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	<title>Pulmonary Fibrosis News Forums | Bill Mattila | Activity</title>
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				<title>Bill Mattila replied to the discussion IPF mucus cough in the forum PF Communities</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38759</link>
				<pubDate>Fri, 22 Aug 2025 19:46:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-mucus-cough/#post-38759"><span class="bb-reply-lable">Reply to</span> IPF mucus cough</a></p> <div class="bb-content-inr-wrap"><p>Make sure that it’s not an attack of the lungs. It’s hard to tell. That’s where the predisone steroids <span>helps.musinex me too.</span></p>
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				<title>Bill Mattila posted an update: Lots of mucus and thick and sticky. What doothers take or [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/45326/</link>
				<pubDate>Sat, 21 Jun 2025 01:22:15 -0500</pubDate>

									<content:encoded><![CDATA[<p>Lots of mucus and thick and sticky. What doothers take or do to rid of it??</p>
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				<title>Bill Mattila replied to the discussion Managing oxygen tubing hacks in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/managing-oxygen-tubing-hacks/#post-38468</link>
				<pubDate>Wed, 04 Jun 2025 19:12:20 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/managing-oxygen-tubing-hacks/#post-38468"><span class="bb-reply-lable">Reply to</span> Managing oxygen tubing hacks</a></p> <div class="bb-content-inr-wrap"><p>Med line soft cannula works for me good luck 4ft.</p>
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				<title>Bill Mattila posted an update: Not too bad. Ialmost died last August. Had a [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/44183/</link>
				<pubDate>Tue, 25 Feb 2025 21:53:27 -0600</pubDate>

									<content:encoded><![CDATA[<p>Not too bad. Ialmost died last August. Had a UTI.and theygave me wrongmeds.I really reacted. Doc didn’t readmychart. Death doesn’t feel good.</p>
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				<title>Bill Mattila: @Charlene Marshall Hi from Michigan im wstill here [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/43340/</link>
				<pubDate>Fri, 01 Nov 2024 00:31:01 -0500</pubDate>

									<content:encoded><![CDATA[<p><a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/charlene1948/' rel="nofollow">@Charlene</a> Marshall </p>
<p>Hi from Michigan im wstill here breathing yet almost died in August from uti and reactions from meds. Will be 82 this mo so let her keep tickling </p>
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				<title>Bill Mattila replied to the discussion Mental health and living with PF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/mental-health-and-living-with-pf/#post-37573</link>
				<pubDate>Thu, 31 Oct 2024 23:32:10 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/mental-health-and-living-with-pf/#post-37573"><span class="bb-reply-lable">Reply to</span> Mental health and living with PF</a></p> <div class="bb-content-inr-wrap"><p>We come and we go. The same for all are equal. Now with lives lived we got in to bad habits. I quit </p>
<p>Them all. But to look back I can’t change a thing and wait for my higher power good luck and god</p>
<p>Speed.</p>
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				<title>Bill Mattila posted an update: Am on oxygen most of time except while sitting. Wow I take [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/39546/</link>
				<pubDate>Tue, 18 Jul 2023 19:41:33 -0500</pubDate>

									<content:encoded><![CDATA[<p>Am on oxygen most of time except while sitting. Wow I take a stroll once in a while. Portable oxygen machines don’t keep up. Can do most things except I have little strength left. At 80 I should of listened to Pa 20 yrs ago. But I’m not crazy YET.  Am taking days @t a time.</p>
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				<title>Bill Mattila replied to the discussion Does anyone get relief from breathlessness in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/does-anyone-get-relief-from-breathlessness/#post-35043</link>
				<pubDate>Wed, 17 May 2023 02:23:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/does-anyone-get-relief-from-breathlessness/#post-35043"><span class="bb-reply-lable">Reply to</span> Does anyone get relief from breathlessness</a></p> <div class="bb-content-inr-wrap"><p>Is important that you make sure that the exacerbation is stopped.<br />
It can go on and on as much as 6 mo.As that was I had read about<br />
This disease. Go hospital if you have to. That what I read about this. Good luck WJM</p>
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				<title>Bill Mattila 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-34602</link>
				<pubDate>Sun, 12 Mar 2023 20:48:31 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/using-supplemental-oxygen/#post-34602"><span class="bb-reply-lable">Reply to</span> Using supplemental oxygen</a></p> <div class="bb-content-inr-wrap"><p>It helped me to carry the portable isn’t hard. If you want to breathe what’s the deal is. I had to talk myself into it. It’s<br />
Crazy your life in a machine. Think about it you need air right.</p>
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				<title>Bill Mattila 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-34529</link>
				<pubDate>Thu, 02 Mar 2023 23:48:05 -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-34529"><span class="bb-reply-lable">Reply to</span> Oxygen Delivery System when needs go up</a></p> <div class="bb-content-inr-wrap"><p>I am replying to my oxygen needs going up. You need to keep your needs even not letting your oxygen levels decline. I have read there is three levels in your body that need a certain level to maintain your body. Organs skin and whole body need proper oxidation.  I hated to wear the cannala. But how can you live with low levels of oxygen ,cause&hellip;<span class="activity-read-more" id="activity-read-more-37693"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-delivery-system-when-needs-go-up/#post-34529" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila posted an update: Short of b all time now machine’s do my ox2…. 2 be [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/35270/</link>
				<pubDate>Thu, 29 Sep 2022 21:29:25 -0500</pubDate>

