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	<title>Pulmonary Fibrosis News Forums | Sarv Punj | Activity</title>
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				<title>Sarv Punj replied to the discussion Oxygen in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/#post-24960</link>
				<pubDate>Tue, 14 Jul 2020 16:37:38 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/page/3/#post-24960"><span class="bb-reply-lable">Reply to</span> Oxygen</a></p> <div class="bb-content-inr-wrap"><p>I have gone through some of the correspondence on the need for Oxygen. I would like to share my experience as I am closely monitoring the condition of my wife. It’s true,Oxygen requirement for individuals suffering from IPF or other COPD disease is unique to individuals. My wife started using oxygen about 1 1/2 yrs back @ 2-3 lpm constant flow&hellip;<span class="activity-read-more" id="activity-read-more-21219"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/oxygen-3/#post-24960" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj posted an update: @charlene-marshall 
Hello Charlene,
I have been [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/20943/</link>
				<pubDate>Thu, 02 Jul 2020 15:28:17 -0500</pubDate>

									<content:encoded><![CDATA[<p>@charlene-marshall<br />
Hello Charlene,<br />
I have been going through various issues relating to IPF but right now I am getting concerned with  alarming  issue of Pulmonary Hypertension as a sequel to IPF. As you know, my wife is a patient of IPF for the last about 8yrs. She was first hospitalised in Feb this year for 10 days. On return from hospital&hellip;<span class="activity-read-more" id="activity-read-more-20943"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/20943/" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion The IPF Patient&#039;s Experience with Prednisone in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/pf-patients-experience-prednisone/#post-24714</link>
				<pubDate>Wed, 24 Jun 2020 01:58:25 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pf-patients-experience-prednisone/page/2/#post-24714"><span class="bb-reply-lable">Reply to</span> The IPF Patient&#039;s Experience with Prednisone</a></p> <div class="bb-content-inr-wrap"><p>Hi everyone. I was reading some news items elsewhere which said that prednisone is generally not used in IPF patients. My wife however is now taking 35 mg prednisone together with Pirfenidone 800 mg twice daily and is on Oxygen 24&#215;7. We tried to titrations prednisone to 30 mg  with the intention of increasing Pirfenidone to 800 mg three times&hellip;<span class="activity-read-more" id="activity-read-more-20760"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/pf-patients-experience-prednisone/#post-24714" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj 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-24488</link>
				<pubDate>Tue, 26 May 2020 14:50:34 -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-24488"><span class="bb-reply-lable">Reply to</span> The Frequency of Changing Your Nasal Cannula</a></p> <div class="bb-content-inr-wrap"><p>HiCharlene,<br />
I read your query about changing the nasal cannula and some of the replies too. As you know, my wife is on Oxygen and uses Oximyzer (pendant type) which has a nasal cannula attached. The manufacturer has specified a months duration for changing the Oximyzer but we feel that it depends more on the upkeep and condition of the&hellip;<span class="activity-read-more" id="activity-read-more-20287"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/the-frequency-of-changing-your-nasal-cannula/#post-24488" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion EGCG Green Tea Extract in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/egcg-green-tea-extract/#post-24218</link>
				<pubDate>Sat, 02 May 2020 04:27:19 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/egcg-green-tea-extract/#post-24218"><span class="bb-reply-lable">Reply to</span> EGCG Green Tea Extract</a></p> <div class="bb-content-inr-wrap"><p>Hello Everybody everybody on the Forum. Various posts on EGGC are very enlightening. I am still not sure which brand of Green Tea Extract I should buy for my wife. There are numerous brands available in India, local as well imported. Also what potency capsules are adequate. I will be grateful if more light is thrown in this regard.<br />
Thanks.</p>
<p>Sarv</p>
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				<title>Sarv Punj replied to the discussion EGCG Green Tea Extract in the forum Clinical Trials</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/egcg-green-tea-extract/#post-24188</link>
				<pubDate>Thu, 30 Apr 2020 16:09:31 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/egcg-green-tea-extract/#post-24188"><span class="bb-reply-lable">Reply to</span> EGCG Green Tea Extract</a></p> <div class="bb-content-inr-wrap"><p>Friends I have read the news about EGCG found to be useful in treatment of IPF. While green tea is easily available, do we have to buy EGCG  (the green tea extract) specially or it is automatically delivered to the body by taking green tea regularly. Kindly educate me on this. Thanks.</p>
<p>sarv</p>
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19429/#acomment-19455</link>
				<pubDate>Mon, 13 Apr 2020 16:22:38 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Charlene,<br />
Thank you so much Charlene for the references. In fact I have already got a post from DrandyHall which is very informative. I am forwarding this to our pulmonologist for his perusal . I believe it will be professionally beneficial to him. Thanks again.</p>
<p>Sarv</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Hello friends, 
I read about laser treatment being used for Corona virus and that research might help evolve some treatment for IPF too. I talked to my wife&#8217;s pulmonologist who was [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19429/#acomment-19454</link>
				<pubDate>Mon, 13 Apr 2020 16:18:58 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Andrew,<br />
Thank you so much for giving a personal account of the treatment undertaken by you for IPF. The link sent by you will surely of interest to our Pulmonologist. I am forwarding the same to him. I am greatly obliged for this information.<br />
Best regards.<br />
Sarv </p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Hello friends, 
I read about laser treatment being used for Corona virus and that research might help evolve some treatment for IPF too. I talked to my wife&#8217;s pulmonologist who was [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj posted an update: Hello friends, 
I read about laser treatment being used [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19429/</link>
				<pubDate>Sun, 12 Apr 2020 16:09:00 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hello friends,<br />
I read about laser treatment being used for Corona virus and that research might help evolve some treatment for IPF too. I talked to my wife&#8217;s pulmonologist who was not aware of this development. He has asked me to share more details about the Later treatment procedure. Could some of the better informed members give&hellip;<span class="activity-read-more" id="activity-read-more-19429"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/19429/" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19334/#acomment-19424</link>
				<pubDate>Sun, 12 Apr 2020 03:14:47 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hello Mark. Great going for you.I thing Lung Transplant is a good option but for relatively younger age group. My wife was not recommended. She is already 77 plus.</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Dear Friends
I have read some other threads in the Forums with interest about patients suffering from IPF and being treated with OFev / Esibret and some using Oxygen too. It [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19334/#acomment-19342</link>
				<pubDate>Thu, 09 Apr 2020 15:09:49 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thank you Mark . It’s rather encouraging that you recovered your lung function by 75% and hopefully you will continue to improve further. This has kindled some hope in us that we can expect similar improvement in my wife’s condion over some time. Thank you again for reassuring.<br />
Sarv</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Dear Friends
I have read some other threads in the Forums with interest about patients suffering from IPF and being treated with OFev / Esibret and some using Oxygen too. It [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj posted an update: Dear Friends
I have read some other threads in the [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19334/</link>
				<pubDate>Thu, 09 Apr 2020 14:27:11 -0500</pubDate>

