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	Comments on: In the Weeds	</title>
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	<link>https://livingwithscleroderma.com/in-the-weeds/</link>
	<description>Reflections on the Messy Complexity of Chronicity</description>
	<lastBuildDate>Wed, 16 Feb 2022 16:37:22 +0000</lastBuildDate>
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		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83381</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Wed, 16 Feb 2022 16:37:22 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83381</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83380&quot;&gt;Janet Blumenshine&lt;/a&gt;.

Good to know. Thank you!]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83380">Janet Blumenshine</a>.</p>
<p>Good to know. Thank you!</p>
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		<item>
		<title>
		By: Janet Blumenshine		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83380</link>

		<dc:creator><![CDATA[Janet Blumenshine]]></dc:creator>
		<pubDate>Wed, 16 Feb 2022 15:08:12 +0000</pubDate>
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					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83371&quot;&gt;Evelyn Herwitz&lt;/a&gt;.

The first two drugs I had taken before I got PAH.  The last two are newer drugs for PAH.  All four drugs open up the blood vessels including my fingers.  I am still careful in keeping my hands and body warm but have not had any sores on my fingers since. My PAH has been in control for the last 3 years.  I have had scleroderma for 8 years.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83371">Evelyn Herwitz</a>.</p>
<p>The first two drugs I had taken before I got PAH.  The last two are newer drugs for PAH.  All four drugs open up the blood vessels including my fingers.  I am still careful in keeping my hands and body warm but have not had any sores on my fingers since. My PAH has been in control for the last 3 years.  I have had scleroderma for 8 years.</p>
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		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83372</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 21:49:36 +0000</pubDate>
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					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83369&quot;&gt;Patricia Osten&lt;/a&gt;.

Patricia, I hope it helps! Acupuncture can also be a big help. I hope you get some relief! It&#039;s always good to read the clinical research about therapies. Here&#039;s a link to a 2020 NIH review of CBD research for controlling chronic pain: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204604/. Take care.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83369">Patricia Osten</a>.</p>
<p>Patricia, I hope it helps! Acupuncture can also be a big help. I hope you get some relief! It&#8217;s always good to read the clinical research about therapies. Here&#8217;s a link to a 2020 NIH review of CBD research for controlling chronic pain: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204604/" rel="nofollow ugc">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204604/</a>. Take care.</p>
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		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83371</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 21:39:59 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83371</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83368&quot;&gt;Janet Blumenshine&lt;/a&gt;.

Thanks, Janet. I hope your PAH is manageable. That&#039;s really interesting, how those meds have stopped your ulcers. Such difficult tradeoffs. Be well!]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83368">Janet Blumenshine</a>.</p>
<p>Thanks, Janet. I hope your PAH is manageable. That&#8217;s really interesting, how those meds have stopped your ulcers. Such difficult tradeoffs. Be well!</p>
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		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83370</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 21:37:49 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83370</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83366&quot;&gt;Linda Russell&lt;/a&gt;.

So glad to hear that, Linda. I hope you are doing well.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83366">Linda Russell</a>.</p>
<p>So glad to hear that, Linda. I hope you are doing well.</p>
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		<title>
		By: Patricia Osten		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83369</link>

		<dc:creator><![CDATA[Patricia Osten]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 20:10:35 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83369</guid>

					<description><![CDATA[This was a providential posting for me.  The major pain issue for me is not really due to any of my Sclerodema/RA/Sj0grens problems but these attacks do make all of the AI symptoms worse. When you mentioned your husband found relief from back pain with CBD cream I was astonished.  I have been dealing with attacks of severe lower back pain since lumbar fusion surgery  in 2018 which has been labeled as &quot;failed back surgery&quot;.  I&#039;ve been on the medical mystery tour of doctors and ensuing tests since 2018 with no cause determined for these attacks and no treatments  except narcotic pain medications that cause nasty side effects. Recently my PCP(who is great) suggested acupuncture.  No one has mentioned trying topical CBD cream. So, thank you for this posting!!! It can&#039;t hurt to try this first.]]></description>
			<content:encoded><![CDATA[<p>This was a providential posting for me.  The major pain issue for me is not really due to any of my Sclerodema/RA/Sj0grens problems but these attacks do make all of the AI symptoms worse. When you mentioned your husband found relief from back pain with CBD cream I was astonished.  I have been dealing with attacks of severe lower back pain since lumbar fusion surgery  in 2018 which has been labeled as &#8220;failed back surgery&#8221;.  I&#8217;ve been on the medical mystery tour of doctors and ensuing tests since 2018 with no cause determined for these attacks and no treatments  except narcotic pain medications that cause nasty side effects. Recently my PCP(who is great) suggested acupuncture.  No one has mentioned trying topical CBD cream. So, thank you for this posting!!! It can&#8217;t hurt to try this first.</p>
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		<item>
		<title>
		By: Janet Blumenshine		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83368</link>

