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	<title>Pulmonary Fibrosis News Forums | Floyd C Montgomery | Activity</title>
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				<title>Floyd C Montgomery replied to the discussion Oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/#post-27214</link>
				<pubDate>Wed, 10 Feb 2021 02:59:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/page/7/#post-27214"><span class="bb-reply-lable">Reply to</span> Oxygen</a></p> <div class="bb-content-inr-wrap"><p>Hi all.  I am 85 years old and I&#8217;m in the final stages of this disease, and have been on oxygen 24/7 for over 3 years.  My needs have increased as it progresses.  I currently use 15l just to walk, and have 2 concentrators hooked in tandem to supply what I need in the home.</p>
<p>My pulmonologist has set my goal to try to stay above 89%, and I can do&hellip;<span class="activity-read-more" id="activity-read-more-25392"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/#post-27214" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery posted an update: I have been on Esbrite for a year now,  and it may [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/24336/</link>
				<pubDate>Fri, 18 Dec 2020 12:09:31 -0600</pubDate>

									<content:encoded><![CDATA[<p> I have been on Esbrite for a year now,  and it may have slowed this disease down, but I&#8217;m to the point that I use 15 l just to walk, and last month, my oxygen supplier brought in a second concentrator and hooked the two together so i can have a flow of 15 l in my apartment.<br />
When i did get a competent doctor, he discussed the use if the&hellip;<span class="activity-read-more" id="activity-read-more-24336"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/24336/" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery replied to the discussion how long can you take Esbriet? in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-long-can-you-take-esbriet/#post-24881</link>
				<pubDate>Tue, 07 Jul 2020 20:51:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-long-can-you-take-esbriet/#post-24881"><span class="bb-reply-lable">Reply to</span> how long can you take Esbriet?</a></p> <div class="bb-content-inr-wrap"><p>I&#8217;ve been on it for 5 months now, and am lucky that i do not suffer any side effects.  My first pulmonologist really knew nothing about IPF, and simply would not put me on anything but some inhalers, which did no good.  By the time i got to a pulmonologist who specializes in IPF, I am on 10l flow on oxygen to walk, and use oxygen 24/7.  The&hellip;<span class="activity-read-more" id="activity-read-more-21051"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-long-can-you-take-esbriet/#post-24881" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery posted an update: I was diagnosed with ipf 2 and a half years ago, but [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18357/</link>
				<pubDate>Thu, 27 Feb 2020 22:06:59 -0600</pubDate>

									<content:encoded><![CDATA[<p>I was diagnosed with ipf 2 and a half years ago, but because my pulmonologist at the time poopooed it, I just started on Esbrite 2 weeks ago when my new pulmonologist started me on it, even though i require a 10 l flow to walk! . She was agast that i had been on prednisone,  and 2 inhalers,  all of which are not effective, and may have&hellip;<span class="activity-read-more" id="activity-read-more-18357"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/18357/" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery replied to the discussion Inhaler Use for Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use-for-pulmonary-fibrosis/#post-21784</link>
				<pubDate>Tue, 29 Oct 2019 15:10:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use-for-pulmonary-fibrosis/page/2/#post-21784"><span class="bb-reply-lable">Reply to</span> Inhaler Use for Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene.  I use both symbiocort and ventolin inhalers twice a day, and have used them for almost a year and half.  I forgot to use then one evening, and really had trouble catching my breath, even though I was on 8l oxygen flow, so they make a difference for me.<br />
Last week I went through a 2 hour series of testing, including a nebulizer,&hellip;<span class="activity-read-more" id="activity-read-more-15919"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/inhaler-use-for-pulmonary-fibrosis/#post-21784" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery replied to the discussion Pulmonary Rehab May Improve Exercise Capacity and Quality of Life in IPF Patients in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-may-improve-exercise-capacity-and-quality-of-life-in-ipf-patients/#post-19944</link>
				<pubDate>Wed, 19 Jun 2019 01:34:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-may-improve-exercise-capacity-and-quality-of-life-in-ipf-patients/#post-19944"><span class="bb-reply-lable">Reply to</span> Pulmonary Rehab May Improve Exercise Capacity and Quality of Life in IPF Patients</a></p> <div class="bb-content-inr-wrap"><p>I am an 83 year old man that was diagnoised with IPF about 2 years ago.  I just completed my seco jnd round of 24 therapy sessions,(twice a week).<br />
I currently am on O2 24/7, and my walking need is 6 liters per minute.<br />
The first day in therapy, at the end of my 6 minute walk with oxygen, my level dropped to 86.  At the end of the sessions,&hellip;<span class="activity-read-more" id="activity-read-more-13191"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pulmonary-rehab-may-improve-exercise-capacity-and-quality-of-life-in-ipf-patients/#post-19944" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery replied to the discussion Laser Therapy Part III in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/laser-therapy-part-iii/#post-17725</link>
				<pubDate>Fri, 15 Mar 2019 13:49:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/laser-therapy-part-iii/#post-17725"><span class="bb-reply-lable">Reply to</span> Laser Therapy Part III</a></p> <div class="bb-content-inr-wrap"><p>I simply cannot find anyone in the Lancaster, PA area that can or will do laser treatment.  There are 2 Chiropractic practices that advertise having levrl IV lasers, but neither have responded to any inquiries I sent them. What would you suggest I  to try to find someone to do the laser treatment? </p>
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				<title>Floyd C Montgomery replied to the discussion Flying with IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17374</link>
				<pubDate>Wed, 06 Mar 2019 18:13:43 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17374"><span class="bb-reply-lable">Reply to</span> Flying with IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Barry.<br />
I was diagnoised with IPF about 2 years ago.  I have been on oxygen for over a year, and currently use a flow of 6l to walk.<br />
Last August my wife and I flew from Lancaster PA to Colorado Springs to see our great grandkids.  I made arrangments through my oxygen suplier for a concentrator in my motel room and oxygen bottles to use&hellip;<span class="activity-read-more" id="activity-read-more-9896"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flying-with-ipf/#post-17374" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery replied to the discussion Dying from IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-16479</link>
				<pubDate>Tue, 05 Feb 2019 02:14:34 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-16479"><span class="bb-reply-lable">Reply to</span> Dying from IPF</a></p> <div class="bb-content-inr-wrap"><p>I am not at the stage yet that I can avail my self of their services, but my wife has been very active in hospice and I won&#8217;t hesitate to use them.</p>
<p>Thanks again for sharing.  I will keep in touch.</p>
<p>Floyd Montgomery</p>
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				<title>Floyd C Montgomery replied to the discussion Dying from IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-16411</link>
				<pubDate>Sat, 02 Feb 2019 16:08:20 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-16411"><span class="bb-reply-lable">Reply to</span> Dying from IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Megan. </p>
<p>I am sorry about your dads death, but I wanted you to kmow how much it meams to me to read about his last 5 months.</p>
<p>I am an 83 year old man that was diagnoised with IPF about 15 months ago, and I am slowly but surely going down hill. Currently I am on 6l of oxygen to walk around and more if I do anything.  I am discouraged about&hellip;<span class="activity-read-more" id="activity-read-more-8371"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-16411" rel="nofollow"> Read more</a></span></p>
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				<title>Floyd C Montgomery updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7762/</link>
				<pubDate>Fri, 04 Jan 2019 19:59:50 -0600</pubDate>

				
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				<title>Floyd C Montgomery became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/2162/</link>
				<pubDate>Tue, 24 Apr 2018 16:40:04 -0500</pubDate>

				
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