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	<title>Pulmonary Fibrosis News Forums | John Kane | Activity</title>
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				<title>John Kane replied to the discussion Ofev issues in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-issues/#post-36667</link>
				<pubDate>Thu, 22 Feb 2024 20:30:58 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-issues/#post-36667"><span class="bb-reply-lable">Reply to</span> Ofev issues</a></p> <div class="bb-content-inr-wrap"><p>I have been on OFEV 150 mgs for 4 1/2 years now. It took me a few months to figure out what I could and could not eat/drink with this medicine.</p>
<p>I followed the instructions but found the biggest diarrhea culprit to be coffee. I have up coffee for over a year, switching to green tea instead. Now I have a coffee from time to time but with a lot&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41667"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-issues/#post-36667" rel="nofollow"> Read more</a></span></p>
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				<title>John Kane replied to the discussion Wristband Pulse Oximeter in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/wristband-pulse-oximeter/#post-33274</link>
				<pubDate>Tue, 11 Oct 2022 23:03:43 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/wristband-pulse-oximeter/#post-33274"><span class="bb-reply-lable">Reply to</span> Wristband Pulse Oximeter</a></p> <div class="bb-content-inr-wrap"><p>I just started looking into wrist worn sensor watches. Whiting s is the only one that says they are FDA approved for the SP02 sensor they use.</p>
<p>More research to be done.</p>
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				<title>John Kane 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-33273</link>
				<pubDate>Tue, 11 Oct 2022 22:59:57 -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/2/#post-33273"><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 had IPF for about 3 1/2 years and take Ofev for it. My wife and I have had the two Covid shots and one booster, last year.</p>
<p>Three months ago we both tested positive for Covid. We both had fatigue(on top of what I already have). My wife had heavy congestion and I had heavy GI issues. Don’t know why we were different but at least I did not&hellip;<span class="activity-read-more" id="activity-read-more-35425"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-33273" rel="nofollow"> Read more</a></span></p>
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				<title>John Kane replied to the discussion travel while on ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-while-on-ofev/#post-33272</link>
				<pubDate>Tue, 11 Oct 2022 22:44:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/travel-while-on-ofev/#post-33272"><span class="bb-reply-lable">Reply to</span> travel while on ofev</a></p> <div class="bb-content-inr-wrap"><p>It took me about a year to minimize the Ofev side effects. What helped me the most was giving up coffee. It seems that the acid, not the caffeine, was the major culprit.<br />
Diet wise, tart or sour tastes, not spicy, would bother me. Dairy does not bother me at all.</p>
<p>Took a while to figure all this out but we traveled when we could.</p>
<p>&nbsp;</p>
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				<title>John Kane replied to the discussion Is ipf genetic? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32674</link>
				<pubDate>Thu, 21 Jul 2022 19:34:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/is-ipf-genetic/#post-32674"><span class="bb-reply-lable">Reply to</span> Is ipf genetic?</a></p> <div class="bb-content-inr-wrap"><p>My mother died of IPF at age 72.  Was diagnosed 3 years ago and am now 72.  Am the oldest of 4 children, and the only one left. One of them died of IPF.</p>
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				<title>John Kane 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-31907</link>
				<pubDate>Tue, 03 May 2022 19:17:07 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/telling-your-family/#post-31907"><span class="bb-reply-lable">Reply to</span> Telling your family</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed in May of 2019. My wife was with me for the post testing discussion with the Pulmonologist. We agreed that it would be best to tell both of our adult kids right away. Very glad that I did and have updated them after each testing testing since then. At this point our friends and relatives also know, the support has been unbelievable.</p>
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				<title>John Kane replied to the discussion Household Chores &#38; IPF! in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/household-chores-ipf/#post-31027</link>
				<pubDate>Thu, 10 Feb 2022 20:34:10 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/household-chores-ipf/#post-31027"><span class="bb-reply-lable">Reply to</span> Household Chores & IPF!</a></p> <div class="bb-content-inr-wrap"><p>Buy the best A/C filter you can find and change it once a month.</p>
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				<title>John Kane replied to the discussion Ofev UK in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-uk/#post-30719</link>
