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	<title>Pulmonary Fibrosis News Forums | Miltont | Activity</title>
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				<title>Miltont replied to the discussion Eastern Medicine alternative in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/eastern-medicine-alternative/#post-23741</link>
				<pubDate>Sun, 29 Mar 2020 14:33:19 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/eastern-medicine-alternative/#post-23741"><span class="bb-reply-lable">Reply to</span> Eastern Medicine alternative</a></p> <div class="bb-content-inr-wrap"><p>Dr Don, are you happy to have a conservation with me about a proposed double blind trial for a non-medical treatment that I have been using to great effect? If so please email me at <a href="mailto:milton.toal@gmail.com" rel="nofollow">milton.toal@gmail.com</a>.</p>
<p>Cheers and thanks in anticipation</p>
<p>&nbsp;</p>
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				<title>Miltont 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-23740</link>
				<pubDate>Sun, 29 Mar 2020 08:51:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/side-effects-of-ofev/#post-23740"><span class="bb-reply-lable">Reply to</span> Side effects of OFEV</a></p> <div class="bb-content-inr-wrap"><p>Hi everyone. I am not on Ofev but reading all your stories reminds me that I keep a container of ginger gums in the glovebox of my boat for anyone who gets seasick and they work. Chewing one is isually enough. Try your supermarket or health food shop. Natural ginger also works but is a bit strong for a lot of palates.</p>
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				<title>Miltont replied to the discussion The Awkwardness of Wearing A Mask In Public in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-awkwardness-of-wearing-a-mask-in-public/#post-23612</link>
				<pubDate>Tue, 24 Mar 2020 14:19:52 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-awkwardness-of-wearing-a-mask-in-public/page/2/#post-23612"><span class="bb-reply-lable">Reply to</span> The Awkwardness of Wearing A Mask In Public</a></p> <div class="bb-content-inr-wrap"><p>I have a high degree of &#8220;not giving a damn &#8221; I guess but I am not the slightest bit self-conscious about wearing a mask. If I need to protect myself that is my business and no-one else&#8217;s. Be strong, people. You must care for yourself.</p>
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				<title>Miltont replied to the discussion Eastern Medicine alternative in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/eastern-medicine-alternative/#post-23562</link>
				<pubDate>Fri, 20 Mar 2020 12:06:15 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/eastern-medicine-alternative/#post-23562"><span class="bb-reply-lable">Reply to</span> Eastern Medicine alternative</a></p> <div class="bb-content-inr-wrap"><p>That eastern medicine sound appropriate for treating cystic fibrosis.</p>
<p>Richard, I had the lump in the throat and the soreness to breathe until my GP put me on a PPI (proton pump inhibitor) to suppress the manufacture of stomah acid. It worked. Ask your doctor if this could be your problem.</p>
<p>&nbsp;</p>
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				<title>Miltont replied to the discussion Sharing Your IPF Story: How Do You Feel About It? in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23561</link>
				<pubDate>Fri, 20 Mar 2020 11:46:03 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23561"><span class="bb-reply-lable">Reply to</span> Sharing Your IPF Story: How Do You Feel About It?</a></p> <div class="bb-content-inr-wrap"><p>I am a very pragmatic person. I face up to and handle reality very well. I don&#8217;t mind sharing. However, when I got the news and was told that at 79 I had an expectancy of 1 &#8211; 3 years without a transplant and I found that the oldest transplant approval was aged 72 I was deeply shocked.  My wife was in the same hospital having just had a&hellip;<span class="activity-read-more" id="activity-read-more-18907"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23561" rel="nofollow"> Read more</a></span></p>
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				<title>Miltont replied to the discussion An Interview With a Pulmonologist in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/an-interview-with-a-pulmonologist/#post-23516</link>
				<pubDate>Wed, 18 Mar 2020 06:02:54 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/an-interview-with-a-pulmonologist/#post-23516"><span class="bb-reply-lable">Reply to</span> An Interview With a Pulmonologist</a></p> <div class="bb-content-inr-wrap"><p>Well done, Mark. I woould like to add some explanation of the scarring problem and also an alert to a new drug to slow progress. I have been studying and treating scarring since 2005 with 100%. What happens and why exercise has to be treated cautiously is this. When the body sustains an injury, it takes some Collagen &#8211; the most abundant protein&hellip;<span class="activity-read-more" id="activity-read-more-18836"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/an-interview-with-a-pulmonologist/#post-23516" rel="nofollow"> Read more</a></span></p>
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				<title>Miltont joined the group Research and Development</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18834/</link>
				<pubDate>Wed, 18 Mar 2020 05:34:08 -0500</pubDate>

				
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				<title>Miltont replied to the discussion Back Muscle Shrinkage Tied to Poor IPF Outcomes, Study Finds in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/back-muscle-shrinkage-tied-to-poor-ipf-outcomes-study-finds/#post-23420</link>
				<pubDate>Sat, 14 Mar 2020 00:01:34 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/back-muscle-shrinkage-tied-to-poor-ipf-outcomes-study-finds/#post-23420"><span class="bb-reply-lable">Reply to</span> Back Muscle Shrinkage Tied to Poor IPF Outcomes, Study Finds</a></p> <div class="bb-content-inr-wrap"><p>&lt;p style=&#8221;text-align: left;&#8221;&gt;I have never heard of this before but I do have a constant fight with the psoas muscles in my back. These are the muscles over the kidneys and when sore, sometimes have sufferers complain of kidney pain. I would never have associated it with IPF but it makes sense, since the timing of IPF symptoms (pre diagnosis)&hellip;<span class="activity-read-more" id="activity-read-more-18715"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/back-muscle-shrinkage-tied-to-poor-ipf-outcomes-study-finds/#post-23420" rel="nofollow"> Read more</a></span></p>
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				<title>Miltont replied to the discussion Public Fears Surrounding COVID-19 in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23419</link>
				<pubDate>Fri, 13 Mar 2020 23:48:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23419"><span class="bb-reply-lable">Reply to</span> Public Fears Surrounding COVID-19</a></p> <div class="bb-content-inr-wrap"><p>My Wife and I have not changed our lives. My children and grandchildren keep urging us to stay indoors but that is not going to happen. I wore a P2 rated mask to screen out smoke during the recent bushfire crisis here in Victoria and NSW which was prudent but I don&#8217;t wear one now. I always practise good hygiene, washing my hand when I cone hom&hellip;<span class="activity-read-more" id="activity-read-more-18714"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/public-fears-surrounding-covid-19/#post-23419" rel="nofollow"> Read more</a></span></p>
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				<title>Miltont replied to the discussion Corona virus in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/corona-virus/#post-23417</link>
				<pubDate>Fri, 13 Mar 2020 23:33:42 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/corona-virus/page/2/#post-23417"><span class="bb-reply-lable">Reply to</span> Corona virus</a></p> <div class="bb-content-inr-wrap"><p>Thanks to Lorraine for forwarding the hints to help prevent infection. I was going to do the same but my access had crashed. The only thing else that I re all the original author saying wad that you touch your mouth or nose on average more than 90 times a day. As he wrote and as Charlene noticed, wearing blue latex gloves reminds you not to&hellip;<span class="activity-read-more" id="activity-read-more-18712"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/corona-virus/#post-23417" rel="nofollow"> Read more</a></span></p>
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				<title>Miltont became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18699/</link>
				<pubDate>Fri, 13 Mar 2020 00:51:54 -0500</pubDate>

				
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