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	<title>Pulmonary Fibrosis News Forums | Renee | Activity</title>
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				<title>Renee replied to the discussion New Zoom meeting - taking the bull by the horn in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-zoom-meeting-taking-the-bull-by-the-horn/#post-33297</link>
				<pubDate>Tue, 18 Oct 2022 13:34:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-zoom-meeting-taking-the-bull-by-the-horn/#post-33297"><span class="bb-reply-lable">Reply to</span> New Zoom meeting - taking the bull by the horn</a></p> <div class="bb-content-inr-wrap"><p>Yes, l would be interested in joining you</p>
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				<title>Renee replied to the discussion travel while on ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-while-on-ofev/#post-33258</link>
				<pubDate>Sat, 08 Oct 2022 21:19:52 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-while-on-ofev/#post-33258"><span class="bb-reply-lable">Reply to</span> travel while on ofev</a></p> <div class="bb-content-inr-wrap"><p>I just made a trip to the Grand Canyon. I was off of my Ofev for 10 days. According to my Doctor it was not a big deal to get off of it because l have no other underlying medical problems. She said if l were on any meds dealing with an infection, that would be a different story.  Overall I am healthy, except for the PF. I am not downplaying&hellip;<span class="activity-read-more" id="activity-read-more-35390"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-while-on-ofev/#post-33258" rel="nofollow"> Read more</a></span></p>
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				<title>Renee replied to the discussion Is ipf genetic? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32791</link>
				<pubDate>Sun, 31 Jul 2022 14:47:02 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32791"><span class="bb-reply-lable">Reply to</span> Is ipf genetic?</a></p> <div class="bb-content-inr-wrap"><p>Exactly Richard, it does matter. Our children and grandchildren are in danger of having this terrible disease. I don&#8217;t want my granddaughter and her offspring to be worried about it. My son has passed so that leaves my worries about our little girl and her future.</p>
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				<title>Renee replied to the discussion Is ipf genetic? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32712</link>
				<pubDate>Sun, 24 Jul 2022 19:54:03 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32712"><span class="bb-reply-lable">Reply to</span> Is ipf genetic?</a></p> <div class="bb-content-inr-wrap"><p>My two brothers have died from IPF. I was diagnosed 2 years ago and my doctor keeps telling me that it isn&#8217;t a hereditary disease.  It appears to me if all of these reporting about different family members testing positive for IPF, then is would be familiar.</p>
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				<title>Renee replied to the discussion Inhaler use in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30389</link>
				<pubDate>Sun, 07 Nov 2021 22:16:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use/#post-30389"><span class="bb-reply-lable">Reply to</span> Inhaler use</a></p> <div class="bb-content-inr-wrap"><p>Hi Liz,</p>
<ol>
<li>I am on Breo once a day but honestly can&#8217;t say if it&#8217;s helpful. I don&#8217;t have asthma so really not sure why I am on it, but doc wants me to stay with it.</li>
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				<title>Renee replied to the discussion Coughing in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/coughing/#post-28089</link>
				<pubDate>Thu, 15 Apr 2021 20:40:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/coughing/#post-28089"><span class="bb-reply-lable">Reply to</span> Coughing</a></p> <div class="bb-content-inr-wrap"><p>Hi Augusta,<br />
 I coughed for a year before finally getting the diagnosis of IPF. I started on Ofev in January of this year and my coughing has almost disappeared. I am convinced that the Ofev has helped. The side effects can be bad at times, but  right now and l will take that over the constant hacking anyday&#x1f600;. Hopefully you can get some&hellip;<span class="activity-read-more" id="activity-read-more-26703"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/coughing/#post-28089" rel="nofollow"> Read more</a></span></p>
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				<title>Renee posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/25481/#acomment-25482</link>
				<pubDate>Sat, 13 Feb 2021 02:33:18 -0600</pubDate>

									<content:encoded><![CDATA[<p>Makes you wonder  if they REALLY know  whether its genetic or not.  More and more people l talk to are saying they too have close family members.  The main reason l want to know for sure is because if my granddaughter.  Could she someday have a diagnosis of IPF???<br />
Scares me witless.</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/chyna/" data-bb-hp-profile="9027" rel="nofollow">Charlene</a> <span class="activity-to">to</span> <a href="https://pulmonaryfibrosisnews.com/forums/members/missnene/" data-bb-hp-profile="12001" rel="nofollow">Renee</a> <a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/renee/' rel="nofollow">@renee</a> 
my mom died w IPF and my brother has it severe anad my pulmonologist says mine is not genetic.   why???					]]></content:encoded>
				
				
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				<title>Renee replied to the discussion New diagnosis age 61 in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-diagnosis-age-61/#post-27220</link>
				<pubDate>Wed, 10 Feb 2021 18:16:05 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-diagnosis-age-61/#post-27220"><span class="bb-reply-lable">Reply to</span> New diagnosis age 61</a></p> <div class="bb-content-inr-wrap"><p>I too was just diagnosed with IPF. I have 2 siblings that had a definite diagnosis of IPF. My doctor says its nit genetic, but still makes me wonder about 3 of 6  developing this horrible disease.  They both only lived less than 3 years after the diagnosis.</p>
<p>&nbsp;</p>
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				<title>Renee posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/24907/#acomment-24951</link>
				<pubDate>Fri, 15 Jan 2021 18:31:42 -0600</pubDate>

									<content:encoded><![CDATA[<p>Thanks Mark. This is not a club anyone wants to belong to, but glad to have any support offered. </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/renee/" data-bb-hp-profile="8801" rel="nofollow">Renee</a> became a registered member					]]></content:encoded>
				
				
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				<title>Renee started the discussion Ofev in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-4/</link>
				<pubDate>Fri, 15 Jan 2021 18:28:33 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-4/">Ofev</a></p> <div class="bb-content-inr-wrap"><ul>
<li>Newbie here. Just</li>
<li>started taking Ofev. So far l have been blessed and the side effects have been very few.  A few headaches and fatigue.  I have only been on it for 8 days, it still has time to hit with a vengeance &#x1f61c;, but praying it wont.</li>
<li></li>
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				<title>Renee became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/24907/</link>
				<pubDate>Thu, 14 Jan 2021 03:27:42 -0600</pubDate>

				
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