<?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 | Doug Jones | Activity</title>
	<link>https://pulmonaryfibrosisnews.com/forums/members/dejones8576/activity/</link>
	<atom:link href="https://pulmonaryfibrosisnews.com/forums/members/dejones8576/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for Doug Jones.</description>
	<lastBuildDate>Sun, 12 Apr 2026 00:23:53 -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">8baf7c2bfd2289e5e1f42c9c43ae1b43</guid>
				<title>Doug Jones replied to the discussion Systemic Enzymes in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/systemic-enzymes/#post-29675</link>
				<pubDate>Wed, 25 Aug 2021 03:11:36 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/systemic-enzymes/#post-29675"><span class="bb-reply-lable">Reply to</span> Systemic Enzymes</a></p> <div class="bb-content-inr-wrap"><p>In the US there are two drugs approved to treat, i.e. slow the progression of IPF&#8211;Ofev and Esbriet (pirfenidone).  Clinical outcomes suggest that neither is better than the other.  So if you are really have trouble with the side effects of Ofev, considering talking with your doctor about Esbriet.</p>
<p>I have been taking Esbriet over 6 yrs&#8211;since it&hellip;<span class="activity-read-more" id="activity-read-more-29144"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/systemic-enzymes/#post-29675" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">779d23ab87e6c7026ee22a3fafca8281</guid>
				<title>Doug Jones replied to the discussion Fibrosis and Esbriet in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-28823</link>
				<pubDate>Thu, 10 Jun 2021 22:50:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-28823"><span class="bb-reply-lable">Reply to</span> Fibrosis and Esbriet</a></p> <div class="bb-content-inr-wrap"><p>The two most common side effects of Esbriet are 1) increased photosensitivity, i.e. more likely to sunburn and 2) gastrointestinal issues including nausea and diarrhea.  Most GI symptoms go away within the the first 3 months as your body adjusts to taking the medicine.  During that time (and afterwards) it is suggested that you take the Esbriet&hellip;<span class="activity-read-more" id="activity-read-more-27684"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fibrosis-and-esbriet/#post-28823" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">63b53358436a24a273b3d80636f71abe</guid>
				<title>Doug Jones replied to the discussion Oxygen concentrators and travel in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28722</link>
				<pubDate>Thu, 03 Jun 2021 20:44:50 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28722"><span class="bb-reply-lable">Reply to</span> Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>Hi Kate&#8211;this is a good topic, especially as many of us with reduced lung capacity begin to travel and fly again.  I have been researching this for some time and suggest the following authoritative resources:</p>
<p>1)  The Pulmonary Fibrosis Foundation has a an informational section on Oxygen Therapy that discusses traveling with oxygen.  See&hellip;<span class="activity-read-more" id="activity-read-more-27515"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28722" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">3b7d38b03d17e6ba8ea27960426e5c7e</guid>
				<title>Doug Jones replied to the discussion Fatigue &#38; Nausea with Esbriet in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fatigue-nausea-with-esbriet/#post-26449</link>
				<pubDate>Thu, 10 Dec 2020 23:12:23 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fatigue-nausea-with-esbriet/#post-26449"><span class="bb-reply-lable">Reply to</span> Fatigue &amp; Nausea with Esbriet</a></p> <div class="bb-content-inr-wrap"><p>Hi Steve&#8211;sorry you are having problems with adverse effects from the 2 authorized IPF drugs.  I have been taking pirfenidone (Esbriet) since November 2014 when FDA first authorized its use in the US.  I am fortunate that I have not had any significant side effects.  One of the major medical databases&#8211;UpToDate&#8211; lists percentage of potential&hellip;<span class="activity-read-more" id="activity-read-more-24098"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fatigue-nausea-with-esbriet/#post-26449" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">3361031ccf67152176f5f271d6c1f9d9</guid>
				<title>Doug Jones replied to the discussion Portable Oxygen Concentators in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen-concentators/#post-26169</link>
				<pubDate>Tue, 17 Nov 2020 21:09:31 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen-concentators/page/2/#post-26169"><span class="bb-reply-lable">Reply to</span> Portable Oxygen Concentators</a></p> <div class="bb-content-inr-wrap"><p>Just a few comments about POCs and some reliable sources of information:</p>