									<content:encoded><![CDATA[<p>Dear Friends<br />
I have read some other threads in the Forums with interest about patients suffering from IPF and being treated with OFev / Esibret and some using Oxygen too. It is gratifying to note that most patients exhibit fairly good exercise tolerance. My wife 77 1/2 who was diagnosed with IPF 8 yrs ago right in the initial stages and has&hellip;<span class="activity-read-more" id="activity-read-more-19334"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/19334/" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23831</link>
				<pubDate>Sun, 05 Apr 2020 12:45:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/5/#post-23831"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Sara,<br />
It is heartening to know that your husband is feeling much better on OFev. Wish him full recovery.You mentioned about OPEN DOOR FOUNDATION . Will it be possible for you to share their email contact so that I could write to them for my wife who is suffering from IPF for the last 8 yrs. She was hospitalised this February for 10 days&hellip;<span class="activity-read-more" id="activity-read-more-19259"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23831" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23830</link>
				<pubDate>Sun, 05 Apr 2020 11:26:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/6/#post-23830"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,<br />
Thank you very much for your prompt reply. I can understand what you said. Different persons may have different experience with the drug. My wife however refuses to restart OFev , In fact presently she is off Pirfenidone too  on Doctor’s advice and taking only Omnacortil 30 mg once a day. We shall restart Pirfenex (Pirfenidone) as&hellip;<span class="activity-read-more" id="activity-read-more-19258"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23830" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19136/#acomment-19167</link>
				<pubDate>Wed, 01 Apr 2020 10:03:56 -0500</pubDate>

									<content:encoded><![CDATA[<p>No worry Mark. I have ordered Kidney and Lever Function tests today which might  be helpful in deciphering her problem. Thanks.</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Friends, as I have reported in my previous posts, my wife is on Nintedanib 150mg bid + Pirfenidone 400mg TDS and Omnacortil  titrated to 20 mg od for the last over one month. Till [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj replied to the discussion Starting Ofev in the forum Ofev (Nintedanib)</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23785</link>
				<pubDate>Wed, 01 Apr 2020 08:17:04 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/page/6/#post-23785"><span class="bb-reply-lable">Reply to</span> Starting Ofev</a></p> <div class="bb-content-inr-wrap"><p>Dear Friends. I am from India. My wife who has been suffering from IPF for about 8 yrs and was doing well with Pirfenidone 800 mg three times a day and 10 mg omnacortil daily but after about 4 yrs of this treatment her breathlessness started going up and she had to use supplemental oxygen @ 2-3lpm day and night.This kept her going but with&hellip;<span class="activity-read-more" id="activity-read-more-19165"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/starting-ofev/#post-23785" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19136/#acomment-19162</link>
				<pubDate>Wed, 01 Apr 2020 07:09:38 -0500</pubDate>

