<?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 | JSR | Activity</title>
	<link>https://pulmonaryfibrosisnews.com/forums/members/jsr/activity/</link>
	<atom:link href="https://pulmonaryfibrosisnews.com/forums/members/jsr/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for JSR.</description>
	<lastBuildDate>Thu, 23 Apr 2026 13:45:40 -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">69ac33a68cef42dafa3144cfc40c7715</guid>
				<title>JSR replied to the discussion Quilting in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/quilting/#post-38115</link>
				<pubDate>Sun, 23 Mar 2025 01:38:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/quilting/#post-38115"><span class="bb-reply-lable">Reply to</span> Quilting</a></p> <div class="bb-content-inr-wrap"><p>I am a long time quilter who went into overdrive when I retired.  I love how quilting gives me an artistic outlet, especially colors.  I especially like doing hand work like English Paper Piecing and hand quilting.  I find them so meditative.  It is a great way to forget your troubles.</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">0851e59fd1fe165790586bf87a0a97de</guid>
				<title>JSR replied to the discussion Streamlining government in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/streamlining-government/#post-37960</link>
				<pubDate>Tue, 18 Feb 2025 20:29:33 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/streamlining-government/#post-37960"><span class="bb-reply-lable">Reply to</span> Streamlining government</a></p> <div class="bb-content-inr-wrap"><p>I have great fears about these cutbacks on my health.  Not only may Social Security and Medicare be gutted, but I also fear that research funding will dry up.  I also want to fight back for my future.</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">af68567085ff843fe98a5e3dde5d10d2</guid>
				<title>JSR replied to the discussion Anyone on Mycophenolate Mofetil (CellCept, Myfortic in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37959</link>
				<pubDate>Tue, 18 Feb 2025 20:20:30 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37959"><span class="bb-reply-lable">Reply to</span> Anyone on Mycophenolate Mofetil (CellCept, Myfortic</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed with Interstitial Lung Disease linked to schleroderma about 2.5 years ago.  It was caught early and I was put on Mycophenolate immediately to control my body&#8217;s over active immune response.  My disease has remained stable during that period.  I use 2 liters of O2 with my cpap at night but do not need it during the day unless I am&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44116"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/anyone-on-mycophenolate-mofetil-cellcept-myfortic/#post-37959" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">910ad02a7702452280eda56b593dd1d6</guid>
				<title>JSR replied to the discussion Dextromethorphan as cure for lung fibrosis? in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dextromethorphan-as-cure-for-lung-fibrosis/#post-37944</link>
				<pubDate>Wed, 12 Feb 2025 00:07:55 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dextromethorphan-as-cure-for-lung-fibrosis/#post-37944"><span class="bb-reply-lable">Reply to</span> Dextromethorphan as cure for lung fibrosis?</a></p> <div class="bb-content-inr-wrap"><p>I have used over the counter Mucinex and Robitussin DM with dextromethorphan to control cough for many years.  I used them on my kids when they were sick.  After reading about this research, I decided to use Mucinex DM on a daily basis.  I have tolerated both very well to thin mucus and control cough over a long period.  Hopefully daily use&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44067"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dextromethorphan-as-cure-for-lung-fibrosis/#post-37944" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">93fc80eced0820152a9eec8fe605c277</guid>
				<title>JSR replied to the discussion Pulmonary rehab - wow or whoa in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-wow-or-whoa/#post-37943</link>
				<pubDate>Tue, 11 Feb 2025 23:22:49 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-wow-or-whoa/#post-37943"><span class="bb-reply-lable">Reply to</span> Pulmonary rehab - wow or whoa</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed with ILD about 2 and a half years ago.  Luckily I was diagnosed fairly early.  I immediately asked for pulmonary therapy.  It was wonderful for me both physically and emotionally.  My periodic testing showed that my benchmarks improved.  When I started I was suffering from the initial gut punch of receiving the diagnosis.  I&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44065"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-wow-or-whoa/#post-37943" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">d969be9e431b0ccff4cbcd7325f76613</guid>
				<title>JSR replied to the discussion Travel and IPF in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-ipf/#post-37146</link>
				<pubDate>Thu, 06 Jun 2024 22:28:12 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-ipf/#post-37146"><span class="bb-reply-lable">Reply to</span> Travel and IPF</a></p> <div class="bb-content-inr-wrap"><p>I have traveled with the Phillips Respironics Simply Go machine.  I need a machine that can do both continuous and pulse oxygen.  It is large enough that I need to use the included cart.  I need to use it at night with my cpap and while at altitude in the airplane.  I was lucky and had electrical outlets that worked so I did not have to&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42500"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-ipf/#post-37146" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">06fe6b6de619173339acc522c8856182</guid>
				<title>JSR replied to the discussion Celcept / Mycophenolate use? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37064</link>
				<pubDate>Tue, 21 May 2024 19:32:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37064"><span class="bb-reply-lable">Reply to</span> Celcept / Mycophenolate use?</a></p> <div class="bb-content-inr-wrap"><p>I am taking 1500 mg daily.  Two 500 tabs in morning and one 500 tab at evening.  I tried 4 but felt very fatigued.  Since my inflammation was in the normal range my doctor let me take the 1500.  I have not had any problems catching viruses or colds.</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">553e2ead817dc77d4736837c06257271</guid>
				<title>JSR replied to the discussion Biggest piece of advice for a new IPF patient in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/biggest-piece-of-ipf-advice-for-a-new-ipf-patient/#post-37054</link>
				<pubDate>Fri, 17 May 2024 02:34:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biggest-piece-of-ipf-advice-for-a-new-ipf-patient/#post-37054"><span class="bb-reply-lable">Reply to</span> Biggest piece of advice for a new IPF patient</a></p> <div class="bb-content-inr-wrap"><p>My best recommendations are use smart watch technology.  I realized that I had low oxygenation because of my smart watch.  Go to the best pulmonologist you can find at a lung center if possible.  Get proper testing, treatment, and go for as much pulmonary therapy as you can get.  It really helps.  Getting the diagnosis is an tough emotional&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42333"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biggest-piece-of-ipf-advice-for-a-new-ipf-patient/#post-37054" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">78d61d82da33a793e567f6496ddc68d0</guid>
				<title>JSR replied to the discussion Celcept / Mycophenolate use? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37053</link>
				<pubDate>Fri, 17 May 2024 02:17:31 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37053"><span class="bb-reply-lable">Reply to</span> Celcept / Mycophenolate use?</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed with interstitial lung disease caused by schleroderma one year and a half ago.  I started mycophenolate immediately.  I am not on a real strong dose so as not to suppress my immune system too much, but my lungs look better and my inflammation is down.  I tolerate it very well.<span>  I only use 2 liters of oxygen at night with my cpap&hellip;</span></p>
<p><span class="activity-read-more" id="activity-read-more-42332"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37053" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">3a499c4c41adf79cb39b5a8b1e1e5156</guid>
				<title>JSR became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/41732/</link>
				<pubDate>Wed, 28 Feb 2024 15:05:12 -0600</pubDate>

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