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	<title>Pulmonary Fibrosis News Forums | Rob | Activity</title>
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				<title>Rob 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-35041</link>
				<pubDate>Tue, 16 May 2023 11:25:29 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-ipf-clinical-trials/#post-35041"><span class="bb-reply-lable">Reply to</span> All IPF Clinical Trials</a></p> <div class="bb-content-inr-wrap"><p>I’m being screened for a Phase 3 Fibroneer trial.   My doctor is also considering an inhaled Teprostinil trial.  Has anyone had any experience with either of these drugs?</p>
<p>Stay well.<br />
Rob</p>
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				<title>Rob replied to the discussion Congestion in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/congestion/#post-33204</link>
				<pubDate>Tue, 04 Oct 2022 14:08:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/congestion/#post-33204"><span class="bb-reply-lable">Reply to</span> Congestion</a></p> <div class="bb-content-inr-wrap"><p>Hi Theresa</p>
<p>I have IPF and take Esbriet.  Also Serrapeptase seems to help.  For nasal congestion I use Omnaris and also saline sprays.  For lung congestion I’ve been inhaling Mucomyst(Acetylcysteine) with a nebulizer for the last 3 years and it has helped greatly.<br />
Stay well.<br />
Rob</p>
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				<title>Rob replied to the discussion Starting Esbriet in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-32166</link>
				<pubDate>Sun, 22 May 2022 17:06:14 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/page/8/#post-32166"><span class="bb-reply-lable">Reply to</span> Starting Esbriet</a></p> <div class="bb-content-inr-wrap"><p>Hi Jim</p>
<p>IPF sucks. I was diagnosed 5 years ago(at 55) and have been on Esbriet for 4 years.  Very little lung decline&#x1f91e;.  Initially had some stomach upset and sun sensitivity lasted a bit longer but now manageable with sunscreen(mostly on hands) and a big hat when I golf.  No idea if Esbriet  has helped but will definitely will continue taking&hellip;<span class="activity-read-more" id="activity-read-more-33534"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-32166" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Supplements in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/supplements/#post-31855</link>
				<pubDate>Thu, 28 Apr 2022 20:43:25 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplements/#post-31855"><span class="bb-reply-lable">Reply to</span> Supplements</a></p> <div class="bb-content-inr-wrap"><p>Has anyone had experience taking quercitin? Supposed to help immune support, respiratory health and now many people have started taking it that have covid.<br />
Stay well.<br />
Rob</p>
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				<title>Rob replied to the discussion Vaccinated PF people and COVID 19 in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-30077</link>
				<pubDate>Tue, 28 Sep 2021 08:30:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-30077"><span class="bb-reply-lable">Reply to</span> Vaccinated PF people and COVID 19</a></p> <div class="bb-content-inr-wrap"><p>I got a third vaccine last week on the basis that Esbriet(and I assume Ofev as well) is an immunosuppressive therapy. My doctor signed my region’s(Halton,Ontario) vaccine referral form and I got the shot at a pharmacy the next day. Previously I had a  COVID spike antibody test to check my immunity from the vaccine(AstraZeneca in March and May.&hellip;<span class="activity-read-more" id="activity-read-more-29802"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/vaccinated-pf-people-and-covid-19/#post-30077" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Do others with IPF cough for 20 minutes every morning? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/#post-30074</link>
				<pubDate>Mon, 27 Sep 2021 23:16:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-others-with-ipf-cough-for-20-minutes-every-morning/page/2/#post-30074"><span class="bb-reply-lable">Reply to</span> Do others with IPF cough for 20 minutes every morning?</a></p> <div class="bb-content-inr-wrap"><p>I used to have a phlegmy cough every morning but it has virtually disappeared since I started inhaling Acetylcysteine solution by nebulizer twice a day for 10 minutes. That was on the advice of Dr David Schwartz in Denver who is a top IPF researcher. Acetylcysteine may be called Mucomyst in the US.</p>
<p>Stay well.<br />
Rob</p>
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				<title>Rob replied to the discussion Getting the Vaccine in Ontario in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-30018</link>
				<pubDate>Thu, 23 Sep 2021 18:27:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-30018"><span class="bb-reply-lable">Reply to</span> Getting the Vaccine in Ontario</a></p> <div class="bb-content-inr-wrap"><p>Just letting you know that if you are on Esbriet(and I assume Ofev as well) you would qualify for the 3rd vaccine dose on the basis that it is an immunosuppressive therapy. Your doctor needs to fill out and sign your region’s vaccine referral form and then you can book the appointment.  I called Shopppers and got my shot the next day.<br />
Be safe</p>
<p>Rob</p>
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				<title>Rob replied to the discussion Starting Esbriet in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-29555</link>
				<pubDate>Mon, 16 Aug 2021 14:06:31 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/page/8/#post-29555"><span class="bb-reply-lable">Reply to</span> Starting Esbriet</a></p> <div class="bb-content-inr-wrap"><p>I’ve been taking Esbriet for 3 years. About a year after being diagnosed with IPF. My pulmonologist started early because I had other immediate family members with IPF. Some early stomach issues and sun rashes that have subsided and still seem to have trouble sleeping. Little drop in lung function&#x1f91e;.</p>
<p>I was recently changed to generic&hellip;<span class="activity-read-more" id="activity-read-more-28978"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-esbriet/#post-29555" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Itchy Skin with Esbriet in the forum Esbriet (Pirfenidone)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/itchy-skin-with-esbriet/#post-29554</link>
				<pubDate>Mon, 16 Aug 2021 13:51:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/itchy-skin-with-esbriet/#post-29554"><span class="bb-reply-lable">Reply to</span> Itchy Skin with Esbriet</a></p> <div class="bb-content-inr-wrap"><p>I had some itchy skin and rashes(from the sun) when first taking Esbriet but they definitely diminished over time. I still have a sunscreen stick to rub on the back of my hands when driving or golfing.</p>
