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	<title>Pulmonary Fibrosis News Forums | Sam Gilmore | Activity</title>
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				<title>Sam Gilmore 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-29189</link>
				<pubDate>Sat, 10 Jul 2021 02:55:28 -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-29189"><span class="bb-reply-lable">Reply to</span> Help for High Oxygen User Nasal Pain</a></p> <div class="bb-content-inr-wrap"><p>That sound good l have found Silver Shield gell works great it softens stuff in nose makes it easy to remove</p>
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				<title>Sam Gilmore 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-29132</link>
				<pubDate>Thu, 08 Jul 2021 00:24:07 -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-29132"><span class="bb-reply-lable">Reply to</span> Help for High Oxygen User Nasal Pain</a></p> <div class="bb-content-inr-wrap"><p>Thank you I have found that a product called Neospoin.. it works greatly a few days in nose couple times s day works thank you</p>
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				<title>Sam Gilmore posted an update: I am on my 10L concentrator I started with concentrator [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/28160/</link>
				<pubDate>Tue, 06 Jul 2021 20:11:28 -0500</pubDate>

									<content:encoded><![CDATA[<p>I am on my 10L concentrator I started with concentrator that is suppose to keep nose and mouth from drying out.so I tryird it out for a few days and it made my nose and mouth extremily dry. I did just the opposite from what it is suppse to go my nose was so dryrd out rediculouse. Any dode else hae this expietence</p>
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				<title>Sam Gilmore replied to the discussion Shortness of breath and normal oxygen reading in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29000</link>
				<pubDate>Thu, 24 Jun 2021 23:05:44 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29000"><span class="bb-reply-lable">Reply to</span> Shortness of breath and normal oxygen reading</a></p> <div class="bb-content-inr-wrap"><p>Sounds familiar Terry except I do have my family to talk to. Im 74 years old. I have had IPf for about 4 years. am on oxygen 24-7 I went from 20L oxygen to now 7L. If I do anything I become short of breath. I haven&#8217;t been out of my house in year and a half. My doctors visits are all virtual. I cant even take a shower now with out&hellip;<span class="activity-read-more" id="activity-read-more-27965"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29000" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Disabled Identity Crisis &#38; Accommodations in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/your-right-to-ada-accommodations/#post-28866</link>
				<pubDate>Tue, 15 Jun 2021 19:50:06 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/your-right-to-ada-accommodations/#post-28866"><span class="bb-reply-lable">Reply to</span> Disabled Identity Crisis &amp; Accommodations</a></p> <div class="bb-content-inr-wrap"><p>I know how your mom feels. I am 73 year old self made man. I was very active and some what prideful in a good way man I came down with IPF like 4 years ago the worst day of my life was the day I was diagnosed. Embarrassed Having to be helped by my family sometimes I feel so helpless on O2 24-7 Not active hardly at all even with Oxygen. The&hellip;<span class="activity-read-more" id="activity-read-more-27758"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/your-right-to-ada-accommodations/#post-28866" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Severe neck and shoulder pain in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/severe-neck-and-shoulder-pain/#post-28818</link>
				<pubDate>Thu, 10 Jun 2021 19:15:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/severe-neck-and-shoulder-pain/#post-28818"><span class="bb-reply-lable">Reply to</span> Severe neck and shoulder pain</a></p> <div class="bb-content-inr-wrap"><p>I have had neck pain for several months now. I use a lotion called Tei-Fu by Natures Sunshine it does help some. My pain comes and goes I dont know if IPF has anything to do with it or not. I have had IPF for 3-4 years and the pain started a few month ago.  I talked to my Dr  and they dont know. So I am dealing with it as best as I can Mine is&hellip;<span class="activity-read-more" id="activity-read-more-27673"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/severe-neck-and-shoulder-pain/#post-28818" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Supplemental Oxygen Questions in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28667</link>
				<pubDate>Thu, 27 May 2021 20:05:29 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28667"><span class="bb-reply-lable">Reply to</span> Supplemental Oxygen Questions</a></p> <div class="bb-content-inr-wrap"><p>I am on oxygen 24-7 I have a home concentrator and a portable concentrator both work very well. How ever I do get brethless when I get active it will go from 98 at rest to 75-85 when active. So I dont get the excursive I need.</p>
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				<title>Sam Gilmore and Jim Parsons are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27367/</link>
				<pubDate>Thu, 27 May 2021 01:30:33 -0500</pubDate>

