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	<title>Pulmonary Fibrosis News Forums | John Fraze | Activity</title>
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				<title>John Fraze replied to the discussion Overdosing on supplemental oxygen in the forum Supplemental Oxygen and PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/overdosing-on-supplemental-oxygen/#post-38178</link>
				<pubDate>Sun, 06 Apr 2025 03:00:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/overdosing-on-supplemental-oxygen/#post-38178"><span class="bb-reply-lable">Reply to</span> Overdosing on supplemental oxygen</a></p> <div class="bb-content-inr-wrap"><p>I tried upping my oxygen from 2 to 3 or 4 at night. It didn’t take long until I developed swollen ankles and calves. I did did some research and found there is such a thing as oxygen toxicity. I reduced my settings back to 2 and my feet and legs went back to normal size. You can look it up on Wikipedia. The damage can be severe. Check with your&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-44517"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/overdosing-on-supplemental-oxygen/#post-38178" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Optimism in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/optimism/#post-37786</link>
				<pubDate>Tue, 31 Dec 2024 21:53:01 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/optimism/#post-37786"><span class="bb-reply-lable">Reply to</span> Optimism</a></p> <div class="bb-content-inr-wrap"><p>Look up the following word on your computer or iPad. </p>
<p>Nerandomilast. Yes it is spelled correctly. </p>
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				<title>John Fraze replied to the discussion Ventless Natural Gas Fireplace in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ventless-natural-gas-fireplace/#post-37529</link>
				<pubDate>Thu, 24 Oct 2024 20:26:14 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ventless-natural-gas-fireplace/#post-37529"><span class="bb-reply-lable">Reply to</span> Ventless Natural Gas Fireplace</a></p> <div class="bb-content-inr-wrap"><p>I have owned a home with two fireplaces. One is vented and the other is ventless. They are completely turned off in the summer, even the pilot lights. I can’t tell they have made any difference whatsoever either in winter or summer in regards to my breathing. </p>
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				<title>John Fraze replied to the discussion Esbriet and fatigue in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/esbriet-and-fatigue/#post-37486</link>
				<pubDate>Thu, 10 Oct 2024 20:20:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/esbriet-and-fatigue/#post-37486"><span class="bb-reply-lable">Reply to</span> Esbriet and fatigue</a></p> <div class="bb-content-inr-wrap"><p>I take OFEV but have the same lack of stamina issues. I struggle to go to the bathroom. It has gotten much worse the last month but has leveled off. </p>
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				<title>John Fraze replied to the discussion Cough help in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cough-help/#post-37447</link>
				<pubDate>Wed, 25 Sep 2024 14:34:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cough-help/#post-37447"><span class="bb-reply-lable">Reply to</span> Cough help</a></p> <div class="bb-content-inr-wrap"><p>I have been able to stop most of the coughing with a 5 day treatment of prednisone. Ask your physician about that. </p>
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				<title>John Fraze replied to the discussion Drug Induced IPF (unknown cause) Meds? in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/drug-induced-ipf-unknown-cause-meds/#post-36961</link>
				<pubDate>Thu, 25 Apr 2024 22:09:11 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/drug-induced-ipf-unknown-cause-meds/#post-36961"><span class="bb-reply-lable">Reply to</span> Drug Induced IPF (unknown cause) Meds?</a></p> <div class="bb-content-inr-wrap"><p>Chest medical journal/flecainide. </p>
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				<title>John Fraze replied to the discussion Low oxygen because I don&#039;t like what it does for my stamina. in the forum Healthcare Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/low-oxygen-because-i-dont-like-what-it-does-for-my-stamina/#post-36933</link>
				<pubDate>Tue, 23 Apr 2024 19:55:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/low-oxygen-because-i-dont-like-what-it-does-for-my-stamina/#post-36933"><span class="bb-reply-lable">Reply to</span> Low oxygen because I don't like what it does for my stamina.</a></p> <div class="bb-content-inr-wrap"><p>There is such a thing as oxygen toxicity. Too much oxygen is as bad as not enough. You can google it you may be astonished. I recommend that you ask your doctor to do an overnight test to determine just how much oxygen you actually need. </p>
