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	<title>Pulmonary Fibrosis News Forums | ARMY PETE | Activity</title>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18792/#acomment-18799</link>
				<pubDate>Tue, 17 Mar 2020 20:37:47 -0500</pubDate>

									<content:encoded><![CDATA[<p>sounds good to me .lol.hate to give up on everything.too many fun things left to do.lol</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/peter/" data-bb-hp-profile="3039" rel="nofollow">ARMY PETE</a> posted an update <a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/reglois/' rel="nofollow">@reglois</a> thanks for you reply. I read about your oxygen going down to the 70 s.be aware that its not just a number.every time you go below 88 or 90,it affects every part of your [&hellip;]					]]></content:encoded>
				
				
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				<title>ARMY PETE posted an update: @reglois thanks for you reply. I read about your [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18792/</link>
				<pubDate>Tue, 17 Mar 2020 19:38:36 -0500</pubDate>

									<content:encoded><![CDATA[<p>@reglois thanks for you reply. I read about your oxygen going down to the 70 s.be aware that its not just a number.every time you go below 88 or 90,it affects every part of your organs which all need that steady flow of oxy.and finally, adjusting the flow and quantety on your own is no bueno!<br />
i just spent a half a day  with those folks.its to&hellip;<span class="activity-read-more" id="activity-read-more-18792"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/18792/" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE posted an update: @reglois holy cow . you can do 3,5 kilometers.better get [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18782/</link>
				<pubDate>Tue, 17 Mar 2020 16:02:39 -0500</pubDate>

									<content:encoded><![CDATA[<p>@reglois holy cow . you can do 3,5 kilometers.better get on your knees and pray.lol.i am lucky to walk 50 feet.&#8217;good luck to you.<br />
peter</p>
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				<title>ARMY PETE posted an update: @jill-tanner 
hi jill. well said.going to the va [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17111/</link>
				<pubDate>Fri, 10 Jan 2020 14:43:08 -0600</pubDate>

									<content:encoded><![CDATA[<p>@jill-tanner<br />
hi jill. well said.going to the va pulmonary folks is just for them i think.they have few answers and nothing seems to do anything.But i got to keep going every 6 month.lol.<br />
regards , peter</p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16851/#acomment-16863</link>
				<pubDate>Mon, 30 Dec 2019 16:11:39 -0600</pubDate>

									<content:encoded><![CDATA[<p>thanks for your reply.happy new year to you also<br />
pete</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/peter/" data-bb-hp-profile="3039" rel="nofollow">ARMY PETE</a> posted an update <a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/hfink2007/' rel="nofollow">@hfink2007</a> 
hi hans
thanks for your message.believe me , i used to be a lot more negative.just ask charlene , lol. now i am just resigned to living my life with the crap that comes [&hellip;]					]]></content:encoded>
				
				
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				<title>ARMY PETE replied to the discussion Phase 3 Trial Shows Ofev Reduces Lung Function Decline In Patients With Fibrotic Lung Diseases in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/phase-3-trial-shows-ofev-reduces-lung-function-decline-in-patients-with-fibrotic-lung-diseases/#post-22344</link>
				<pubDate>Mon, 30 Dec 2019 16:08:32 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phase-3-trial-shows-ofev-reduces-lung-function-decline-in-patients-with-fibrotic-lung-diseases/#post-22344"><span class="bb-reply-lable">Reply to</span> Phase 3 Trial Shows Ofev Reduces Lung Function Decline In Patients With Fibrotic Lung Diseases</a></p> <div class="bb-content-inr-wrap"><p>Amen , Jillt</p>
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				<title>ARMY PETE posted an update: @hfink2007 
hi hans
thanks for your message.believe me , [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16851/</link>
				<pubDate>Sun, 29 Dec 2019 18:18:11 -0600</pubDate>