				
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				<title>Sam Gilmore replied to the discussion Supplemental Oxygen Questions in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28364</link>
				<pubDate>Tue, 18 May 2021 20:43:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28364"><span class="bb-reply-lable">Reply to</span> Supplemental Oxygen Questions</a></p> <div class="bb-content-inr-wrap"><p>I have been diagnosed IPF 3 years ago. Using oxygen for about 2 years I&#8217;m on 7-24 now set at 5 I&#8217;m at 95&#8211;98 resting but as soon as I get up and walk 5ft it drops to 65-75  I have. Difficulty moving from room to room. I am looking into getting a Motorized Chair so I can get around. I know I don&#8217;t have to much time left I am making of it the&hellip;<span class="activity-read-more" id="activity-read-more-27223"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28364" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion No Oxygen and extremely bad breathing in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/no-oxygen-and-extremely-bad-breathing/#post-28171</link>
				<pubDate>Tue, 27 Apr 2021 20:49:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/no-oxygen-and-extremely-bad-breathing/#post-28171"><span class="bb-reply-lable">Reply to</span> No Oxygen and extremely bad breathing</a></p> <div class="bb-content-inr-wrap"><p>Sorry to hear about your mom . I am dealing with the oxygen too I am on it 24-7 even then I get breathless. Your Doc will need to prescribe oxygen for you they have suppliers that they go through. Hope that helps </p>
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				<title>Sam Gilmore replied to the discussion &#039;Scanxiety&#039; Among IPF Patients in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/scanxiety-among-ipf-patients/#post-28111</link>
				<pubDate>Tue, 20 Apr 2021 21:15:45 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/scanxiety-among-ipf-patients/#post-28111"><span class="bb-reply-lable">Reply to</span> 'Scanxiety' Among IPF Patients</a></p> <div class="bb-content-inr-wrap"><p>No not really My last appointments have been virtual. However I did go in for a CT scan but I could not do it I cant lay flat my head needs to be elevated and my arms over my head, and also lay on my stomach I cant do any of those things.  As they started to put me in the tube I said no cant do this pull me out.. So I did not get the CT so Im&hellip;<span class="activity-read-more" id="activity-read-more-26756"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/scanxiety-among-ipf-patients/#post-28111" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Supplemental Oxygen Questions in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/#post-28060</link>
				<pubDate>Tue, 13 Apr 2021 23:33:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplemental-oxygen-questions/page/2/#post-28060"><span class="bb-reply-lable">Reply to</span> Supplemental Oxygen Questions</a></p> <div class="bb-content-inr-wrap"><p>I have been on Oxygen 24-7 for several months now. While I am at rest my level is 85-98 but if I get up to do anything it drops between 78-85 while on oxygen. I am considering getting a Mobility scooter to help me get around the house from room to room. Anyone have experience with the scooters? Than you Sam G</p>
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				<title>Sam Gilmore posted an update: I have had IPF for about 2yeras I am on oxygen 24-7 [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/26485/</link>
				<pubDate>Fri, 02 Apr 2021 19:18:29 -0500</pubDate>

									<content:encoded><![CDATA[<p>I have had IPF for about 2yeras I am on oxygen 24-7 my question is while on oxygen if I get up to go to next room my level goes from, 97 to 76 and I get very short winded.  This just started like a month ago. My Doctor told me to go to 5 on my machine but even that does not seem to help.  I think this is just a sign that my journey is about&hellip;<span class="activity-read-more" id="activity-read-more-26485"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/26485/" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion WEI Institute Natural Care of Chronic Lung Diseases in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/wei-institute-natural-care-of-chronic-lung-diseases/#post-27244</link>
				<pubDate>Thu, 11 Feb 2021 22:09:45 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/wei-institute-natural-care-of-chronic-lung-diseases/#post-27244"><span class="bb-reply-lable">Reply to</span> WEI Institute Natural Care of Chronic Lung Diseases</a></p> <div class="bb-content-inr-wrap"><p>Thank you for your input about WEI it is very expensive and from what I have read I don&#8217;t think it will help me much. I am going on my 5th year with this thing IPF it has affected my life allot but I am still doing pretty good am on oxygen when I  some what  active life. not like before. I am enjoying my family and my 9 year old and 3 month old&hellip;<span class="activity-read-more" id="activity-read-more-25443"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/wei-institute-natural-care-of-chronic-lung-diseases/#post-27244" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore started the discussion WEI Institute Natural Care of Chronic Lung Diseases in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/wei-institute-natural-care-of-chronic-lung-diseases/</link>
				<pubDate>Tue, 09 Feb 2021 22:02:28 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/wei-institute-natural-care-of-chronic-lung-diseases/">WEI Institute Natural Care of Chronic Lung Diseases</a></p> <div class="bb-content-inr-wrap"><p>Has anyone had experience with the WEI Institute?  From my research it sounds promising but it is expensive.  Any information that you may share would be helpful.  I am considering trying the program. Thank you Sam Gilmore</p>
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				<title>Sam Gilmore posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/24682/#acomment-24692</link>
				<pubDate>Sat, 02 Jan 2021 16:14:21 -0600</pubDate>

