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	<title>Pulmonary Fibrosis News Forums | Burma | Activity</title>
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				<title>Burma replied to the discussion Sudden deterioration in breathing in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/sudden-deterioration-in-breathing/#post-27495</link>
				<pubDate>Thu, 25 Feb 2021 22:07:10 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sudden-deterioration-in-breathing/#post-27495"><span class="bb-reply-lable">Reply to</span> Sudden deterioration in breathing</a></p> <div class="bb-content-inr-wrap"><p>I am sorry to hear your father is having a problem with shortness of breath.  It is very scary, I know.  I have been diagnosed with Pulmonary Fibrosis (2018) and take OFEV.  I am on 4 L oxygen., 24/7, for about a year now.  I was having a very hard time breathing just by taking a couple steps.  My Oximeter would go down to 74 and it would&hellip;<span class="activity-read-more" id="activity-read-more-25730"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sudden-deterioration-in-breathing/#post-27495" rel="nofollow"> Read more</a></span></p>
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				<title>Burma replied to the discussion Head aches in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/head-aches/#post-26184</link>
				<pubDate>Thu, 19 Nov 2020 01:03:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/head-aches/#post-26184"><span class="bb-reply-lable">Reply to</span> Head aches</a></p> <div class="bb-content-inr-wrap"><p>Hello All,</p>
<p>I too have been fighting headaches and I contribute it to possibly lack of oxygen and/or dry sinuses, if not both.  I am on oxygen and I do use a humidifier on my concentrator and that has helped.  I would wake up every morning with a headache.  My morning routine includes a few doses of saline spray and then it would seem to go&hellip;<span class="activity-read-more" id="activity-read-more-23622"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/head-aches/#post-26184" rel="nofollow"> Read more</a></span></p>
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				<title>Burma replied to the discussion Cold Weather and Fatigue for IPF Patients. in the forum Canadians With PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26027</link>
				<pubDate>Thu, 05 Nov 2020 20:26:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26027"><span class="bb-reply-lable">Reply to</span> Cold Weather and Fatigue for IPF Patients.</a></p> <div class="bb-content-inr-wrap"><p>Hello Charlene!  I am one of those that dread the wintertime.  Not so much because of my compromised lungs and the cold temps, but because here in western Pennsylvania, we have a whole LOT of cloudy, dreary days and it just seems to suck the energy out of me.  I seem to be tired, have brain fog, loss of ambition, and quite lethargic on those&hellip;<span class="activity-read-more" id="activity-read-more-23345"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cold-weather-fatigue-ipf-patients/#post-26027" rel="nofollow"> Read more</a></span></p>
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				<title>Burma 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-24465</link>
				<pubDate>Thu, 21 May 2020 19:20:13 -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-24465"><span class="bb-reply-lable">Reply to</span> The Frequency of Changing Your Nasal Cannula</a></p> <div class="bb-content-inr-wrap"><p>I am on oxygen 24/7 but I only change my canula every other month, and the oxygen tubing about every six months.  I clean the canula every day with vinegar and soap and then rinse with hot water. Use the vinegar first and then the soap and water.  Rinsing it will take away the vinegar smell. As for the long tubing, I gather it up, plug the&hellip;<span class="activity-read-more" id="activity-read-more-20236"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-24465" rel="nofollow"> Read more</a></span></p>
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				<title>Burma replied to the discussion The Awkwardness of Wearing A Mask In Public in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-awkwardness-of-wearing-a-mask-in-public/#post-22840</link>
				<pubDate>Wed, 05 Feb 2020 01:05:17 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-awkwardness-of-wearing-a-mask-in-public/#post-22840"><span class="bb-reply-lable">Reply to</span> The Awkwardness of Wearing A Mask In Public</a></p> <div class="bb-content-inr-wrap"><p>If I feel the need to wear a mask, I do and I really don&#8217;t pay any attention to anyone&#8217;s opinion.  They aren&#8217;t fighting to breath!  I use a VOG mask.  A little pricey but worth it.  Although, I don&#8217;t wear my mask into the bank.  Don&#8217;t want to scare anyone.  LOL  I also purchased two &#8220;Gators&#8221; on Amazon, which work well.  (You can also pull the&hellip;<span class="activity-read-more" id="activity-read-more-17777"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-awkwardness-of-wearing-a-mask-in-public/#post-22840" rel="nofollow"> Read more</a></span></p>
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				<title>Burma posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17419/#acomment-17420</link>
				<pubDate>Thu, 23 Jan 2020 21:22:30 -0600</pubDate>

									<content:encoded><![CDATA[<p>Janis, be sure to eat protein when you take OFEV.  Every time.  Protein takes longer to digest.  The Open Door suggested it to me and it has helped my stomach settle down.  Good luck. </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/janis-henry-gorsline/" data-bb-hp-profile="4163" rel="nofollow">janis gorsline</a> and <a href="https://pulmonaryfibrosisnews.com/forums/members/casey/" data-bb-hp-profile="3786" rel="nofollow">Karen Martin</a> are now connected					]]></content:encoded>
				
				
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				<title>Burma replied to the discussion Is it time to give up Christmas? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-it-time-to-give-up-christmas/#post-22428</link>
				<pubDate>Tue, 07 Jan 2020 16:49:29 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-it-time-to-give-up-christmas/#post-22428"><span class="bb-reply-lable">Reply to</span> Is it time to give up Christmas?</a></p> <div class="bb-content-inr-wrap"><p>You are not a Grinch or Scrooge. Christmas Eve 2018, I ended up in the hospital. They thought I had pneumonia.  As usual, I was supposed to host Christmas dinner for the family. My son, his wife and his three adult sons.  Because I was in the hospital, family Christmas fell apart.  I was released the 27th and felt fine, thankfully&#8230;they were&hellip;<span class="activity-read-more" id="activity-read-more-17017"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-it-time-to-give-up-christmas/#post-22428" rel="nofollow"> Read more</a></span></p>
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				<title>Burma replied to the discussion Aloha from Hawaii in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21621</link>
				<pubDate>Fri, 11 Oct 2019 15:55:46 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21621"><span class="bb-reply-lable">Reply to</span> Aloha from Hawaii</a></p> <div class="bb-content-inr-wrap"><p>Charlene, so happy for you!  And thank you for sharing your adventures and your pictures.  You enjoy your dream vacation.  You deserve it!!</p>
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				<title>Burma replied to the discussion Hair thinning: a side effect of Ofev? in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hair-thinning-a-side-effect-of-ofev/#post-20380</link>
				<pubDate>Fri, 19 Jul 2019 18:11:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hair-thinning-a-side-effect-of-ofev/#post-20380"><span class="bb-reply-lable">Reply to</span> Hair thinning: a side effect of Ofev?</a></p> <div class="bb-content-inr-wrap"><p>I have been wondering about this.  I seemed to have lost quite a bit of hair the last several months.  While I was at my last hair appointment, my hair dresser said I was losing my hair, and maybe should have my thyroid tested.  I did have it tested and the thyroid is just fine.  I mentioned it to my GP and he said it might be a side effect of&hellip;<span class="activity-read-more" id="activity-read-more-13832"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hair-thinning-a-side-effect-of-ofev/#post-20380" rel="nofollow"> Read more</a></span></p>
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				<title>Burma became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13820/</link>
				<pubDate>Fri, 19 Jul 2019 16:23:59 -0500</pubDate>

				
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