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	<title>Pulmonary Fibrosis News Forums | Bob Hodges | Activity</title>
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				<title>Bob Hodges replied to the discussion Vaccinated PF people and COVID 19 in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-29754</link>
				<pubDate>Tue, 31 Aug 2021 19:49:43 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-29754"><span class="bb-reply-lable">Reply to</span> Vaccinated PF people and COVID 19</a></p> <div class="bb-content-inr-wrap"><p>Ihad the maderna vaccine back in February. Tested positive for COVID yesterday and getting the infusion IV right now.  My symptoms have been slight runny nose, low energy, and mild congestion. No headache, normal temperature. Diagnosed with IPF 4 years ago. Not on oxygen yet.</p>
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				<title>Bob Hodges posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27652/#acomment-27676</link>
				<pubDate>Thu, 10 Jun 2021 19:53:36 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thanks for welcome. </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/seaboberraol-com/" data-bb-hp-profile="11204" rel="nofollow">Bob Hodges</a> became a registered member					]]></content:encoded>
				
				
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				<title>Bob Hodges replied to the discussion Fibrosis and Esbriet in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-28820</link>
				<pubDate>Thu, 10 Jun 2021 19:51:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-28820"><span class="bb-reply-lable">Reply to</span> Fibrosis and Esbriet</a></p> <div class="bb-content-inr-wrap"><p>Have been on Esbirit for a year and a half and only side affect is a lack of energy possible from it. My FVC have been remaining fairly stable with just a slight decrease in volume. Diagnosed 3 yrs ago. Took OFEV for a year and couldn’t handle all the side affects.</p>
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				<title>Bob Hodges became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27652/</link>
				<pubDate>Wed, 09 Jun 2021 15:38:25 -0500</pubDate>

				
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