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	<title>Pulmonary Fibrosis News Forums | Kate Smithson | Activity</title>
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				<title>Kate Smithson replied to the discussion Fibrosis and Esbriet in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-29425</link>
				<pubDate>Thu, 05 Aug 2021 13:50:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-29425"><span class="bb-reply-lable">Reply to</span> Fibrosis and Esbriet</a></p> <div class="bb-content-inr-wrap"><p>Hello Yolanda:</p>
<p>As I’m not always hungry at the time I’m due to take my ESBRIET tablet,  I have found that eating 1/2 a banana or a piece of cheese works. So far no nausea while doing this.  I’ve been able to maintain the full dose for two years now and in the 3 years since my diagnosis, my PF test results have remained stable.  Best wishes&hellip;<span class="activity-read-more" id="activity-read-more-28758"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-29425" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson replied to the discussion Progression of IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28752</link>
				<pubDate>Sat, 05 Jun 2021 06:05:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28752"><span class="bb-reply-lable">Reply to</span> Progression of IPF</a></p> <div class="bb-content-inr-wrap"><p>Carol:</p>
<p>Are you walking/exercising WITH oxygen?</p>
<p>My pulmonologist prescribed using oxygen during exercise, to try to keep the saturation levels above 88.  Mine had dropped to 78 while I was doing the 6 minutes test and while I walked outdoors for exercise. I said I stopped when I felt out of breath and resumed walking when the oxygen&hellip;<span class="activity-read-more" id="activity-read-more-27560"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28752" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson replied to the discussion Oxygen concentrators and travel in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28751</link>
				<pubDate>Sat, 05 Jun 2021 04:45:08 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28751"><span class="bb-reply-lable">Reply to</span> Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>Thank you all who responded to my question re POC’s.  I am so appreciative of the information shared.  Your comments have given me much to read before getting set up.<br />
In checking with an equipment supplier, I learned that the OxyGo 5 is manufactured by Inogen and is the name used for the Canadian brand. Apparently they are the same.</p>
<p>I re-read&hellip;<span class="activity-read-more" id="activity-read-more-27559"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28751" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson started the discussion Oxygen concentrators and travel in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/</link>
				<pubDate>Thu, 03 Jun 2021 00:11:15 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/">Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>I have been searching old columns and forums for information on oxygen concentrators, as I&#8217;m sure this has been aired before.   Please help me out, as I seem to recall Charlene writing about a POC that she used for travel. [I am also living in Ontario, Canada.]</p>
<p>I was diagnosed with IPF in August 2018, almost 3 years ago, and am not yet&hellip;<span class="activity-read-more" id="activity-read-more-27494"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson replied to the discussion Excessive cough during sleeping time in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25349</link>
				<pubDate>Tue, 25 Aug 2020 17:00:14 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25349"><span class="bb-reply-lable">Reply to</span> Excessive cough during sleeping time</a></p> <div class="bb-content-inr-wrap"><p>Sorry for all of us ‘coughers’, (and those who have to listen to us!), but glad to read the comments!<br />
I was diagnosed with IPF two years ago.  The cough was what led to my diagnosis but it was quite mild until the past 6 months, when it became more frequent and lasted longer.  At times now I wake, coughing.<br />
Life is still pretty normal for me,&hellip;<span class="activity-read-more" id="activity-read-more-22030"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25349" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson and Mark Koziol are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17585/</link>
				<pubDate>Tue, 28 Jan 2020 22:25:57 -0600</pubDate>

				
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				<title>Kate Smithson replied to the discussion Friend Requests in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/friend-requests/#post-22720</link>
				<pubDate>Tue, 28 Jan 2020 15:30:43 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/friend-requests/#post-22720"><span class="bb-reply-lable">Reply to</span> Friend Requests</a></p> <div class="bb-content-inr-wrap"><p>Dear Steve, Charlene and Mark:</p>
<p>It is Kate Smithson here, and I am a registered member of PF News. I sent that message to Steve as I am searching for travel insurance information.   I had a question  for him and didn’t feel comfortable communicating on the public forum, so sent the “friend” request.<br />
I trust that you can reassure him that I’m a&hellip;<span class="activity-read-more" id="activity-read-more-17541"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/friend-requests/#post-22720" rel="nofollow"> Read more</a></span></p>
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				<title>Kate Smithson became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12371/</link>
				<pubDate>Thu, 23 May 2019 20:17:17 -0500</pubDate>

				
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