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	<title>Pulmonary Fibrosis News Forums | Heather | Activity</title>
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				<title>Heather replied to the discussion The Harsh Realities of Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-33767</link>
				<pubDate>Fri, 02 Dec 2022 17:25:17 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/page/2/#post-33767"><span class="bb-reply-lable">Reply to</span> The Harsh Realities of Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>I am so grateful for this forum and all of these posts. We learned yesterday that my husband&#8217;s (48, diagnosed in March 2020) IPF has gotten worse and his pulmonologist has suggested he start the process of getting on the transplant list. While I knew this would happen eventually, I honestly thought there would be more time. I had it in my&hellip;<span class="activity-read-more" id="activity-read-more-36333"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-harsh-realities-of-lung-transplantation/#post-33767" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion Shortness of breath and normal oxygen reading in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29010</link>
				<pubDate>Fri, 25 Jun 2021 13:41:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29010"><span class="bb-reply-lable">Reply to</span> Shortness of breath and normal oxygen reading</a></p> <div class="bb-content-inr-wrap"><p>Hi Terry &#8211; What jumped out to me was that your doctor doesn&#8217;t seem to be giving you the information you want/need to feel informed about your condition. I would encourage you to have a conversation with your doctor about that. Tell him/her you want to learn more and what level of information you need. If nothing changes perhaps you could&hellip;<span class="activity-read-more" id="activity-read-more-27975"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-normal-oxygen-reading/#post-29010" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion New to discussions questions about cough in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-discussions-questions-about-cough/#post-28651</link>
				<pubDate>Wed, 26 May 2021 19:21:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-discussions-questions-about-cough/#post-28651"><span class="bb-reply-lable">Reply to</span> New to discussions questions about cough</a></p> <div class="bb-content-inr-wrap"><p>My husband is the patient and his cough started a year before his PF diagnosis. It was more of a tickle ana alight throat clearing but it was constant. Now, 2 years later it&#8217;s a constant cough. Gaba didn&#8217;t help him but he is now taking an off-label anti-depressant (A tri-cyclide but I can&#8217;t recall the name.) While it helps, he still coughs all&hellip;<span class="activity-read-more" id="activity-read-more-27353"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-to-discussions-questions-about-cough/#post-28651" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion Second opinion referral suggestions? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/second-opinion-referral-suggestions/#post-27736</link>
				<pubDate>Tue, 16 Mar 2021 19:47:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/second-opinion-referral-suggestions/#post-27736"><span class="bb-reply-lable">Reply to</span> Second opinion referral suggestions?</a></p> <div class="bb-content-inr-wrap"><p>Hi James &#8211; I&#8217;m on the forum here as a spouse of an IPF patient. I have found this to be immensely helpful. As for getting a second opinion, I am on the east coast so can&#8217;t really help with anything in-person, but Dr. Cheilonda Johnson at UPenn is amazing and maybe she will do a&hellip;<span class="activity-read-more" id="activity-read-more-26108"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/second-opinion-referral-suggestions/#post-27736" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion Dad was placed on end-of-life care in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dad-was-placed-on-end-of-life-care/#post-27735</link>
				<pubDate>Tue, 16 Mar 2021 19:42:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dad-was-placed-on-end-of-life-care/#post-27735"><span class="bb-reply-lable">Reply to</span> Dad was placed on end-of-life care</a></p> <div class="bb-content-inr-wrap"><p>Hello Vishal &#8211; Thank you for sharing this with us. I&#8217;m wishing you, your dad, and entire family well during this difficult time.</p>
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				<title>Heather replied to the discussion Gabapentin is a Proven Treatment for Refractory Chronic Cough in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-27675</link>
