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	<title>Pulmonary Fibrosis News Forums | Glenda Rouland | Activity</title>
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				<title>Glenda Rouland replied to the discussion PFTs and a Reduction in DLCO Number. in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-a-reduction-in-dlco-number/#post-22839</link>
				<pubDate>Tue, 04 Feb 2020 23:15:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-a-reduction-in-dlco-number/page/2/#post-22839"><span class="bb-reply-lable">Reply to</span> PFTs and a Reduction in DLCO Number.</a></p> <div class="bb-content-inr-wrap"><p>I am having same problem DLCO has gone down to 34 from 49 which I had for 3 years. So much more trouble breathing now with no change in ct or X-ray   Just evaluated for list at Vanderbilt and no PH. Don’t get what’s going on</p>
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				<title>Glenda Rouland replied to the discussion IPF-Related Medication Side Effects: Impact on Skin in the forum PF Life: Young Adults</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-related-medication-side-effects-impact-on-skin/#post-21893</link>
				<pubDate>Thu, 07 Nov 2019 15:09:39 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-related-medication-side-effects-impact-on-skin/#post-21893"><span class="bb-reply-lable">Reply to</span> IPF-Related Medication Side Effects: Impact on Skin</a></p> <div class="bb-content-inr-wrap"><p>I take Esbriet and have developed primoral dermatitis    Never ever had sensitive skin or rashes before.   Also my skin very dry</p>
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				<title>Glenda Rouland replied to the discussion PFF Summit 2019 in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pff-summit-2019/#post-21745</link>
				<pubDate>Thu, 24 Oct 2019 17:44:12 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pff-summit-2019/#post-21745"><span class="bb-reply-lable">Reply to</span> PFF Summit 2019</a></p> <div class="bb-content-inr-wrap"><p>I am attending the Summit</p>
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				<title>Glenda Rouland replied to the discussion Overheating as a Patient with Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/overheating-as-a-patient-with-pulmonary-fibrosis/#post-21512</link>
				<pubDate>Thu, 03 Oct 2019 17:47:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/overheating-as-a-patient-with-pulmonary-fibrosis/#post-21512"><span class="bb-reply-lable">Reply to</span> Overheating as a Patient with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>I have noticed that I sweat a lot more with physical activity.  Never used to. Dr said because having to work to breathe so everything working harder.   I also go to UAB and being evaluated at Vanderbilt</p>
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				<title>Glenda Rouland replied to the discussion PFTs and a Reduction in DLCO Number. in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-a-reduction-in-dlco-number/#post-21032</link>
				<pubDate>Tue, 27 Aug 2019 16:27:06 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-a-reduction-in-dlco-number/#post-21032"><span class="bb-reply-lable">Reply to</span> PFTs and a Reduction in DLCO Number.</a></p> <div class="bb-content-inr-wrap"><p>This sounds like my story. Got diagnosed in 2015 but cray shied in 2013 but dr never got it.  My DLCO has been stable starting at 50  always testing  between 48-50 which is stable.  In May of this year it was in the low 40’s and recently it was 34. Concerning the drop  wondering if I had exerbation.    My FVC has stayed low 70’s this year  I&hellip;<span class="activity-read-more" id="activity-read-more-14789"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-a-reduction-in-dlco-number/#post-21032" rel="nofollow"> Read more</a></span></p>
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				<title>Glenda Rouland replied to the discussion Tips for Carrying Multiple Items as a Patient with PF. in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-carrying-multiple-items-as-a-patient-with-pf/#post-19910</link>
				<pubDate>Tue, 18 Jun 2019 03:12:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-carrying-multiple-items-as-a-patient-with-pf/#post-19910"><span class="bb-reply-lable">Reply to</span> Tips for Carrying Multiple Items as a Patient with PF.</a></p> <div class="bb-content-inr-wrap"><p>There are no portables to go to 5l continuous. I have sequal eclipse that will go to 3  continuous and 9 setting for pulse. The setting numbers are not liters</p>
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				<title>Glenda Rouland replied to the discussion Clearing Throat in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/clearing-throat/#post-19425</link>
				<pubDate>Tue, 28 May 2019 14:12:45 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/clearing-throat/#post-19425"><span class="bb-reply-lable">Reply to</span> Clearing Throat</a></p> <div class="bb-content-inr-wrap"><p>Yes all the time sometimes when I lay down keep doing until through is sore.   Bought Grossan nasal irrigator on amazon at dr advice makes a huge difference.</p>
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				<title>Glenda Rouland replied to the discussion Tips for Carrying Multiple Items as a Patient with PF. in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-carrying-multiple-items-as-a-patient-with-pf/#post-19064</link>
				<pubDate>Fri, 10 May 2019 14:54:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-carrying-multiple-items-as-a-patient-with-pf/#post-19064"><span class="bb-reply-lable">Reply to</span> Tips for Carrying Multiple Items as a Patient with PF.</a></p> <div class="bb-content-inr-wrap"><p>I have the better breathers backpack ordered on amazon. It has pockets and pouches to carry everything I use in my purse</p>
<p>when I use my wheeled sequal concentrator I use a small computer bag over the handle and pull it.</p>
<p>I am on 4 lpm soo do use tanks locally in my backpack .</p>
<p>i also got an iPhone case that has a door on back to hold license&hellip;<span class="activity-read-more" id="activity-read-more-12094"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-carrying-multiple-items-as-a-patient-with-pf/#post-19064" rel="nofollow"> Read more</a></span></p>
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				<title>Glenda Rouland replied to the discussion Six-Minute Walk Tests in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/six-minute-walk-tests/#post-18328</link>
				<pubDate>Thu, 11 Apr 2019 14:13:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/six-minute-walk-tests/#post-18328"><span class="bb-reply-lable">Reply to</span> Six-Minute Walk Tests</a></p> <div class="bb-content-inr-wrap"><p>I always walk as fast as I can on 6 minute walk test so I have an idea of oxygen I need when walking fast. Last time I did 1568 feet. I keep track of the feet I walk alo.  Don’t know why they don’t do a stair walking test for oxygen</p>
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				<title>Glenda Rouland changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/8856/</link>
				<pubDate>Wed, 13 Feb 2019 16:41:44 -0600</pubDate>

