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	<title>Pulmonary Fibrosis News Forums | James | Activity</title>
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				<title>James replied to the discussion Vaccinated PF people and COVID 19 in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-34778</link>
				<pubDate>Tue, 28 Mar 2023 19:17:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/page/3/#post-34778"><span class="bb-reply-lable">Reply to</span> Vaccinated PF people and COVID 19</a></p> <div class="bb-content-inr-wrap"><p>I have IPF and was stuck for the COVID twice since 2020 booster 2022 and tested positive two weeks ago, no symptoms though.</p>
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				<title>James replied to the discussion After month on 0fev 100; first day on 150 in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/after-month-on-0fev-100-first-day-on-150/#post-34450</link>
				<pubDate>Thu, 16 Feb 2023 20:48:40 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/after-month-on-0fev-100-first-day-on-150/#post-34450"><span class="bb-reply-lable">Reply to</span> After month on 0fev 100; first day on 150</a></p> <div class="bb-content-inr-wrap"><p>I can&#8217;t complain.  150 for me and my liver panel is clean, no effects yet.</p>
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				<title>James replied to the discussion Oxygen Delivery System when needs go up in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-delivery-system-when-needs-go-up/#post-34449</link>
				<pubDate>Thu, 16 Feb 2023 20:47:17 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-delivery-system-when-needs-go-up/#post-34449"><span class="bb-reply-lable">Reply to</span> Oxygen Delivery System when needs go up</a></p> <div class="bb-content-inr-wrap"><p>my numbers change like the wind. I run on 6 ltrs on my concentrator during waking hours and 3 at night.  my saturation averages 80-85% with some lows hovering in the upper 40&#8217;s. No joke.  I tend to push things a bit but I am well aware of my limits.</p>
<p>All I can say is just keep monitoring her numbers and adjust as required to maintain comfort. &hellip;<span class="activity-read-more" id="activity-read-more-37536"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-delivery-system-when-needs-go-up/#post-34449" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion Painful Sneezes since IPF Diagnosis. in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/painful-sneezes-since-ipf-diagnosis/#post-34004</link>
				<pubDate>Thu, 05 Jan 2023 02:48:49 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/painful-sneezes-since-ipf-diagnosis/#post-34004"><span class="bb-reply-lable">Reply to</span> Painful Sneezes since IPF Diagnosis.</a></p> <div class="bb-content-inr-wrap"><p>At any other time I would consider my sneezing to be funny, but the pain and overall bone jarring and teeth rattling is shear misery.  The sneezing hits me with five to eight hard sneezes in rapid fire, so fast that they actually sound like one sneeze! My tongue gets caught between my teeth and my jaw slams in the same manor as the sneezing.  I&hellip;<span class="activity-read-more" id="activity-read-more-36795"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/painful-sneezes-since-ipf-diagnosis/#post-34004" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion Congestion in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/congestion/#post-33207</link>
				<pubDate>Tue, 04 Oct 2022 19:34:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/congestion/#post-33207"><span class="bb-reply-lable">Reply to</span> Congestion</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed IPF in 2017.  I am sure that I have expelled several dozen gallons of mucus since then.  I use face cloths to cough into&#8230; they are soaked within an hour or so.  Ofev 150 x 2 a day and Guaifenesin 400 mg x 3 a day to make coughs more productive, that it does&#8230;. it works better than nothing I suppose.</p>
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				<title>James replied to the discussion Telling your family in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31752</link>
				<pubDate>Thu, 21 Apr 2022 19:20:57 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31752"><span class="bb-reply-lable">Reply to</span> Telling your family</a></p> <div class="bb-content-inr-wrap"><p>my, next to telling my bride, that was really hard&#8230; no, rough to do.</p>
<p>My son and his wife, my two daughters and their husbands, each got a phone call as they live many miles away.  I made sure their spouses were with them as I told them&#8230; as an engineer I tend to be frank, which I feel lessened the shock of a flowery explanation.  I could&hellip;<span class="activity-read-more" id="activity-read-more-32834"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31752" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion For sale in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/for-sale/#post-31750</link>
				<pubDate>Thu, 21 Apr 2022 19:14:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/for-sale/#post-31750"><span class="bb-reply-lable">Reply to</span> For sale</a></p> <div class="bb-content-inr-wrap"><p>15 years???? I&#8217;ll have what you are taking!!  That is awesome and hope you have another 15 years.</p>
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				<title>James replied to the discussion Buying an Oxygen concentrator in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31659</link>
				<pubDate>Tue, 12 Apr 2022 19:58:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31659"><span class="bb-reply-lable">Reply to</span> Buying an Oxygen concentrator</a></p> <div class="bb-content-inr-wrap"><p>first, get a prescription as the concentrator is considered a medical device and regulated by our wonderful, compassionate government&#8230;.. anyway, I have an inogen one g5 i use all day long. I have batteries and wall power.  it is good for 6 ltr hr pulsed. I fly quite a bit and you need one for flying, can&#8217;t use tanks.  I had to pay for mine&hellip;<span class="activity-read-more" id="activity-read-more-32651"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/buying-an-oxygen-concentrator/#post-31659" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-31570</link>