									<content:encoded><![CDATA[<p>@hfink2007<br />
hi hans<br />
thanks for your message.believe me , i used to be a lot more negative.just ask charlene , lol. now i am just resigned to living my life with the crap that comes with it.i tryed ofev and it gave me to many side effects .and no none of the pills that countered the effect helped enough. i decided to stop.i rather enjoy what time&hellip;<span class="activity-read-more" id="activity-read-more-16851"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/16851/" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE posted an update: @charlene-marshall 
thank you charlene.makes sense.i [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16776/</link>
				<pubDate>Sat, 21 Dec 2019 15:28:59 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
thank you charlene.makes sense.i dropped 6 pouds + in the last month and yes i do eat a lot less.<br />
take care</p>
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				<title>ARMY PETE posted an update: @charlene-marshall 
hi charlene.just a note wishing you [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16773/</link>
				<pubDate>Sat, 21 Dec 2019 15:00:15 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
hi charlene.just a note wishing you a merry christmas and  a happy new year .<br />
peter<br />
oh , i forgot. is weight loss part of ipf?</p>
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				<title>ARMY PETE posted an update: @tschnatz This is not the time to discuss me and my IPF [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16753/</link>
				<pubDate>Thu, 19 Dec 2019 19:31:26 -0600</pubDate>

									<content:encoded><![CDATA[<p>@tschnatz This is not the time to discuss me and my IPF but reading toms profile reminds me about my own  fragility.I am not on a lot but if you feel like talking, I am a good listener ,I think.<br />
peter</p>
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				<title>ARMY PETE posted an update: @tschnatz   although I never spoke to tom ,I can [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16752/</link>
				<pubDate>Thu, 19 Dec 2019 19:21:24 -0600</pubDate>

									<content:encoded><![CDATA[<p>@tschnatz   although I never spoke to tom ,I can only imagine the loss you experience .It  is even more painful  that he couldn&#8217;t be here a little longer  and have this holiday with you.<br />
I hope that you will have family and friends around you during this stressful time<br />
regards<br />
Peter</p>
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				<title>ARMY PETE posted an update: @charlene-marshall 
hi Charlene.thanks for your [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16583/</link>
				<pubDate>Mon, 09 Dec 2019 17:58:37 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
hi Charlene.thanks for your kind words.same holiday wishes for you and yours.<br />
peter</p>
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				<title>ARMY PETE posted an update: @charlene-marshall 
hi Charlene
I am doing ok for the [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16554/</link>
				<pubDate>Thu, 05 Dec 2019 16:24:31 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
hi Charlene<br />
I am doing ok for the most part. seems the hardest part is switching from the vertical to the horizontal positionand vsa versa.lots of coughing , choking etc..ttyl.<br />
peter</p>
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				<title>ARMY PETE posted an update: @charlene-marshall 
hi there thanks for your reply [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16466/</link>
				<pubDate>Fri, 29 Nov 2019 20:32:18 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
hi there thanks for your reply regarding ofev and sharing the news from your seminar.hope all is well.<br />
peter</p>
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				<title>ARMY PETE and Kristin are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/16395/</link>
				<pubDate>Tue, 26 Nov 2019 19:40:46 -0600</pubDate>

				
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				<title>ARMY PETE replied to the discussion Phase 3 Trial Shows Ofev Reduces Lung Function Decline In Patients With Fibrotic Lung Diseases in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/phase-3-trial-shows-ofev-reduces-lung-function-decline-in-patients-with-fibrotic-lung-diseases/#post-22079</link>
				<pubDate>Tue, 26 Nov 2019 19:13:23 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phase-3-trial-shows-ofev-reduces-lung-function-decline-in-patients-with-fibrotic-lung-diseases/#post-22079"><span class="bb-reply-lable">Reply to</span> Phase 3 Trial Shows Ofev Reduces Lung Function Decline In Patients With Fibrotic Lung Diseases</a></p> <div class="bb-content-inr-wrap"><p>hello,  my name is pete.i was on ofev for about 9 weeks and finaly gave up .I was definatly in that 66% .i.e. living in the bathroom.ive been told by many that espriet is not much different .what is lacking in all the studies and trials is the out come with the meds.no one seems to be able to put it intp lay mans terms.I.e. if I die in 4&hellip;<span class="activity-read-more" id="activity-read-more-16394"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phase-3-trial-shows-ofev-reduces-lung-function-decline-in-patients-with-fibrotic-lung-diseases/#post-22079" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE replied to the discussion Aloha from Hawaii in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21510</link>
				<pubDate>Thu, 03 Oct 2019 14:33:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/aloha-from-hawaii/#post-21510"><span class="bb-reply-lable">Reply to</span> Aloha from Hawaii</a></p> <div class="bb-content-inr-wrap"><p>hey charlene</p>
<p>I am so happy for you. you go girl. now stay of the computer and have fun .lol.</p>
<p>&#8220;see you&#8221; when you get back.</p>
<p>army pete</p>
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				<title>ARMY PETE posted an update: thanks for your message.i will do my best.the "blow [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15240/</link>
				<pubDate>Tue, 17 Sep 2019 14:54:58 -0500</pubDate>

