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	<title>Pulmonary Fibrosis News Forums | John14392 | Activity</title>
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				<title>John14392 replied to the discussion POC rental for airplane in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/poc-rental-for-airplane/#post-39344</link>
				<pubDate>Fri, 20 Feb 2026 21:34:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/poc-rental-for-airplane/#post-39344"><span class="bb-reply-lable">Reply to</span> POC rental for airplane</a></p> <div class="bb-content-inr-wrap"><p>Plane cabin pressure is about 8000 ft.   I think I would rather have it with me and not need it, then need it and not have it.</p>
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<p>Let us know how your flying after transplant goes.</p>
<p>John</p>
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				<title>John14392 replied to the discussion Are you going through lack of oxygen and palpitations? in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/are-you-going-through-lack-of-oxygen-and-palpitations/#post-39296</link>
				<pubDate>Fri, 06 Feb 2026 21:46:51 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/are-you-going-through-lack-of-oxygen-and-palpitations/#post-39296"><span class="bb-reply-lable">Reply to</span> Are you going through lack of oxygen and palpitations?</a></p> <div class="bb-content-inr-wrap"><p>Also I sleep in my armchair as I get exhausted climbing stairs and our bedroom is 2.5 stair levels up from my den where my armchair is.  When I sleep my O2 is at level 20.</p>
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				<title>John14392 replied to the discussion Are you going through lack of oxygen and palpitations? in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/are-you-going-through-lack-of-oxygen-and-palpitations/#post-39295</link>
				<pubDate>Fri, 06 Feb 2026 21:44:47 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/are-you-going-through-lack-of-oxygen-and-palpitations/#post-39295"><span class="bb-reply-lable">Reply to</span> Are you going through lack of oxygen and palpitations?</a></p> <div class="bb-content-inr-wrap"><p>I am on no drugs to slow my scarring.  I experienced the same problem.  I am on O2 all the time.  I am on the transplant list and will probably be transplanted either this summer or next summer.  Resting at level 10 I get to 90-92 blood O2, but at level 20 I get to 98-99 which feels much better, so I use level 20 when resting in my armchair. &hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-46818"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/are-you-going-through-lack-of-oxygen-and-palpitations/#post-39295" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Determining when it&#039;s time to stop working in the forum Employment &#38; Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/determining-when-its-time-to-stop-working/#post-39256</link>
				<pubDate>Fri, 23 Jan 2026 22:49:07 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/determining-when-its-time-to-stop-working/#post-39256"><span class="bb-reply-lable">Reply to</span> Determining when it's time to stop working</a></p> <div class="bb-content-inr-wrap"><p>I have 20% good lungs left, I am on 10-25 O2 levels depending on what I am doing.  At home watching TV I can get by on level 10, but when I move out of my recliner I need more.  I have 3 level 10 floor oxygen concentrators at home so all my home is covered.  I am on O2 24/7.  I have a work office outside my home and a home office.  If I get up&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-46728"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/determining-when-its-time-to-stop-working/#post-39256" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Night time Oxygen Concentrators in the forum Healthcare Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/night-time-oxygen-concentrators/#post-39096</link>
				<pubDate>Fri, 19 Dec 2025 20:32:50 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/night-time-oxygen-concentrators/#post-39096"><span class="bb-reply-lable">Reply to</span> Night time Oxygen Concentrators</a></p> <div class="bb-content-inr-wrap"><p>I use level 10 floor oxygen concentrators all the time now.  At night I have 30 ft hose and put the concentrator in an adjacent room and shut both doors, with the cord going under the doors (in the middle so they don&#8217;t get kinked in the corners of the door).</p>
<p>I am on the transplant list and I need 3 floor concentrators to reach everywhere in my&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-46461"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/night-time-oxygen-concentrators/#post-39096" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Veterans and IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/veterans-and-ipf/#post-39001</link>