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				<title>John Fraze replied to the discussion New with so many questions in the forum Caregivers and Spouses</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36785</link>
				<pubDate>Mon, 18 Mar 2024 00:45:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36785"><span class="bb-reply-lable">Reply to</span> New with so many questions</a></p> <div class="bb-content-inr-wrap"><p>My Afib was not caused by OFEV. I’ve had Afib for over 20 years. </p>
<p>One of the side effects of OFEV is diarrhea,  Imodium helps control the diarrhea and can be purchased at Costco for a much cheaper price. </p>
<p>Also, if the diarrhea is very severe the his doctor might lower the dose from 150 milligrams twice per day to 100 milligrams twice per day.&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41894"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36785" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion New with so many questions in the forum Caregivers and Spouses</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36745</link>
				<pubDate>Tue, 12 Mar 2024 23:10:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36745"><span class="bb-reply-lable">Reply to</span> New with so many questions</a></p> <div class="bb-content-inr-wrap"><p>Hello Margo,</p>
<p>My name is John. I have had IPF for 7 years. I have been taking OFEV for over 5 years. I also have a heart condition know as Afib. </p>
<p>I have been to Hawaii many times. If you do go to Hawaii you will need to fly. Planes are all pressurized for 8,000 feet. So it feels like you are at 8,000 when you are really at 35,000 feet. People&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41836"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-with-so-many-questions/#post-36745" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion The End in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-end/#post-36674</link>
				<pubDate>Thu, 22 Feb 2024 23:39:07 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-end/#post-36674"><span class="bb-reply-lable">Reply to</span> The End</a></p> <div class="bb-content-inr-wrap"><p>You might talk to your pulmonologist about the amount of oxygen you are using. There is such a thing as oxygen toxicity. Too much is as bad or worse than not enough. You can also look it up on <a target='_blank' href="http://www.mayoclinic.com" rel="nofollow">http://www.mayoclinic.com</a>.  I was amazed when I checked into it. </p>
<div class="bb-link-preview-container"><div class="bb-link-preview-image"><div class="bb-link-preview-image-cover"><a href="http://www.mayoclinic.com" target="_blank"><img src="https://pulmonaryfibrosisnews.com/forums/wp-content/uploads/2024/02/MC_TwitterCard_120x120.jpg" /></a></div></div><div class="bb-link-preview-info"><p class="bb-link-preview-link-name">mayoclinic.com</p><p class="bb-link-preview-title"><a href="http://www.mayoclinic.com" target="_blank" rel="nofollow">Top-ranked Hospital in the Nation</a></p><div class="bb-link-preview-excerpt"><p>Top-ranked Hospital in the Nation</p></div></div></div></div>]]></content:encoded>
				
				
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				<title>John Fraze 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-36586</link>
				<pubDate>Fri, 09 Feb 2024 01:53:44 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-cost-and-assistance/#post-36586"><span class="bb-reply-lable">Reply to</span> OFEV cost and assistance</a></p> <div class="bb-content-inr-wrap"><p>Open Doors has a cost support program as indicated in a previous reply. I have found it useful. 866 673 6366. </p>
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				<title>John Fraze replied to the discussion Saracatinib in the forum Canadians With PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/saracatinib/#post-35968</link>
				<pubDate>Thu, 21 Sep 2023 01:40:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saracatinib/#post-35968"><span class="bb-reply-lable">Reply to</span> Saracatinib</a></p> <div class="bb-content-inr-wrap"><p>If you want to try this drug as a Guinea pig. You can read up on the right to try law passed in 2017 and signed by President Trump. </p>
<p></p>
<p><a target='_blank' href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title</a></p>
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<div class="bb-link-preview-container"><div class="bb-link-preview-info"><p class="bb-link-preview-link-name">ncbi.nlm.nih.gov</p><p class="bb-link-preview-title"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title" target="_blank" rel="nofollow">Page not available - PMC</a></p><div class="bb-link-preview-excerpt"><p>Page not available - PMC</p></div></div></div></div>]]></content:encoded>
				
				
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				<title>John Fraze replied to the discussion Saracatinib in the forum Canadians With PF</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/saracatinib/#post-35966</link>