									<content:encoded><![CDATA[<p>thanks for your message.i will do my best.the &#8220;blow test &#8220;lady is worse the a drill sergeant</p>
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				<title>ARMY PETE posted an update: @mark-koziol  hey mark , 
i posted a reply to you on [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15231/</link>
				<pubDate>Mon, 16 Sep 2019 15:00:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>@mark-koziol  hey mark ,<br />
i posted a reply to you on the Spain and other county s site .don&#8217;t know wy i was there .lol<br />
peter</p>
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				<title>ARMY PETE posted an update: @mark-koziol 
hey mark. seems like i am using [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15225/</link>
				<pubDate>Sun, 15 Sep 2019 22:38:24 -0500</pubDate>

									<content:encoded><![CDATA[<p>@mark-koziol<br />
hey mark. seems like i am using my concentrator more then before and that  happend in the last few weeks.its ok after sitting a while but as soon i do something , even light stuff, it drops down to the low 80s or less.but i recover quickly.cough more ,sometimes dry,sometimes with mucus.next appt. is in october .dont know how i&hellip;<span class="activity-read-more" id="activity-read-more-15225"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/15225/" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE posted an update: @stulef   I agree with your suggestion</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15116/</link>
				<pubDate>Tue, 10 Sep 2019 15:39:46 -0500</pubDate>

									<content:encoded><![CDATA[<p>@stulef   I agree with your suggestion</p>
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				<title>ARMY PETE posted an update: @ohiocher slowly falling apart LOL</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15115/</link>
				<pubDate>Tue, 10 Sep 2019 15:35:37 -0500</pubDate>

									<content:encoded><![CDATA[<p>@ohiocher slowly falling apart LOL</p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15106/#acomment-15114</link>
				<pubDate>Tue, 10 Sep 2019 15:34:25 -0500</pubDate>

									<content:encoded><![CDATA[<p>have a great time.finally .I will be&#8221; suffering &#8220;with you here in the sunshine state.lol</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/charlene-marshall/" data-bb-hp-profile="170" rel="nofollow">Charlene</a> posted an update Hello friends!
I officially leave for Hawaii in two weeks tomorrow and trying to figure out how I can bring all of you &#8220;along&#8221; with me &#8211; whether it be through video&#8217;s, photos, [&hellip;]					]]></content:encoded>
				
				
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/1154/#acomment-15113</link>
				<pubDate>Tue, 10 Sep 2019 15:30:38 -0500</pubDate>

									<content:encoded><![CDATA[<p>I am on oxygen.a six minute walk would drop me down to 80 0r less..thats with out ox. I was told to hook up when I go below 88.thats seems to be happening a lot.i have a portable tank but have not used it outside YET.hope this helps?your dr.is wise.quality is the most important thing for me.tried ofev but it took my quality down to&hellip;<span class="activity-read-more" id="activity-read-more-15113"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/1154/#acomment-15113" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/jim-mccool/" rel="nofollow">Jim McCool</a> became a registered member					]]></content:encoded>
				
				
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				<title>ARMY PETE posted an update: @ohiocher  hi .
I was diagnosed about the same time.gave [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15112/</link>
				<pubDate>Tue, 10 Sep 2019 15:20:50 -0500</pubDate>

