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	<title>Pulmonary Fibrosis News Forums | Robert Morgan | Activity</title>
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				<title>Robert Morgan replied to the discussion Help for High Oxygen User Nasal Pain in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/help-for-high-oxygen-user-nasal-pain/#post-27764</link>
				<pubDate>Thu, 18 Mar 2021 20:07:57 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/help-for-high-oxygen-user-nasal-pain/#post-27764"><span class="bb-reply-lable">Reply to</span> Help for High Oxygen User Nasal Pain</a></p> <div class="bb-content-inr-wrap"><p>I have similar problems. I use Arm and Hammer Simple Saline mist several times a day. Nasal rinses in the morning or as needed. Mist and saline gel at night. The gel stays in my nostrils as I sleep.  I also have used saline mist gel but not convinced how much it helps. At night I have a high-end AirOSwiss humidifier to keep the bedroom air&hellip;<span class="activity-read-more" id="activity-read-more-26155"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/help-for-high-oxygen-user-nasal-pain/#post-27764" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Skin Irritations Caused by Oxygen Cannulas. in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/skin-irritations-caused-oxygen-cannulas/#post-26144</link>
				<pubDate>Sat, 14 Nov 2020 20:09:29 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/skin-irritations-caused-oxygen-cannulas/#post-26144"><span class="bb-reply-lable">Reply to</span> Skin Irritations Caused by Oxygen Cannulas.</a></p> <div class="bb-content-inr-wrap"><p>I am on high oxygen and experiencing irritation of my nasal tissues, including crusty accumulations of bloody tissueand soreness. Two treatments have helped. Simply Saline by Arm &amp; Hammer injects a fine saline mist deeply into each nostril. It has no additives, which some reports say are damaging to the tissues. I use it several times a day.&hellip;<span class="activity-read-more" id="activity-read-more-23533"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/skin-irritations-caused-oxygen-cannulas/#post-26144" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Low BMI Might Be a Risk Factor for Gastrointestinal Side Effects in IPF Patients on Ofev in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/low-bmi-might-be-a-risk-factor-for-gastrointestinal-side-effects-in-ipf-patients-on-ofev/#post-21429</link>
				<pubDate>Wed, 25 Sep 2019 19:13:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/low-bmi-might-be-a-risk-factor-for-gastrointestinal-side-effects-in-ipf-patients-on-ofev/#post-21429"><span class="bb-reply-lable">Reply to</span> Low BMI Might Be a Risk Factor for Gastrointestinal Side Effects in IPF Patients on Ofev</a></p> <div class="bb-content-inr-wrap"><p>Great. IPF has reduced my appetite and food consumption, and consequently caused significant weight loss and lower BMI. It is a vicious circle. Taking famotidine, the generic Pepsid AC, has helped with acid reflux and increased my appetite somewhat. I am taking 100 Mg OFEV twice a day along with 801 mg Esbriet three times daily.</p>
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				<title>Robert Morgan replied to the discussion Introducing The Pulmonary Fibrosis News Multimedia Initiative in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/introducing-the-pulmonary-fibrosis-news-multimedia-initiative/#post-20702</link>
				<pubDate>Tue, 06 Aug 2019 19:37:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/introducing-the-pulmonary-fibrosis-news-multimedia-initiative/#post-20702"><span class="bb-reply-lable">Reply to</span> Introducing The Pulmonary Fibrosis News Multimedia Initiative</a></p> <div class="bb-content-inr-wrap"><p>This needs work. 1) Do not bury the lead. The introduction is way too long, includes too many names and details of the source of the information being presented before getting to the meat of the podcast. It is far more beneficial to summarize the results first. 2) Content is very technical with a lot of medical terminology, abbreviated&hellip;<span class="activity-read-more" id="activity-read-more-14236"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/introducing-the-pulmonary-fibrosis-news-multimedia-initiative/#post-20702" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion clinical trials for new meds in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/clinical-trials-for-new-meds/#post-20684</link>
				<pubDate>Tue, 06 Aug 2019 16:50:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/clinical-trials-for-new-meds/#post-20684"><span class="bb-reply-lable">Reply to</span> clinical trials for new meds</a></p> <div class="bb-content-inr-wrap"><p>There are clinical trials for just about every disease. PFF has a clinical trial finder for pulmonary fibrosis here:<br />
