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	<title>Comments on: My Portal Hypertension Journey</title>
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	<link>http://www.portal-hypertension.com</link>
	<description>A resource guide for those diagnosed with portal hypertension or portal vein thrombosis (PVT) by Clint Steenson</description>
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		<title>By: Clint</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2766</link>
		<dc:creator>Clint</dc:creator>
		<pubDate>Tue, 17 Jan 2012 01:42:40 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2766</guid>
		<description>Hi Again Yvonne!

Appreciate you getting back to me.  Sincerely glad that your father has had another bleed.  I am very intested in knowing the reasoning behind the vitamin supplements.  I can understand the logic behind the Vitamin D3, magnesium, and zinc, however I am not sure about the other products.  I also think the low sodium, meat, and dairy free diet is a good thing for him considering what he is up against besides the portal hypertension (esophogeal varices).  One thing I am concerned about, and maybe you have not considered this - is the vitamin E. Not to say Vitamin E is a bad thing, but if your father is on blood thinners already (especially Coumadin aka Warfarin) it acts as a natural blood thinner and it may throw off his I&amp;R readings.  I&#039;m not on Coumadin because it does not work for me, but I am on Fragmin (needles) so I don&#039;t have to have my readings monitored, however I try to avoid Vitamin E as it can worsen a bleed if that happens.  Also Vitamin &quot;K&quot; which is found naturally in some foods (ie Spinach) can affect I&amp;R readings - from what I have learned.  These are just a few things I have found out through the years.  As yet, and believe me I have asked (specialists/family doctor), I have never been given a diet to follow, except to cut down on sodium - which is never good for anyone.  When I asked my family doctor last year about vitamins, he told me that basically we get most of what we need in a balanced diet with the 4 main food groups.  For the most part he is right, but I beg to differ as I think extra vitamins in some sense can be very beneficial for most people - especially those not watching their diets or those with health conditions.  My hematologist told me to take Vitamin B50 or B75 for the homocystine levels in my blood, and on my last visit he told me to take 4000 IU of vitamin D as new research is showing some good benefits to that.  Calcium Citrate in particular is better absorbed than the other one (sorry can&#039;t remember the name).  A few weeks ago I had a doctor who also has portal hypertension come on this blog and leave a comment, and he told me that he thought the meds were important, but that Western medicine did not look to herbal treatments the same way they do in European or eastern cultures.  There is value in both.  

Thanks again for your comments ... one never knows how any of this may help, but it is good to keep abreast of this most disconcerting condition and lend support wherever we can. 

Peace,  Clint</description>
		<content:encoded><![CDATA[<p>Hi Again Yvonne!</p>
<p>Appreciate you getting back to me.  Sincerely glad that your father has had another bleed.  I am very intested in knowing the reasoning behind the vitamin supplements.  I can understand the logic behind the Vitamin D3, magnesium, and zinc, however I am not sure about the other products.  I also think the low sodium, meat, and dairy free diet is a good thing for him considering what he is up against besides the portal hypertension (esophogeal varices).  One thing I am concerned about, and maybe you have not considered this &#8211; is the vitamin E. Not to say Vitamin E is a bad thing, but if your father is on blood thinners already (especially Coumadin aka Warfarin) it acts as a natural blood thinner and it may throw off his I&#038;R readings.  I&#8217;m not on Coumadin because it does not work for me, but I am on Fragmin (needles) so I don&#8217;t have to have my readings monitored, however I try to avoid Vitamin E as it can worsen a bleed if that happens.  Also Vitamin &#8220;K&#8221; which is found naturally in some foods (ie Spinach) can affect I&#038;R readings &#8211; from what I have learned.  These are just a few things I have found out through the years.  As yet, and believe me I have asked (specialists/family doctor), I have never been given a diet to follow, except to cut down on sodium &#8211; which is never good for anyone.  When I asked my family doctor last year about vitamins, he told me that basically we get most of what we need in a balanced diet with the 4 main food groups.  For the most part he is right, but I beg to differ as I think extra vitamins in some sense can be very beneficial for most people &#8211; especially those not watching their diets or those with health conditions.  My hematologist told me to take Vitamin B50 or B75 for the homocystine levels in my blood, and on my last visit he told me to take 4000 IU of vitamin D as new research is showing some good benefits to that.  Calcium Citrate in particular is better absorbed than the other one (sorry can&#8217;t remember the name).  A few weeks ago I had a doctor who also has portal hypertension come on this blog and leave a comment, and he told me that he thought the meds were important, but that Western medicine did not look to herbal treatments the same way they do in European or eastern cultures.  There is value in both.  </p>
<p>Thanks again for your comments &#8230; one never knows how any of this may help, but it is good to keep abreast of this most disconcerting condition and lend support wherever we can. </p>
<p>Peace,  Clint</p>
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		<title>By: Yvonne</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2762</link>
		<dc:creator>Yvonne</dc:creator>
		<pubDate>Mon, 16 Jan 2012 21:50:47 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2762</guid>
		<description>Thanks Clint,