									<content:encoded><![CDATA[<p>@ohiocher  hi .<br />
I was diagnosed about the same time.gave up on ofev with too many bath room visits and close calls .I find myself on oxygen now .every thing got worse in the  last 2 month&#8230;…..are you on oxygen ?<br />
peter</p>
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				<title>ARMY PETE replied to the discussion How do you feel? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21163</link>
				<pubDate>Wed, 04 Sep 2019 15:23:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/page/2/#post-21163"><span class="bb-reply-lable">Reply to</span> How do you feel?</a></p> <div class="bb-content-inr-wrap"><p>darn it ,cant see what I am typing</p>
<p>nagging</p>
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				<title>ARMY PETE replied to the discussion How do you feel? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21162</link>
				<pubDate>Wed, 04 Sep 2019 15:22:57 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21162"><span class="bb-reply-lable">Reply to</span> How do you feel?</a></p> <div class="bb-content-inr-wrap"><p>hey Charlene,</p>
<p>you are never nqagging.lol</p>
<p>peter</p>
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				<title>ARMY PETE replied to the discussion How do you feel? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21136</link>
				<pubDate>Tue, 03 Sep 2019 20:13:22 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21136"><span class="bb-reply-lable">Reply to</span> How do you feel?</a></p> <div class="bb-content-inr-wrap"><p>thank you for caring.</p>
<p>the air in the house is ok as far as i knowissues with coughing .we keep the ac on.showering causes even with the exaust fan on.were in fla.air is probebly better the in a big city.for what its worth, i just went outside to unplug my charger and put it into my shed.my oxy.went to 76.my wife is giving me hell for not&hellip;<span class="activity-read-more" id="activity-read-more-14980"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21136" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE replied to the discussion How do you feel? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21115</link>
				<pubDate>Tue, 03 Sep 2019 16:05:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21115"><span class="bb-reply-lable">Reply to</span> How do you feel?</a></p> <div class="bb-content-inr-wrap"><p>hi to every one</p>
<p>I have not been on for a while .I can attest to the unfortunate fact that I have the same experience.what concerns me is the speed of the symptoms progression.my next appt.is in October.it almost feels like a waste of time to go only to hear what I already know.with in the last 3 month or so I have been on oxygen , for&hellip;<span class="activity-read-more" id="activity-read-more-14950"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/how-do-you-feel/#post-21115" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE joined the group Research and Development</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13736/</link>
				<pubDate>Tue, 16 Jul 2019 15:52:45 -0500</pubDate>

				
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				<title>ARMY PETE updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13669/</link>
				<pubDate>Thu, 11 Jul 2019 16:43:33 -0500</pubDate>

				
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				<title>ARMY PETE and Jan Riche are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12963/</link>
				<pubDate>Mon, 10 Jun 2019 19:37:56 -0500</pubDate>

				
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				<title>ARMY PETE posted an update: seems like i all ways mess up when and where to [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12932/</link>
				<pubDate>Sun, 09 Jun 2019 16:20:18 -0500</pubDate>

									<content:encoded><![CDATA[<p>seems like i all ways mess up when and where to post comments and or updates or messages..i am much more comfortable wth direct messaging like e mail.maybe i am getting to old/confused to navigate here .i never know who reads or gets my comments .lol. just gone stay on the sidelines for a while .</p>
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				<title>ARMY PETE posted an update: @kmoel327     i am allways curious as to how difficult it [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12930/</link>
				<pubDate>Sun, 09 Jun 2019 15:49:33 -0500</pubDate>

									<content:encoded><![CDATA[<p>@kmoel327     i am allways curious as to how difficult it is to survive past that magical 2-3 year prediction of survivebility.i was diagnosed 3/2017 </p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11775/#acomment-12262</link>
				<pubDate>Mon, 20 May 2019 18:39:53 -0500</pubDate>

									<content:encoded><![CDATA[<p>hello again.i am wondering about your doctor.stay away from kids?????what if you had kids ,does he want to rid of them? i ave a cat and i am ok i .get a litle out of breath when i clean her litter box.i also cough less at night.takes a few minutes to adjust to laying down ,cough more then for a fea min.<br />
good luck<br />
peter</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/jeannie-finley/" data-bb-hp-profile="3168" rel="nofollow">Jeannie</a> became a registered member					]]></content:encoded>
				
				
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				<title>ARMY PETE replied to the discussion A condition with no clear diagnostic criteria - Idiopathic in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19102</link>
				<pubDate>Sun, 12 May 2019 16:27:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19102"><span class="bb-reply-lable">Reply to</span> A condition with no clear diagnostic criteria - Idiopathic</a></p> <div class="bb-content-inr-wrap"><p>hi charlene , we &#8220;spoke before&#8221;so far my diagnosis is ipf.honey coam slowly progressing.ofev made me sick after 7 weeks i quit it.scared to try the other drug.dont want to go through living in bathroom again.as of late , i am out of breath  making the bed or taking out the garbage ,even showering is difficult.i have ptsd .i am a vietnam vet&hellip;<span class="activity-read-more" id="activity-read-more-12123"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19102" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE posted an update: @johnl i had been on ofev for 7 weeks or so and  i [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11931/</link>
				<pubDate>Sun, 05 May 2019 16:48:30 -0500</pubDate>