<p>1)  The Pulmonary Paper organization prepares an annual comparison of oxygen concentrators with detailed specifications from many companies. Latest is 2019.  Included are both continuous flow and pulse flow models as well as models such as the Simply/Go that Charlene&hellip;<span class="activity-read-more" id="activity-read-more-23589"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen-concentators/#post-26169" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">dde9e63a9b165e66cd32cc2e714c7754</guid>
				<title>Doug Jones replied to the discussion PFTS and coughing in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25834</link>
				<pubDate>Thu, 15 Oct 2020 21:52:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25834"><span class="bb-reply-lable">Reply to</span> PFTS and coughing</a></p> <div class="bb-content-inr-wrap"><p>Hi Jackie&#8211;Sorry to hear about your IPF diagnosis but welcome to the club!  I have had episodes of coughing over my 5 years with this disease.  For me, coughing comes and goes&#8211;but you may never have this symptom.  Is your doctor prescribing anything for the GERD?  GERD is apparently common in as many as 80% of pulmonary fibrosis&hellip;<span class="activity-read-more" id="activity-read-more-22944"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25834" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">617912adcef37e390412ff3a8e014cde</guid>
				<title>Doug Jones replied to the discussion PFTS and coughing in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25797</link>
				<pubDate>Tue, 13 Oct 2020 19:36:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25797"><span class="bb-reply-lable">Reply to</span> PFTS and coughing</a></p> <div class="bb-content-inr-wrap"><p>Hi Cindy&#8211;I struggle with the same problem. A couple of small tips that help me are the following:</p>
<p>1)  I spray my throat with Chloraseptic sore throat spray beforehand.  It has 1.4% phenol which is a mild anesthetic.  I&#8217;m sure there are other brands including generics.</p>
<p>2) I bring a water bottle with me and take regular sips to keep my throat&hellip;<span class="activity-read-more" id="activity-read-more-22886"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pfts-and-coughing/#post-25797" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">6ef3a09580254ba31423fcf67ce7baad</guid>
				<title>Doug Jones replied to the discussion Getting oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25796</link>
				<pubDate>Tue, 13 Oct 2020 19:22:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25796"><span class="bb-reply-lable">Reply to</span> Getting oxygen</a></p> <div class="bb-content-inr-wrap"><p>Bob and Trixie&#8211;Sorry about the &#8220;messiness&#8221; of my response.  I copied the info from the PFF and it included all the formatting.  the phone number to call  is 844-825-5733 for the PFF Support Line.  Doug</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">b232bd7e4c8bb2e62096a2f4b06055a8</guid>
				<title>Doug Jones replied to the discussion Getting oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25795</link>
				<pubDate>Tue, 13 Oct 2020 19:18:18 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25795"><span class="bb-reply-lable">Reply to</span> Getting oxygen</a></p> <div class="bb-content-inr-wrap"><p>Hi Bob&#8211;as Mark mentioned, you will need a prescription from your doctor for oxygen.  I have IPF and need oxygen.  Medical facilities have developed COVID-19 protocols which protect both patients and staff when procedures such as a Pulmonary Function Test ((PFT) and 6 Minute Walk Test (6MWT).  I had a PFT performed in July 2020 and have another&hellip;<span class="activity-read-more" id="activity-read-more-22884"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-oxygen/#post-25795" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">4edb3a9152055e8047773e7e86905309</guid>
				<title>Doug Jones replied to the discussion Public Fears Surrounding COVID-19 in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23505</link>
				<pubDate>Tue, 17 Mar 2020 23:50:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23505"><span class="bb-reply-lable">Reply to</span> Public Fears Surrounding COVID-19</a></p> <div class="bb-content-inr-wrap"><p>1)  Charlene&#8211;gentle clarification re: COVID-19 terminology.  COVID-19 is the name given to the disease which is caused by a particular NEW corona virus&#8211;&lt;span style=&#8221;color: #000000; font-family: &#8216;Open Sans&#8217;, apple-system, blinkmacsystemfont, &#8216;Segoe UI&#8217;, &#8216;Helvetica Neue&#8217;, arial, sans-serif; font-size: 17px;&#8221;&gt; &lt;/span&gt;&lt;span style=&#8221;color: #000000;&hellip;<span class="activity-read-more" id="activity-read-more-18822"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23505" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">49e050bc8e0b0ca9f2070a33040c7ea5</guid>
				<title>Doug Jones replied to the discussion fits of cough in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/fits-of-cough/#post-23335</link>
