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	<title>Pulmonary Fibrosis News Forums | Gordon White | Activity</title>
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				<title>Gordon White replied to the discussion Aloha from Hawaii in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21540</link>
				<pubDate>Fri, 04 Oct 2019 19:58:58 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21540"><span class="bb-reply-lable">Reply to</span> Aloha from Hawaii</a></p> <div class="bb-content-inr-wrap"><p>Thanks for sharing your trip.  The great memories will last a lifetime.</p>
<p>Kona is my very favorite coffee.  Wonderful stuff!</p>
<p>One question or observation &#8211;  If you breath better there and need less oxygen, what is the elevation?  I am now living in Florida at an elevation of 60 feet above sea level and breathe much better than I did when I&hellip;<span class="activity-read-more" id="activity-read-more-15534"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21540" rel="nofollow"> Read more</a></span></p>
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				<title>Gordon White posted an update: Can Pulmonary Fibrosis improve your vision?
I have [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/14709/</link>
				<pubDate>Fri, 23 Aug 2019 20:50:59 -0500</pubDate>

									<content:encoded><![CDATA[<p>Can Pulmonary Fibrosis improve your vision?<br />
I have worn glasses for over 75 years and the best corrected vision in my right eye is 20-200.  My Pulmonary Fibrosis is in the final stage and last week I was checked by my Pulmonologist.  He reviewed my records and said, &#8220;Gordon, it is my opinion that you will live long enough to see 20-20&#8221;  &hellip;<span class="activity-read-more" id="activity-read-more-14709"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/14709/" rel="nofollow"> Read more</a></span></p>
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				<title>Gordon White replied to the discussion Overheating as a Patient with Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/overheating-as-a-patient-with-pulmonary-fibrosis/#post-20846</link>
				<pubDate>Fri, 16 Aug 2019 17:00:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/overheating-as-a-patient-with-pulmonary-fibrosis/#post-20846"><span class="bb-reply-lable">Reply to</span> Overheating as a Patient with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>I have Mayo Clinic diagnosed Idiopathic Pulmonary Fibrosis since 2012 and use O2 24/7.  For the past 4 years, the wife says the house is too hot and I say it&#8217;s too cold.   She can tolerate the thermostat set at 79 degrees F and I do too with the use of a long sleeve flannel shirt.</p>
<p>Never once have I considered the cold intolerance to be a side&hellip;<span class="activity-read-more" id="activity-read-more-14475"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/overheating-as-a-patient-with-pulmonary-fibrosis/#post-20846" rel="nofollow"> Read more</a></span></p>
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				<title>Gordon White updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4582/</link>
				<pubDate>Tue, 07 Aug 2018 15:13:19 -0500</pubDate>

				
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				<title>Gordon White became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4580/</link>
				<pubDate>Tue, 07 Aug 2018 14:48:30 -0500</pubDate>

				
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