									<content:encoded><![CDATA[<p>@johnl i had been on ofev for 7 weeks or so and  i started living in the bathroom.going shopping was frightfull&#8230;&#8230;..i quit.<br />
how ever , my dr. told me and this forum platform.agrees i think, that no two patients are alike and some people tolerate either of the two major&#8221;pills&#8221;. you just gone have to try.<br />
peter in palmetto</p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10582/#acomment-11923</link>
				<pubDate>Sat, 04 May 2019 14:57:00 -0500</pubDate>

									<content:encoded><![CDATA[<p>I am 71 and  I am not taking a risk with concidering a transfer.way too many requirements  .besides , I would rather have a younger person get a lung.also ihate waiting and die before ,if at all,they have lung available.but I am content and LIVE for now.im not a pessimist ,just a realist.its all good (sort 0f lol)</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/crysshay/" data-bb-hp-profile="3032" rel="nofollow">Crystal M</a> became a registered member					]]></content:encoded>
				
				
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				<title>ARMY PETE and Marianne are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11902/</link>
				<pubDate>Fri, 03 May 2019 18:30:20 -0500</pubDate>

				
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				<title>ARMY PETE posted an update: @betty-edwards my doc. had me on ofev and i quit after [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11388/</link>
				<pubDate>Tue, 16 Apr 2019 23:53:03 -0500</pubDate>

									<content:encoded><![CDATA[<p>@betty-edwards my doc. had me on ofev and i quit after 2 month or so.we had a good discussion last week and i came away with the fact that those two meds. work for some and not for others.if you can stomache either its worth a try .i for one gone do with out.most people will have some side effects ..betty , you are a lucky lady .its just not&hellip;<span class="activity-read-more" id="activity-read-more-11388"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/11388/" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE posted an update: @lowe i kind of envy you for the weight loss.i [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11278/</link>
				<pubDate>Mon, 15 Apr 2019 13:07:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>@lowe i kind of envy you for the weight loss.i stopped smoking and didnt loose a pound sinse</p>
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				<title>ARMY PETE posted an update: @lowe hello,just read about your (i think?) cbd [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11277/</link>
				<pubDate>Mon, 15 Apr 2019 13:00:21 -0500</pubDate>

									<content:encoded><![CDATA[<p>@lowe hello,just read about your (i think?) cbd use.been thinking about it.bought some for my wife but she wants something stronger&#8230;&#8230;..<br />
i got the water soluteble.</p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10908/#acomment-10948</link>
				<pubDate>Thu, 04 Apr 2019 18:14:36 -0500</pubDate>

									<content:encoded><![CDATA[<p>hey Charlene<br />
You make a great Diplomat.You should be an Ambassador.lol<br />
thanks<br />
Peter<br />
peter</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/peter/" data-bb-hp-profile="3039" rel="nofollow">ARMY PETE</a> posted an update I am curious.I was diagnosed about 2017 ,closer to 2018.had a triple bypass last may and lost track of time&#8230;&#8230;was put on ofev and i stopped after about 2 month dues to [&hellip;]					]]></content:encoded>
				
				
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10908/#acomment-10923</link>
				<pubDate>Wed, 03 Apr 2019 22:36:06 -0500</pubDate>

									<content:encoded><![CDATA[<p>hi charlene,I did try ofev for 7 weeks and it made me sick.Maybe these forums are just not for me.I am retired army and have a backgreound in lawenforcement.I cant deal with maybe or could &#8230;&#8230;I want facts and or proof.I am not a guineapig.We are giving a lot of false hopes .Maybe thats human nature but Nothing here is a sure shot.So , I&hellip;<span class="activity-read-more" id="activity-read-more-10923"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/10908/#acomment-10923" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/peter/" data-bb-hp-profile="3039" rel="nofollow">ARMY PETE</a> posted an update I am curious.I was diagnosed about 2017 ,closer to 2018.had a triple bypass last may and lost track of time&#8230;&#8230;was put on ofev and i stopped after about 2 month dues to [&hellip;]					]]></content:encoded>
				