				
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				<title>Glenda Rouland and Charlene are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7584/</link>
				<pubDate>Sat, 29 Dec 2018 15:28:20 -0600</pubDate>

				
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				<title>Glenda Rouland and Steve Dragoo are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7566/</link>
				<pubDate>Sat, 29 Dec 2018 00:50:28 -0600</pubDate>

				
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				<title>Glenda Rouland and Bob are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7564/</link>
				<pubDate>Sat, 29 Dec 2018 00:31:47 -0600</pubDate>

				
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				<title>Glenda Rouland replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15872</link>
				<pubDate>Fri, 28 Dec 2018 21:37:06 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/2/#post-15872"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Charlene and Bob I am living in Birmingham AL. Been here 18 years originally from Michigan and hubby from IL.  I was diagnosed in with IPF in oct  2015 but had in 2013 dr never saw X-ray. I went on oxygen last Jan and have gone from 2L to last 3 months 4L.  I go to UAB which is a center of excellence so I am lucky there although my doctor has&hellip;<span class="activity-read-more" id="activity-read-more-7560"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15872" rel="nofollow"> Read more</a></span></p>
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				<title>Glenda Rouland replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15832</link>
				<pubDate>Thu, 27 Dec 2018 17:17:11 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/2/#post-15832"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Did look up muscle and joint pain is a possible side effect. I will call manufacturer</p>
<p>thanks</p>
<p>Charlene and Bob</p>
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				<title>Glenda Rouland joined the group Research and Development</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7468/</link>
				<pubDate>Tue, 25 Dec 2018 22:25:30 -0600</pubDate>

				
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				<title>Glenda Rouland replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15809</link>
				<pubDate>Tue, 25 Dec 2018 22:22:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/2/#post-15809"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Had been on Esbriet for 2.5 years  had a decline so doctor switched me to Ofev. Been taking 2 months getting bad joint pain and muscle pain. Anyone else experience and did it go away after a bit</p>
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				<title>Glenda Rouland became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7465/</link>
				<pubDate>Tue, 25 Dec 2018 22:14:09 -0600</pubDate>

				
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