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	<title>
	Comments on: Winter Blooms	</title>
	<atom:link href="https://livingwithscleroderma.com/winter-blooms/feed/" rel="self" type="application/rss+xml" />
	<link>https://livingwithscleroderma.com/winter-blooms/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Tue, 28 Jan 2020 21:47:59 +0000</lastBuildDate>
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		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78571</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 21:47:59 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78571</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/winter-blooms/#comment-78568&quot;&gt;Heather Milligan&lt;/a&gt;.

You are most welcome! :)]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/winter-blooms/#comment-78568">Heather Milligan</a>.</p>
<p>You are most welcome! 🙂</p>
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		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78570</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 21:47:35 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78570</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/winter-blooms/#comment-78566&quot;&gt;Patricia Bizzell&lt;/a&gt;.

It was a beautiful show, as always.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/winter-blooms/#comment-78566">Patricia Bizzell</a>.</p>
<p>It was a beautiful show, as always.</p>
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		<item>
		<title>
		By: Heather Milligan		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78568</link>

		<dc:creator><![CDATA[Heather Milligan]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 18:55:06 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78568</guid>

					<description><![CDATA[So lovely.  Thank you for taking the time to post.]]></description>
			<content:encoded><![CDATA[<p>So lovely.  Thank you for taking the time to post.</p>
]]></content:encoded>
		
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		<item>
		<title>
		By: Patricia Bizzell		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78566</link>

		<dc:creator><![CDATA[Patricia Bizzell]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 16:39:46 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78566</guid>

					<description><![CDATA[Thanks for posting so many photos from &quot;Flora in Winter,&quot; Evie. I enjoyed this show again this year, and enjoyed re-visiting it with your photos, but oh darn! You didn&#039;t pick any of my favorites! Mine were the arrangements for the Scholar&#039;s Stone, the Madonna of Humility, and the Saint Sebastian. Really liked the ones you picked, too, of course. Second from the top, especially--I forget the name of the painting, but I thought the floral arrangement met an interesting challenge in responding to an abstract, and edgy, work.]]></description>
			<content:encoded><![CDATA[<p>Thanks for posting so many photos from &#8220;Flora in Winter,&#8221; Evie. I enjoyed this show again this year, and enjoyed re-visiting it with your photos, but oh darn! You didn&#8217;t pick any of my favorites! Mine were the arrangements for the Scholar&#8217;s Stone, the Madonna of Humility, and the Saint Sebastian. Really liked the ones you picked, too, of course. Second from the top, especially&#8211;I forget the name of the painting, but I thought the floral arrangement met an interesting challenge in responding to an abstract, and edgy, work.</p>
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		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78562</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 16:19:35 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78562</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/winter-blooms/#comment-78561&quot;&gt;Deanna&lt;/a&gt;.

Hi Deanna,

Thanks for your question. No, I am not on disability. I work for myself. Ten years ago, when I was laid off from my job, I spent about 6 months looking for work and then realized I would be much happier and healthier starting my own consulting practice. It takes a lot of persistence and tolerance for uncertainty, and cash flow is not always predictable, but I prefer this to working for someone else. It really helps to be able to set my own hours.  See https://www.herwitzassociates.com/.

I fully empathize with your struggle with chronic ulcers and infections, and know exactly what you mean about sensitive, deformed hands. I&#039;m sorry to hear of your hospitalizations and amputations. I, too, had partial amputations of several fingers a couple of years ago. 
     
I find the Apple &quot;chiclets&quot; keyboard essential to my ability to type. I used Dragon software when my hands fell apart a couple of years ago, but I prefer typing, because I can write faster that way. 

My best advice is to take stock of what you can do, and what you love to do and care about most, and craft work around that. With the internet, there is so much opportunity to be a creative solo entrepreneur. Be realistic about your energy and managing pain, and factor that in, but don&#039;t let it stop you from experimenting to find the right fit. I hope this helps! 

Best of luck, and be well,
Evelyn]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/winter-blooms/#comment-78561">Deanna</a>.</p>
<p>Hi Deanna,</p>
<p>Thanks for your question. No, I am not on disability. I work for myself. Ten years ago, when I was laid off from my job, I spent about 6 months looking for work and then realized I would be much happier and healthier starting my own consulting practice. It takes a lot of persistence and tolerance for uncertainty, and cash flow is not always predictable, but I prefer this to working for someone else. It really helps to be able to set my own hours.  See <a href="https://www.herwitzassociates.com/" rel="nofollow ugc">https://www.herwitzassociates.com/</a>.</p>
<p>I fully empathize with your struggle with chronic ulcers and infections, and know exactly what you mean about sensitive, deformed hands. I&#8217;m sorry to hear of your hospitalizations and amputations. I, too, had partial amputations of several fingers a couple of years ago. </p>
<p>I find the Apple &#8220;chiclets&#8221; keyboard essential to my ability to type. I used Dragon software when my hands fell apart a couple of years ago, but I prefer typing, because I can write faster that way. </p>
<p>My best advice is to take stock of what you can do, and what you love to do and care about most, and craft work around that. With the internet, there is so much opportunity to be a creative solo entrepreneur. Be realistic about your energy and managing pain, and factor that in, but don&#8217;t let it stop you from experimenting to find the right fit. I hope this helps! </p>
<p>Best of luck, and be well,<br />
Evelyn</p>
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			</item>
		<item>
		<title>
		By: Deanna		</title>
		<link>https://livingwithscleroderma.com/winter-blooms/#comment-78561</link>

		<dc:creator><![CDATA[Deanna]]></dc:creator>
		<pubDate>Tue, 28 Jan 2020 14:25:02 +0000</pubDate>
		<guid isPermaLink="false">https://www.livingwithscleroderma.com/?p=6613#comment-78561</guid>

					<description><![CDATA[Hello Evelyn...please forgive me for reaching out to you as you have probably already answered these questions elsewhere, I just simply haven&#039;t found them. I am wondering if you can work full time or are you on disability. I am on disability as I have many of the issues associated with the disease also, but my biggest problem is also chronic digital ulcers ( resulting in two lengthy hospital stays for Infection and amputation on a few toes) anyway I find working in most capacities is painful to my somewhat deformed hands and the residual pain from the previous ulcers etc.. I too am college educated, and have written a book ( mostly by talk to text software) anyway.....have you had to deal with this issue. I miss working....
Any ideas?]]></description>
			<content:encoded><![CDATA[<p>Hello Evelyn&#8230;please forgive me for reaching out to you as you have probably already answered these questions elsewhere, I just simply haven&#8217;t found them. I am wondering if you can work full time or are you on disability. I am on disability as I have many of the issues associated with the disease also, but my biggest problem is also chronic digital ulcers ( resulting in two lengthy hospital stays for Infection and amputation on a few toes) anyway I find working in most capacities is painful to my somewhat deformed hands and the residual pain from the previous ulcers etc.. I too am college educated, and have written a book ( mostly by talk to text software) anyway&#8230;..have you had to deal with this issue. I miss working&#8230;.<br />
Any ideas?</p>
]]></content:encoded>
		
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