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				<title>Rob replied to the discussion Tyvaso for IPF in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28207</link>
				<pubDate>Sat, 01 May 2021 10:16:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28207"><span class="bb-reply-lable">Reply to</span> Tyvaso for IPF</a></p> <div class="bb-content-inr-wrap"><p>Dr David Schwartz at University of Colorado Medicine.</p>
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				<title>Rob replied to the discussion Tyvaso for IPF in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28203</link>
				<pubDate>Fri, 30 Apr 2021 20:14:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28203"><span class="bb-reply-lable">Reply to</span> Tyvaso for IPF</a></p> <div class="bb-content-inr-wrap"><p>I’m not in a trial but Dr Schwartz has a group in Denver inhaling Acetylcysteine(NAC) and got my pulmonologist in Canada on board. I’ve been inhaling 8ml by nebulizer for 10 minutes twice a day for 2 years. My lung congestion is greatly improved and if that is an issue for you I would recommend it.</p>
<p>Stay well</p>
<p>Rob</p>
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				<title>Rob replied to the discussion Tyvaso for IPF in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28197</link>
				<pubDate>Thu, 29 Apr 2021 21:07:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tyvaso-for-ipf/#post-28197"><span class="bb-reply-lable">Reply to</span> Tyvaso for IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene</p>
<p>No Tyvasco experience but I inhale liquid Acetylcysteine twice a day and take Esbriet. Noticeably less mucous and relatively stable.  &#x1f91e;Recommended to me by Dr David Schwartz in Denver who is a top IPF expert.<br />
Be well</p>
<p>Rob</p>
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				<title>Rob replied to the discussion Getting the Vaccine in Ontario in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28079</link>
				<pubDate>Thu, 15 Apr 2021 00:55:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28079"><span class="bb-reply-lable">Reply to</span> Getting the Vaccine in Ontario</a></p> <div class="bb-content-inr-wrap"><p>Thanks for the replies. Looks like we got an appointment for Friday.  &#x1f91e;</p>
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				<title>Rob replied to the discussion Getting the Vaccine in Ontario in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28040</link>
				<pubDate>Tue, 13 Apr 2021 18:11:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28040"><span class="bb-reply-lable">Reply to</span> Getting the Vaccine in Ontario</a></p> <div class="bb-content-inr-wrap"><p>Thanks John.  Organ transplant is on the list and I’m just worried the doctor’s letter stating IPF is highest risk won’t get be enough.</p>
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				<title>Rob replied to the discussion Getting the Vaccine in Ontario in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28038</link>
				<pubDate>Tue, 13 Apr 2021 15:03:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28038"><span class="bb-reply-lable">Reply to</span> Getting the Vaccine in Ontario</a></p> <div class="bb-content-inr-wrap"><p>I have IPF and have spent the last year at home. I just received my first AstraZeneca shot.  In the Ontario guidelines it says that people in the highest risk category and a caregiver can qualify for a vaccine in some areas. Of course IPF isn’t on the list but I have a doctor’s letter stating I’m at highest risk and my caregiver has a&hellip;<span class="activity-read-more" id="activity-read-more-26635"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/getting-the-vaccine-in-ontario/#post-28038" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Trying to Win the Battle Against Allergy Season in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/trying-to-win-the-battle-against-allergy-season/#post-24936</link>
				<pubDate>Sun, 12 Jul 2020 17:40:06 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/trying-to-win-the-battle-against-allergy-season/#post-24936"><span class="bb-reply-lable">Reply to</span> Trying to Win the Battle Against Allergy Season</a></p> <div class="bb-content-inr-wrap"><p>Agreed my nasal congestion is especially bad this year.  Spraying up my nose with full stream saline spray(I use Hydrasense) helps me a lot.</p>
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				<title>Rob replied to the discussion Book Club in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24669</link>
				<pubDate>Sat, 20 Jun 2020 00:48:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/page/2/#post-24669"><span class="bb-reply-lable">Reply to</span> Book Club</a></p> <div class="bb-content-inr-wrap"><p>Thanks to great support from all readers my wife’s book, The Jane Austen Society, has been at the top of the Toronto Star and Globe &amp; Mail’s Canadian bestseller list for the last 2 weeks and #7 on the LA Times hardcover bestseller list. We’ve been able to support the Firestone Institute for Respiratory Health’s COVID Response Fund as a&hellip;<span class="activity-read-more" id="activity-read-more-20699"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24669" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Book Club in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24493</link>
				<pubDate>Tue, 26 May 2020 18:24:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24493"><span class="bb-reply-lable">Reply to</span> Book Club</a></p> <div class="bb-content-inr-wrap"><p>P.S.</p>
<p>A portions of sales from the book are being donated to the Firestone Institute for Respiratory Health in Hamilton.</p>
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				<title>Rob replied to the discussion Book Club in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24492</link>
				<pubDate>Tue, 26 May 2020 18:06:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24492"><span class="bb-reply-lable">Reply to</span> Book Club</a></p> <div class="bb-content-inr-wrap"><p>My wife and I opened a small bookstore in late 2015. Four months later I was diagnosed with IPF so at the end of 2016 we shut down the store to focus on bucket list trips and my health. After our Tuscany and my golf trip she went to visit Jane Austen’s(her fave author) home in Chawton, UK and that trip became the basis of her first published&hellip;<span class="activity-read-more" id="activity-read-more-20293"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-24492" rel="nofollow"> Read more</a></span></p>
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				<title>Rob posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19409/#acomment-19741</link>
				<pubDate>Sun, 26 Apr 2020 15:37:14 -0500</pubDate>

