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	<title>Pulmonary Fibrosis News Forums | Polly Kanto | Activity</title>
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				<title>Polly Kanto replied to the discussion Post-nasal Drip: Another Ailment to Deal With in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-37711</link>
				<pubDate>Fri, 29 Nov 2024 23:34:41 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-37711"><span class="bb-reply-lable">Reply to</span> Post-nasal Drip: Another Ailment to Deal With</a></p> <div class="bb-content-inr-wrap"><p>I’ve had PF for almost 3 years. As my oxygen level gradually increased from 2 L to 6, I noticed an awful lot of PND, constantly having to take out my cannula and blow my nose. My pulmonologist started me with a palliative care nurse, and she said the problem is your nose is responding to having a foreign object in it, the cannula tubes, and is&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-43533"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/post-nasal-drip-another-ailment-to-deal-with/#post-37711" rel="nofollow"> Read more</a></span></p>
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				<title>Polly Kanto replied to the discussion Issue contacting BI Cares regarding OFEV in the forum Healthcare Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/issue-contacting-bi-cares-regarding-ofev/#post-37682</link>
				<pubDate>Fri, 22 Nov 2024 22:53:42 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/issue-contacting-bi-cares-regarding-ofev/#post-37682"><span class="bb-reply-lable">Reply to</span> Issue contacting BI Cares regarding OFEV</a></p> <div class="bb-content-inr-wrap"><p>I called to re-order my prescription and we were told that they did not have my account information. Have been getting Ofev for over 2 1/2 years and never had a problem. They said that they were going with a new pharmacy and a lot of information got lost in the transfer. The first time we were on hold for an hour and a half, had to call again&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-43489"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/issue-contacting-bi-cares-regarding-ofev/#post-37682" rel="nofollow"> Read more</a></span></p>
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				<title>Polly Kanto replied to the discussion New user to Pirfenidone in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/new-user-to-pirfenidone/#post-37067</link>
				<pubDate>Tue, 21 May 2024 20:33:22 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-user-to-pirfenidone/#post-37067"><span class="bb-reply-lable">Reply to</span> New user to Pirfenidone</a></p> <div class="bb-content-inr-wrap"><p>Hi Riley. My sister has IPF and tried Esbriet after being diagnosed at the Mayo Clinic four years ago. She said the medication “nearly killed her.” After seeing her pulmonologist again she went on Ofev and after going down from 150 mg to 100 mg is doing very well. A little over two years ago I was diagnosed with ILD, and went on Ofev. The 150&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42365"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/new-user-to-pirfenidone/#post-37067" rel="nofollow"> Read more</a></span></p>
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				<title>Polly Kanto replied to the discussion Celcept / Mycophenolate use? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37051</link>
				<pubDate>Thu, 16 May 2024 21:17:51 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37051"><span class="bb-reply-lable">Reply to</span> Celcept / Mycophenolate use?</a></p> <div class="bb-content-inr-wrap"><p>Hi George. I was diagnosed with I LD a little over two years ago. In an attempt to get off a low daily maintenance of prednisone, I tried CellCept. I had a very bad reaction when I worked up to the highest dose of the day and had to stop taking it. After some time, I was advised to try it again and had the same results. I was just sick all&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42330"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/celcept-mycophenolate-use/#post-37051" rel="nofollow"> Read more</a></span></p>
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				<title>Polly Kanto became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/37674/</link>
				<pubDate>Wed, 01 Mar 2023 14:21:53 -0600</pubDate>

				
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