									<content:encoded><![CDATA[<p>Short of b all time now machine’s do my ox2…. 2 be continued I hope&#x1f440;</p>
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				<title>Bill Mattila replied to the discussion Why the Word &#039;Rest&#039; Triggers Me in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/why-the-word-rest-triggers-me/#post-33189</link>
				<pubDate>Thu, 29 Sep 2022 21:24:36 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/why-the-word-rest-triggers-me/#post-33189"><span class="bb-reply-lable">Reply to</span> Why the Word 'Rest' Triggers Me</a></p> <div class="bb-content-inr-wrap"><p><strong>This is all true, but everyone is defensive about their Disability to move like they used too. You have to accept the reality of it&#x1f440;. I have to think about all the rest of my problems Catheter and all no breathe. I have had problems for 15+ years and still alive and almost 80. So I like to Whine about the Doctor that did a shxxxxd job on&hellip;</strong><span class="activity-read-more" id="activity-read-more-35269"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/why-the-word-rest-triggers-me/#post-33189" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila replied to the discussion OFEV and Surgery in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-surgery/#post-32505</link>
				<pubDate>Fri, 01 Jul 2022 19:51:54 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ofev-and-surgery/#post-32505"><span class="bb-reply-lable">Reply to</span> OFEV and Surgery</a></p> <div class="bb-content-inr-wrap"><p>OFEV does cause bleeding ,so I stopped a number of times for procedures and too many side effects. Don’t fear a short stoppage.</p>
<p>Also see Doctor and and ask him or her.</p>
<p>&nbsp;</p>
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				<title>Bill Mattila posted an update: I haven’t been commenting on my ipf cause it is worsting. [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/34134/</link>
				<pubDate>Fri, 01 Jul 2022 19:42:18 -0500</pubDate>

									<content:encoded><![CDATA[<p>I haven’t been commenting on my ipf cause it is worsting. Time to use my oxygen more.<br />
I have other issues that I’m dealing with too. Like a subcatheter and bleeding from my line and going to get it changed. Not a good feeling. But the right MA does a good job.<br />
Shorter breath is hard to accept, but part of disease. So I posted some news.wjm</p>
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				<title>Bill Mattila posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/23739/#acomment-30233</link>
				<pubDate>Fri, 29 Oct 2021 17:19:41 -0500</pubDate>

									<content:encoded><![CDATA[<p>Welcome to the forum Hans.</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/hansfink2007/" data-bb-hp-profile="8383" rel="nofollow">Hans M. Fink</a> became a registered member					]]></content:encoded>
				
				
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				<title>Bill Mattila posted an update: Well I have a new attachment in my life as a doctors [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/30232/</link>
				<pubDate>Fri, 29 Oct 2021 17:06:38 -0500</pubDate>

									<content:encoded><![CDATA[<p>Well I have a new attachment in my life as a doctors bone head misQ on a procedure has given me a A life time of misery, called a catheter direct to my bladder;( with all the<br />
rest of my issues that’s all I needed. Nothing new as I spend attached to a line. That I have stretched TOOFAR now have to heal it up. I have the same issues that the&hellip;<span class="activity-read-more" id="activity-read-more-30232"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/30232/" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila and Libby are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/26609/</link>
				<pubDate>Sat, 10 Apr 2021 02:18:07 -0500</pubDate>