				<pubDate>Thu, 05 Mar 2020 23:26:23 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fits-of-cough/#post-23335"><span class="bb-reply-lable">Reply to</span> fits of cough</a></p> <div class="bb-content-inr-wrap"><p>For those interested in the formal recommendations from the American College of Chest Physicians, you may want to check out this article from CHEST&#8211;their official, refereed publication from 2018; below is an abstract of the article..</p>
<p>Doug Jones</p>
<p>Treatment of Interstitial Lung Disease Associated Cough:  CHEST Guideline and Expert Panel Report. &hellip;<span class="activity-read-more" id="activity-read-more-18566"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/fits-of-cough/#post-23335" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">3754b0168890efb9044aea84f39e9ed7</guid>
				<title>Doug Jones replied to the discussion Gabapentin is a Proven Treatment for Refractory Chronic Cough in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-23139</link>
				<pubDate>Tue, 25 Feb 2020 23:37:02 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-23139"><span class="bb-reply-lable">Reply to</span> Gabapentin is a Proven Treatment for Refractory Chronic Cough</a></p> <div class="bb-content-inr-wrap"><p>These response are interesting; glad that gabapentin may work for some.  I note that the research study cited from Lancet EXLCLUDED chronic coughers who had a respiratory disease so its effectiveness for IPF patients may not be the same&#8211;see excerpt below.  The medical literature shows mixed results for gabapentin in controlling cough&#8211;plus a&hellip;<span class="activity-read-more" id="activity-read-more-18302"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-23139" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">b634d5060f6a928b238057bf9961d2d9</guid>
				<title>Doug Jones replied to the discussion Using Elderberry to Combat Cold and Flu Symptoms in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/using-elderberry-to-combat-cold-and-flu-symptoms/#post-22460</link>
				<pubDate>Thu, 09 Jan 2020 18:48:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/using-elderberry-to-combat-cold-and-flu-symptoms/#post-22460"><span class="bb-reply-lable">Reply to</span> Using Elderberry to Combat Cold and Flu Symptoms</a></p> <div class="bb-content-inr-wrap"><p>Consumer Reports recently reported on &#8220;The Best Flu Treatment for You&#8221;  which includes many of the suggestions noted in the previous comments.  However, Elderberry has very limited research support so I would be skeptical of that.  See the full report at <a target='_blank' href="https://www.consumerreports.org/flu/the-best-flu-treatment-for-you/" rel="nofollow">https://www.consumerreports.org/flu/the-best-flu-treatment-for-you/</a><br />
&lt;p style=&#8221;box-sizing:&hellip;<span class="activity-read-more" id="activity-read-more-17071"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/using-elderberry-to-combat-cold-and-flu-symptoms/#post-22460" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">664349deb3accf690696eab151c56486</guid>
				<title>Doug Jones replied to the discussion Gabapentin For IPF-Related Cough? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-for-ipf-related-cough/#post-21715</link>
				<pubDate>Wed, 23 Oct 2019 01:06:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-for-ipf-related-cough/#post-21715"><span class="bb-reply-lable">Reply to</span> Gabapentin For IPF-Related Cough?</a></p> <div class="bb-content-inr-wrap"><p>Regarding &#8220;Off-label&#8221; use of a drug, the October 2019 issue of AARP Bulletin (page 36) has the following information and link to determine if a drug is being used &#8220;off-label&#8221;, that is, for a purpose it was not originally validated to treat.</p>
<p>&#8220;At DailyMed.nim.nih.gov   you can check if the drugs you&#8217;re currently taking are off-label for your&hellip;<span class="activity-read-more" id="activity-read-more-15805"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-for-ipf-related-cough/#post-21715" rel="nofollow"> Read more</a></span></p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">ab1ed5e276f0e0b95dac0e4f91cfc904</guid>
				<title>Doug Jones replied to the discussion PFF Summit 2019 in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pff-summit-2019/#post-21714</link>
				<pubDate>Tue, 22 Oct 2019 17:00:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pff-summit-2019/#post-21714"><span class="bb-reply-lable">Reply to</span> PFF Summit 2019</a></p> <div class="bb-content-inr-wrap"><p>I will be attending the PFF Summit and plan to take some informal notes to share with my local Pulmonary Fibrosis Support Group.  Doug</p>
</div>]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">9eadb270d92351e1f8d7173704ce64c1</guid>
				<title>Doug Jones became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/14368/</link>
				<pubDate>Sat, 10 Aug 2019 21:37:27 -0500</pubDate>

				
									<slash:comments>1</slash:comments>
				
							</item>
		
	</channel>
</rss>
		