									<content:encoded><![CDATA[<p>Thank you for your reply. My problem is I don&#8217;t get enough exercise. I don&#8217;t have much energy. Each day has its own challenge doesn&#8217;t it . Take care stay safe. Sam </p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/samgilmore/" data-bb-hp-profile="6979" rel="nofollow">Sam Gilmore</a> posted an update Sleep I have been diagnosed with IPF for about 4 years now.  Not doing to bad am on oxygen about 50% of the time. My question is about sleep. I do not sleep well. I to When I do go [&hellip;]					]]></content:encoded>
				
				
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				<title>Sam Gilmore posted an update: Sleep I have been diagnosed with IPF for about 4 years [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/24682/</link>
				<pubDate>Sat, 02 Jan 2021 10:57:05 -0600</pubDate>

									<content:encoded><![CDATA[<p>Sleep I have been diagnosed with IPF for about 4 years now.  Not doing to bad am on oxygen about 50% of the time. My question is about sleep. I do not sleep well. I to When I do go to bed its like 2:am and don&#8217;t fall a sleep until about 4am but then I will sleep some times until 5apm. Any one else have this issue?</p>
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				<title>Sam Gilmore replied to the discussion Too much oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/too-much-oxygen/#post-26652</link>
				<pubDate>Sun, 27 Dec 2020 07:42:25 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/too-much-oxygen/#post-26652"><span class="bb-reply-lable">Reply to</span> Too much oxygen</a></p> <div class="bb-content-inr-wrap"><p>What a great topic. I have been on oxygen for about year have had IPF for about 4 years. I use oxygen when I am active but when I am resting I  do not use it all the time only when I feel a need for or get panicky which happens. I will use it to bring my lungs back to the 90s. I do think its important to try an strengthen the lungs as much as&hellip;<span class="activity-read-more" id="activity-read-more-24500"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/too-much-oxygen/#post-26652" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion results experienced after Wei Labs products usage in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/results-experienced-after-wei-labs-products-usage/#post-26409</link>
				<pubDate>Tue, 08 Dec 2020 22:10:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/results-experienced-after-wei-labs-products-usage/#post-26409"><span class="bb-reply-lable">Reply to</span> results experienced after Wei Labs products usage</a></p> <div class="bb-content-inr-wrap"><p>I have not read any thing new about Wei but would like to know more Can anybody share</p>
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				<title>Sam Gilmore replied to the discussion Portable Oxygen Concentators in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen-concentators/#post-26116</link>
				<pubDate>Fri, 13 Nov 2020 00:49:07 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen-concentators/#post-26116"><span class="bb-reply-lable">Reply to</span> Portable Oxygen Concentators</a></p> <div class="bb-content-inr-wrap"><p>I have a portable oxygen concentrator called a OxyGo Next It&#8217;s lightweight and fits in a bag to carry around very convenient weighs 4.7 pounds.  Through my insurance I pay 37.00 a month and that includes the Home concentrator also.  Hope this helps.</p>
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				<title>Sam Gilmore replied to the discussion Cold Weather and Fatigue for IPF Patients. in the forum Canadians With PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26019</link>
				<pubDate>Thu, 05 Nov 2020 05:16:38 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26019"><span class="bb-reply-lable">Reply to</span> Cold Weather and Fatigue for IPF Patients.</a></p> <div class="bb-content-inr-wrap"><p>Thank you I do better in cooler temps.  When I first came down the IPF the cold really bothered  me but know the warmer temps  do.  Texas is good place for us, most of the time. Y&#8217;all take care.</p>
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				<title>Sam Gilmore replied to the discussion Cold Weather and Fatigue for IPF Patients. in the forum Canadians With PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26001</link>
				<pubDate>Tue, 03 Nov 2020 20:26:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26001"><span class="bb-reply-lable">Reply to</span> Cold Weather and Fatigue for IPF Patients.</a></p> <div class="bb-content-inr-wrap"><p>I live in Texas so we don&#8217;t get below 45 degrees hardly ever. But I feel better when its cold. But here we are averaging 70-75 so far early Nov and thats ok better than 100+ like we get in the summer ..</p>
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				<title>Sam Gilmore replied to the discussion How does taking Prednisone help IPF patients in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-does-taking-prednisone-help-ipf-patients/#post-25963</link>
