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	<title>Pulmonary Fibrosis News Forums | Richard Martin | Activity</title>
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				<title>Richard Martin replied to the discussion Wrestling with the End Stage of Pulmonary Fibrosis in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/wrestling-end-stage-pulmonary-fibrosis/#post-31147</link>
				<pubDate>Wed, 23 Feb 2022 14:37:26 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/wrestling-end-stage-pulmonary-fibrosis/#post-31147"><span class="bb-reply-lable">Reply to</span> Wrestling with the End Stage of Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>As a current IPF patient I want to thank you for your research and article. Not pleasant but very informative and helpful.  I have asked a half dozen doctors the questions you asked and got nowhere as you also experienced.<br />
Again a big thanks for your efforts<br />
Rich </p>
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				<title>Richard Martin posted an update: Charlene
Do you or any of your readers own a personal [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11189/</link>
				<pubDate>Sun, 14 Apr 2019 16:40:28 -0500</pubDate>

									<content:encoded><![CDATA[<p>Charlene<br />
Do you or any of your readers own a personal home spirometry machine to determine FVC for IPF patients.. I am interested in knowing if they are considered to be of value to the user?  Thanks and again a big thanks for all the research and writing that you do.</p>
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				<title>Richard Martin posted an update: Charlene
In response to suggested reading on Pf, the [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4812/</link>
				<pubDate>Fri, 17 Aug 2018 20:21:37 -0500</pubDate>

									<content:encoded><![CDATA[<p>Charlene<br />
In response to suggested reading on Pf, the five books you listed, it appears that the majority are written for the medical, clinical or scientific practitioner.<br />
Yes there may be some information  valuable to the patient but in my opinion more valuable to the physician, etc.</p>
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				<title>Richard Martin posted an update: In response to your question, the rash etc. had [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4730/</link>
				<pubDate>Tue, 14 Aug 2018 23:17:52 -0500</pubDate>

									<content:encoded><![CDATA[<p>In response to your question, the rash etc. had no connection with heart or cardiovascular areas as far as we know.  Doctors all believe rash was my extreme sensitivity to Esbriet  and sun.  However,  do the doctors really know??  I am not sure.</p>
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				<title>Richard Martin posted an update: Charlene  
A few words about Esbriet.  Started it  [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/4712/</link>
				<pubDate>Tue, 14 Aug 2018 14:55:02 -0500</pubDate>

									<content:encoded><![CDATA[<p>Charlene<br />
A few words about Esbriet.  Started it  April 2018 and discontinued June 2018 due to severe rash (sunburn) where my entire body peeled.  A few other side effects but nothing severe.  Considered Opev but since i have atrial fibrillation and take a blood thinner I was advised not to start Opev as it does have a small history of&hellip;<span class="activity-read-more" id="activity-read-more-4712"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/4712/" rel="nofollow"> Read more</a></span></p>
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				<title>Richard Martin updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/3980/</link>
				<pubDate>Fri, 06 Jul 2018 16:53:18 -0500</pubDate>

				
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				<title>Richard Martin became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/3978/</link>
				<pubDate>Fri, 06 Jul 2018 16:50:56 -0500</pubDate>

				
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