You are very good to respond. We are about two weeks out from the original bleed. I believe my father is now on a low dose of propranolol, original dose was too much and affected his blood pressure ( too low). He is actually going back to the doctor tomorrow to check on the bands that were placed around the veins. 

With regards to the rest of his Meds, most of which are natural

1) selenium, zinc, magnesium 
2) vitamin A, E 
3) milk thistle, essiac tea, beta glucan, 
4) vitamin D3
5)  shiitake and reishi mushroom extract

He is also on a low sodium, meat and dairy free diet

We are hopeful this will help to strengthen him and fight off the cancer, minimize the potential of another bleed and also just help the cirrhosis,

Thanks again Clint. I will keep checking back in to stay uptodate on everyone&#039;s progress

Yvonne</description>
		<content:encoded><![CDATA[<p>Thanks Clint,</p>
<p>You are very good to respond. We are about two weeks out from the original bleed. I believe my father is now on a low dose of propranolol, original dose was too much and affected his blood pressure ( too low). He is actually going back to the doctor tomorrow to check on the bands that were placed around the veins. </p>
<p>With regards to the rest of his Meds, most of which are natural</p>
<p>1) selenium, zinc, magnesium<br />
2) vitamin A, E<br />
3) milk thistle, essiac tea, beta glucan,<br />
4) vitamin D3<br />
5)  shiitake and reishi mushroom extract</p>
<p>He is also on a low sodium, meat and dairy free diet</p>
<p>We are hopeful this will help to strengthen him and fight off the cancer, minimize the potential of another bleed and also just help the cirrhosis,</p>
<p>Thanks again Clint. I will keep checking back in to stay uptodate on everyone&#8217;s progress</p>
<p>Yvonne</p>
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		<title>By: Clint</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2440</link>
		<dc:creator>Clint</dc:creator>
		<pubDate>Mon, 02 Jan 2012 01:01:28 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2440</guid>
		<description>Hello Yvonne,

Thanks for your inquiry.  For everyone who comments or for that matter reads this blog and they themselves or a loved is dealing with portal hypertension - I am &lt;strong&gt;always saddened &lt;/strong&gt;to learn about their struggles.  In particular it can be very confusing and uncertain when I person first learns of this, and you are no exception to that if you have been reading the comments posted here.  In the 2 years I have now managed this blog I have been in touch with many people who have successfully survived banding and continue to live many years beyond the diagnosis.  To date I have not come across anyone who is dealing with the 2 added complications that your Dad is dealing with, so I have no one to compare him with.  If this is a 3 day course of meds I would be interested in knowing what he is on - if you know that as that may be helpful to others in the event they are dealing with the same issue.  I am sure he will be on a beta blocker to lower his blood pressure in case of additional bleeds (if there are other varices known) and that seems to be the standard treatment for those of us with this condition.  I can&#039;t even begin to imagine how you are feeling right now as you said you are on pins and needles - all I can offer (and I hope you don&#039;t mind) is for me to uphold your Dad in prayer.   Overall I would appreciate knowing how the treatment is working, so if you can update me that would be great.  

