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	<title>Pulmonary Fibrosis News Forums | Rose M. | Activity</title>
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				<title>Rose M. replied to the discussion The Relationship Between PAH &#38; Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-relationship-between-pah-pulmonary-fibrosis/#post-19111</link>
				<pubDate>Tue, 14 May 2019 12:30:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-relationship-between-pah-pulmonary-fibrosis/#post-19111"><span class="bb-reply-lable">Reply to</span> The Relationship Between PAH & Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,</p>
<p>I didn&#8217;t have an echocardiogram done till a year after the IPF was found on my chest x-ray (May 2013).  And I&#8217;m not sure how long I had the IPF  before that chest x-ray.  My echo done in the spring of 2014 showed I had a mean arterial pressure of 28-30.  But my pulmonary doctor was not concerned, he felt we could keep an eye on&hellip;<span class="activity-read-more" id="activity-read-more-12145"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-relationship-between-pah-pulmonary-fibrosis/#post-19111" rel="nofollow"> Read more</a></span></p>
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				<title>Rose M. replied to the discussion Six-Minute Walk Tests in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/six-minute-walk-tests/#post-18282</link>
				<pubDate>Wed, 10 Apr 2019 06:20:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/six-minute-walk-tests/#post-18282"><span class="bb-reply-lable">Reply to</span> Six-Minute Walk Tests</a></p> <div class="bb-content-inr-wrap"><p>Hi All,</p>
<p>I&#8217;ve only had one 6 minute walk test.  That was given to me in January 2015 at UCLA.  (I am returning to their ILD clinic in May)  My test was done for 6 minutes, and I just kept walking till the end.  I was able to maintain a sat in the low to mid 90&#8217;s during the test.  I recovered quickly from any shortness of breath.  I did 440&hellip;<span class="activity-read-more" id="activity-read-more-11058"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/six-minute-walk-tests/#post-18282" rel="nofollow"> Read more</a></span></p>
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				<title>Rose M. updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9376/</link>
				<pubDate>Sun, 24 Feb 2019 07:03:29 -0600</pubDate>

				
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				<title>Rose M. replied to the discussion New Study Correlates to Forum Discussion re: Vitamin D Deficiency in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-study-correlates-to-forum-discussion-re-vitamin-d-deficiency/#post-17035</link>
				<pubDate>Sun, 24 Feb 2019 07:00:05 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-study-correlates-to-forum-discussion-re-vitamin-d-deficiency/#post-17035"><span class="bb-reply-lable">Reply to</span> New Study Correlates to Forum Discussion re: Vitamin D Deficiency</a></p> <div class="bb-content-inr-wrap"><p>My previous primary doc never tested my Vit D level.  Neither did my pulmonologist.  I have a new primary as my previous one retired.  He tested my Vit D level last August, and it was low.  He waited a couple of months and retested it, and it was still low.  Put me on Vit D 5000 units each week.   I see him in a couple of weeks for repeat&hellip;<span class="activity-read-more" id="activity-read-more-9375"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-study-correlates-to-forum-discussion-re-vitamin-d-deficiency/#post-17035" rel="nofollow"> Read more</a></span></p>
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				<title>Rose M. updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/6245/</link>
				<pubDate>Fri, 26 Oct 2018 02:40:48 -0500</pubDate>

				
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				<title>Rose M. replied to the discussion How to Decide When to Stop Working with Pulmonary Fibrosis. in the forum Employment &#38; Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-14998</link>
				<pubDate>Fri, 26 Oct 2018 02:13:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-14998"><span class="bb-reply-lable">Reply to</span> How to Decide When to Stop Working with Pulmonary Fibrosis.</a></p> <div class="bb-content-inr-wrap"><p>I am retired.  I stopped working in Oct. 2014, at the age of 63.  I was a full time critical care nurse in a Cath Lab.  My last year of work was part time, as I could no longer keep up working full time, nor could I keep up with the &#8216;on call&#8217; schedule.  I was always exhausted.  I had an hour commute each way to work.  It was a difficult&hellip;<span class="activity-read-more" id="activity-read-more-6244"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-14998" rel="nofollow"> Read more</a></span></p>
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				<title>Rose Moore became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/6241/</link>
				<pubDate>Fri, 26 Oct 2018 01:49:29 -0500</pubDate>

				
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