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	<title>Pulmonary Fibrosis News Forums | Mark | Activity</title>
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				<title>Mark 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-39003</link>
				<pubDate>Fri, 14 Nov 2025 22:13:40 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/veterans-and-ipf/#post-39003"><span class="bb-reply-lable">Reply to</span> Veterans and IPF</a></p> <div class="bb-content-inr-wrap"><p>I was in the Air Force 1973-1976, worked in munitions </p>
<p>I was drain 2015, my comment to the doctor was. Well that’s what I get for 30 years smoking, he said nope not from smoking, but from after the military, and maybe before</p>
<p>Driving into the LA area in 1960’s and 70’s your eyes would start stinging and you probably start coughing</p>
<p></p>
<p>My dad worked as&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-46274"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/veterans-and-ipf/#post-39003" rel="nofollow"> Read more</a></span></p>
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				<title>Mark replied to the discussion Where do you live, receive care, and are you in  a local support group? in the forum Polls &#38; Quizzes</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/where-do-you-live-receive-care-and-are-you-in-a-local-support-group/page/3/#post-38250</link>
				<pubDate>Fri, 25 Apr 2025 23:18:57 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/where-do-you-live-receive-care-and-are-you-in-a-local-support-group/page/3/#post-38250"><span class="bb-reply-lable">Reply to</span> Where do you live, receive care, and are you in  a local support group?</a></p> <div class="bb-content-inr-wrap"><p>Good evening </p>
<p>I current live just east of St. Louis for the last 7 years, before that Tucson Az, and Southern California .</p>
<p>I was diagnosed with ILD and PF.  In 2015 at the VA in Tucson, I also have every form of Arthritis and Zollinger Ellison condition.</p>
<p>I was on OFEV for about 2 years, only side affect was decreased appetite </p>
<p>Lost close to 90&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44687"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/where-do-you-live-receive-care-and-are-you-in-a-local-support-group/page/3/#post-38250" rel="nofollow"> Read more</a></span></p>
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				<title>Mark replied to the discussion No lung transplant in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/no-lung-transplant/#post-38028</link>
				<pubDate>Tue, 04 Mar 2025 21:00:33 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/no-lung-transplant/#post-38028"><span class="bb-reply-lable">Reply to</span> No lung transplant</a></p> <div class="bb-content-inr-wrap"><p>Hello wizard </p>
<p>I was diagnosed with PF and ILD, along with RA in 2015.</p>
<p>I will turn 70 this fall, at the time of diagnosis, I had a discussion about all the options and treatments.  A lung transplant is one the few major surgeries that will take considerable toll on you for years after, depending on how well you react to the procedure.</p>
<p>In 2013 I&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44227"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/no-lung-transplant/#post-38028" rel="nofollow"> Read more</a></span></p>
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				<title>Mark replied to the discussion Lung Biopsy in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/lung-biopsy/#post-34422</link>
				<pubDate>Tue, 14 Feb 2023 22:22:11 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/lung-biopsy/#post-34422"><span class="bb-reply-lable">Reply to</span> Lung Biopsy</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed in 2016, the first thing the doctor wanted to do was a open lung biopsy.</p>
<p>no CT scan, no PFT.</p>
<p>as I researched everything I could about this surgical procedure.  I asked the following questions</p>
<p>would my treatment change?</p>
<p>would it change the diagnosis?</p>
<p>then help me understand, I have compromised lungs, you now want to cunt&hellip;<span class="activity-read-more" id="activity-read-more-37477"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/lung-biopsy/#post-34422" rel="nofollow"> Read more</a></span></p>
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				<title>Mark 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/#post-30868</link>
				<pubDate>Thu, 27 Jan 2022 21:55:51 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30868"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Like many who have responded, I did a lot of research about my medical issues.  I was diagnosed in 2016.  I am currently 66 and only stared supplemental oxygen 2/22/2022 and only 2L when exercising, and doing extensive yard or house work.  I do not take any medication for my lung issues, although I do take several for my RA and&hellip;<span class="activity-read-more" id="activity-read-more-31293"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-30868" rel="nofollow"> Read more</a></span></p>
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				<title>Mark replied to the discussion Cardiopulmonary exercise (CPET) in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cardiopulmonary-exercise-cpet/#post-30548</link>
				<pubDate>Thu, 02 Dec 2021 20:29:00 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cardiopulmonary-exercise-cpet/#post-30548"><span class="bb-reply-lable">Reply to</span> Cardiopulmonary exercise (CPET)</a></p> <div class="bb-content-inr-wrap"><p>I have not had this test, as part of my polumnary tests.</p>
<p>i did do a similar test as an athlete and stress study while in high school and college.</p>
<p>from what I researched and remember it is testing how oxygen is being used in the body.</p>
<p>could be Canadian, or just your medical team.</p>
<p>my medical team is with the VA here in the US.</p>
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				<title>Mark replied to the discussion Biopsy… yes or no? in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-30492</link>
				<pubDate>Thu, 18 Nov 2021 20:30:10 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-30492"><span class="bb-reply-lable">Reply to</span> Biopsy… yes or no?</a></p> <div class="bb-content-inr-wrap"><p>Martha</p>
<p>when I was first diagnosed with ILD and PF, the polumnologist in Tucson wanted to do a full open lung biopsy.  I did a lot of research and talked to a few who had been through such, then asked this question</p>
<p>why would I agree to have my chest cut into, my lungs cut into in multiple places, to get a scraping to verify the diagnosis, oh&hellip;<span class="activity-read-more" id="activity-read-more-30542"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-30492" rel="nofollow"> Read more</a></span></p>
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				<title>Mark replied to the discussion Inhaler use in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30425</link>
				<pubDate>Thu, 11 Nov 2021 20:11:38 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30425"><span class="bb-reply-lable">Reply to</span> Inhaler use</a></p> <div class="bb-content-inr-wrap"><p>Happy Veterans Day to all</p>
<p>a polumnologist I had in Arizona had me using symbicort twice a day and albuterol as needed for labored breathing.</p>
<p>i since moved to the St. Louis area, my new polumnologist asked about the inhalers, I said the symbicort just made nausea and tired many times, she said, stop and see what happens, now off that for the&hellip;<span class="activity-read-more" id="activity-read-more-30437"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30425" rel="nofollow"> Read more</a></span></p>
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				<title>Mark became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27978/</link>
				<pubDate>Fri, 25 Jun 2021 14:43:35 -0500</pubDate>

				
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