<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
		>

<channel>
	<title>Pulmonary Fibrosis News Forums | Bcoddy | Activity</title>
	<link>https://pulmonaryfibrosisnews.com/forums/members/bcoddy/activity/</link>
	<atom:link href="https://pulmonaryfibrosisnews.com/forums/members/bcoddy/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for Bcoddy.</description>
	<lastBuildDate>Wed, 22 Apr 2026 16:32:15 -0500</lastBuildDate>
	<generator>https://buddypress.org/?v=2.20.0</generator>
	<language>en-US</language>
	<ttl>30</ttl>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>2</sy:updateFrequency>
		
								<item>
				<guid isPermaLink="false">65ea139384efb1be01e83c2ff1e26f77</guid>
				<title>Bcoddy replied to the discussion Jascayd pricing and insurance coverage in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/jascayd-pricing-and-insurance-coverage/#post-39237</link>
				<pubDate>Tue, 20 Jan 2026 21:09:41 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/jascayd-pricing-and-insurance-coverage/#post-39237"><span class="bb-reply-lable">Reply to</span> Jascayd pricing and insurance coverage</a></p> <div class="bb-content-inr-wrap"><p>My UHC part D covers it. January was about $2k but now my deductible is met for the year. You have to have your doctor submit for approval. </p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">06f5031eb751143f2e060c8f7040960b</guid>
				<title>Bcoddy started the discussion Jascayd and Esbriet in the forum Jascayd (nerandomilast)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/jascayd-and-esbriet/</link>
				<pubDate>Tue, 16 Dec 2025 20:55:17 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/jascayd-and-esbriet/">Jascayd and Esbriet</a></p> <div class="bb-content-inr-wrap"><p>I’ve been on the combo for about 6 weeks now. I’m having a runny nose and repeated headaches almost every morning (along with the continued gastric issues of Esbriet).  Anyone else having these symptoms?</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">e5c3bb8d4231244b13e952687acb4635</guid>
				<title>Bcoddy replied to the discussion Medical Marijuana in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/medical-marijuana/#post-38756</link>
				<pubDate>Fri, 22 Aug 2025 19:16:02 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/medical-marijuana/#post-38756"><span class="bb-reply-lable">Reply to</span> Medical Marijuana</a></p> <div class="bb-content-inr-wrap"><p>I take edibles. It really helps me with the anxiety. I doubt that it is helping my disease. I would never consider vaping or smoking as even strong perfumes give me fits at times. My Dr knows I use regularly and has said nothing about it affecting transplant except I would have to stop some weeks prior. I am unsure if I want to endure that anyway. </p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">0738c658b0cdb766f221be1276962b6c</guid>
				<title>Bcoddy replied to the discussion IPF mucus cough in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38738</link>
				<pubDate>Tue, 19 Aug 2025 19:39:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38738"><span class="bb-reply-lable">Reply to</span> IPF mucus cough</a></p> <div class="bb-content-inr-wrap"><p>I have this issue as well predominantly in the mornings. It’s annoying and sometimes it’s very thick and colorful.  And I have had it lead to bronchitis.  Pulmonary rehab really does help and although I’ve not done nebulizer treatments, I do have an iptotropium, nasal spray that is effective and stopping the nose run that occurs after the&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-45773"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38738" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">313b092d05df2a59ecaa11e34c87bd2c</guid>
				<title>Bcoddy replied to the discussion Runny nose in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/runny-nose/#post-38294</link>
				<pubDate>Tue, 06 May 2025 19:15:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/runny-nose/#post-38294"><span class="bb-reply-lable">Reply to</span> Runny nose</a></p> <div class="bb-content-inr-wrap"><p>Yes. Whenever I over exert. After recovering I sometimes use iptotropium spray. I also have allergies so I get the spray for that. </p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">1423d054f45ebfe1f6ebe822c5de9771</guid>
				<title>Bcoddy replied to the discussion Is there a way to tell what the charge/discharge level is with the Inogen 1 G5? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-there-a-way-to-tell-what-the-charge-discharge-level-is-with-the-inogen-1-g5/#post-37776</link>
				<pubDate>Tue, 24 Dec 2024 23:22:16 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-there-a-way-to-tell-what-the-charge-discharge-level-is-with-the-inogen-1-g5/#post-37776"><span class="bb-reply-lable">Reply to</span> Is there a way to tell what the charge/discharge level is with the Inogen 1 G5?</a></p> <div class="bb-content-inr-wrap"><p>The display screen shows a percentage. The G5 has a VERY basic app that you can see the value in minutes. But you may have to contact your provider for a code to connect via Bluetooth. The battery itself also has a button that light up to the nearest 25%. It flashes if it’s discharged or close. </p>
<p></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">3814ce0fdf3af1fd778e6bc060f10f21</guid>
				<title>Bcoddy replied to the discussion New user to Pirfenidone in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-user-to-pirfenidone/#post-37065</link>
				<pubDate>Tue, 21 May 2024 19:42:08 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-user-to-pirfenidone/#post-37065"><span class="bb-reply-lable">Reply to</span> New user to Pirfenidone</a></p> <div class="bb-content-inr-wrap"><p>I cannot tolerate the generic form of the drug and have been able to get a pass on the brand-name Esbriet. I’ve been on it for almost 2 years now with few side effects after the first six months.  Always eat with meals.</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">a8e3703d3af4b5c026dc69069cbf30b1</guid>
				<title>Bcoddy became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/40882/</link>
				<pubDate>Mon, 27 Nov 2023 14:48:03 -0600</pubDate>

				
									<slash:comments>0</slash:comments>
				
							</item>
		
	</channel>
</rss>
		