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	<title>Pulmonary Fibrosis News Forums | Rod Danner | Activity</title>
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				<title>Rod Danner replied to the discussion Painful hand and leg cramps in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/painful-hand-and-leg-cramps/#post-32548</link>
				<pubDate>Thu, 07 Jul 2022 19:33:45 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/painful-hand-and-leg-cramps/#post-32548"><span class="bb-reply-lable">Reply to</span> Painful hand and leg cramps</a></p> <div class="bb-content-inr-wrap"><p>I have found that the absolute best thing for quickly dealing with cramps is a magnesium foam called &#8220;Theraworx&#8221; it is available at pharmacies and some sporting goods stores. Just spray some on and rub it in. It helps provide almost immediate relief. Also, hydration and magnesium supplements may help some too, the hydration for sure.</p>
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				<title>Rod Danner replied to the discussion Top 4 Words You&#039;d Use to Describe IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/top-4-words-youd-use-to-describe-ipf/#post-31766</link>
				<pubDate>Fri, 22 Apr 2022 16:02:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/top-4-words-youd-use-to-describe-ipf/#post-31766"><span class="bb-reply-lable">Reply to</span> Top 4 Words You'd Use to Describe IPF</a></p> <div class="bb-content-inr-wrap"><p>Smothering, progressive, incurable, and terminal.  It&#8217;s certainly not a pretty picture.</p>
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				<title>Rod Danner replied to the discussion How are long-term (4+ years) OFEV users doing? in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-are-long-term-4-years-ofev-users-doing/#post-31680</link>
				<pubDate>Wed, 13 Apr 2022 16:19:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-are-long-term-4-years-ofev-users-doing/#post-31680"><span class="bb-reply-lable">Reply to</span> How are long-term (4+ years) OFEV users doing?</a></p> <div class="bb-content-inr-wrap"><p>I have been on OFEV for 6 years as of two days ago. The only actual side effects that have been a problem have been some stomach cramping and the associated diarrhea. I have been able to keep the diarrhea mostly under control with Loperamide (Immodium) by just taking one when the first sign of loose stools appears. If I am going to be&hellip;<span class="activity-read-more" id="activity-read-more-32676"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-are-long-term-4-years-ofev-users-doing/#post-31680" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner replied to the discussion OFEV low 02 levels in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-low-02-levels/#post-31233</link>
				<pubDate>Fri, 04 Mar 2022 00:59:20 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-low-02-levels/#post-31233"><span class="bb-reply-lable">Reply to</span> OFEV low 02 levels</a></p> <div class="bb-content-inr-wrap"><p>I agree with Paul Lakeland. The drop in O2 levels is most likely from the progression of the disease.</p>
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				<title>Rod Danner changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/30466/</link>
				<pubDate>Fri, 12 Nov 2021 15:42:30 -0600</pubDate>

				
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				<title>Rod Danner replied to the discussion Inhaler use in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30442</link>
				<pubDate>Fri, 12 Nov 2021 15:40:04 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30442"><span class="bb-reply-lable">Reply to</span> Inhaler use</a></p> <div class="bb-content-inr-wrap"><p>I use Albuterol on occasion before exercise and before bed. It does seem to help. I also use a nebulizer with Albuterol when I seem more &#8220;choked up&#8221; than usual. It also does seem to offer some relief. They also test me with Albuterol during my PFTs and it does show some improvement post-use.</p>
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				<title>Rod Danner replied to the discussion Phlegm in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26958</link>
				<pubDate>Fri, 22 Jan 2021 15:54:07 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26958"><span class="bb-reply-lable">Reply to</span> Phlegm</a></p> <div class="bb-content-inr-wrap"><p>Hello Ted,</p>
<p>It seems that oscillating pressure is a treatment that is common in the southern hemisphere. I have been using a device called an Air-Physio that is made in Australia. It is the same concept with the steel ball vibrating as you exhale. I have found that when I use it before bed especially, it tends to cut down on some of the&hellip;<span class="activity-read-more" id="activity-read-more-25077"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26958" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner replied to the discussion Do others with IPF cough for 20 minutes every morning? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/#post-26436</link>
