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	<title>Pulmonary Fibrosis News Forums | Kathy Medina | Activity</title>
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				<title>Kathy Medina replied to the discussion Pedometer, SpO2 bracelets/watches in the forum Polls &#38; Quizzes</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pedometer-spo2-bracelets-watches/#post-20682</link>
				<pubDate>Tue, 06 Aug 2019 15:52:43 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pedometer-spo2-bracelets-watches/#post-20682"><span class="bb-reply-lable">Reply to</span> Pedometer, SpO2 bracelets/watches</a></p> <div class="bb-content-inr-wrap"><p>Hi Linda,</p>
<p>&nbsp;</p>
<p>I was telling my pulmonary doctor last year that I didn&#8217;t care about a fit bit but I we should invent something like that that would monitor your O2 levels!  I was in the Dr office about a month ago and found a ad for a unit called H.E.l.O).  It claims to monitor heart rate, sleep, blood pressure, calories, mood, energy, steps,&hellip;<span class="activity-read-more" id="activity-read-more-14223"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pedometer-spo2-bracelets-watches/#post-20682" rel="nofollow"> Read more</a></span></p>
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				<title>Kathy Medina replied to the discussion Episodic Dizziness &#38; Pulmonary Fibrosis in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/episodic-dizziness-pulmonary-fibrosis/#post-18780</link>
				<pubDate>Fri, 26 Apr 2019 14:54:15 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/episodic-dizziness-pulmonary-fibrosis/#post-18780"><span class="bb-reply-lable">Reply to</span> Episodic Dizziness & Pulmonary Fibrosis</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene</p>
<p>I was surprised to see this.  I experience dizziness myself.  I have been so dizzy everytime I stood up that I honestly lost all touch with reality.  I was very afraid that I may pass out.  I have been to my doctor who referred me to a ENT and when all was good there he referred me to a balance test then when all was well there I&hellip;<span class="activity-read-more" id="activity-read-more-11716"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/episodic-dizziness-pulmonary-fibrosis/#post-18780" rel="nofollow"> Read more</a></span></p>
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				<title>Kathy Medina replied to the discussion Recently diagnosed with IPF &#38; Honeycomb Lung in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/recently-diagnosed-with-ipf-honeycomb-lung/#post-18506</link>
				<pubDate>Tue, 16 Apr 2019 14:48:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/recently-diagnosed-with-ipf-honeycomb-lung/#post-18506"><span class="bb-reply-lable">Reply to</span> Recently diagnosed with IPF &amp; Honeycomb Lung</a></p> <div class="bb-content-inr-wrap"><p>Hi John</p>
<p>Welcome to the forum.  I am on Esbriet.  The side effects are not good.  The one that I notice the most is I have to take it with food or it will give me the worst heartburn symptoms you can imagine.  It is also very difficult for me to eat 3 meals a day.  I know it says to try to take it at the same time each day but, I feel an&hellip;<span class="activity-read-more" id="activity-read-more-11349"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/recently-diagnosed-with-ipf-honeycomb-lung/#post-18506" rel="nofollow"> Read more</a></span></p>
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				<title>Kathy Medina posted an update: Hi everyone! I am new to the forum and have no clue what [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/11235/</link>
				<pubDate>Mon, 15 Apr 2019 00:51:07 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone! I am new to the forum and have no clue what I am doing.  I recently moved from Utah to Nevada for the air quality and I hate snow anyway.  Sometimes I find it frustrating when you see all these ads on TV for cures for different diseases but nothing for IPF.  I enjoy this column and there are so many good ideas.  I would like to find&hellip;<span class="activity-read-more" id="activity-read-more-11235"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/11235/" rel="nofollow"> Read more</a></span></p>
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				<title>Kathy Medina became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/9575/</link>
				<pubDate>Wed, 27 Feb 2019 20:33:59 -0600</pubDate>

				
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