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	<title>Pulmonary Fibrosis News Forums | sally williams | Activity</title>
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				<title>sally williams replied to the discussion Nerandomilast approved by the FDA in the forum Treatments and Science</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/nerandomilast-approved-by-the-fda/#post-38944</link>
				<pubDate>Tue, 14 Oct 2025 20:39:07 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nerandomilast-approved-by-the-fda/#post-38944"><span class="bb-reply-lable">Reply to</span> Nerandomilast approved by the FDA</a></p> <div class="bb-content-inr-wrap"><p>My pumonologist told me that the drug would be best for those who cannot tolerate either Esbriet or OFEV&#8230;the results are the same with the new drug.  I tolerate Edbriet well, I am relatively stable after 5 years, I will not be trying this new drug.</p>
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				<title>sally williams replied to the discussion Pirfenidone (Generic for Esbriet) CostPlus in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pirfenidone-generic-for-esbriet-costplus/#post-36348</link>
				<pubDate>Tue, 19 Dec 2023 21:44:04 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pirfenidone-generic-for-esbriet-costplus/#post-36348"><span class="bb-reply-lable">Reply to</span> Pirfenidone (Generic for Esbriet) CostPlus</a></p> <div class="bb-content-inr-wrap"><p>The $30.80 is for 30 pills so $92.40 for a month&#8230;still a much better price.</p>
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				<title>sally williams started the discussion Altitude and IPF in the forum Healthcare Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/altitude-and-ipf/</link>
				<pubDate>Sat, 23 Sep 2023 18:50:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/altitude-and-ipf/">Altitude and IPF</a></p> <div class="bb-content-inr-wrap"><p>I am 82 and living at 4000 ft elevation. Will moving  to a lower elevation make it easier to breathe?  I have been told that it will for a while but I will eventually acclimate&#8230;</p>
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				<title>sally williams replied to the discussion Did you get Study drug or Placebo? in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/did-you-get-study-drug-or-placebo/#post-35707</link>
				<pubDate>Wed, 23 Aug 2023 15:42:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/did-you-get-study-drug-or-placebo/#post-35707"><span class="bb-reply-lable">Reply to</span> Did you get Study drug or Placebo?</a></p> <div class="bb-content-inr-wrap"><p>Thank you Pete,  will talk to my doc.  I have been participating in trials since diagnosis, but the other trials didn’t pan out…keep up the fight.  We WILL win.</p>
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				<title>sally williams replied to the discussion Did you get Study drug or Placebo? in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/did-you-get-study-drug-or-placebo/#post-35700</link>
				<pubDate>Tue, 22 Aug 2023 21:37:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/did-you-get-study-drug-or-placebo/#post-35700"><span class="bb-reply-lable">Reply to</span> Did you get Study drug or Placebo?</a></p> <div class="bb-content-inr-wrap"><p>I too am on the Tyvaso trial and they have offered the open label upon completion (six more months). If the trial is not over at that time, should I take the extension if I don&#8217;t know if the drug was beneficial for IPF?</p>
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				<title>sally williams replied to the discussion All IPF Clinical Trials in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/all-ipf-clinical-trials/#post-35048</link>
				<pubDate>Tue, 16 May 2023 20:29:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-ipf-clinical-trials/#post-35048"><span class="bb-reply-lable">Reply to</span> All IPF Clinical Trials</a></p> <div class="bb-content-inr-wrap"><p>I am participating in the Trepostinil trial.  I am in week 10 of 1 year.  Pretty easy, inhailing the drug or placebo 4 times a day.  Not too many side effects, occasional headache, dizziness.  This is my second trial.  I believe that we need to do whatever we can to get rid of this dread disease.  I only participate in the ones that allow me to&hellip;<span class="activity-read-more" id="activity-read-more-38724"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-ipf-clinical-trials/#post-35048" rel="nofollow"> Read more</a></span></p>
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				<title>sally williams replied to the discussion Starting out with Esbriet in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-out-with-esbriet/#post-33923</link>
				<pubDate>Tue, 20 Dec 2022 20:29:30 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-out-with-esbriet/#post-33923"><span class="bb-reply-lable">Reply to</span> Starting out with Esbriet</a></p> <div class="bb-content-inr-wrap"><p>I have been on Esbriet for almost a year. I think the key is a really gradual increase in the number of pills per day…it took me over 2 months to get up to the full day dosage.  Good luck.</p>
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				<title>sally williams posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/35975/#acomment-36285</link>
				<pubDate>Tue, 29 Nov 2022 21:23:36 -0600</pubDate>

