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	<title>Pulmonary Fibrosis News Forums | ChArles Bietsch | Activity</title>
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				<title>ChArles Bietsch replied to the discussion Sleeping with head elevated in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32629</link>
				<pubDate>Thu, 14 Jul 2022 23:10:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32629"><span class="bb-reply-lable">Reply to</span> Sleeping with head elevated</a></p> <div class="bb-content-inr-wrap"><p>The primary purpose of head elevation is to prevent silent acid reflux from entering the lungs.  There is a strong correlation between GERD and IPF. And several peer reviewed  studies have been done to establish the connection </p>
<p>If you have not had a 24 hour reflux test you may consider it to verify. If proven that you do. There are remedies&hellip;<span class="activity-read-more" id="activity-read-more-34364"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32629" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion CT Scan Reads Compatible with Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ct-scan-reads-compatible-with-pulmonary-fibrosis/#post-32479</link>
				<pubDate>Thu, 30 Jun 2022 21:41:15 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ct-scan-reads-compatible-with-pulmonary-fibrosis/#post-32479"><span class="bb-reply-lable">Reply to</span> CT Scan Reads Compatible with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>Hi I don’t know where you live , or if you are using a local / standard pulmonologist for evaluation </p>
<p>There are a variety of types / conditions that cause fibrosis in the lungs.  Ie infection, autoimmune diseases, etc </p>
<p>To set you mind at ease find a pulmonary fibrosis center of excellence near you.  Usually they are a specialized ILD&hellip;<span class="activity-read-more" id="activity-read-more-34094"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ct-scan-reads-compatible-with-pulmonary-fibrosis/#post-32479" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-32441</link>
				<pubDate>Mon, 27 Jun 2022 23:26:02 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-32441"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>I can say after having a single 4 1/2 years ago my ipf cough all but disappeared.  Still cough occasionally, but no where as debilitating as before.  The new lung will take over the primary  function . And the native lung will slowly fade…. Though mine has been relatively stable. My view, not a big issue to worry about.  I was 72 at time of Tx&hellip;<span class="activity-read-more" id="activity-read-more-34037"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-32441" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion Drinking Wine with Pulmonary Fibrosis. in the forum PF Life: Young Adults</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/drinking-wine-with-pulmonary-fibrosis/#post-32134</link>
				<pubDate>Thu, 19 May 2022 20:51:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/drinking-wine-with-pulmonary-fibrosis/#post-32134"><span class="bb-reply-lable">Reply to</span> Drinking Wine with Pulmonary Fibrosis.</a></p> <div class="bb-content-inr-wrap"><p>Charlene…. It would depend upon what type of medication you are on. Some such as cellcept and prednisone are toxic to the liver and kidneys and preservation of their function is necessary for king yet survival.  Alcohol of any kind is not recommended </p>
<p>Same if one is contemplating a transplant. Liver and kidneys need to be fully functional to be&hellip;<span class="activity-read-more" id="activity-read-more-33473"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/drinking-wine-with-pulmonary-fibrosis/#post-32134" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-31596</link>
				<pubDate>Mon, 04 Apr 2022 23:29:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/page/2/#post-31596"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>If they suggested a stent it will likely not disqualify you.  If they do it before you will likely have to wait for approx six months as you will be on blood thinners.    Sometimes they take care of it during the Tx surgery depending upon age.</p>
<p>&nbsp;</p>
<p>at my evaluation I had two over 60%, did not have stents , still don’t and that was 4 1/2 years&hellip;<span class="activity-read-more" id="activity-read-more-32552"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-31596" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30903</link>
				<pubDate>Sat, 29 Jan 2022 01:11:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30903"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Hi… Char</p>
<p>I responded to your article from the standpoint of a person who has gone through the process, and to share my experience and views</p>
<p>The title of the article was the “harsh realities”of lung transplant…, which could infer that your points are fact, and apply to all cases.</p>
<p>While some May experience issues you mention, many do&hellip;<span class="activity-read-more" id="activity-read-more-31339"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30903" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30870</link>
				<pubDate>Thu, 27 Jan 2022 22:45:26 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30870"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Mark….</p>
<p>Some comments  on your post….</p>
<p>Sure your immune system is depressed.  However, you don’t have to move in a bubble.  I have navigated the last two years with no issues and have led no less normal life than others.</p>
<p>It is no more dangerous than navigating the landscape with ipf.  One virus could wipe you out as well. Just be&hellip;<span class="activity-read-more" id="activity-read-more-31295"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30870" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30867</link>
				<pubDate>Thu, 27 Jan 2022 21:50:49 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30867"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Charlene.  Hi, read your article and sense this is coming from a place of uncertainty and/or fear.</p>
<p>I have to disagree with you on several points…. In particular the title of the article “harsh” reality????</p>
<p>what could be more harsh than living with IPF and not being able to do anything about it???</p>
<p>First, the statement trading one disease for&hellip;<span class="activity-read-more" id="activity-read-more-31292"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30867" rel="nofollow"> Read more</a></span></p>
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				<title>ChArles Bietsch became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/31289/</link>
				<pubDate>Thu, 27 Jan 2022 21:25:01 -0600</pubDate>

				
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