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	<title>Pulmonary Fibrosis News Forums | MikeC | Activity</title>
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				<title>MikeC replied to the discussion New in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new/#post-38490</link>
				<pubDate>Tue, 10 Jun 2025 19:36:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new/#post-38490"><span class="bb-reply-lable">Reply to</span> New</a></p> <div class="bb-content-inr-wrap"><p>Hello, </p>
<p>If you&#8217;re experiencing shortness of breath during exertion you may want to talk to your doctor about pulmonary rehab. It did wonders for me. </p>
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				<title>MikeC replied to the discussion Cost of Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cost-of-ofev/#post-34327</link>
				<pubDate>Tue, 07 Feb 2023 20:19:39 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cost-of-ofev/#post-34327"><span class="bb-reply-lable">Reply to</span> Cost of Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Deb,</p>
<p>As Phil said you can contact BI Cares to receive the medication at no cost provided you do not exceed the earnings limit. I am on Medicare and do not pay for my OFEV.</p>
<p>Best wishes, Mike</p>
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				<title>MikeC replied to the discussion Telling your family in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31919</link>
				<pubDate>Wed, 04 May 2022 00:53:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31919"><span class="bb-reply-lable">Reply to</span> Telling your family</a></p> <div class="bb-content-inr-wrap"><p>Hi Michael, I think your children should know, for your sake as well as theirs. I was diagnosed with IPF in March 2020 and heard the terrible prognosis &#8220;3-5 years&#8221;. I made an appointment with the pulmonary department at the University of Michigan who confirmed my diagnosis of moderately severe IPF, but told me that 3-5 year expected&hellip;<span class="activity-read-more" id="activity-read-more-33092"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31919" rel="nofollow"> Read more</a></span></p>
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				<title>MikeC became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/31712/</link>
				<pubDate>Fri, 18 Feb 2022 15:51:53 -0600</pubDate>

				
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