				<pubDate>Thu, 21 Sep 2023 01:31:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saracatinib/#post-35966"><span class="bb-reply-lable">Reply to</span> Saracatinib</a></p> <div class="bb-content-inr-wrap"><p><a target='_blank' href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title&lt;div&gt;This" rel="nofollow">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title&lt;div&gt;This</a> article discusses the right to try law. Lots of reading but interesting. &lt;/div&gt;&lt;div&gt;<br />&lt;/div&gt;&lt;div&gt;John&lt;/div&gt;&lt;div&gt;<br />&lt;/div&gt;</p>
<div class="bb-link-preview-container"><div class="bb-link-preview-image"><div class="bb-link-preview-image-cover"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title" target="_blank"><img src="https://pulmonaryfibrosisnews.com/forums/wp-content/uploads/2023/08/favicon-57.png" /></a></div></div><div class="bb-link-preview-info"><p class="bb-link-preview-link-name">ncbi.nlm.nih.gov</p><p class="bb-link-preview-title"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416898/#S14title" target="_blank" rel="nofollow">Page not available - PMC</a></p><div class="bb-link-preview-excerpt"><p>Page not available - PMC</p></div></div></div></div>]]></content:encoded>
				
				
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				<title>John Fraze replied to the discussion How quickly can pulmonary fibrosis progress? in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-35393</link>
				<pubDate>Thu, 13 Jul 2023 20:19:08 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-35393"><span class="bb-reply-lable">Reply to</span> How quickly can pulmonary fibrosis progress?</a></p> <div class="bb-content-inr-wrap"><p>I would recommend Imodium to you folks having diarrhea type side effects from Ofev. I have been on ofev for almost 5 years and I have been able to blunt the side effects to a manageable degree. When it gets too bad I skip a dose of ofev to make better, probably only maybe once a month. There is a generic version of Imodium which is much&hellip;<span class="activity-read-more" id="activity-read-more-39488"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-quickly-can-pulmonary-fibrosis-progress/#post-35393" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Split Ofev doseages in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/split-ofev-doseages/#post-35304</link>
				<pubDate>Fri, 30 Jun 2023 00:04:30 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/split-ofev-doseages/page/2/#post-35304"><span class="bb-reply-lable">Reply to</span> Split Ofev doseages</a></p> <div class="bb-content-inr-wrap"><p>I would suggest that you try taking one Imodium per day to help with the diarrhea. I did and it helped. I take one every day and on Sunday, Tuesday, Thursday and Saturday I take an additional one half Imodium. After several years of experimenting this works best. If it gets too bad I skip an ofev dose but not very often, maybe once a month. I&hellip;<span class="activity-read-more" id="activity-read-more-39294"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/split-ofev-doseages/#post-35304" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze 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-34521</link>
				<pubDate>Thu, 02 Mar 2023 21:22:58 -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-34521"><span class="bb-reply-lable">Reply to</span> Oxygen Delivery System when needs go up</a></p> <div class="bb-content-inr-wrap"><p>You might want to try a humidifier to relieve some of the nose dryness. Also spray her nose with saline solution as it will clean her nose, prevent infection and relieve dryness in her nostrils. Best of luck.</p>
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				<title>John Fraze replied to the discussion Leaving the house on 4LPM oxygen? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/leaving-the-house-on-4lpm-oxygen/#post-33265</link>
				<pubDate>Tue, 11 Oct 2022 19:37:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/leaving-the-house-on-4lpm-oxygen/#post-33265"><span class="bb-reply-lable">Reply to</span> Leaving the house on 4LPM oxygen?</a></p> <div class="bb-content-inr-wrap"><p>I have an Ogen one G5 that goes up to 6 LPM. </p>
<p>Good luck. They are pricy. </p>
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				<title>John Fraze replied to the discussion CONFUSED BY LATEST LUNG FUNCTION RESULTS in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/confused-by-latest-lung-function-results/#post-32941</link>
				<pubDate>Wed, 24 Aug 2022 00:54:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/confused-by-latest-lung-function-results/#post-32941"><span class="bb-reply-lable">Reply to</span> CONFUSED BY LATEST LUNG FUNCTION RESULTS</a></p> <div class="bb-content-inr-wrap"><p>The numbers can change for a variety of reasons. The temperature, humidity, state of his health such as a bad cold or just the sniffles.<br />
