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	<title>Pulmonary Fibrosis News Forums | Celia | Activity</title>
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				<title>Celia replied to the discussion What portable oxygen concentrator do you recommend? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/what-portable-oxygen-concentrator-do-you-recommend/#post-38771</link>
				<pubDate>Tue, 26 Aug 2025 12:34:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-portable-oxygen-concentrator-do-you-recommend/#post-38771"><span class="bb-reply-lable">Reply to</span> What portable oxygen concentrator do you recommend?</a></p> <div class="bb-content-inr-wrap"><p>Howdy! I am on O2 24/7 and I need 6 to 8 litres to walk .</p>
<p>However, when I am seated -which can be at home or in the car- I can use a concentrator .  </p>
<p>It is true that the concentrator is not the same thing as an O2 tank, but personally I have found that using the concentrator for a car ride woks and is a great way to save on the tanks.  I&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45846"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-portable-oxygen-concentrator-do-you-recommend/#post-38771" rel="nofollow"> Read more</a></span></p>
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				<title>Celia replied to the discussion OFEV Thoughts in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-thoughts/#post-38751</link>
				<pubDate>Wed, 20 Aug 2025 17:27:32 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-thoughts/#post-38751"><span class="bb-reply-lable">Reply to</span> OFEV Thoughts</a></p> <div class="bb-content-inr-wrap"><p>GO for it, friends!</p>
<p>Hello!</p>
<p>I am on Ofev.  at first I was ill a lot, (vomit, diarrhea and cramping) but I have focused on different dietary things and now I have very few symptoms.  I definitely found that higher protein helps. For me breakfast is HB egg, on bread with cheese (I know, dairy, but it works for me) and sometimes add salmon. I often&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45806"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-thoughts/#post-38751" rel="nofollow"> Read more</a></span></p>
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				<title>Celia 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-37971</link>
				<pubDate>Tue, 18 Feb 2025 21:35:22 -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-37971"><span class="bb-reply-lable">Reply to</span> Anyone on Mycophenolate Mofetil (CellCept, Myfortic</a></p> <div class="bb-content-inr-wrap"><p>hi!</p>
<p>I am on it. Worked up to 2000 per day (1K am and 1K pm).  <br />I find that taking a fiber supplement helps my mild GI symptoms with it-obviously it has to be timed with the meds/ all the other stuff.  This med is taken on en empty stomach.  No problems really. </p>
<p>My dx is interstitial lung disease and RA.</p>
<p>I feel like it helps my RA, I have no idea&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44128"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37971" rel="nofollow"> Read more</a></span></p>
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				<title>Celia replied to the discussion Mental health and living with PF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/mental-health-and-living-with-pf/#post-37953</link>
				<pubDate>Fri, 14 Feb 2025 22:20:15 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/mental-health-and-living-with-pf/#post-37953"><span class="bb-reply-lable">Reply to</span> Mental health and living with PF</a></p> <div class="bb-content-inr-wrap"><p>ah hello.</p>
<p>I have been thinking this (the idea of how long to stay on treatment) &#8211; I have RA and PF diagnosed June 2023. no known risks or cause. Lung function has gotten much worse over last three months and I&#8221;m new to being on o2 (LTOT). To walk 20 feet I need 6 liters. Insurance is a NIGHTMARE.  They have several times refused antfibrotic&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44094"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/mental-health-and-living-with-pf/#post-37953" rel="nofollow"> Read more</a></span></p>
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				<title>Celia became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/41437/</link>
				<pubDate>Wed, 31 Jan 2024 15:06:11 -0600</pubDate>

				
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