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	<title>Pulmonary Fibrosis News Forums | Jane McBride | Activity</title>
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				<title>Jane McBride replied to the discussion Leaving the house on 4LPM oxygen? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/leaving-the-house-on-4lpm-oxygen/#post-34212</link>
				<pubDate>Sat, 21 Jan 2023 05:02:38 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/leaving-the-house-on-4lpm-oxygen/page/2/#post-34212"><span class="bb-reply-lable">Reply to</span> Leaving the house on 4LPM oxygen?</a></p> <div class="bb-content-inr-wrap"><p>Ihave been using the Inogen portables for several years. I started at 3. I am now using the Inogen that goes up to 6. I was unaware of the discrepa0ncies mention in these replies because the Inogens seem to work for me. I have car chargers in all of our cars and take an extra battery with me now for occasions like this afternoon when&hellip;<span class="activity-read-more" id="activity-read-more-37117"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/leaving-the-house-on-4lpm-oxygen/#post-34212" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride replied to the discussion Fluctuating Body Temperatures - Cold &#38; Hot in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fluctuating-body-temperatures-cold-hot/#post-28043</link>
				<pubDate>Tue, 13 Apr 2021 19:35:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fluctuating-body-temperatures-cold-hot/#post-28043"><span class="bb-reply-lable">Reply to</span> Fluctuating Body Temperatures - Cold &amp; Hot</a></p> <div class="bb-content-inr-wrap"><p>This was of great interest. I am on Ofev and since it seems to be stabilizing the IPF at the moment I am just trying to find ways to deal with the side effects comfortably. There seem to be any number of us dealing with the temperature range so I think of it as a side effect without official medical affirmation.<br />
Almost every evening, I have&hellip;<span class="activity-read-more" id="activity-read-more-26642"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fluctuating-body-temperatures-cold-hot/#post-28043" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride replied to the discussion Tips to Combat the Effects of the Cold Dry Winter Air in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-to-combat-the-effects-of-the-cold-dry-winter-air/#post-22617</link>
				<pubDate>Wed, 22 Jan 2020 01:32:56 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-to-combat-the-effects-of-the-cold-dry-winter-air/#post-22617"><span class="bb-reply-lable">Reply to</span> Tips to Combat the Effects of the Cold Dry Winter Air</a></p> <div class="bb-content-inr-wrap"><p>Thanks for this subject, Mark. I am facing a very cold winter here in Illinois and would like some info on how to best handle my Inogen 3.  The hose and canula get very stiff as well. Wrapping the tubing up under scarves etc. helps but was hoping someone might have a suggestion as to acquiring tubing that gets hard and doesn&#8217;t start pulling&hellip;<span class="activity-read-more" id="activity-read-more-17362"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-to-combat-the-effects-of-the-cold-dry-winter-air/#post-22617" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride replied to the discussion Post-meal fatigue in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/post-meal-fatigue/#post-22616</link>
				<pubDate>Wed, 22 Jan 2020 00:55:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-meal-fatigue/#post-22616"><span class="bb-reply-lable">Reply to</span> Post-meal fatigue</a></p> <div class="bb-content-inr-wrap"><p>Hi Fred and Wendy,</p>
<p>I find smaller meals helps with fatigue as well. The only draw back is balancing the meals and the Ofev dosage, which requires a &#8220;full meal&#8221; according to the instructions (has a similar problem with previous meds). Found I can balance both smaller meals and stave off some of the side effects of Ofev at the same time but&hellip;<span class="activity-read-more" id="activity-read-more-17361"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-meal-fatigue/#post-22616" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride replied to the discussion What you need to know about Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/need-know-ofev/#post-21355</link>
				<pubDate>Thu, 19 Sep 2019 16:29:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/need-know-ofev/#post-21355"><span class="bb-reply-lable">Reply to</span> What you need to know about Ofev</a></p> <div class="bb-content-inr-wrap"><p>@janette</p>
<p>&nbsp;</p>
<p>Hi Janette,</p>
<p>Like you Ofev seems to have stabilized the progression of my IPF, lovely to hear. However, I too had difficulty with the intestinal side effects on the 300mg a day.  Not as badly as you but badly enough to plan my life around whether or not I could plan to go out with friends etc. My doctor changed the dosage to 200&hellip;<span class="activity-read-more" id="activity-read-more-15276"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/need-know-ofev/#post-21355" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride replied to the discussion The Frequency of Changing Your Nasal Cannula in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20835</link>
				<pubDate>Fri, 16 Aug 2019 14:44:50 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20835"><span class="bb-reply-lable">Reply to</span> The Frequency of Changing Your Nasal Cannula</a></p> <div class="bb-content-inr-wrap"><p>Thanks for the tip of wearing the cannula at the back. It has really given my ears a rest and doesn&#8217;t dangle down the front getting in the way of everything.  I wear it 24/7 and this suggestion was really a relief. Plan to  rig some kind of easy belt to help with walking around doing housework, etc.</p>
<p>Am going to experiment with the cannula on my&hellip;<span class="activity-read-more" id="activity-read-more-14466"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20835" rel="nofollow"> Read more</a></span></p>
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				<title>Jane McBride posted an update: This evening is the first time I have been aware of [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13648/</link>
				<pubDate>Wed, 10 Jul 2019 01:36:58 -0500</pubDate>

									<content:encoded><![CDATA[<p>This evening is the first time I have been aware of lazer therapy for IPF. May I please have some more information? </p>
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				<title>Jane McBride replied to the discussion Pulmonary Rehab May Improve Exercise Capacity and Quality of Life in IPF Patients in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-may-improve-exercise-capacity-and-quality-of-life-in-ipf-patients/#post-19985</link>
				<pubDate>Thu, 20 Jun 2019 20:20:25 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-may-improve-exercise-capacity-and-quality-of-life-in-ipf-patients/#post-19985"><span class="bb-reply-lable">Reply to</span> Pulmonary Rehab May Improve Exercise Capacity and Quality of Life in IPF Patients</a></p> <div class="bb-content-inr-wrap"><p>Would appreciate recommendations for Pulmonary Rehab in Northern Illinois.</p>
<p>&nbsp;</p>
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				<title>Jane McBride posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13210/#acomment-13235</link>
				<pubDate>Thu, 20 Jun 2019 20:17:19 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you Charlene.<br />
I have just moved to northern Illinois. Can anyone recommend a good pulmanologist with IPF interests? </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/janenmcbride/" data-bb-hp-profile="3395" rel="nofollow">Jane McBride</a> became a registered member					]]></content:encoded>
				
				
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				<title>Jane McBride became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13210/</link>
				<pubDate>Thu, 20 Jun 2019 11:31:51 -0500</pubDate>

				
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