				<pubDate>Tue, 11 Jan 2022 21:13:40 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-uk/#post-30719"><span class="bb-reply-lable">Reply to</span> Ofev UK</a></p> <div class="bb-content-inr-wrap"><p>Teri, is your paleontologist looking for Jurassic or Mezazoic requirements?</p>
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				<title>John Kane 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-30319</link>
				<pubDate>Fri, 29 Oct 2021 13:35:15 -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-30319"><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>Two years ago, when we were trying to figure out what Washington with me, I took myself to an Allergist. All the testing came out negative but she prescribed Azelastine for my sinus/ runny nose issue. This works very well for me, better than the Flonase I was using. IMHO anyway…</p>
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				<title>John Kane replied to the discussion What&#039;s Worked for me with OFEV in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/whats-worked-for-me-with-ofev/#post-30132</link>
				<pubDate>Tue, 05 Oct 2021 21:22:08 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/whats-worked-for-me-with-ofev/#post-30132"><span class="bb-reply-lable">Reply to</span> What's Worked for me with OFEV</a></p> <div class="bb-content-inr-wrap"><p>Joy, I have been on Ofev for just about two years now. I always eat before I take the pill, oatmeal with nuts and fruit or toast and eggs in the morning. I find that overall the oatmeal works best. For the evening pill I make a peanut butter sandwich or Greek yogurt and nuts and fruit. I take my pills at 9am and 9 pm ish. A lot of the GI&hellip;<span class="activity-read-more" id="activity-read-more-29900"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/whats-worked-for-me-with-ofev/#post-30132" rel="nofollow"> Read more</a></span></p>
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				<title>John Kane 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-30095</link>
				<pubDate>Wed, 29 Sep 2021 01:41:14 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/abdominal-cramps-with-ofev/#post-30095"><span class="bb-reply-lable">Reply to</span> abdominal cramps with Ofev</a></p> <div class="bb-content-inr-wrap"><p>Have been on Ofev for two years 150 mg x 2. Y gastric issues were very strong and constant until I stopped drinking coffee…Now I would say that they have been reduced by half, as far as cramps go. The diarrhea continues, but not as bad as before. I believe that the acidity of the coffee added to my side effects.</p>
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				<title>John Kane replied to the discussion Breathing Issues and Started OFEV This Week in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-issues-and-started-ofev-this-week/#post-25099</link>
				<pubDate>Wed, 29 Jul 2020 03:48:44 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-issues-and-started-ofev-this-week/#post-25099"><span class="bb-reply-lable">Reply to</span> Breathing Issues and Started OFEV This Week</a></p> <div class="bb-content-inr-wrap"><p>Hi Cheryl, I have been on 150 mg Ofev tablets since Nov 2019. My main side effect is GI and this varies by what I eat with the medicine. A salad doesn’t cut it, but protein in any form seems to minimize the distress. I also note some fatigue, although this seems to be minor yet consistent. Hope this helps.</p>
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				<title>John Kane replied to the discussion Just got approved for Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/just-got-approved-for-ofev/#post-24702</link>
				<pubDate>Tue, 23 Jun 2020 22:10:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/just-got-approved-for-ofev/page/2/#post-24702"><span class="bb-reply-lable">Reply to</span> Just got approved for Ofev</a></p> <div class="bb-content-inr-wrap"><p>I have been taking Ofev, 150 mg pills twice a day, for 9 months. I take my morning pills at 9 with breakfast. We eat dinner at normal times, around 6 ish and I take my second pill at 9pm with a moderate snack. Usually yogurt or a peanut butter sandwich does the trick. Snacking too light tends to aggravate the stomach. Hope this helps.</p>
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				<title>John Kane replied to the discussion OFEV and milk in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-milk/#post-24159</link>
				<pubDate>Tue, 28 Apr 2020 14:38:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-milk/#post-24159"><span class="bb-reply-lable">Reply to</span> OFEV and milk</a></p> <div class="bb-content-inr-wrap"><p>I have been on Ofev for 6 months, 150 mg twice a day. Five days a week I have oatmeal made with milk and have not had any issues. The other days I have an omelette, or some eggs.</p>
<p>I haven’t noticed any taste changes, or loss of appetite.</p>
<p>Yogurt was ok but left me feeling hungry, even with fruit.</p>
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				<title>John Kane posted an update: What can trigger an exacerbation?</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19575/</link>
				<pubDate>Fri, 17 Apr 2020 19:11:04 -0500</pubDate>

									<content:encoded><![CDATA[<p>What can trigger an exacerbation?</p>
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				<title>John Kane replied to the discussion Nintedanib... Dosage in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/#post-23688</link>