Take care,

Clint</description>
		<content:encoded><![CDATA[<p>Hello Yvonne,</p>
<p>Thanks for your inquiry.  For everyone who comments or for that matter reads this blog and they themselves or a loved is dealing with portal hypertension &#8211; I am <strong>always saddened </strong>to learn about their struggles.  In particular it can be very confusing and uncertain when I person first learns of this, and you are no exception to that if you have been reading the comments posted here.  In the 2 years I have now managed this blog I have been in touch with many people who have successfully survived banding and continue to live many years beyond the diagnosis.  To date I have not come across anyone who is dealing with the 2 added complications that your Dad is dealing with, so I have no one to compare him with.  If this is a 3 day course of meds I would be interested in knowing what he is on &#8211; if you know that as that may be helpful to others in the event they are dealing with the same issue.  I am sure he will be on a beta blocker to lower his blood pressure in case of additional bleeds (if there are other varices known) and that seems to be the standard treatment for those of us with this condition.  I can&#8217;t even begin to imagine how you are feeling right now as you said you are on pins and needles &#8211; all I can offer (and I hope you don&#8217;t mind) is for me to uphold your Dad in prayer.   Overall I would appreciate knowing how the treatment is working, so if you can update me that would be great.  </p>
<p>Take care,</p>
<p>Clint</p>
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		<title>By: Yvonne</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2436</link>
		<dc:creator>Yvonne</dc:creator>
		<pubDate>Sun, 01 Jan 2012 23:08:11 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2436</guid>
		<description>Hi Clint 

I am so glad I came across your site today. My father has been battling liver cancer for the last seven months, through alternative, integrative therapies and was doing very well. Unfortunately he also has portal hypertension and cirrhosis. Today was the first time he ever experienced bleeding and was informed of the concept of Esophageal varices , all very scary as you well know. We had no idea this was going to be part of his journey. Doctors immediately carried out the banding treatment and he is on a three day course of Meds. We are on pins and needles waiting to see how everything turns out. After reading your site I am hopeful he has a chance of managing this. Have you come across anyone on your journey who is also battling liver cancer (tumor) and cirrhosis ?