		<dc:creator><![CDATA[Janet Blumenshine]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 18:09:16 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83368</guid>

					<description><![CDATA[I can&#039;t imagine what you are going through with your ulcers. I know you have great doctors.  My experience with ulcers--I haven&#039;t had any since I started taking meds for my pulmonary arterial hypertension...nifedipine, sildenafil, opsumit and uptravi.  But, of course, you don&#039;t want PAH.
Thinking of you.]]></description>
			<content:encoded><![CDATA[<p>I can&#8217;t imagine what you are going through with your ulcers. I know you have great doctors.  My experience with ulcers&#8211;I haven&#8217;t had any since I started taking meds for my pulmonary arterial hypertension&#8230;nifedipine, sildenafil, opsumit and uptravi.  But, of course, you don&#8217;t want PAH.<br />
Thinking of you.</p>
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		<item>
		<title>
		By: Linda Russell		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83366</link>

		<dc:creator><![CDATA[Linda Russell]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 17:27:02 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83366</guid>

					<description><![CDATA[Thank you so very much for your in depth stories of the past two weeks. I have known the pain of nerve ending spasms. Your writings are so extremely helpful.]]></description>
			<content:encoded><![CDATA[<p>Thank you so very much for your in depth stories of the past two weeks. I have known the pain of nerve ending spasms. Your writings are so extremely helpful.</p>
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		<item>
		<title>
		By: Evelyn Herwitz		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83365</link>

		<dc:creator><![CDATA[Evelyn Herwitz]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 16:52:47 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83365</guid>

					<description><![CDATA[In reply to &lt;a href=&quot;https://livingwithscleroderma.com/in-the-weeds/#comment-83361&quot;&gt;Patricia Bizzell&lt;/a&gt;.

Indeed! 
Re masking pain . . . there&#039;s an important distinction to be made between masking pain, as in blocking the sensations without addressing the cause, and managing pain, which is my focus here. I&#039;ve learned from very hard experience with infected ulcers over the decades that you have to get ahead of the pain and stay on top of it with whatever means are safe and effective, or the pain becomes much more intense and harder to control. I agree, pain is the body&#039;s warning system, but once you identify and deal with the cause, the pain requires careful management until the problem resolves. To all readers who struggle with this issue, I hope my experience is helpful.]]></description>
			<content:encoded><![CDATA[<p>In reply to <a href="https://livingwithscleroderma.com/in-the-weeds/#comment-83361">Patricia Bizzell</a>.</p>
<p>Indeed!<br />
Re masking pain . . . there&#8217;s an important distinction to be made between masking pain, as in blocking the sensations without addressing the cause, and managing pain, which is my focus here. I&#8217;ve learned from very hard experience with infected ulcers over the decades that you have to get ahead of the pain and stay on top of it with whatever means are safe and effective, or the pain becomes much more intense and harder to control. I agree, pain is the body&#8217;s warning system, but once you identify and deal with the cause, the pain requires careful management until the problem resolves. To all readers who struggle with this issue, I hope my experience is helpful.</p>
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		<item>
		<title>
		By: Patricia Bizzell		</title>
		<link>https://livingwithscleroderma.com/in-the-weeds/#comment-83361</link>

		<dc:creator><![CDATA[Patricia Bizzell]]></dc:creator>
		<pubDate>Tue, 15 Feb 2022 15:50:23 +0000</pubDate>
		<guid isPermaLink="false">https://livingwithscleroderma.com/?p=8253#comment-83361</guid>

					<description><![CDATA[So sorry to hear about this ordeal, Evie, but relieved that you discovered a new way to manage the pain. My chiropractor recommended CBD cream several years ago for my arthritic joint pain and it works wonderfully well, just as you describe. It even eased the pain of a bad bruise I got on my foot after stumbling into a table. I use it only infrequently, maybe once or twice a month at most, although I am not aware of any negative consequences of more frequent use. The one caution my husband has expressed: any time a person masks pain, they may be masking a condition that they need to attend to. But in the case of your painful thumb and other joint issues, Evie, it&#039;s clear that you know what&#039;s going on and address it medically. In my case, one goal is to postpone joint surgery as long as possible, a goal approved by my rheumatologist. Good luck to us both!]]></description>
			<content:encoded><![CDATA[<p>So sorry to hear about this ordeal, Evie, but relieved that you discovered a new way to manage the pain. My chiropractor recommended CBD cream several years ago for my arthritic joint pain and it works wonderfully well, just as you describe. It even eased the pain of a bad bruise I got on my foot after stumbling into a table. I use it only infrequently, maybe once or twice a month at most, although I am not aware of any negative consequences of more frequent use. The one caution my husband has expressed: any time a person masks pain, they may be masking a condition that they need to attend to. But in the case of your painful thumb and other joint issues, Evie, it&#8217;s clear that you know what&#8217;s going on and address it medically. In my case, one goal is to postpone joint surgery as long as possible, a goal approved by my rheumatologist. Good luck to us both!</p>
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