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	<title>Pulmonary Fibrosis News Forums | Gina | Activity</title>
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				<title>Gina replied to the discussion OFEV Side Effect reduced! in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-side-effect-reduced/#post-36081</link>
				<pubDate>Tue, 24 Oct 2023 19:59:11 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-side-effect-reduced/#post-36081"><span class="bb-reply-lable">Reply to</span> OFEV Side Effect reduced!</a></p> <div class="bb-content-inr-wrap"><p>Harold, that is great news. I have a very similar situation. Do you eat your cinnamon raisin bread dry or add butter. I could use some relief as well. I’m willing to try anything after my 21/2 years of running to the bathroom. Thanks </p>
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				<title>Gina replied to the discussion OFEV cost and assistance in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-cost-and-assistance/#post-33098</link>
				<pubDate>Fri, 16 Sep 2022 13:22:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-cost-and-assistance/#post-33098"><span class="bb-reply-lable">Reply to</span> OFEV cost and assistance</a></p> <div class="bb-content-inr-wrap"><p>Hi John?</p>
<p>I was diagnosed last year and was turned down multiple times for help. I finally found “The Assistance Fund” (tafcares.org) and was accepted after a short time on their waitlist. They pay the balance after insurance. Hope this helps. Good luck</p>
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				<title>Gina replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32386</link>
				<pubDate>Wed, 22 Jun 2022 10:57:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32386"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Annette,<br />
HRCT is a high resolution CAT scan. They are diagnostic for IPF. UIP (usual interstitial pneumonitis) as seen on the HRCT confirms IPF. Idiopathic pulmonary fibrosis has no known cause, hence “idiopathic.” Mine is familiar as well. My brother was also diagnosed recently. Radiologists can differentiate between UIP vs NSIP&hellip;<span class="activity-read-more" id="activity-read-more-33947"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32386" rel="nofollow"> Read more</a></span></p>
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				<title>Gina replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32349</link>
				<pubDate>Mon, 13 Jun 2022 16:39:42 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32349"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>hi Annette,</p>
<p>I have been on Ofev 150 since January. I also deal with diarrhea and occasional nausea. The nausea usually passes within 15 minutes. The diarrhea, unfortunately, has gotten worse. I am still experimenting with different foods. I also just started a new clinical trial, so I’m thinking these new pills are a major factor.</p>
<p>My PFT and&hellip;<span class="activity-read-more" id="activity-read-more-33825"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-32349" rel="nofollow"> Read more</a></span></p>
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				<title>Gina replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-30813</link>
				<pubDate>Thu, 20 Jan 2022 21:12:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-30813"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene and Jean,</p>
<p>i was granted funding from</p>
<p>TAFCARES. .Org (the assistance foundation) multiple other foundations said I made too much money. Check them out online.</p>
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				<title>Gina replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-30811</link>
				<pubDate>Thu, 20 Jan 2022 20:57:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-30811"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Pauline,</p>
<p>I’m glad you made it through the difficulties you were having. I was diagnosed with IPF in May, 2021. I have been on Ofev since July with minimal side effects. I am currently transitioning from 100mg to 150mg twice daily. My question to you is what Medicare part D plan is covering the cost? My current plan leaves me a $3000 copay.&hellip;<span class="activity-read-more" id="activity-read-more-31203"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-30811" rel="nofollow"> Read more</a></span></p>
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				<title>Gina became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27401/</link>
				<pubDate>Fri, 28 May 2021 00:58:35 -0500</pubDate>

				
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