				<pubDate>Thu, 10 Dec 2020 06:22:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/page/2/#post-26436"><span class="bb-reply-lable">Reply to</span> Do others with IPF cough for 20 minutes every morning?</a></p> <div class="bb-content-inr-wrap"><p>Hi Susan. I have already been using a wedge pillow and the head of my bed has been raised. I decided to try an experiment last night and sleep flat. It was with less coughing as I had been experiencing with the wedge. It was successful and I’ll give it another try tonight. It’s the same way for me with the cramps. I also get them when not coughing.</p>
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				<title>Rod Danner replied to the discussion Do others with IPF cough for 20 minutes every morning? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/#post-26406</link>
				<pubDate>Tue, 08 Dec 2020 21:43:23 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/page/2/#post-26406"><span class="bb-reply-lable">Reply to</span> Do others with IPF cough for 20 minutes every morning?</a></p> <div class="bb-content-inr-wrap"><p>I have a cough, although it doesn&#8217;t go on quite as long as with the OP. Mine is most prevalent at bedtime and in the morning, but will also occur during the day. I often cough so hard and long to expel mucus that it causes cramps in my intercostal muscles in the back and in my transversus thoracic muscle. The cramps are quite painful. I&hellip;<span class="activity-read-more" id="activity-read-more-24020"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/#post-26406" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner replied to the discussion How The Apple Watch Can Assist Patients with Pulmonary Fibrosis in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22453</link>
				<pubDate>Thu, 09 Jan 2020 14:56:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/page/2/#post-22453"><span class="bb-reply-lable">Reply to</span> How The Apple Watch Can Assist Patients with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>The Breathe app is native. It will already be on your watch.</p>
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				<title>Rod Danner replied to the discussion How The Apple Watch Can Assist Patients with Pulmonary Fibrosis in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22447</link>
				<pubDate>Wed, 08 Jan 2020 14:33:30 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/page/2/#post-22447"><span class="bb-reply-lable">Reply to</span> How The Apple Watch Can Assist Patients with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>I thought I would give an update on my experience with the Apple Watch 5 that was under the tree on Christmas. I have been exploring the use and potential over the last two weeks. I have found it to be extremely useful in any number of ways both health and related to life in general. It works relatively seamlessly with my iPhone, although,&hellip;<span class="activity-read-more" id="activity-read-more-17046"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22447" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner replied to the discussion How The Apple Watch Can Assist Patients with Pulmonary Fibrosis in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22224</link>
				<pubDate>Fri, 13 Dec 2019 14:14:19 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22224"><span class="bb-reply-lable">Reply to</span> How The Apple Watch Can Assist Patients with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>I had not really been interested in an Apple watch until the series 4 &amp; 5.  The new capabilities will be useful and they keep adding more with each update. I agree that O2 saturation would be a real benefit. I will be seeing one under the tree for Christmas.  Be careful Lorraine, the quality and performance of your iPhone may lead you down a&hellip;<span class="activity-read-more" id="activity-read-more-16640"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-the-apple-watch-can-assist-patients-with-pulmonary-fibrosis/#post-22224" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner replied to the discussion Do you take OFEV? Take our poll! in the forum Polls &#38; Quizzes</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/take-ofev-take-poll/#post-22078</link>
				<pubDate>Tue, 26 Nov 2019 17:50:14 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/take-ofev-take-poll/#post-22078"><span class="bb-reply-lable">Reply to</span> Do you take OFEV? Take our poll!</a></p> <div class="bb-content-inr-wrap"><p>I have been on OFEV for almost three years. It is the first and only IPF medication I have used. I live in Florida and bicycle a lot, so Esbriet was a non-starter for me.  Of course, the effectiveness of the medication is quite subjective. I do believe that it has slowed progression, but then, how fast would it progress without? Anyway,&hellip;<span class="activity-read-more" id="activity-read-more-16391"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/take-ofev-take-poll/#post-22078" rel="nofollow"> Read more</a></span></p>
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				<title>Rod Danner became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5004/</link>
				<pubDate>Thu, 23 Aug 2018 17:09:01 -0500</pubDate>

				
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