				
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				<title>Bill Mattila replied to the discussion Progression of IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28005</link>
				<pubDate>Thu, 08 Apr 2021 20:39:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28005"><span class="bb-reply-lable">Reply to</span> Progression of IPF</a></p> <div class="bb-content-inr-wrap"><p>Bernard I’m sorry that they do that. I guess money is more important, we get Charged 11 thousand US dollars a month. My insurance is good so I only pay a low copay. I too suffer from side effects that most people do even the gas and bloating. I have had exrabations a few times it isn’t nice. I’ve had the IPF for at least 15yrs or so and I&hellip;<span class="activity-read-more" id="activity-read-more-26583"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/progression-of-ipf/#post-28005" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila replied to the discussion Phlegm in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26926</link>
				<pubDate>Tue, 19 Jan 2021 23:33:04 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26926"><span class="bb-reply-lable">Reply to</span> Phlegm</a></p> <div class="bb-content-inr-wrap"><p>I have fits with my mucus. I do Mucinex  everyday at least the maximum (2400mg a day) so it’s a bear to regulate. I also have a vibrating vest that works. But you have to do it at least 1hr a day or more. I have had IPF for a long time, but didn’t do anything about it. I didn’t know I had it. So I went to lung man and got the news but now I’m&hellip;<span class="activity-read-more" id="activity-read-more-25016"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/phlegm/#post-26926" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila replied to the discussion Oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-4/#post-26713</link>
				<pubDate>Thu, 31 Dec 2020 23:36:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-4/#post-26713"><span class="bb-reply-lable">Reply to</span> Oxygen</a></p> <div class="bb-content-inr-wrap"><p>I had to kinda of remind my Doctor that I was short of O2 on working. He wrote a 2liter constant flow so now I haul a 22lb machine around with me. They said that the small machines won’t work on constant flow and where only on demand which was a lie.</p>
<p>They will do that and up to 5liter. Now I’m stuck with boat anchor.<br />
Now should I spend 2000$&hellip;<span class="activity-read-more" id="activity-read-more-24626"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-4/#post-26713" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila replied to the discussion Side effects of OFEV in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/side-effects-of-ofev/#post-24794</link>
				<pubDate>Wed, 01 Jul 2020 01:54:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/side-effects-of-ofev/page/2/#post-24794"><span class="bb-reply-lable">Reply to</span> Side effects of OFEV</a></p> <div class="bb-content-inr-wrap"><p>Dear suffering OFEV users. I have been on OFEV for 2.5 years. First year no side effects.</p>
<p>Now I have them all right down to the rash. Elevated alt and my thyroid test is messed up a little. I take 15omg twice a day I have diarrhea and sickness too. I skip a dose to reset my tract. Will be calling Doctor about my rash and other meds cause&hellip;<span class="activity-read-more" id="activity-read-more-20918"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/side-effects-of-ofev/#post-24794" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila posted an update: Also Charlene THANK YOU for hosting this forum. You are [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17817/</link>
				<pubDate>Thu, 06 Feb 2020 21:25:13 -0600</pubDate>

									<content:encoded><![CDATA[<p>Also Charlene THANK YOU for hosting this forum. You are a god sent angel.</p>
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				<title>Bill Mattila posted an update: Got use to cpap machine yeah ! Also read I too [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17816/</link>
				<pubDate>Thu, 06 Feb 2020 21:21:34 -0600</pubDate>

									<content:encoded><![CDATA[<p>Got use to cpap machine yeah ! Also read I too take simvestation . Have taken statins for many years now. Who knows<br />
What helps anymore? Take my meds and feel good for what is wrong and not worry about everything&#8230;..</p>
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				<title>Bill Mattila posted an update: My Ofev has slowed my IPF way down. But now Cpap machine [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/17441/</link>
				<pubDate>Fri, 24 Jan 2020 01:12:04 -0600</pubDate>

									<content:encoded><![CDATA[<p>My Ofev has slowed my IPF way down. But now Cpap machine is helping me breathe So I do it every night. I hate it but so welcome to disease. At least it has a good side effect.</p>
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				<title>Bill Mattila and A. Houghton are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12222/</link>
				<pubDate>Thu, 16 May 2019 20:26:35 -0500</pubDate>