				<pubDate>Thu, 31 Mar 2022 20:37:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-31570"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Mine is a strange story I guess.  I was diagnosed in mid 2017, and started getting sick, coughing, vomiting, chest pains&#8230;. running the gauntlet of things that could be thrown at me.  It turned out as was determined in late January 2018 that I was having heart attacks right at the time of the diagnosis.  I had a triple bypass and an aortic&hellip;<span class="activity-read-more" id="activity-read-more-32518"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-31570" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion Traveling with Pulmonary Fibrosis in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-with-pulmonary-fibrosis/#post-31568</link>
				<pubDate>Thu, 31 Mar 2022 20:05:29 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-with-pulmonary-fibrosis/#post-31568"><span class="bb-reply-lable">Reply to</span> Traveling with Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>I am a frequent flyer.  I average for to eight flights a week.  I have flown all but three weeks since January 2, 2022. I have flown virtually every week since the pandemic started and many many weeks before&#8230; years actually.</p>
<p>I was diagnosed IPF mid 2017 and given the usual 5 to 7 year prognosis. I was placed on oxygen and I managed to get&hellip;<span class="activity-read-more" id="activity-read-more-32515"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-with-pulmonary-fibrosis/#post-31568" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion Salty phlegm issue in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/salty-phlegm-issue/#post-30433</link>
				<pubDate>Thu, 11 Nov 2021 22:09:10 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/salty-phlegm-issue/#post-30433"><span class="bb-reply-lable">Reply to</span> Salty phlegm issue</a></p> <div class="bb-content-inr-wrap"><p>sorry to say, but get used to the coughing and the endless phlegm.  After taking the OFEV, I have about a 30 minute grace period before I cough to the point of vomiting.  I carry a towel around so I have something to catch my product.  My doctors have tried every combination of pills, capsules and sprays to stop the mucus and cough but nothing&hellip;<span class="activity-read-more" id="activity-read-more-30449"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/salty-phlegm-issue/#post-30433" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion MRI to diagnose PF in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/mri-to-diagnose-pf/#post-30432</link>
				<pubDate>Thu, 11 Nov 2021 22:03:04 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/mri-to-diagnose-pf/#post-30432"><span class="bb-reply-lable">Reply to</span> MRI to diagnose PF</a></p> <div class="bb-content-inr-wrap"><p>I don&#8217;t know why it takes so long for a C.T.    I have had the M.R.I. but my doctor says the C.T. has better definition. I get my treatment from the vet admin., and they are faster than my regular doctor for treatment.</p>
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				<title>James 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-29096</link>
				<pubDate>Sat, 03 Jul 2021 02:28:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-29096"><span class="bb-reply-lable">Reply to</span> Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>oxygentogo.com is who handles my poc via delta</p>
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				<title>James 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-28822</link>
				<pubDate>Thu, 10 Jun 2021 20:58:14 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28822"><span class="bb-reply-lable">Reply to</span> Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>The government considers the POC to be a medical device and only administered with a prescription from a medical physician. To sell it or trade it off to someone who does not have a prescription is considered illegal and can be prosecuted although I have not heard of anyone actually being arrested for it. It is based on a percentage of oxygen&hellip;<span class="activity-read-more" id="activity-read-more-27680"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28822" rel="nofollow"> Read more</a></span></p>
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				<title>James 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-28724</link>
				<pubDate>Thu, 03 Jun 2021 20:19:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28724"><span class="bb-reply-lable">Reply to</span> Oxygen concentrators and travel</a></p> <div class="bb-content-inr-wrap"><p>I have been flying with an oxygen concentrator twice a month for the last year. I have to call in to get my Inogen cleared each time I fly with my airline. Besides that, it is not a problem flying with them. You still have to wear a mask for the most part on the flights. I have to certify that I have enough battery power for at least one and&hellip;<span class="activity-read-more" id="activity-read-more-27511"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-concentrators-and-travel/#post-28724" rel="nofollow"> Read more</a></span></p>
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				<title>James replied to the discussion Increased Throat Clearing in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/increased-throat-clearing/#post-27766</link>
				<pubDate>Thu, 18 Mar 2021 20:34:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/increased-throat-clearing/#post-27766"><span class="bb-reply-lable">Reply to</span> Increased Throat Clearing</a></p> <div class="bb-content-inr-wrap"><p>I started with the clearing 2 years before I had a positive diagnosis.  I have a solid cough, productive most of the time&#8230;  my last CT shows a rather agressive progression since last year. I&#8217;m still here&#8230;. lol&#8230;  Clive</p>
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				<title>James posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19211/#acomment-19220</link>
				<pubDate>Fri, 03 Apr 2020 11:03:19 -0500</pubDate>

									<content:encoded><![CDATA[<p>t.y. just trying to learn more about this condition.</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/magician/" data-bb-hp-profile="5137" rel="nofollow">James</a> became a registered member					]]></content:encoded>
				
				
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				<title>James became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19211/</link>
				<pubDate>Fri, 03 Apr 2020 02:34:46 -0500</pubDate>

				
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