									<content:encoded><![CDATA[<p>Take the Esbriet even slower then recommended to give your body a chance to adjust…back off if you have to.  I took almost 2 months to get to 3 three times a day.</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/garryg/" data-bb-hp-profile="14642" rel="nofollow">Garry Garcia</a> became a registered member					]]></content:encoded>
				
				
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				<title>sally williams replied to the discussion Traveling long distances in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-long-distances/#post-31917</link>
				<pubDate>Wed, 04 May 2022 00:05:24 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-long-distances/#post-31917"><span class="bb-reply-lable">Reply to</span> Traveling long distances</a></p> <div class="bb-content-inr-wrap"><p>Allen, I believe that since you live at a fairly high elevation and a river cruise will be at sea level, you should be fine without supplemental oxygen.  I live at a slightly lower elevation and always feel fantastic at sea level.  I say don’t worry about the flight.  I fly fine without oxygen, although my longest flight has only been 4&hellip;<span class="activity-read-more" id="activity-read-more-33090"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/traveling-long-distances/#post-31917" rel="nofollow"> Read more</a></span></p>
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				<title>sally williams replied to the discussion Remembering if you took Medications in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/remembering-if-you-took-medications/#post-30329</link>
				<pubDate>Mon, 01 Nov 2021 20:53:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/remembering-if-you-took-medications/#post-30329"><span class="bb-reply-lable">Reply to</span> Remembering if you took Medications</a></p> <div class="bb-content-inr-wrap"><p>Count them out in the morning and place them in 3 small containers&#8230;I have 3 very small saucers that I use, easy to see right away if I need to take the next dosage</p>
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				<title>sally williams replied to the discussion N115 nasal spray in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/n115-nasal-spray/#post-30253</link>
				<pubDate>Thu, 21 Oct 2021 20:10:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/n115-nasal-spray/#post-30253"><span class="bb-reply-lable">Reply to</span> N115 nasal spray</a></p> <div class="bb-content-inr-wrap"><ol>
<li>In a Phase III Clinical Trial with patients with Pulmonary Fibrosis, there was a statistically and clinically significant improvement in all lung functions, compared to baseline, including an increase in FEV-1, SaO, FVC, FEV-1/FVC ratios (from 52% to 86%) and a reduction in coughing and fatigue.</li>
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<p>Very exciting results, I believe they are&hellip;<span class="activity-read-more" id="activity-read-more-30147"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/n115-nasal-spray/#post-30253" rel="nofollow"> Read more</a></span></p>
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				<title>sally williams replied to the discussion Tyvaso for IPF in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28204</link>
				<pubDate>Fri, 30 Apr 2021 20:35:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28204"><span class="bb-reply-lable">Reply to</span> Tyvaso for IPF</a></p> <div class="bb-content-inr-wrap"><p>Rob, is Dr Schwartz at National Jewish? I see a Michael D. Schwartz listed..same man?</p>
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				<title>sally williams replied to the discussion Leg muscle weakness side effect of OFEV in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/leg-muscle-weakness-side-effect-of-ofev/#post-28107</link>
				<pubDate>Tue, 20 Apr 2021 19:24:34 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/leg-muscle-weakness-side-effect-of-ofev/#post-28107"><span class="bb-reply-lable">Reply to</span> Leg muscle weakness side effect of OFEV</a></p> <div class="bb-content-inr-wrap"><p>I do not suffer from that, bu I do Pilates and maybe that stretching helps. Good luck, not walking isn’t good.</p>
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				<title>sally williams replied to the discussion New to IPF in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf/#post-28086</link>
				<pubDate>Thu, 15 Apr 2021 20:23:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-ipf/#post-28086"><span class="bb-reply-lable">Reply to</span> New to IPF</a></p> <div class="bb-content-inr-wrap"><p>To Steven and Christie, Anecdotal information.  My brother had a kidney transplant due to a hereditary disease.  (Polycystic kidney). After 12 years there has been no sign of cysts</p>
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				<title>sally williams became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/25959/</link>
				<pubDate>Tue, 09 Mar 2021 02:18:03 -0600</pubDate>

				
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