				
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				<title>Bill Mattila posted an update: Running more out of breath. Going to doc. Next month.</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11546/</link>
				<pubDate>Sun, 21 Apr 2019 01:10:56 -0500</pubDate>

									<content:encoded><![CDATA[<p>Running more out of breath. Going to doc. Next month.</p>
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				<title>Bill Mattila and Mark Koziol are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10849/</link>
				<pubDate>Tue, 02 Apr 2019 17:54:49 -0500</pubDate>

				
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				<title>Bill Mattila posted an update: reply about the taking of OFEV  Seems that it gets [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10836/</link>
				<pubDate>Tue, 02 Apr 2019 12:59:39 -0500</pubDate>

									<content:encoded><![CDATA[<p>reply about the taking of OFEV  Seems that it gets your gastric moving from a hr after until next dose. I try to take it on a full meal. Not always the<br />
situation you will be in. Good luck everyone.</p>
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				<title>Bill Mattila posted an update: My taking Ofev is getting interesting. I now have more [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10817/</link>
				<pubDate>Mon, 01 Apr 2019 22:44:53 -0500</pubDate>

									<content:encoded><![CDATA[<p>My taking Ofev is getting interesting. I now have more side effects. Take Ofev with your meal. That’s my plan lots of food take at same time everyday. Gives me sore butt too. Sorry about that.the terminology.</p>
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				<title>Bill Mattila and Laura Bush are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9734/</link>
				<pubDate>Sat, 02 Mar 2019 23:00:54 -0600</pubDate>

				
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				<title>Bill Mattila posted an update: @charlene-marshall  You found a new job in LIFE. LOL [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9660/</link>
				<pubDate>Fri, 01 Mar 2019 14:42:41 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall  You found a new job in LIFE. LOL your hands are full. Did I tell you I have had this IPF for at least 15 yrs or more.</p>
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				<title>Bill Mattila posted an update: @charlene-marshall  Not much to maintain. change filter [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9659/</link>
				<pubDate>Fri, 01 Mar 2019 14:39:56 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall  Not much to maintain. change filter in compressor. And keep vest clean. You have to adjust the straps on occastion. Doctor recommends vibrating twice a day . One hour total. It comes with pre programmed. Push button and shake it.</p>
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				<title>Bill Mattila posted an update: @charlene-marshall  Glad you are back. I love the forums. [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9653/</link>
				<pubDate>Fri, 01 Mar 2019 13:03:43 -0600</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall  Glad you are back. I love the forums. I have trouble getting oked for my OFEV. every three months same jump through the HOOPS.</p>
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				<title>Bill Mattila: @raymond-c-king  yes Ray you probably can’t use the vest. [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9646/</link>
				<pubDate>Fri, 01 Mar 2019 02:17:53 -0600</pubDate>

									<content:encoded><![CDATA[<p><a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/raymond-c-king/' rel="nofollow">@raymond-c-king</a>  yes Ray you probably can’t use the vest. Cause it does vibrate stomach too. It was prescribed by the doctor. Try the mucinex. Don’t take too much. I used to live on it before I was diagnosed with the IPF. I take the cheap stuff. Just Kirkland from Amazon 400mg quick release.  One Ihave had the IPF for almost twenty yrs. two&hellip;<span class="activity-read-more" id="activity-read-more-9646"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/9646/" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila and Raymond C. King are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9607/</link>
				<pubDate>Thu, 28 Feb 2019 15:10:08 -0600</pubDate>

				
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				<title>Bill Mattila replied to the discussion Dealing with Phlegm. in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-phlegm/#post-17105</link>
				<pubDate>Tue, 26 Feb 2019 21:29:50 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-phlegm/page/2/#post-17105"><span class="bb-reply-lable">Reply to</span> Dealing with Phlegm.</a></p> <div class="bb-content-inr-wrap"><p>I handle my excess with a vibrating vest. And mucinex works for me. I mentioned to the lung man and he agreed but don’t take too long.</p>
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				<title>Bill Mattila posted an update: Has anyone tried mucinex for your excess mucus?? It [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9493/</link>
				<pubDate>Tue, 26 Feb 2019 21:25:07 -0600</pubDate>