									<content:encoded><![CDATA[<p>Thanks Mark. As I said before my wife was on both OFev and Esbriet concurrently but since she has been feeling very low for the last 3-4 days , the first reaction was that the only change in medication is addition of Ofev which could have caused this indisposition and she stopped OFev.I called her Pulmonologist who has advised to stop both&hellip;<span class="activity-read-more" id="activity-read-more-19162"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/19136/#acomment-19162" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Friends, as I have reported in my previous posts, my wife is on Nintedanib 150mg bid + Pirfenidone 400mg TDS and Omnacortil  titrated to 20 mg od for the last over one month. Till [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj replied to the discussion Dying from IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-23769</link>
				<pubDate>Tue, 31 Mar 2020 14:23:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/page/3/#post-23769"><span class="bb-reply-lable">Reply to</span> Dying from IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Magan,<br />
It’s really enlightening how patiently you dealt with your late dad’s illness during his last five months. I have read the thread partially though but seem to have gained a lot. I am 81 and my wife is in late 77 yrs and is suffering from this life threatening IPF. I admire your courage too to have gone through the pain of losing your&hellip;<span class="activity-read-more" id="activity-read-more-19140"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-23769" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19136/#acomment-19137</link>
				<pubDate>Tue, 31 Mar 2020 13:37:31 -0500</pubDate>

									<content:encoded><![CDATA[<p>In continuation of my post above, I want to add that I am not really convinced as to why Nintedanib 150 mg bid can not be replaced by Nintedanib 100 mg three times a day , since the total dosage for the day remains 300mg and better distributed over the day in 3 doses of 100 mg each. </p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/sarvpunj/" data-bb-hp-profile="5000" rel="nofollow">Sarv Punj</a> posted an update Friends, as I have reported in my previous posts, my wife is on Nintedanib 150mg bid + Pirfenidone 400mg TDS and Omnacortil  titrated to 20 mg od for the last over one month. Till [&hellip;]					]]></content:encoded>
				
				
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				<title>Sarv Punj posted an update: Friends, as I have reported in my previous posts, my wife [&#133;]</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/19136/</link>
				<pubDate>Tue, 31 Mar 2020 13:29:11 -0500</pubDate>

									<content:encoded><![CDATA[<p>Friends, as I have reported in my previous posts, my wife is on Nintedanib 150mg bid + Pirfenidone 400mg TDS and Omnacortil  titrated to 20 mg od for the last over one month. Till now she did not feel much difference in her general disposition. Instead for the last week or so she got multiple blisters in her tongue which made it difficult for&hellip;<span class="activity-read-more" id="activity-read-more-19136"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/19136/" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion Nintedanib... Dosage in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/#post-23693</link>
				<pubDate>Thu, 26 Mar 2020 16:31:59 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/#post-23693"><span class="bb-reply-lable">Reply to</span> Nintedanib... Dosage</a></p> <div class="bb-content-inr-wrap"><p>Dear Dr Salzberg,<br />
Thank you very much for providing the contact details of OFEV Open Door, I will surely try to call them. I believe the number given by you is U S number. You also mentioned that 150 mg bid is more beneficial. I wanted to know if 100 mg three times a day (ie total dosage for the day is 300 mg) will give the same benefit or&hellip;<span class="activity-read-more" id="activity-read-more-19050"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/#post-23693" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj started the discussion Nintedanib... Dosage in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/</link>
				<pubDate>Thu, 26 Mar 2020 13:43:16 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/">Nintedanib... Dosage</a></p> <div class="bb-content-inr-wrap"><p>Hi friends. I am a new member having joined the Forum only yesterday. In my introduction I had stated about my 77 yrs old wife who has been a patient of IPF for the last 8 yrs. She was diagnosed at very early stage of IPF and was put on Prednisine 40 mg daily which was titrated toa maintenance dose of 10 mg which was going up and down according&hellip;<span class="activity-read-more" id="activity-read-more-19037"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/nintedanib-dosage/" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj replied to the discussion Sharing Your IPF Story: How Do You Feel About It? in the forum Pulmonary Fibrosis Awareness &#38; Advocacy</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23646</link>
				<pubDate>Wed, 25 Mar 2020 11:08:45 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23646"><span class="bb-reply-lable">Reply to</span> Sharing Your IPF Story: How Do You Feel About It?</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,</p>
<p>pits heartening as well as heart rending to read experiences of different IPF patients. I shared the story of my wife yesterday. She was started on Cyendiv 150 mg twice daily ( Same as OFev)  last month in combination with Perfenidone 400 mg three times a day after being hospitalised for 10 days due to sudden sudden exacerbation&hellip;<span class="activity-read-more" id="activity-read-more-19020"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sharing-your-ipf-story-how-do-you-feel-about-it/#post-23646" rel="nofollow"> Read more</a></span></p>
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				<title>Sarv Punj became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18958/</link>
				<pubDate>Mon, 23 Mar 2020 15:23:53 -0500</pubDate>

				
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