mar 2024 14:50:20 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=9846#comment-88384</guid>

					<description><![CDATA[I have been reading your blog for nearly twelve years now since I was initially diagnosed with Systemic Scleroderma at the age of fifty. Eight years subsequent to my initial diagnosis I experienced a full blown, near fatal scleroderma renal crisis. I have since mostly recovered, but I wanted you to know that, throughout my journey, I have always appreciated your informative and insightful writing. Keep up the good fight Evelyn and know that your wisdom is helpful to those of us who stand with you.]]></description>
			<content:encoded><![CDATA[<p>I have been reading your blog for nearly twelve years now since I was initially diagnosed with Systemic Scleroderma at the age of fifty. Eight years subsequent to my initial diagnosis I experienced a full blown, near fatal scleroderma renal crisis. I have since mostly recovered, but I wanted you to know that, throughout my journey, I have always appreciated your informative and insightful writing. Keep up the good fight Evelyn and know that your wisdom is helpful to those of us who stand with you.</p>
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