				<pubDate>Thu, 26 Mar 2020 15:38:58 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/#post-23688"><span class="bb-reply-lable">Reply to</span> Nintedanib... Dosage</a></p> <div class="bb-content-inr-wrap"><p>Call the manufacturer and ask about an Assistance Fund.</p>
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				<title>John Kane replied to the discussion I Did Everything Right, So Why Did I End Up With Pulmonary Fibrosis? in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/i-did-everything-right-so-why-did-i-end-up-with-pulmonary-fibrosis/#post-22999</link>
				<pubDate>Fri, 14 Feb 2020 23:25:24 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/i-did-everything-right-so-why-did-i-end-up-with-pulmonary-fibrosis/#post-22999"><span class="bb-reply-lable">Reply to</span> I Did Everything Right, So Why Did I End Up With Pulmonary Fibrosis?</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed with IPF last June. My father died of COPD/ emphysema and my mother did also, I was told. Both were heavy smokers. Last week, I found my mother’s death certificate which I had never seen before. IPF was listed as her cause of death.<br />
Knowing what I know now about this disease, I am amazed that she had it. Never saw her near any&hellip;<span class="activity-read-more" id="activity-read-more-18047"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/i-did-everything-right-so-why-did-i-end-up-with-pulmonary-fibrosis/#post-22999" rel="nofollow"> Read more</a></span></p>
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				<title>John Kane updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17330/</link>
				<pubDate>Tue, 21 Jan 2020 15:23:14 -0600</pubDate>

				
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				<title>John Kane replied to the discussion Am I Too Old for A Lung Transplant? in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/am-i-too-old-for-a-lung-transplant/#post-22111</link>
				<pubDate>Thu, 28 Nov 2019 16:09:04 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/am-i-too-old-for-a-lung-transplant/#post-22111"><span class="bb-reply-lable">Reply to</span> Am I Too Old for A Lung Transplant?</a></p> <div class="bb-content-inr-wrap"><p>The Mayo Clinic told me that 70 is their usual cut off age, but, since there is nothing else wrong with me (yet), they can consider an exception&#8230;I had a great visit there.</p>
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				<title>John Kane replied to the discussion Do You Identify With Being &#039;Disabled&#039;? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-identify-with-being-disabled/#post-21585</link>
				<pubDate>Tue, 08 Oct 2019 14:32:20 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-identify-with-being-disabled/#post-21585"><span class="bb-reply-lable">Reply to</span> Do You Identify With Being 'Disabled'?</a></p> <div class="bb-content-inr-wrap"><p>I also do not consider myself disabled, but I believe that I am early on in this disease. I did get a handicap tag but only use it if I have to walk a longer distance. I passed up a handicapped spot at the grocery store the other day. The gentleman who did take the spot was in far more need than me.</p>
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				<title>John Kane replied to the discussion What you need to know about Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/need-know-ofev/#post-21434</link>
				<pubDate>Thu, 26 Sep 2019 15:14:52 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/need-know-ofev/#post-21434"><span class="bb-reply-lable">Reply to</span> What you need to know about Ofev</a></p> <div class="bb-content-inr-wrap"><p>Charlene, I am about to start Ofev. Where can I find actual studies/stats on the success for this drug. I watched the manufacturers video, but that is their spin. Thanks, John</p>
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				<title>John Kane replied to the discussion Harmonica Class / Pulmonary Rehab in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/harmonica-class-pulmonary-rehab/#post-20848</link>
				<pubDate>Fri, 16 Aug 2019 18:09:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/harmonica-class-pulmonary-rehab/#post-20848"><span class="bb-reply-lable">Reply to</span> Harmonica Class / Pulmonary Rehab</a></p> <div class="bb-content-inr-wrap"><p>I already have a good harmonica but the pulmonica looks interesting. I wonder if this is prescribed as therapy whether Medicare would pick up some of the cost&#8230;.</p>
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				<title>John Kane replied to the discussion The Frequency of Changing Your Nasal Cannula in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20839</link>
				<pubDate>Fri, 16 Aug 2019 15:40:20 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-20839"><span class="bb-reply-lable">Reply to</span> The Frequency of Changing Your Nasal Cannula</a></p> <div class="bb-content-inr-wrap"><p>Charlene, I also use the Respironics Simply Go concentrator. It did not come with a backpack, just the shoulder bag. I did find, and buy a back pack for this unit, by Philips, on Amazon. My med supplier needed to order this, but I got it through Prime in 2 days. And less expensively.</p>
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				<title>John Kane became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13390/</link>
				<pubDate>Wed, 26 Jun 2019 23:08:20 -0500</pubDate>

				
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