The percentage of oxygen in the air is the same but cold dry air is much more compact than warm moist air so in summer it’s much easier to breathe in cool air conditioning than outdoors in warm humid&hellip;<span class="activity-read-more" id="activity-read-more-34897"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/confused-by-latest-lung-function-results/#post-32941" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Good Saturated Oxygen Levels Yet With Labored Breathing in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32760</link>
				<pubDate>Thu, 28 Jul 2022 19:45:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32760"><span class="bb-reply-lable">Reply to</span> Good Saturated Oxygen Levels Yet With Labored Breathing</a></p> <div class="bb-content-inr-wrap"><p>I have two types of oxygen concentrators. One is continuing flow and the other is a pulse flow. I don’t know what you have but when you use a pulse flow machine breathing fast actually slows it down. The instructions with mine say not to breathe fast or deeply as that interferes with the rhythm of the machine. Just to turn the number of liters&hellip;<span class="activity-read-more" id="activity-read-more-34592"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32760" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Good Saturated Oxygen Levels Yet With Labored Breathing in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32734</link>
				<pubDate>Tue, 26 Jul 2022 19:46:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32734"><span class="bb-reply-lable">Reply to</span> Good Saturated Oxygen Levels Yet With Labored Breathing</a></p> <div class="bb-content-inr-wrap"><p>Check your filters on your oxygen machine. You might need to clean them.<br />
check to see if your medical records show any stenosis in your pulmonary veins that run from your lungs to your heart.  There are four of them. If you have had a heart ablation there is a possibility your pulmonary veins have stenosis. A symptom of this is shortness&hellip;<span class="activity-read-more" id="activity-read-more-34542"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/good-saturated-oxygen-levels-yet-with-labored-breathing/#post-32734" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Need to start all over in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/need-to-start-all-over/#post-32128</link>
				<pubDate>Thu, 19 May 2022 19:24:06 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/need-to-start-all-over/#post-32128"><span class="bb-reply-lable">Reply to</span> Need to start all over</a></p> <div class="bb-content-inr-wrap"><p>I just read that it is coming out in generic. It didn’t say when it would be available to get an Rx for the generic version but I assume it should be soon. They will need some time to get the manufacturing process going and then the actual distribution to pharmacies. Ask your doctor or pharmacy when it will be available.  </p>
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				<title>John Fraze replied to the discussion COVID ON TOP OF IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/covid-on-top-of-ipf/#post-31957</link>
				<pubDate>Thu, 05 May 2022 20:35:11 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/covid-on-top-of-ipf/#post-31957"><span class="bb-reply-lable">Reply to</span> COVID ON TOP OF IPF</a></p> <div class="bb-content-inr-wrap"><p>I am 84 years old. I have had two shots plus a booster. And a flu shot every year for probably 30 or 40 years. I was diagnosed wit IPF in November 2018. I have been taking Ofev since January 1, 2019.</p>
<p>I contracted Covid-19 either late January or early February of 2022. Symptoms were mild as were my wife’s. We both tested positive with a home kit&hellip;<span class="activity-read-more" id="activity-read-more-33173"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/covid-on-top-of-ipf/#post-31957" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Dealing with Side Effects in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-side-effects/#post-31756</link>
				<pubDate>Thu, 21 Apr 2022 20:25:52 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-side-effects/#post-31756"><span class="bb-reply-lable">Reply to</span> Dealing with Side Effects</a></p> <div class="bb-content-inr-wrap"><p>Has anyone experienced the effects ofev has on nose bleeds?  I’ve been having considerable difficulty with nose bleeds lately. A nose bleed every day for 10 days.  They have taken me off eliquis and ofev temporarily until the bleeding issue is resolved.</p>
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				<title>John Fraze replied to the discussion Ofev and anticoagulants in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-anticoagulants/#post-31660</link>
