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	<title>Pulmonary Fibrosis News Forums | Lisa Powers | Activity</title>
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				<title>Lisa Powers replied to the discussion Flying with IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17737</link>
				<pubDate>Fri, 15 Mar 2019 16:45:16 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/page/2/#post-17737"><span class="bb-reply-lable">Reply to</span> Flying with IPF</a></p> <div class="bb-content-inr-wrap"><p>Pamela, your story is a very serious eye opener.  One never knows if this all comes from the IPF &#8211; directly/indirectly &#8211; or if medications or other health conditions &#8211; known or unknown &#8211; contribute to these surprising  and critical potential problems. It&#8217;s good that the airlines require a letter from our doctors stating that we are &#8220;okay to&hellip;<span class="activity-read-more" id="activity-read-more-10314"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17737" rel="nofollow"> Read more</a></span></p>
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				<title>Lisa Powers replied to the discussion Natural Relief for Mucus in the Lungs? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/natural-relief-for-mucous-in-the-lungs/#post-17686</link>
				<pubDate>Thu, 14 Mar 2019 06:28:44 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/natural-relief-for-mucous-in-the-lungs/#post-17686"><span class="bb-reply-lable">Reply to</span> Natural Relief for Mucus in the Lungs?</a></p> <div class="bb-content-inr-wrap"><p>You can get Bromelain in capsule form and skip the acidic problems, and unfortunately, the delicious fruit flavor. I have used Goldenseal for colds to help dry up sinus and post nasal drip, but I don&#8217;t know if this also works for mucous in the lungs. It might, but I&#8217;d like to hear a doctor or naturopath&#8217;s thoughts about it for IPF.</p>
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				<title>Lisa Powers replied to the discussion Flying with IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17637</link>
				<pubDate>Wed, 13 Mar 2019 02:24:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17637"><span class="bb-reply-lable">Reply to</span> Flying with IPF</a></p> <div class="bb-content-inr-wrap"><p>@caneelbay1  In the Pulmonary Rehab classes we talked about germs on planes. Someone had asked a Flight Attendant how they stayed well. Their answer &#8211; rub antibiotic ointment in your nostrils. She was serious. I usually travel with masks so if someone is coughing, or there&#8217;s a small child nearby, I&#8217;m comfortable wearing it.  I have N95 masks&hellip;<span class="activity-read-more" id="activity-read-more-10216"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17637" rel="nofollow"> Read more</a></span></p>
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				<title>Lisa Powers replied to the discussion Flying with IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17616</link>
				<pubDate>Tue, 12 Mar 2019 22:29:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/page/2/#post-17616"><span class="bb-reply-lable">Reply to</span> Flying with IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene, I wanted to share our experiences with flying to Hawaii. My husband was officially diagnosed at UCSF in 2014, but a pulmonologist he’d been seeing had been writing PF on his visit summaries for 3 to 4 years before that. Strangely he never talked to us about it, or its implications, only that he had the crackling sounds. But he&hellip;<span class="activity-read-more" id="activity-read-more-10198"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17616" rel="nofollow"> Read more</a></span></p>
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				<title>Lisa Powers posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9949/#acomment-9998</link>
				<pubDate>Fri, 08 Mar 2019 20:04:06 -0600</pubDate>

									<content:encoded><![CDATA[<p>Charlene, can you help me post this to the forum on travel and flying?</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/lisapowers/" data-bb-hp-profile="2949" rel="nofollow">Lisa Powers</a> became a registered member					]]></content:encoded>
				
				
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				<title>Lisa Powers posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9949/#acomment-9997</link>
				<pubDate>Fri, 08 Mar 2019 20:03:32 -0600</pubDate>

									<content:encoded><![CDATA[<p>I meant to add that the cost for the concentrator rentals was for 3 weeks each. They average between $100 and $150 per week, and I remember now that the 2018 price in June was $150 per week.</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/lisapowers/" data-bb-hp-profile="2949" rel="nofollow">Lisa Powers</a> became a registered member					]]></content:encoded>
				
				
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				<title>Lisa Powers changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9994/</link>
				<pubDate>Fri, 08 Mar 2019 19:40:00 -0600</pubDate>

				
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				<title>Lisa Powers posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9949/#acomment-9993</link>
				<pubDate>Fri, 08 Mar 2019 19:37:19 -0600</pubDate>

									<content:encoded><![CDATA[<p>Hi Charlene,  I wanted to share our experiences with flying to Hawaii. I&#8217;m not sure how to post it to the topic, but you mentioned you were hoping to go to Hawaii soon. My husband was officially diagnosed at UCSF in 2014, but a pulmonologist he&#8217;d been seeing had been writing PF on his visit summaries for 3 to 4 years before that. Strangely&hellip;<span class="activity-read-more" id="activity-read-more-9993"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/9949/#acomment-9993" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/lisapowers/" data-bb-hp-profile="2949" rel="nofollow">Lisa Powers</a> became a registered member					]]></content:encoded>
				
				
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				<title>Lisa Powers became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9949/</link>
				<pubDate>Fri, 08 Mar 2019 13:42:18 -0600</pubDate>

				
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