				<pubDate>Thu, 29 Oct 2020 20:37:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-does-taking-prednisone-help-ipf-patients/#post-25963"><span class="bb-reply-lable">Reply to</span> How does taking Prednisone help IPF patients</a></p> <div class="bb-content-inr-wrap"><p>I have had IPF for 4 years at first I had no quality of life.  After talking to my Dr. He put me on Prednisone been on it for about two years at 10mg what a difference I know there are side effects but to me the benefits out way the side effects. I also know that there is no cure at this time.  Just take a day at a time.  You will have good&hellip;<span class="activity-read-more" id="activity-read-more-23202"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-does-taking-prednisone-help-ipf-patients/#post-25963" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Afraid of the unknown in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/afraid-of-the-unknown/#post-25896</link>
				<pubDate>Thu, 22 Oct 2020 22:42:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/afraid-of-the-unknown/#post-25896"><span class="bb-reply-lable">Reply to</span> Afraid of the unknown</a></p> <div class="bb-content-inr-wrap"><p>I know how you feel when I had no energy to even get out of bed no quality life. I was first diagnosed with IPF 4 years ago I am 74 years old . My first doctor was not very encouraging my wife and I left his office feeling hopeless and afraid I felt like a was given a death sentence. After a few months I decided to find another doctor&hellip;<span class="activity-read-more" id="activity-read-more-23065"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/afraid-of-the-unknown/#post-25896" rel="nofollow"> Read more</a></span></p>
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				<title>Sam Gilmore replied to the discussion Getting oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25829</link>
				<pubDate>Thu, 15 Oct 2020 19:21:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25829"><span class="bb-reply-lable">Reply to</span> Getting oxygen</a></p> <div class="bb-content-inr-wrap"><p>My United Healthcare insurance covers Oxygen it cost me about 37 a month for a portable and a stay at home Oxygen devices.</p>
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				<title>Sam Gilmore replied to the discussion Getting oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25826</link>
				<pubDate>Thu, 15 Oct 2020 19:13:02 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25826"><span class="bb-reply-lable">Reply to</span> Getting oxygen</a></p> <div class="bb-content-inr-wrap"><p><em> </em>I have IPF for 4 years now and doing good I do use Oxygen as needed not all the time. But yes it does help when I become tired or short of breath. Your Doctor does have to prescribe it but its not a big deal . Talk to your Doctor.</p>
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				<title>Sam Gilmore replied to the discussion Laser Therapy Results in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/laser-therapy-results/#post-25232</link>
				<pubDate>Thu, 13 Aug 2020 19:08:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/laser-therapy-results/page/5/#post-25232"><span class="bb-reply-lable">Reply to</span> Laser Therapy Results</a></p> <div class="bb-content-inr-wrap"><p>I have not heard of Laser therapy is it new? Where can I get more information about it? Thank you</p>
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				<title>Sam Gilmore posted an update: I have not heard about Laser therapy.  Where can get [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/21840/</link>
				<pubDate>Thu, 13 Aug 2020 19:06:30 -0500</pubDate>

									<content:encoded><![CDATA[<p>I have not heard about Laser therapy.  Where can get more info and is this new </p>
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				<title>Sam Gilmore replied to the discussion Tailored Exercise Programs Beneficial for Patients with IPF/PF in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tailored-exercise-programs-beneficial-for-patients-with-ipf-pf/#post-25176</link>
				<pubDate>Thu, 06 Aug 2020 20:39:42 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tailored-exercise-programs-beneficial-for-patients-with-ipf-pf/#post-25176"><span class="bb-reply-lable">Reply to</span> Tailored Exercise Programs Beneficial for Patients with IPF/PF</a></p> <div class="bb-content-inr-wrap"><p>I do not have a tailored program I do walk and ride exercycle for about 10 &#8211; 15 min. a day Because of energy level that&#8217;s about all I can do.  So many days I do not have enough energy to do much more. I am 73 years old had IPF for 4 years but am doing pretty good just tired many times.</p>
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				<title>Sam Gilmore became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/21697/</link>
				<pubDate>Thu, 06 Aug 2020 20:34:09 -0500</pubDate>

				
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