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	<title>Pulmonary Fibrosis News Forums | Paula Gee | Activity</title>
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				<title>Paula Gee 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-36443</link>
				<pubDate>Tue, 09 Jan 2024 20:22:18 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-36443"><span class="bb-reply-lable">Reply to</span> New to IPF</a></p> <div class="bb-content-inr-wrap"><p>Pops were you able to get the oxygen you needed? That was the most challenging part of my treatment because of Medicare requirements you be seen in person to get a prescription. I have tried Ofev and discontinued it because of harsh side affects. I have Hypersensitive Pnuemonitis diagnosed by biopsy but I have been treated for ILD since 2015.&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41259"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf-2/#post-36443" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee replied to the discussion Hard time Breathing in the mornings. in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hard-time-breathing-in-the-mornings/#post-36384</link>
				<pubDate>Thu, 28 Dec 2023 20:16:30 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hard-time-breathing-in-the-mornings/#post-36384"><span class="bb-reply-lable">Reply to</span> Hard time Breathing in the mornings.</a></p> <div class="bb-content-inr-wrap"><p>Hi there. My name is Paula. I have hypersensitive pnuemonitis which is caused by mold. I was diagnosed in 2015. Starting using oxygen in 2019. Has your Dr suggested or tested you for needing oxygen?</p>
<p>Tried Ofev. Too harsh for me. I use Cell Cept, azithromycin 3 x a week, and 10-20 mg of prednisone. Seasonal allergies affect my breathing but being&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41160"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hard-time-breathing-in-the-mornings/#post-36384" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee 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-35439</link>
				<pubDate>Thu, 20 Jul 2023 21:22:48 -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-35439"><span class="bb-reply-lable">Reply to</span> How quickly can pulmonary fibrosis progress?</a></p> <div class="bb-content-inr-wrap"><p>Jayme,</p>
<p>Have you been offered Cell Cept or<br />
Prednisone. I was diagnosed in 2015 with ILD and a biopsy in 2019 showed exposure to mold. So I started to need oxygen in 2019 but it is portable and comes in many forms. I was on Ofev for a short while but chose not to deal with side affects. I got enrolled in a drug trial<br />
At my hospital University&hellip;<span class="activity-read-more" id="activity-read-more-39579"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-35439" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee replied to the discussion Deciphering spring allergies from worsening PF symptoms in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/deciphering-spring-allergies-from-worsening-pf-symptoms/#post-34830</link>
				<pubDate>Wed, 05 Apr 2023 16:40:46 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/deciphering-spring-allergies-from-worsening-pf-symptoms/#post-34830"><span class="bb-reply-lable">Reply to</span> Deciphering spring allergies from worsening PF symptoms</a></p> <div class="bb-content-inr-wrap"><p>I have recently started one generic anahistamine morning and night and my seasonal allergies are better under control. I still have some sinus drainage but don’t feel the energy drain like before. I am on daily dose of 10 mg of prednisone. In the fall I have found that upping that to 20 mg during the allergy season really helped. I live in&hellip;<span class="activity-read-more" id="activity-read-more-38209"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/deciphering-spring-allergies-from-worsening-pf-symptoms/#post-34830" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee replied to the discussion Rolling cart in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/rolling-cart/#post-32868</link>
				<pubDate>Tue, 09 Aug 2022 20:41:18 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/rolling-cart/#post-32868"><span class="bb-reply-lable">Reply to</span> Rolling cart</a></p> <div class="bb-content-inr-wrap"><p>I use a walker with a seat on it and put my portable concentrator on the seat to move around in the house. I also use the walker to carry my laundry to the laundry room, trays to the kitchen etc. it really gives me a lot of confidence having it to help with the energy usage. I also try to use the wine bottle size oxygen bottles when I am out for&hellip;<span class="activity-read-more" id="activity-read-more-34734"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/rolling-cart/#post-32868" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/33020/#acomment-33137</link>
				<pubDate>Wed, 04 May 2022 15:43:18 -0500</pubDate>

									<content:encoded><![CDATA[<p>Christie thanks so much. I find these forums are so helpful. Thanks for reaching out. </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/paula/" data-bb-hp-profile="13453" rel="nofollow">Paula Gee</a> became a registered member					]]></content:encoded>
				
				
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				<title>Paula Gee replied to the discussion Buying an Oxygen concentrator in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31877</link>
				<pubDate>Fri, 29 Apr 2022 14:30:36 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31877"><span class="bb-reply-lable">Reply to</span> Buying an Oxygen concentrator</a></p> <div class="bb-content-inr-wrap"><p>I have not flown with a portable oxygen concentrator yet but I was making plans for a trip to Scotland. I have a Caire Freedom Style portable and use a setting of 2. When I talked to United Airlines they told me my machine was not on the approved FAA list even though I told her the machine has an FAA approved label on the bottom of the machine.&hellip;<span class="activity-read-more" id="activity-read-more-33022"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31877" rel="nofollow"> Read more</a></span></p>
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				<title>Paula Gee became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/33020/</link>
				<pubDate>Fri, 29 Apr 2022 13:23:13 -0500</pubDate>

				
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