				<pubDate>Fri, 14 Nov 2025 20:37:42 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/veterans-and-ipf/#post-39001"><span class="bb-reply-lable">Reply to</span> Veterans and IPF</a></p> <div class="bb-content-inr-wrap"><p>I am a Vietnam veteran with IPF &#8211; with no identifiable cause.  I am 69 yrs old and the VA is covering all my IPF costs &#8211; I have no other disability &#8211; my IPF is not linked to my service.  I am on the lung transplant wait list right now.  They said as long as I applied for a transplant before age 70 I would qualify for a transplant.&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-46270"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/veterans-and-ipf/#post-39001" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Life span in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38863</link>
				<pubDate>Tue, 16 Sep 2025 19:54:39 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38863"><span class="bb-reply-lable">Reply to</span> Life span</a></p> <div class="bb-content-inr-wrap"><p>I was also told 3-5 years at diagnosis.  1 year later told 1-2 years, now at 1.75 years I&#8217;m on the transplant list and without a transplant have less than 1 year to live.   I was on OFEV, initially it helped slow the progression but then as my body got used to it the progression came back aggressively.</p>
<p>PF is lung scarring as if you have cuts&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45995"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38863" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion How quickly can pulmonary fibrosis progress? in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-38859</link>
				<pubDate>Fri, 12 Sep 2025 22:18:32 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-38859"><span class="bb-reply-lable">Reply to</span> How quickly can pulmonary fibrosis progress?</a></p> <div class="bb-content-inr-wrap"><p>As a type 2 diabetic I was on 500 mg Metformin &#8211; 1 pill a day.  The lowest dose possible and it kept my a1c low.  But also taking any more caused diarrhea.  I am 69, on 8-10 liters supplemental O2 needed almost all the time to keep above 90 blood O2, I have lost weight with IPF and also during my prep for getting on the transplant list&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45984"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-38859" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Life span in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38853</link>
				<pubDate>Thu, 11 Sep 2025 05:46:35 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38853"><span class="bb-reply-lable">Reply to</span> Life span</a></p> <div class="bb-content-inr-wrap"><p>I have extensively researched PF and the 2 slowing progression drugs and the studies and the drugs reversing scarring in mice and everyone else about PF and all the types of it.  If it was on the internet I&#8217;ve read it. </p>
<p>The 3-5 years came from a old study done !y the Mayo Clinic and as Mayo Clinic is the gold standard most Pulmonologists&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45975"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/4/#post-38853" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Successful lungs transplant stories in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/successful-lungs-transplant-stories/#post-38845</link>
				<pubDate>Tue, 09 Sep 2025 07:54:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/successful-lungs-transplant-stories/#post-38845"><span class="bb-reply-lable">Reply to</span> Successful lungs transplant stories</a></p> <div class="bb-content-inr-wrap"><p>Hi Everyone</p>
<p>My name is John, age 69, O blood type, in excellent health outside my lungs, on transplant list since 7/2/25, agreed to Hep C lungs, using 10 liters O2 at home can get by on 8 &#8211;  and this thread is extremely helpful to me.  This thread is really informative to me as it gives me information what may happen go me post transplant and&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45963"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/successful-lungs-transplant-stories/#post-38845" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 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/page/2/#post-38839</link>
				<pubDate>Sat, 06 Sep 2025 05:00:36 -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-38839"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>&lt;div&gt;What influenced my decision to transplant or not &#8211; my deciding factors -&lt;/div&gt;</p>
<p></p>
<p>I was diagnosed 2 years ago at 68, got the standard 3-5 years to live IPF diagnosis.  O blood type.  Last Dec (1 yr 2 months later).got new lifespan diagnoses 1-2 years go live, on OFEV from May 2024. Married, 2 adult kids, 2 young grandkids.</p>
<p>Told you have to be&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45941"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/page/2/#post-38839" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion smells, smoke, fumes, etc. in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/smells-smoke-fumes-etc/#post-38833</link>
				<pubDate>Fri, 05 Sep 2025 20:26:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/smells-smoke-fumes-etc/#post-38833"><span class="bb-reply-lable">Reply to</span> smells, smoke, fumes, etc.</a></p> <div class="bb-content-inr-wrap"><p>Any fumes make my cough and lower my blood O2.</p>