									<content:encoded><![CDATA[<p>Have you looked at genetic testing.  My family is lousy with IPF as well and the genetic test gave me some info.  </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/jarr/" data-bb-hp-profile="5221" rel="nofollow">Jerry</a> posted an update Hello, all just wanted to give you my history i lost my mother to pulmonary fibrosis in 2001 i have since lost 3 brothers because of this terrible disease one in 2013  he was 57 one in [&hellip;]					]]></content:encoded>
				
				
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				<title>Rob replied to the discussion Boosting the immune system in the forum Healthy Recipe Sharing</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/boosting-the-immune-system/#post-22512</link>
				<pubDate>Wed, 15 Jan 2020 14:10:03 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/boosting-the-immune-system/#post-22512"><span class="bb-reply-lable">Reply to</span> Boosting the immune system</a></p> <div class="bb-content-inr-wrap"><p>I take Zinc, Vit C, Vit D and Oregano Oil daily for immune boosting.  I wear a device called an Airtamer(bought on Amazon)  whenever I’m in public near other people.  It’s supposed to repel germs and I believe it works.  I always have an individually wrapped medical mask with me if I’m in a train, theatre&#8230;  I’ll put it on if people near me&hellip;<span class="activity-read-more" id="activity-read-more-17207"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/boosting-the-immune-system/#post-22512" rel="nofollow"> Read more</a></span></p>
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				<title>Rob replied to the discussion Supplements in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/supplements/#post-20557</link>
				<pubDate>Tue, 30 Jul 2019 13:29:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplements/#post-20557"><span class="bb-reply-lable">Reply to</span> Supplements</a></p> <div class="bb-content-inr-wrap"><p>Hello Ruth</p>
<p>My mother had IPF and she believed NAC helped her.  I also have IPF and was told by a top researcher(Dr David Schwartz- just got a $10 million IPF research grant)that NAC in pill form shown little effect but recommended I inhale the liquid form(Acetycysteine or Mucomyst) by nebulizer.  I had a terrible persistent phlegmy cough that&hellip;<span class="activity-read-more" id="activity-read-more-14076"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/supplements/#post-20557" rel="nofollow"> Read more</a></span></p>
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				<title>Rob posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12710/#acomment-12719</link>
				<pubDate>Sun, 02 Jun 2019 12:24:40 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hello Marianne<br />
My coughing problem was definitely phlegm related and  the mucomyst treatment has helped significantly. Not sure it would help with  dry cough. Also found taking Serrapeptase May help.<br />
Be well.<br />
Rob</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/marianne/" data-bb-hp-profile="3010" rel="nofollow">Marianne</a> posted an update <a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/obleek/' rel="nofollow">@obleek</a> &#8211; Rob
Do you think the treatment you use for your cough would help with a dry chronic cough.  It has been worse lately but I figure it might be due to the fact that I am using [&hellip;]					]]></content:encoded>
				
