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	<title>Pulmonary Fibrosis News Forums | Maureen | Activity</title>
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				<title>Maureen started the discussion Cardiopulmonary exercise (CPET) in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cardiopulmonary-exercise-cpet/</link>
				<pubDate>Wed, 01 Dec 2021 10:24:05 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cardiopulmonary-exercise-cpet/">Cardiopulmonary exercise (CPET)</a></p> <div class="bb-content-inr-wrap"><p>My respiralogist just ordered this test to diagnose IPF plus a CT scan. Just wondering if others had this procedure to diagnose.<br />
I&#8217;m from Canada &#8211; could this be a Canadian thing??</p>
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				<title>Maureen started the discussion MRI to diagnose PF in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/mri-to-diagnose-pf/</link>
				<pubDate>Thu, 11 Nov 2021 17:50:35 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/mri-to-diagnose-pf/">MRI to diagnose PF</a></p> <div class="bb-content-inr-wrap"><p>Wondering if using an MRI test is being used to diagnose PF.  This would be a test I would pay for a diagnosis, instead of having to wait so long for another CT.</p>
<p>thanks for any feedback!</p>
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				<title>Maureen 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-30102</link>
				<pubDate>Thu, 30 Sep 2021 15:09:31 -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-30102"><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>Morning James<br />
I have a Chinese acupuncturist who put me on cough medicine called Nin Jiom Pei Pa Koa. It works well for me cause I have Restless Legs so I can’t take “off the counter cough meds”.</p>
<p>&nbsp;</p>
<p>I tried to take a picture of it, but can’t figure out how to include it!!</p>
<p>thanks for sharing James!</p>
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				<title>Maureen replied to the discussion Body aches in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29955</link>
				<pubDate>Fri, 17 Sep 2021 15:01:33 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29955"><span class="bb-reply-lable">Reply to</span> Body aches</a></p> <div class="bb-content-inr-wrap"><p>Rebecca, thanks for sharing! I will take your advice &amp; start monitoring what I’m eating to see if there is a correlation. I didn’t think of that!!</p>
<p>&nbsp;</p>
<p>Stay safe!</p>
<p>Maureen</p>
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				<title>Maureen replied to the discussion Body aches in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29954</link>
				<pubDate>Thu, 16 Sep 2021 14:22:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29954"><span class="bb-reply-lable">Reply to</span> Body aches</a></p> <div class="bb-content-inr-wrap"><p>Thanks Patricia for sharing your experience. My O2 (oxygen) has registered normal. What was/is your readings? I take CBD &amp; it is very effective to ease the pain. I need to wait till January for a 2nd CT scan to confirm the diagnosis. I do have a Cpap that I use every day.</p>
<p>I am so grateful that you shared your experience. I don’t feel so alone&hellip;<span class="activity-read-more" id="activity-read-more-29599"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29954" rel="nofollow"> Read more</a></span></p>
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				<title>Maureen replied to the discussion Body aches in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29788</link>
				<pubDate>Thu, 02 Sep 2021 16:04:36 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/#post-29788"><span class="bb-reply-lable">Reply to</span> Body aches</a></p> <div class="bb-content-inr-wrap"><p>Madonna, that sounds very painful. Mine feels like the muscles ache. No joint pain. I use CBD oil several times a day. It does control the full body aches. Just not sure this relates to PF that’s why I am asking.</p>
<p>Hope today is a pain free day for you Madonna!</p>
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				<title>Maureen started the discussion Body aches in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/</link>
				<pubDate>Wed, 01 Sep 2021 15:33:32 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/body-aches/">Body aches</a></p> <div class="bb-content-inr-wrap"><p>Anyone have any suggestions about body aches. I wake up during the night with them or it will hit during the day. It feels like getting the flu- with body aches. Yes I have been checked for COVID-negative. Do others have this?</p>
<p>Thanks in Advance</p>
<p>Maureen</p>
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				<title>Maureen replied to the discussion What to ask the doctor? in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/what-to-ask-the-doctor/#post-29234</link>
				<pubDate>Thu, 15 Jul 2021 19:03:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-to-ask-the-doctor/#post-29234"><span class="bb-reply-lable">Reply to</span> What to ask the doctor?</a></p> <div class="bb-content-inr-wrap"><p>I am waiting too for a diagnosis- which is leaning towards PF. My respiralogist said I need a second CT scan (1yr apart) to confirm. So they may not have all the answers at your 1st visit. Keep us updated!</p>
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				<title>Maureen replied to the discussion Looking for answers in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/looking-for-answers/#post-29160</link>
				<pubDate>Thu, 08 Jul 2021 15:50:09 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/looking-for-answers/#post-29160"><span class="bb-reply-lable">Reply to</span> Looking for answers</a></p> <div class="bb-content-inr-wrap"><p>I am on this crazy road of diagnosis. My GP said all signs are looking like PF. My respiralogist says my ERV at 16% is due to abdominal fat pressing on my diaphragm ( like a pregnant woman). She says the person who interrupted my breathing test used the wrong word when he wrote &#8221; severely  reduced 0.16L&#8221; so now I have to wait for a 2nd CT scan&hellip;<span class="activity-read-more" id="activity-read-more-28250"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/looking-for-answers/#post-29160" rel="nofollow"> Read more</a></span></p>
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				<title>Maureen and Charlene are now connected</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/28009/</link>
				<pubDate>Sat, 26 Jun 2021 11:22:39 -0500</pubDate>

				
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				<title>Maureen posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27977/#acomment-28008</link>
				<pubDate>Sat, 26 Jun 2021 10:48:20 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thanks Charlene. Waiting anxiously to talk to my respiralogist on Wednesday. The GP said the breathing test results are pointing to PF because my ERV is severely low. She already told me that the 2 drugs available aren’t very effective. She also said it would be early stage. I am very much into alternative medicine to help with my doctors.&hellip;<span class="activity-read-more" id="activity-read-more-28008"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/27977/#acomment-28008" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/gamo/" data-bb-hp-profile="11309" rel="nofollow">Maureen</a> became a registered member					]]></content:encoded>
				
				
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				<title>Maureen became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/27977/</link>
				<pubDate>Fri, 25 Jun 2021 14:42:30 -0500</pubDate>

				
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