<p></p>
<p>No cooking in our kitchen, my wife cooks in the garage on tabletop.appliances and a hot plate now, being a Chef level cook who loves to cook and bake, my IPF has taken those away from her.</p>
<p>I can&#8217;t breathe fumes of any type. Even smells of food cooked in the garage, but brought into the kitchen table&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45934"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/smells-smoke-fumes-etc/#post-38833" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Let&#039;s talk about supplemental oxygen in the forum Supplemental Oxygen and PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/lets-talk-about-supplemental-oxygen/#post-38818</link>
				<pubDate>Tue, 02 Sep 2025 20:33:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/lets-talk-about-supplemental-oxygen/#post-38818"><span class="bb-reply-lable">Reply to</span> Let's talk about supplemental oxygen</a></p> <div class="bb-content-inr-wrap"><p>&lt;div&gt;Here are some  of my tips -&lt;/div&gt;</p>
<p></p>
<p>I have had PF for about 2 years now, I am 69 and listed for a transplant.  I am on level 10 resting.  I have bone from level 4 to 6 to 8 to 10.  I have 5 blood O2 finger meters, so I have one where ever I&#8217;m at so not to have to carry one around at home or work &#8211; I still work most of my week full time.  I&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45919"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/lets-talk-about-supplemental-oxygen/#post-38818" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion IPF mucus cough in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38794</link>
				<pubDate>Fri, 29 Aug 2025 20:24:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38794"><span class="bb-reply-lable">Reply to</span> IPF mucus cough</a></p> <div class="bb-content-inr-wrap"><p>Taking a drink of water helps me.</p>
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				<title>John14392 replied to the discussion IPF mucus cough in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38739</link>
				<pubDate>Tue, 19 Aug 2025 19:51:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38739"><span class="bb-reply-lable">Reply to</span> IPF mucus cough</a></p> <div class="bb-content-inr-wrap"><p>I use Delsym DM cough syrup.  It works.</p>
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				<title>John14392 replied to the discussion Is anyone taking multivitamins to help boast fatigue? in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-anyone-taking-multivitamins-to-help-boast-fatigue/#post-38694</link>
				<pubDate>Fri, 01 Aug 2025 23:31:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-anyone-taking-multivitamins-to-help-boast-fatigue/#post-38694"><span class="bb-reply-lable">Reply to</span> Is anyone taking multivitamins to help boast fatigue?</a></p> <div class="bb-content-inr-wrap"><p>Daily I take a Costco Multi and a Vit D suppliment.</p>
<p>To help with fatigue and O2 levels I take a energy booster with caffine in it too.</p>
<p></p>
<p>All this helps a great deal</p>
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				<title>John14392 replied to the discussion Telling your family in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-38587</link>
				<pubDate>Sun, 29 Jun 2025 06:39:04 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-38587"><span class="bb-reply-lable">Reply to</span> Telling your family</a></p> <div class="bb-content-inr-wrap"><p>I am a born again Christian who walks his talk.  For me, death lets me go to my forever home &#8211; Heaven.  My family are born again Christians who know they are going to Heaven as they also have made Jesus their personal Lord and Savior.  So although their hearts hurt when I told them, in their heads they knew they would see me again in Heaven.  I&hellip;<span class="activity-read-more" id="activity-read-more-45404"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-38587" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 replied to the discussion Ofev in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-10/#post-38576</link>
				<pubDate>Tue, 24 Jun 2025 20:31:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-10/#post-38576"><span class="bb-reply-lable">Reply to</span> Ofev</a></p> <div class="bb-content-inr-wrap"><p>I&#8217;ve been on Ofev for about 1.5 years, the only way it is free is to be a Vet and get it through the Veterans Pulmonologists.  However, if your Dr medicare or private insurance Dr will prescribe you Ofev or Esbriet, my Medicare supplement referred me to the online Canadian prescription drug store, and by faxing them my prescription I found&hellip;<span class="activity-read-more" id="activity-read-more-45373"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-10/#post-38576" rel="nofollow"> Read more</a></span></p>
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				<title>John14392 became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/40981/</link>
				<pubDate>Wed, 06 Dec 2023 14:27:22 -0600</pubDate>

				
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