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	<title>Pulmonary Fibrosis News Forums | Buddy38 | Activity</title>
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				<title>Buddy38 replied to the discussion relationship - fatigue &#38; oxygen in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/relationship-fatigue-oxygen/#post-38121</link>
				<pubDate>Tue, 25 Mar 2025 21:20:32 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/relationship-fatigue-oxygen/#post-38121"><span class="bb-reply-lable">Reply to</span> relationship - fatigue &amp; oxygen</a></p> <div class="bb-content-inr-wrap"><p>It really was not that hard. I just quit using it. I carried my oxyemeter with me and went as far as I could without oxygen. Then stopped and sat a little while till my reading gotback to 96 and kept going . I thane pretty much knew my limits and I can lead a pretty normal life without oxygen!!! </p>
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				<title>Buddy38 replied to the discussion relationship - fatigue &#38; oxygen in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/relationship-fatigue-oxygen/#post-38113</link>
				<pubDate>Sat, 22 Mar 2025 00:25:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/relationship-fatigue-oxygen/#post-38113"><span class="bb-reply-lable">Reply to</span> relationship - fatigue &amp; oxygen</a></p> <div class="bb-content-inr-wrap"><p>I am probably older than the rest of you, 86. I was diagnosed in 2015. At the time I went to rehab and it got rid of any symptoms. In 2019 it came back and I was put on OFEV and oxygen. After 2 years on OFEV I had to get off. The side effects were too much. I also weaned myself off of oxygen </p>
<p>I use oxygen only before I go to bed for about&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44387"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/relationship-fatigue-oxygen/#post-38113" rel="nofollow"> Read more</a></span></p>
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				<title>Buddy38 replied to the discussion Anyone on Mycophenolate Mofetil (CellCept, Myfortic in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37973</link>
				<pubDate>Tue, 18 Feb 2025 21:55:27 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37973"><span class="bb-reply-lable">Reply to</span> Anyone on Mycophenolate Mofetil (CellCept, Myfortic</a></p> <div class="bb-content-inr-wrap"><p>I am 86 !! I found out I had IPF in 2020. I was told that I have had it since 2015. I took OFEV for about 2 years. I could not take it anymore. It had me almost bedridden. I was on oxygen for about two years. I weaned myself off of oxygen. I manage my IPF on my on. I know my limits!! I hope I can make 90!!! </p>
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				<title>Buddy38 posted an update: Oxygen TherabyI see so many posts that state that when [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/43558/</link>
				<pubDate>Tue, 03 Dec 2024 21:09:00 -0600</pubDate>

									<content:encoded><![CDATA[<p>Oxygen Theraby</p>
<p>I see so many posts that state that when they were diagnosed with IPF, the doctor started them on Oxygen 24/7. That was not the treatment on my case. I had previously one of the very best pulmonologist in the country. I was not on oxygen and still not on oxygen after 10 yrs. I did take Ofev for about two years . I could not take&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-43558"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/43558/" rel="nofollow"> Read more</a></span></p>
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				<title>Buddy38 replied to the discussion stem cell therapy in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/stem-cell-therapy-2/#post-37633</link>
				<pubDate>Tue, 12 Nov 2024 21:40:25 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/stem-cell-therapy-2/#post-37633"><span class="bb-reply-lable">Reply to</span> stem cell therapy</a></p> <div class="bb-content-inr-wrap"><p>Denny, I woulzlike to know how to order that drug from Russia. Do you have more information on it</p>
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				<title>Buddy38 replied to the discussion New to IPF in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37244</link>
				<pubDate>Tue, 02 Jul 2024 22:22:16 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37244"><span class="bb-reply-lable">Reply to</span> New to IPF</a></p> <div class="bb-content-inr-wrap"><p>Tysaco is approved only for pulmonary hypertension!!! It is about two to phase 3 trials for I P F. How do your doctor prescribe this for you. I have been trying to figure a way to get the medication!!! How does the Tysaco work on you!! How about side effects!! Please answer!!!</p>
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				<title>Buddy38 replied to the discussion New to IPF in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37235</link>
				<pubDate>Mon, 01 Jul 2024 20:39:58 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37235"><span class="bb-reply-lable">Reply to</span> New to IPF</a></p> <div class="bb-content-inr-wrap"><p>The drugs name is Tabasco!!!!</p>
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				<title>Buddy38 replied to the discussion New to IPF in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37234</link>
				<pubDate>Mon, 01 Jul 2024 20:33:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-37234"><span class="bb-reply-lable">Reply to</span> New to IPF</a></p> <div class="bb-content-inr-wrap"><p>Tabasco has been approved for pulmonary hypertension!!! The company has gone directly to phase 3 trials for I PF!!! They are opportunistic that this will work!! Wondering if anyone has got there doctor to give it to them with a diagnosis of pulmonary hypertension!!!!</p>
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				<title>Buddy38 replied to the discussion Medscape - The Future of IPF in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/medscape-the-future-of-ipf/#post-36999</link>
				<pubDate>Fri, 03 May 2024 23:02:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/medscape-the-future-of-ipf/#post-36999"><span class="bb-reply-lable">Reply to</span> Medscape - The Future of IPF</a></p> <div class="bb-content-inr-wrap"><p>I read on this website and through other media about many new drugs for IPF. Most of the are in phase 2-3. They have had very good results with a lot of them. But , with the FDA, they will not be available for 5 years. By that time most of us suffering from this disease will be dead!!! Why can’t the more serious cases of IPF have these new drugs&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42247"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/medscape-the-future-of-ipf/#post-36999" rel="nofollow"> Read more</a></span></p>
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				<title>Buddy38 replied to the discussion Worse after OFEV? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/worse-after-ofev/#post-36985</link>
				<pubDate>Tue, 30 Apr 2024 22:06:28 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/worse-after-ofev/#post-36985"><span class="bb-reply-lable">Reply to</span> Worse after OFEV?</a></p> <div class="bb-content-inr-wrap"><p>Hi I started talking OFEV after I had IPD for 5 years and did not know it!!! The first 6 months I did not have a side effects taking the large dose of OFEV. I the beginning to feel terrible all the time!! We switched to the smaller dose and that worked for about 6 months! I got off OFEV entirely a couple of years ago. I feel good !! IPF has&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42222"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/worse-after-ofev/#post-36985" rel="nofollow"> Read more</a></span></p>
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				<title>Buddy38 replied to the discussion breathing device in the forum Healthcare Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-device/#post-36944</link>
				<pubDate>Tue, 23 Apr 2024 23:19:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-device/#post-36944"><span class="bb-reply-lable">Reply to</span> breathing device</a></p> <div class="bb-content-inr-wrap"><p>I have two Imogene !! One goes to 3 the other goes to 6. They are both portable!! I have had IPF since 2016! About 2020 I started using oxygen with tanks and Imogene machines!! I used them for about 1 year. I weaned myself off of oxygen altogether. I I’m 85 1/2 years old. I can do whatever I want. I do not exert myself. I ride the scooter in the&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42160"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-device/#post-36944" rel="nofollow"> Read more</a></span></p>
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				<title>Buddy38 became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/40476/</link>
				<pubDate>Wed, 11 Oct 2023 14:39:40 -0500</pubDate>

				
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