				<pubDate>Thu, 11 Mar 2021 16:40:08 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-27675"><span class="bb-reply-lable">Reply to</span> Gabapentin is a Proven Treatment for Refractory Chronic Cough</a></p> <div class="bb-content-inr-wrap"><p>Chiming in on the use of gabapentin. My husband was diagnosed a year ago (at 45), and several months ago he tried gaba to control his cough which has gotten progressively worse. He didn&#8217;t feel it was helping, and because he&#8217;s not big on taking medications (he takes a lot of pills now- Esbriet, the GERD one, etc.), he tapered off. Now that&hellip;<span class="activity-read-more" id="activity-read-more-26020"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/gabapentin-is-a-proven-treatment-for-refractory-chronic-cough/#post-27675" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion Common Characteristics of Pulmonary Fibrosis and COVID-19 in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/25570/#post-25610</link>
				<pubDate>Mon, 21 Sep 2020 18:48:19 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/25570/#post-25610"><span class="bb-reply-lable">Reply to</span> Common Characteristics of Pulmonary Fibrosis and COVID-19</a></p> <div class="bb-content-inr-wrap"><p>This is timely as my husband &#8211; diagnosed in March 2020 &#8211; and I haven&#8217;t told anyone yet about his diagnosis. We need to though. For one thing, he was diagnosed with a genetic condition called short telomere syndrome which is likely the root cause of his PF (though the docs still call it IPF). We need to tell his sister (who has children) about&hellip;<span class="activity-read-more" id="activity-read-more-22542"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/25570/#post-25610" rel="nofollow"> Read more</a></span></p>
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				<title>Heather changed their profile picture</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/22413/</link>
				<pubDate>Mon, 14 Sep 2020 13:21:11 -0500</pubDate>

				
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				<title>Heather replied to the discussion Neurontin (Gabapentin) in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/neurontin-gabapentin/#post-25555</link>
				<pubDate>Mon, 14 Sep 2020 13:18:35 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/neurontin-gabapentin/#post-25555"><span class="bb-reply-lable">Reply to</span> Neurontin (Gabapentin)</a></p> <div class="bb-content-inr-wrap"><p>Thanks for this information. I am looking into it for my husband. His cough has gotten so bad that he has rib pain. Thank you all for sharing.</p>
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				<title>Heather replied to the discussion Excessive cough during sleeping time in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25478</link>
				<pubDate>Thu, 03 Sep 2020 17:45:39 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25478"><span class="bb-reply-lable">Reply to</span> Excessive cough during sleeping time</a></p> <div class="bb-content-inr-wrap"><p>I&#8217;d like to help my husband manage his &#8220;dry cough&#8221; &#8212; it was the first indicator that something was wrong. It&#8217;s gotten so bad that his co-workers ask/comment on it and he&#8217;s not comfortable telling them that he has IPF. I want him to be able to have meetings and phone calls without the persistent cough. I really appreciate all the tips and will&hellip;<span class="activity-read-more" id="activity-read-more-22234"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/excessive-cough-during-sleeping-time/#post-25478" rel="nofollow"> Read more</a></span></p>
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				<title>Heather replied to the discussion Food aversions &#38; loss of appetite in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/food-aversions-loss-of-appetite/#post-25477</link>
				<pubDate>Thu, 03 Sep 2020 17:35:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/food-aversions-loss-of-appetite/#post-25477"><span class="bb-reply-lable">Reply to</span> Food aversions &amp; loss of appetite</a></p> <div class="bb-content-inr-wrap"><p>Hi All,</p>
<p>I&#8217;m here because my husband was diagnosed with IPF in March 2020, at the age of 45. I&#8217;m learning from everyone here. He went on Ofev in March, and it made it him so ill he had to stop taking it (dropped 10 pounds off his already lean frame.)  During that time he had no appetite and developed an aversion to eggs. We used to eat eggs&hellip;<span class="activity-read-more" id="activity-read-more-22233"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/food-aversions-loss-of-appetite/#post-25477" rel="nofollow"> Read more</a></span></p>
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				<title>Heather became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/21455/</link>
				<pubDate>Mon, 27 Jul 2020 17:47:57 -0500</pubDate>

				
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