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	<title>Pulmonary Fibrosis News Forums | Judy | Activity</title>
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				<title>Judy posted an update: @charlene-marshall I have a question. Here in Florida we [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/21034/</link>
				<pubDate>Mon, 06 Jul 2020 23:23:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall I have a question. Here in Florida we are supposed to wear face masks in public buildings. I go out very seldom and have worn a mask. I called my oxygen company to see if they had received new orders from my pulmonologist yet as we have found sometimes the faxes don&#8217;t go through. Back to question she told me that I was&hellip;<span class="activity-read-more" id="activity-read-more-21034"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/21034/" rel="nofollow"> Read more</a></span></p>
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				<title>Judy replied to the discussion The Frequency of Changing Your Nasal Cannula in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-24506</link>
				<pubDate>Thu, 28 May 2020 16:55:46 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/page/2/#post-24506"><span class="bb-reply-lable">Reply to</span> The Frequency of Changing Your Nasal Cannula</a></p> <div class="bb-content-inr-wrap"><p>Entered before finishing comment. Anyhow there was a mention regarding dry nose, which is irritating to say the least. Shortly after I started o2 24/7 i recognized that  needed something but knew I couldn&#8217;t use Vaseline. A friend of my daughter has a young very ill son who has been on o2 most of his life. When asked she recommended Rhinase&hellip;<span class="activity-read-more" id="activity-read-more-20333"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-24506" rel="nofollow"> Read more</a></span></p>
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				<title>Judy replied to the discussion Changing Furnace Filters &#38; Spring Cleaning For PF Patients in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/changing-furnace-filters-spring-cleaning-for-pf-patients/#post-23893</link>
				<pubDate>Fri, 10 Apr 2020 00:12:58 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/changing-furnace-filters-spring-cleaning-for-pf-patients/#post-23893"><span class="bb-reply-lable">Reply to</span> Changing Furnace Filters & Spring Cleaning For PF Patients</a></p> <div class="bb-content-inr-wrap"><p>`living in Florida I change tge heat/air conditioning filter at least every 2 months and usually every month. The system works better and is much better for my lubgs. I also have air purifiers running 24/7 and change that filter as called for. </p>
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				<title>Judy replied to the discussion PSA Safe Grocery Shopping in COVID-19 Pandemic – UPDATED!!! - YouTube in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/psa-safe-grocery-shopping-in-covid-19-pandemic-updated-youtube/#post-23813</link>
				<pubDate>Fri, 03 Apr 2020 00:09:29 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/psa-safe-grocery-shopping-in-covid-19-pandemic-updated-youtube/#post-23813"><span class="bb-reply-lable">Reply to</span> PSA Safe Grocery Shopping in COVID-19 Pandemic – UPDATED!!! - YouTube</a></p> <div class="bb-content-inr-wrap"><p>There are so many seniors in our area that stores are really busy during that tine. My children don&#8217;t want me to go out,  and I am lucky enough that they can get what I need. Must admit that I miss going to the store as staying is boring and I like to shop </p>
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				<title>Judy replied to the discussion Hobbies for COVID-19 Quarantine in the forum Coronavirus (COVID-19) and Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hobbies-for-covid-19-quarantine/#post-23802</link>
				<pubDate>Thu, 02 Apr 2020 19:11:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hobbies-for-covid-19-quarantine/#post-23802"><span class="bb-reply-lable">Reply to</span> Hobbies for COVID-19 Quarantine</a></p> <div class="bb-content-inr-wrap"><p>I have been sewing, reading, computer games and Other crafts to keep busy. Take each day as it comes.  Not used to staying in.</p>
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				<title>Judy replied to the discussion Definitive test for diagnosis? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/definitive-test-for-diagnosis/#post-23270</link>
				<pubDate>Wed, 04 Mar 2020 10:05:57 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/definitive-test-for-diagnosis/#post-23270"><span class="bb-reply-lable">Reply to</span> Definitive test for diagnosis?</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed about a year ago, but not conclusively. I have been on o2 since last year as my levels drop without it. I was on prednizone 10 mg. I was taken off that in January of this year to do testing see what the changes were with ct and pft.. Put on ofev but couldn&#8217;t tolerate the side effects. I was going to have lung biopsy, but&hellip;<span class="activity-read-more" id="activity-read-more-18502"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/definitive-test-for-diagnosis/#post-23270" rel="nofollow"> Read more</a></span></p>