				
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				<title>Rob replied to the discussion Taking Precautions When Traveling by Air in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/19164/#post-19208</link>
				<pubDate>Sat, 18 May 2019 22:43:28 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/19164/#post-19208"><span class="bb-reply-lable">Reply to</span> Taking Precautions When Traveling by Air</a></p> <div class="bb-content-inr-wrap"><p>All good precautions.</p>
<p>We also turn the air vent on high.</p>
<p>I wear a device called an Airtamer A310(available on Amazon) when I’m on a plane , train, in a theatre or any crowded place.  I know people who fly frequently that swear by  it but who knows.</p>
<p>Stay well</p>
<p>Rob</p>
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				<title>Rob replied to the discussion Breathing Treatments in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-treatments/#post-18928</link>
				<pubDate>Sun, 05 May 2019 12:45:58 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-treatments/#post-18928"><span class="bb-reply-lable">Reply to</span> Breathing Treatments</a></p> <div class="bb-content-inr-wrap"><p>Thanks David ( @davidaswain ).  I’m currently taking 240,000 but may try to bump up.  Do you always take it on an empty stomach?</p>
<p>Rob</p>
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				<title>Rob replied to the discussion Breathing Treatments in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-treatments/#post-18907</link>
				<pubDate>Fri, 03 May 2019 13:49:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathing-treatments/#post-18907"><span class="bb-reply-lable">Reply to</span> Breathing Treatments</a></p> <div class="bb-content-inr-wrap"><p>I am taking Esbriet for IPF but had developed frequent and painful sinus congestion recently.  I started taking Serrapeptase(along with saline spray)to help that problem but I do believe my breathing has improved as well.  I’m normally a skeptic about supplements but would like to hear other IPF patients response to Serrapeptase.   Rob</p>
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				<title>Rob posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10775/#acomment-11875</link>
				<pubDate>Thu, 02 May 2019 15:11:00 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thanks Mark. That got more Google and social media response outside of PF News than we thought.  Will look at it again later. Rob</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/obleek/" data-bb-hp-profile="3058" rel="nofollow">Rob</a> became a registered member					]]></content:encoded>
				
				
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				<title>Rob posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10775/#acomment-11867</link>
				<pubDate>Thu, 02 May 2019 11:28:34 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hello Mark<br />
Is there any way to delete my Book Club post. </p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/obleek/" data-bb-hp-profile="3058" rel="nofollow">Rob</a> became a registered member					]]></content:encoded>
				
				
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				<title>Rob updated their profile</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11591/</link>
				<pubDate>Mon, 22 Apr 2019 13:46:39 -0500</pubDate>

				
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				<title>Rob replied to the discussion IPF patient wonders if current symptoms are IPF related or not in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-patient-wonders-if-current-symptoms-are-ipf-related-or-not/#post-18686</link>
				<pubDate>Mon, 22 Apr 2019 13:37:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-patient-wonders-if-current-symptoms-are-ipf-related-or-not/#post-18686"><span class="bb-reply-lable">Reply to</span> IPF patient wonders if current symptoms are IPF related or not</a></p> <div class="bb-content-inr-wrap"><p>Hello Merle ( @sandford ),</p>
<p>I am 57 diagnosed with IPF 2 years ago and am on Esbriet. I constantly suffered with a phlegmy cough but a year ago started inhaling Acetylcysteine solution(Mucomyst) 10ml twice daily by nebulizer and now cough rarely and feel much better.</p>
<p>Rob</p>
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				<title>Rob changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11072/</link>
				<pubDate>Wed, 10 Apr 2019 15:42:55 -0500</pubDate>

				
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				<title>Rob changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11068/</link>
				<pubDate>Wed, 10 Apr 2019 15:33:57 -0500</pubDate>

				
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				<title>Rob changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11067/</link>
				<pubDate>Wed, 10 Apr 2019 15:32:59 -0500</pubDate>

				
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				<title>Rob changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11059/</link>
				<pubDate>Wed, 10 Apr 2019 12:16:38 -0500</pubDate>

				
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				<title>Rob posted an update: Hello IPF Forum
I’m new here and just wanted to share a [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10963/</link>
				<pubDate>Fri, 05 Apr 2019 15:21:12 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hello IPF Forum<br />
I’m new here and just wanted to share a treatment that has significantly reduced my coughing and lung congestion.<br />
I inhale 10 ml of Acetylcysteine solution(Mucomyst in the US) twice per day using a nebulizer.  Since starting this treatment my significant coughing has almost completely disappeared.  This was recommended by Dr&hellip;<span class="activity-read-more" id="activity-read-more-10963"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/10963/" rel="nofollow"> Read more</a></span></p>
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				<title>Rob became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10775/</link>
				<pubDate>Sun, 31 Mar 2019 11:25:20 -0500</pubDate>

				
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