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	<title>Pulmonary Fibrosis News Forums | Patricia Anne Hughes | Activity</title>
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				<title>Patricia Anne Hughes replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15012</link>
				<pubDate>Fri, 26 Oct 2018 14:56:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15012"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi,</p>
<p>my wife started OFEV recently but unfortunately had to stop due to an adverse affect on her liver. She is now about to start on Esbriet instead to see if that’s any better. We are advised that whilst both drugs apparently serve the same purpose the Esbriet is a little easier  to monitor side effects in the early stages in so much that you&hellip;<span class="activity-read-more" id="activity-read-more-6258"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-15012" rel="nofollow"> Read more</a></span></p>
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				<title>Patricia Anne Hughes posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5893/#acomment-5909</link>
				<pubDate>Sat, 06 Oct 2018 15:34:41 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi again,<br />
Seems to be standard practice here in the Uk whereas patients on ofev have regular monthly full blood checks due to the potency of ofev having a detrimental affect  on other organs of the body. I must say Pat was feeling pretty rotten after only 3 weeks on ofev. The problem is of course is it’s difficult to know how effective the drug&hellip;<span class="activity-read-more" id="activity-read-more-5909"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/5893/#acomment-5909" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/anthony-hughes/" data-bb-hp-profile="1531" rel="nofollow">Patricia Anne Hughes</a> posted an update Hi
Think everyone agrees that the worst  part of IPF is the persistent coughing.
Just wondering whether anyone has come across some treatment or drugs that actually work [&hellip;]					]]></content:encoded>
				
				
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				<title>Patricia Anne Hughes posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5893/#acomment-5906</link>
				<pubDate>Sat, 06 Oct 2018 15:07:51 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thanks Charlene.<br />
I see you are also fighting this horrible illness. As perhaps you have guessed I,m the carer husband for Pat and probably like other carers it’s just as terrible to be an onlooker seeing a loved one suffer knowing there is nothing you can do to help.<br />
Unfortunately pats had to temporarily stop the ofev tablets as her liver count&hellip;<span class="activity-read-more" id="activity-read-more-5906"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/5893/#acomment-5906" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/anthony-hughes/" data-bb-hp-profile="1531" rel="nofollow">Patricia Anne Hughes</a> posted an update Hi
Think everyone agrees that the worst  part of IPF is the persistent coughing.
Just wondering whether anyone has come across some treatment or drugs that actually work [&hellip;]					]]></content:encoded>
				
				
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				<title>Patricia Anne Hughes posted an update: Hi
Think everyone agrees that the worst  part of IPF is [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5893/</link>
				<pubDate>Fri, 05 Oct 2018 21:09:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
Think everyone agrees that the worst  part of IPF is the persistent coughing.<br />
Just wondering whether anyone has come across some treatment or drugs that actually work in treating this cough?</p>
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				<title>Patricia Anne Hughes replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-14684</link>
				<pubDate>Fri, 28 Sep 2018 15:46:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-14684"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>I,ve just started OFEV and suffering sickness etc. Really bad dry cough which is the worst symptom. Also recently started supplementary  oxygen. We seem to be fortunate in the UK where the drugs and oxygen are free ( although of course pre-paid the compulsory national health insurance contributions of a few pounds a week throughout my&hellip;<span class="activity-read-more" id="activity-read-more-5815"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-14684" rel="nofollow"> Read more</a></span></p>
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				<title>Patricia Anne Hughes updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5803/</link>
				<pubDate>Fri, 28 Sep 2018 15:16:04 -0500</pubDate>

				
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				<title>Anthony Hughes became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5801/</link>
				<pubDate>Fri, 28 Sep 2018 15:14:08 -0500</pubDate>

				
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