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	<title>Pulmonary Fibrosis News Forums | Richard Halderman | Activity</title>
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				<title>Richard Halderman replied to the discussion Using supplemental oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/using-supplemental-oxygen/#post-34646</link>
				<pubDate>Thu, 16 Mar 2023 20:15:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/using-supplemental-oxygen/#post-34646"><span class="bb-reply-lable">Reply to</span> Using supplemental oxygen</a></p> <div class="bb-content-inr-wrap"><p>My self I have small bottles that fit in a hydration back pack to use when I am out and yes it helps keep my o2 levels at 90+. I run it on 3 and it does great. At home when I sit down and rest I run at 2.5. I only use as need Which is getting moer frequent. But to answer &#8216;yes&#8217; ut does help.</p>
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				<title>Richard Halderman replied to the discussion Life span in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/#post-34571</link>
				<pubDate>Thu, 09 Mar 2023 21:39:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/3/#post-34571"><span class="bb-reply-lable">Reply to</span> Life span</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed in 2014 and am still in the moderate range. Text book longevity is not accurate. I will add you to my prayer list. It out of our hands now.</p>
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				<title>Richard Halderman replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-34548</link>
				<pubDate>Tue, 07 Mar 2023 21:26:27 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/8/#post-34548"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed in 2015 and started OFEV in 2022. My p<br />
PF is Idiopathic and at the start of OFEV I was in the moderate range. Unfortunately I could not tolerate it. After 5 months of starts and stops and loss of 45 lbs. due to gastrointestinal reactions had to finaly give up. Hopefully another med will come along that I can tolerate. </p>
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				<title>Richard Halderman replied to the discussion The inevitable.... in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-inevitable/#post-34473</link>
				<pubDate>Tue, 21 Feb 2023 23:05:03 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-inevitable/#post-34473"><span class="bb-reply-lable">Reply to</span> The inevitable....</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed in 2014 at that time I read life expectancy was 2 to 4 years. At that time I realized I needed to get right with life and my creator. I settled it in my heart how this disease ended. No cure nothing. I realize this is a very devastating disease believe me I know. But I have maintained a relationship with my creator and my wife.&hellip;<span class="activity-read-more" id="activity-read-more-37604"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-inevitable/#post-34473" rel="nofollow"> Read more</a></span></p>
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				<title>Richard Halderman replied to the discussion Rituxamab Infusion Treatment in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/rituxamab-infusion-treatment/#post-33922</link>
				<pubDate>Tue, 20 Dec 2022 20:22:12 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/rituxamab-infusion-treatment/#post-33922"><span class="bb-reply-lable">Reply to</span> Rituxamab Infusion Treatment</a></p> <div class="bb-content-inr-wrap"><p>I have been through the Rituximab infusion. Every 6 mo for 2 years and had no problem with the treatments. The main thing is it kills your immune system. You have to be very careful where you go and who you are around. My infusions were more for ANCA Vasculitis and it worked tremendously. Added benefit is it slows the IPF by killing your immune system. </p>
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				<title>Richard Halderman 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-33819</link>
				<pubDate>Thu, 08 Dec 2022 23:07:36 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/page/2/#post-33819"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>I was offered the option the first part of this year ad my 70th b/day was mid June and I would not be eligible after that. I researched the process and in light of the enormous cost,the %s of success longevity a post transplant and post care and forever being on a seeming covid lock down it just didn&#8217;t seem desirable to me. So I declined&hellip;<span class="activity-read-more" id="activity-read-more-36427"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-33819" rel="nofollow"> Read more</a></span></p>
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				<title>Richard Halderman replied to the discussion Where do you live, receive care, and are you in  a local support group? in the forum Polls &#38; Quizzes</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/where-do-you-live-receive-care-and-are-you-in-a-local-support-group/#post-33601</link>
				<pubDate>Thu, 17 Nov 2022 22:57:05 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/where-do-you-live-receive-care-and-are-you-in-a-local-support-group/page/3/#post-33601"><span class="bb-reply-lable">Reply to</span> Where do you live, receive care, and are you in  a local support group?</a></p> <div class="bb-content-inr-wrap"><p>I&#8217;m a 70 year old mele diagnosed in 2015 I live in Yakima Wa. and recieve treatment in Seattle Wa. about a 3 hr. drive. As far as I know there are no social support groups local. IPF is not bad as yet, I have limitations on activities but it what it is.</p>
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				<title>Richard Halderman posted an update: @christie-patient Thank you for your welcome. I am not [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/35718/</link>
				<pubDate>Thu, 27 Oct 2022 02:14:54 -0500</pubDate>

									<content:encoded><![CDATA[<p>@christie-patient Thank you for your welcome. I am not much of conversationalist but, thanks.</p>
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				<title>Richard Halderman became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/35107/</link>
				<pubDate>Fri, 16 Sep 2022 13:24:57 -0500</pubDate>

				
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