				<pubDate>Tue, 12 Apr 2022 20:22:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-anticoagulants/#post-31660"><span class="bb-reply-lable">Reply to</span> Ofev and anticoagulants</a></p> <div class="bb-content-inr-wrap"><p>I have IPF and Afib, I Have been taking OFEV since January 1, 2019 (almost 3 1/2 years.)  I have had 4 ablations for AFIB since 2009. I have been taking eliquis since then. When I started taking OFEV they cut my eliquis from 5 mg twice a day to 2 1/2 mg twice a day. I also take flecainide 50 mg twice per day for my AFIB. So far so good. Hope&hellip;<span class="activity-read-more" id="activity-read-more-32652"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-anticoagulants/#post-31660" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Post-nasal Drip: Another Ailment to Deal With in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30287</link>
				<pubDate>Tue, 26 Oct 2021 19:49:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30287"><span class="bb-reply-lable">Reply to</span> Post-nasal Drip: Another Ailment to Deal With</a></p> <div class="bb-content-inr-wrap"><p>My cardiologist has forbidden me to take Benadryl. I have a fib </p>
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				<title>John Fraze replied to the discussion abdominal cramps with Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/abdominal-cramps-with-ofev/#post-30286</link>
				<pubDate>Tue, 26 Oct 2021 19:36:50 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/abdominal-cramps-with-ofev/#post-30286"><span class="bb-reply-lable">Reply to</span> abdominal cramps with Ofev</a></p> <div class="bb-content-inr-wrap"><p>I have been on OFEV for almost 3 years. I take 150 mg twice per day. At first I had minor abdominal cramps and still do. I started have diarrhea to the extent it was aggravating so I started taking Imodium.  It controlled it somewhat. I started taking one every other day and it helped some. I changed to one every day and and that helped even&hellip;<span class="activity-read-more" id="activity-read-more-30194"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/abdominal-cramps-with-ofev/#post-30286" rel="nofollow"> Read more</a></span></p>
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				<title>John Fraze replied to the discussion Post-nasal Drip: Another Ailment to Deal With in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30264</link>
				<pubDate>Fri, 22 Oct 2021 02:03:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30264"><span class="bb-reply-lable">Reply to</span> Post-nasal Drip: Another Ailment to Deal With</a></p> <div class="bb-content-inr-wrap"><p>Remember the formula for water is H2O. </p>
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				<title>John Fraze replied to the discussion Post-nasal Drip: Another Ailment to Deal With in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30263</link>
				<pubDate>Fri, 22 Oct 2021 02:00:35 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-30263"><span class="bb-reply-lable">Reply to</span> Post-nasal Drip: Another Ailment to Deal With</a></p> <div class="bb-content-inr-wrap"><p>I have found that the ipratropium helps a lot.</p>
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				<title>John Fraze posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/29503/#acomment-29682</link>
				<pubDate>Wed, 22 Sep 2021 02:19:55 -0500</pubDate>

									<content:encoded><![CDATA[<p>I recently purchased a portable oxygen concentrator. It weighs 5.7 pounds with a double battery, with a single battery it weighs only 4.7 pounds. It comes with a shoulder bag  that allows you to carry it. It is also certified to use on commercial airliners so now I can fly again.  They are expensive, mine costs $2665. No tax, no shipping costs.&hellip;<span class="activity-read-more" id="activity-read-more-29682"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/29503/#acomment-29682" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/flowers123/" data-bb-hp-profile="11514" rel="nofollow">Diane Shaughnessy</a> posted an update I live in IL with my two dogs are used to love walking but now I can’t walk much anymore because of my pulmonary fibrosis I wonder if anybody has any suggestions where oxygen [&hellip;]					]]></content:encoded>
				
				
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				<title>John Fraze replied to the discussion End of Life in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/end-of-life/#post-30006</link>
				<pubDate>Wed, 22 Sep 2021 01:58:34 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/end-of-life/#post-30006"><span class="bb-reply-lable">Reply to</span> End of Life</a></p> <div class="bb-content-inr-wrap"><p>I feel so bad for that lady and have great fear of putting my wife through something similar. I’m 84 and she is 81. We have been married 63 years and dated 3 years before getting married. I was diagnosed in November 2018 and on OFEV since January 1, 2019. Doing pretty well so far.</p>
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				<title>John Fraze became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/29671/</link>
				<pubDate>Tue, 21 Sep 2021 20:47:47 -0500</pubDate>

				
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