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				<title>Judy replied to the discussion Book Club in the forum Hobbies &#38; Projects</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-22785</link>
				<pubDate>Fri, 31 Jan 2020 00:10:14 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/book-club/#post-22785"><span class="bb-reply-lable">Reply to</span> Book Club</a></p> <div class="bb-content-inr-wrap"><p>I have been an avid reader since i waa a child.  I love different genres depending on mymood. My favorite author is J D Robb. I have been reading her for years.  I also enjoy  Lee Child, Michael Connelly,  Karen Kingsbury among others.  Since I have been so fatigued of late I have been reading alot. </p>
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				<title>Judy replied to the discussion Friend Requests in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/friend-requests/#post-22731</link>
				<pubDate>Tue, 28 Jan 2020 18:07:26 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/friend-requests/#post-22731"><span class="bb-reply-lable">Reply to</span> Friend Requests</a></p> <div class="bb-content-inr-wrap"><p>I too received the friend request and it went nowhere.  Hlad to know about the spammers and that you are taking care of them. Really appreciate your work.  I hadn&#8217;t thought about a possible spammer when I received  I now know to delete.  Many thanks </p>
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				<title>Judy replied to the discussion Do you take OFEV? Take our poll! in the forum Polls &#38; Quizzes</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/take-ofev-take-poll/#post-22638</link>
				<pubDate>Thu, 23 Jan 2020 16:21:00 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/take-ofev-take-poll/page/2/#post-22638"><span class="bb-reply-lable">Reply to</span> Do you take OFEV? Take our poll!</a></p> <div class="bb-content-inr-wrap"><p>Just started ofev this week. Some slight nausea so far.  To soon to give much feedback. </p>
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				<title>Judy replied to the discussion Chest cramps in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/chest-cramps/#post-22614</link>
				<pubDate>Tue, 21 Jan 2020 23:59:43 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/chest-cramps/#post-22614"><span class="bb-reply-lable">Reply to</span> Chest cramps</a></p> <div class="bb-content-inr-wrap"><p>Thank you for talking about the he cramping. I too suffer from the chest cramping also cramping in my legs and feet.  I had asked my dr regarding them. Didn&#8217;t know if it was related to my fibrosis or not. One dr thought it was a bruised rib. After reading the above i feel better about them. At least have a reason.  For my chest area I usually&hellip;<span class="activity-read-more" id="activity-read-more-17359"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/chest-cramps/#post-22614" rel="nofollow"> Read more</a></span></p>
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				<title>Judy posted an update: I was writing re the inhalers and their lack of [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/15982/</link>
				<pubDate>Fri, 01 Nov 2019 17:58:58 -0500</pubDate>

									<content:encoded><![CDATA[<p>I was writing re the inhalers and their lack of working. .but I wondered about stuffiness, I live in Florida and it is humid. Additionally does anyone have a problem that I like to drool I&#8217;m my. I do have post nasal drip and it sometimes bags me.</p>
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				<title>Judy replied to the discussion Periodic Muscle Cramps &#38; Pain Since IPF Diagnosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/periodic-muscle-cramps-pain-since-ipf-diagnosis/#post-21076</link>
				<pubDate>Fri, 30 Aug 2019 18:16:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/periodic-muscle-cramps-pain-since-ipf-diagnosis/#post-21076"><span class="bb-reply-lable">Reply to</span> Periodic Muscle Cramps & Pain Since IPF Diagnosis</a></p> <div class="bb-content-inr-wrap"><p>I am new to having pulmonary fibrosis.  Been on oxygen for about 3 months.  Before oxygen i was a couch potato.  Now i can do things again.  Prior to oxygen i had cramping on rib cage. I also have been experiencing leg and foot cramps periodically.  After starting the oxygen,  the rib cramping stopped until this week,  when i started feeling&hellip;<span class="activity-read-more" id="activity-read-more-14867"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/periodic-muscle-cramps-pain-since-ipf-diagnosis/#post-21076" rel="nofollow"> Read more</a></span></p>
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				<title>Judy became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/13486/</link>
				<pubDate>Tue, 02 Jul 2019 17:04:47 -0500</pubDate>

				
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