									<content:encoded><![CDATA[<p>Has anyone tried mucinex for your excess mucus?? It works for me and frees my breathing up.</p>
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				<title>Bill Mattila 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-16730</link>
				<pubDate>Wed, 13 Feb 2019 18:48:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/#post-16730"><span class="bb-reply-lable">Reply to</span> Taking ofev a year!</a></p> <div class="bb-content-inr-wrap"><p><strong>Do not take Ofev with stool softeners. HA HA.</strong></p>
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				<title>Bill Mattila started the discussion Taking ofev a year! in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/</link>
				<pubDate>Tue, 22 Jan 2019 16:59:45 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/taking-ofev-a-year/">Taking ofev a year!</a></p> <div class="bb-content-inr-wrap"><p>After a year of OFEV It has slowed the progress of the fiberosis a lot. It now costs 109 thousand a year. 9100.00 a month.</p>
<p>Thank GOD that my insurance co pay is only 42$ a month.</p>
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				<title>Bill Mattila replied to the discussion Indigestion &#38; Acid Reflux in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/indigestion-acid-reflux/#post-16184</link>
				<pubDate>Tue, 22 Jan 2019 16:50:21 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/indigestion-acid-reflux/page/3/#post-16184"><span class="bb-reply-lable">Reply to</span> Indigestion &amp; Acid Reflux</a></p> <div class="bb-content-inr-wrap"><p>My acid reflux had a lot to do with my lung condition. Causing lots of inflamation.</p>
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				<title>Bill Mattila posted an update: Feeling good at times and so so at other times cant [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/8038/</link>
				<pubDate>Tue, 22 Jan 2019 16:47:33 -0600</pubDate>

									<content:encoded><![CDATA[<p>Feeling good at times and so so at other times cant exersize at a hard level.  Antibiotics are to be used only for infections.</p>
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				<title>Bill Mattila posted an update: Have been to doctor feeling so so at times and great [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7397/</link>
				<pubDate>Fri, 21 Dec 2018 21:53:03 -0600</pubDate>

									<content:encoded><![CDATA[<p>Have been to doctor feeling so so at times and great other times. Asked doctor about antibiotics and he prescribed a regement of a week of 3 times a day for week. I was keeping for reserve for sinus or lung infections. Is this wise?<br />
Also am excersizing at least bowling and walking. Could be worse. My saturation is good at rest and fair with&hellip;<span class="activity-read-more" id="activity-read-more-7397"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/7397/" rel="nofollow"> Read more</a></span></p>
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				<title>Bill Mattila posted an update: Hi just a quick update about all. Yes it hasn’t progressed [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/7027/</link>
				<pubDate>Fri, 30 Nov 2018 15:39:24 -0600</pubDate>

									<content:encoded><![CDATA[<p>Hi just a quick update about all. Yes it hasn’t progressed in a year. Yes short of breath on excersise. But breath deep and blow through mouth. It helps. Had a sinus infection, which doctor treated with 850mg amoxicillin twice a day for 7<br />
Days. Made my lungs feel sooo much better. Anyone experiencing this would I would like to know. Thanks Bill</p>
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				<title>Bill Mattila and Charlene are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5112/</link>
				<pubDate>Sun, 26 Aug 2018 14:06:15 -0500</pubDate>

				
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				<title>Bill Mattila posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5044/#acomment-5053</link>
				<pubDate>Fri, 24 Aug 2018 18:04:07 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you for the welcome! I want to say that inflammation has had a bearing on my condition. As the gurd I have had all my life has got in my lungs and didn’t help my condition. Added that I had smoked for 25yrs and worked in bad air for along time. Also a number of people that worked close by ended up with iPad.</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/bill-mattila/" rel="nofollow">Bill Mattila</a> became a registered member					]]></content:encoded>
				
				
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				<title>Bill Mattila posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5044/#acomment-5052</link>
				<pubDate>Fri, 24 Aug 2018 17:56:22 -0500</pubDate>

									<content:encoded><![CDATA[<p>Yes I have been floating around the forum. I have had IPF for many years. Not knowing or caring to go to another doctor. So I’m here in a declining stage wondering why I didn’t go. Regular attacks now happen, so have to be careful what I do.</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/bill-mattila/" rel="nofollow">Bill Mattila</a> became a registered member					]]></content:encoded>
				
				
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				<title>Bill Mattila updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5050/</link>
				<pubDate>Fri, 24 Aug 2018 17:47:07 -0500</pubDate>

				
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				<title>Bill Mattila became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/5044/</link>
				<pubDate>Fri, 24 Aug 2018 17:40:16 -0500</pubDate>

				
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