<a target='_blank' href="https://trials.pulmonaryfibrosis.org" rel="nofollow">https://trials.pulmonaryfibrosis.org</a>.  You can find sources for other types of clinical trials through Google or other search engine.</p>
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				<title>Robert Morgan replied to the discussion Statins and PF/IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/statins-and-pf-ipf/#post-19834</link>
				<pubDate>Fri, 14 Jun 2019 14:38:20 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/statins-and-pf-ipf/#post-19834"><span class="bb-reply-lable">Reply to</span> Statins and PF/IPF</a></p> <div class="bb-content-inr-wrap"><p>I have been taking simvastatin for many years and do not believe it interacts with Esbriet, the medicine I am on for IPF. Statins reduce cholesterol which can clog blood vessels and put strain on the heart. IPF reduces lung function which also puts strain on the heart. For that reason, I think it would be a bad idea to stop taking your&hellip;<span class="activity-read-more" id="activity-read-more-13050"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/statins-and-pf-ipf/#post-19834" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Portable oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14727</link>
				<pubDate>Tue, 02 Oct 2018 18:12:44 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14727"><span class="bb-reply-lable">Reply to</span> Portable oxygen</a></p> <div class="bb-content-inr-wrap"><p>This web site provides specs for Portable Oxygen Concentrators including both pulsed and continuous flow models. The continuous models have a limited range of flow, up to a maximum of 3 liters per minute.  <strong><a target='_blank' href="https://www.portableoxygensolutions.com/portable-oxygen-concentrator-comparison-guide/" rel="nofollow">https://www.portableoxygensolutions.com/portable-oxygen-concentrator-comparison-guide/</a> When I travel within the US, I make arrangements&hellip;</strong><span class="activity-read-more" id="activity-read-more-5846"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14727" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Portable oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14483</link>
				<pubDate>Wed, 19 Sep 2018 18:24:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14483"><span class="bb-reply-lable">Reply to</span> Portable oxygen</a></p> <div class="bb-content-inr-wrap"><p>I discovered a website that provides a comparison among the most popular models of Portable Oxygen Concentrators. https://www.portableoxygensolutions.com/portable-oxygen-concentrator-comparison-guide/  There are many tradeoffs of weight, cost and battery life. Your oxygen supplier will likely offer only some of them. Although most come with a&hellip;<span class="activity-read-more" id="activity-read-more-5607"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14483" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Portable oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14305</link>
				<pubDate>Tue, 04 Sep 2018 20:40:03 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14305"><span class="bb-reply-lable">Reply to</span> Portable oxygen</a></p> <div class="bb-content-inr-wrap"><p>I need a POC for travel and it is complicated! My oxygen supplier, LinCare, says there is a backlog in getting them. We have a trip planned in mid October, and I may have to rent one for about $125 a week. There are several websites that rate the different makes and models. Inogen One G3 is highly rated in most reviews, but LinCare won&#8217;t carry&hellip;<span class="activity-read-more" id="activity-read-more-5375"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-14305" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan replied to the discussion Starting Esbriet in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-14116</link>
				<pubDate>Sun, 26 Aug 2018 20:10:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/page/2/#post-14116"><span class="bb-reply-lable">Reply to</span> Starting Esbriet</a></p> <div class="bb-content-inr-wrap"><p>My pulmonologist recently switched my IPF medication from OFEV, which I took for a year and a half, to Esbriet. This was in response to a recent study that indicated taking a combination of the two was more effective at slowing the deterioration of the lungs than either alone. I am in my third month of Esbriet and have not yet been directed by&hellip;<span class="activity-read-more" id="activity-read-more-5129"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-14116" rel="nofollow"> Read more</a></span></p>
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				<title>Robert Morgan became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4739/</link>
				<pubDate>Wed, 15 Aug 2018 17:15:25 -0500</pubDate>

				
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