				
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				<title>ARMY PETE posted an update: I am curious.I was diagnosed about 2017 ,closer to [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10908/</link>
				<pubDate>Wed, 03 Apr 2019 17:04:02 -0500</pubDate>

									<content:encoded><![CDATA[<p>I am curious.I was diagnosed about 2017 ,closer to 2018.had a triple bypass last may and lost track of time&#8230;&#8230;was put on ofev and i stopped after about 2 month dues to side affects.(bathroom,cramps ,feeling like crap.i read about members telling me they are doing well on either of the 2 major meds.By what measure are they doing well? What&hellip;<span class="activity-read-more" id="activity-read-more-10908"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/10908/" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE replied to the discussion Taking ofev a year! in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-18094</link>
				<pubDate>Tue, 02 Apr 2019 18:20:34 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-18094"><span class="bb-reply-lable">Reply to</span> Taking ofev a year!</a></p> <div class="bb-content-inr-wrap"><p>You are very kind.thank you.I am on prozac , trazedone and blood pressure drugs and a few more for what ailes me .The ofev just buriied me .lol</p>
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				<title>ARMY PETE replied to the discussion What You Enjoy... in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/what-you-enjoy/#post-18093</link>
				<pubDate>Tue, 02 Apr 2019 18:16:19 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-you-enjoy/#post-18093"><span class="bb-reply-lable">Reply to</span> What You Enjoy...</a></p> <div class="bb-content-inr-wrap"><p>WE ARE IN FLORIDA . MINUTES FROM THE BAY AND A FEW LONGER MINUTES TO THE GULF.DONT WORRY .WHEN YOU GO TO HAWAII YOU SEE WHAT I MEAN .LOL</p>
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				<title>ARMY PETE replied to the discussion Taking ofev a year! in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-18083</link>
				<pubDate>Tue, 02 Apr 2019 17:59:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-18083"><span class="bb-reply-lable">Reply to</span> Taking ofev a year!</a></p> <div class="bb-content-inr-wrap"><p>Being somewhat of a cynic,I see that the good germans ,and I am one , raked in over 20 billion dolars sinse 2017.Much of there studys are trials and the results are measured by the amounts of air you can exhale /inhale.I do that test every few month.It  does not show ay &#8220;real life&#8221; qualiy of life changes .At least in my case , living with ofev&hellip;<span class="activity-read-more" id="activity-read-more-10852"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-18083" rel="nofollow"> Read more</a></span></p>
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				<title>ARMY PETE replied to the discussion What You Enjoy... in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/what-you-enjoy/#post-18081</link>
				<pubDate>Tue, 02 Apr 2019 17:59:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-you-enjoy/#post-18081"><span class="bb-reply-lable">Reply to</span> What You Enjoy...</a></p> <div class="bb-content-inr-wrap"><p>I enjoy eating out at a waterfront restaurant with my wife.</p>
<p>Having coffee or wine on the patio</p>
<p>Watching movies on Netflix , amazon , hulu etc.alone.She does not like tv.</p>
<p>Driving our Cadillac</p>
<p>Going to my weekly Ptsd group</p>
<p>Do I dare say , being intimate with my wife?</p>
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				<title>ARMY PETE posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10623/#acomment-10661</link>
				<pubDate>Wed, 27 Mar 2019 19:01:02 -0500</pubDate>

									<content:encoded><![CDATA[<p>from what hear and have read,there is not much difference between the two meds. At this point my symptoms are manageable .I use simbicort ,which I dont think helps much.my air/pulse is mostly in the low 90s or upper 80s.it varies depending on my exertion&#8230;..I am somewhat of an odd duck. I am retired army and a nam. vet.ive  been through a lot&hellip;<span class="activity-read-more" id="activity-read-more-10661"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/10623/#acomment-10661" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/peter/" data-bb-hp-profile="3039" rel="nofollow">ARMY PETE</a> posted an update hello everyone.i think my profile gives some info about me. I dont want to come across as a negative  influence on any one but I have tried ofev for 2 month plus and I quit.at first [&hellip;]					]]></content:encoded>
				
				
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