Thanks Clint

Yvonne</description>
		<content:encoded><![CDATA[<p>Hi Clint </p>
<p>I am so glad I came across your site today. My father has been battling liver cancer for the last seven months, through alternative, integrative therapies and was doing very well. Unfortunately he also has portal hypertension and cirrhosis. Today was the first time he ever experienced bleeding and was informed of the concept of Esophageal varices , all very scary as you well know. We had no idea this was going to be part of his journey. Doctors immediately carried out the banding treatment and he is on a three day course of Meds. We are on pins and needles waiting to see how everything turns out. After reading your site I am hopeful he has a chance of managing this. Have you come across anyone on your journey who is also battling liver cancer (tumor) and cirrhosis ?</p>
<p>Thanks Clint</p>
<p>Yvonne</p>
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		<title>By: Clint</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2169</link>
		<dc:creator>Clint</dc:creator>
		<pubDate>Tue, 20 Dec 2011 02:54:20 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2169</guid>
		<description>The above message translated ...  Hi guys I am also patients with portal hypertension, I&#039;m 29 years old now .. and when the portal hypertension was diagnosed I was 3 chronon.Einai a condition difficult and treacherous, but anyone can address whether the removal prosechei.Ekana splenomegaly when I was 5 years old and splinonefriki epanastomosi by warren after bleeding varices 2 major surgeon in Greece ... but the problem does not stop now every six months I do checkups with blood and gastroscopy .. I take medication only Interal propanololy .. 4 tablets a day .. of course it must be careful not to get tired and do not put this epidinonei pounds because of portal hypertension .. I wish them all anarosi to parents of children COURAGE because everything will pass, I&#039;m sure that scientists are close to the treatment of portal hypertension which will take a few years to come ... Thank you all and especially Clint who did this istiologio to speak .. Well christougena!</description>
		<content:encoded><![CDATA[<p>The above message translated &#8230;  Hi guys I am also patients with portal hypertension, I&#8217;m 29 years old now .. and when the portal hypertension was diagnosed I was 3 chronon.Einai a condition difficult and treacherous, but anyone can address whether the removal prosechei.Ekana splenomegaly when I was 5 years old and splinonefriki epanastomosi by warren after bleeding varices 2 major surgeon in Greece &#8230; but the problem does not stop now every six months I do checkups with blood and gastroscopy .. I take medication only Interal propanololy .. 4 tablets a day .. of course it must be careful not to get tired and do not put this epidinonei pounds because of portal hypertension .. I wish them all anarosi to parents of children COURAGE because everything will pass, I&#8217;m sure that scientists are close to the treatment of portal hypertension which will take a few years to come &#8230; Thank you all and especially Clint who did this istiologio to speak .. Well christougena!</p>
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		<title>By: Θεοδωρος Κεκελης</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-2160</link>
		<dc:creator>Θεοδωρος Κεκελης</dc:creator>
		<pubDate>Mon, 19 Dec 2011 10:25:29 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-2160</guid>
		<description>Γεια σας παιδια ειμαι και εγω ασθενης με πυλαια υπερταση,ειμαι 29 χρονων τωρα..Ενω οταν διαγνωστηκε η πυλαια υπερταση ημουν 3 χρονων.Ειναι μια παθηση δυσκολη και υπουλη αλλα μπορει ο καθενας να την αντιμετωπισει αν προσεχει.Εκανα αφαιρεση σπληνομεγαλιας οταν ημουν 5 χρονων και σπληνονεφρικη επαναστομωση κατα warren μετα απο αιμοραγια κιρσων 2 μεγαλα χειρουργια στην Ελλαδα...Αλλα το προβλημα δεν σταματαει τωρα καθε εξι μηνες κανω ελεγχο με αιματολογικες και γαστροσκοπησεις..Παιρνω φαρμακευτικη αγωγη μονο Interal propanololy..4 δισκια την ημερα..Βεβαια πρεπει να προσεχετε να μην κουραζεστε και να μην βαλετε κιλα γιατι αυτο επιδινωνει την πυλαια υπερταση..Ευχομαι σε ολους καλη αναρωση στους γονεις των παιδιων κουραγιο γιατι ολα θα περασουν,ειμαι σιγουρος οτι οι επιστημονες ειναι κοντα στην θεραπεια της πυλαιας υπερτασης η οποια θα διαρκεσει λιγα χρονια ακομα...Ευχαριστω ολους και τον Clint ιδιαιτερα που εκανε αυτο το ιστιολογιο για να μιλαμε..Καλα χριστουγενα!!!</description>
		<content:encoded><![CDATA[<p>Γεια σας παιδια ειμαι και εγω ασθενης με πυλαια υπερταση,ειμαι 29 χρονων τωρα..Ενω οταν διαγνωστηκε η πυλαια υπερταση ημουν 3 χρονων.Ειναι μια παθηση δυσκολη και υπουλη αλλα μπορει ο καθενας να την αντιμετωπισει αν προσεχει.Εκανα αφαιρεση σπληνομεγαλιας οταν ημουν 5 χρονων και σπληνονεφρικη επαναστομωση κατα warren μετα απο αιμοραγια κιρσων 2 μεγαλα χειρουργια στην Ελλαδα&#8230;Αλλα το προβλημα δεν σταματαει τωρα καθε εξι μηνες κανω ελεγχο με αιματολογικες και γαστροσκοπησεις..Παιρνω φαρμακευτικη αγωγη μονο Interal propanololy..4 δισκια την ημερα..Βεβαια πρεπει να προσεχετε να μην κουραζεστε και να μην βαλετε κιλα γιατι αυτο επιδινωνει την πυλαια υπερταση..Ευχομαι σε ολους καλη αναρωση στους γονεις των παιδιων κουραγιο γιατι ολα θα περασουν,ειμαι σιγουρος οτι οι επιστημονες ειναι κοντα στην θεραπεια της πυλαιας υπερτασης η οποια θα διαρκεσει λιγα χρονια ακομα&#8230;Ευχαριστω ολους και τον Clint ιδιαιτερα που εκανε αυτο το ιστιολογιο για να μιλαμε..Καλα χριστουγενα!!!</p>
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		<title>By: Rachel Johnson</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-1651</link>
		<dc:creator>Rachel Johnson</dc:creator>
		<pubDate>Tue, 22 Nov 2011 18:18:14 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-1651</guid>
		<description>Hi, I hope I&#039;m not crashing your party but yours is the most hopeful source of information I have found in searching for help with symptoms of portal hypertension. I&#039;ve been reading through your blog for a while and haven&#039;t come across anyone with a Hepatitis C diagnosis. In 2004 I was diagnosed with HepC, did 11 months of chemo+antiviral treatment that did nothing helpful. In 2006 I was diagnosed with portal hypertension. I&#039;ve had no more treatment than medication to control acid reflux. In the last year I&#039;ve developed an excruciating chest pain that is always in the same spot. I&#039;ve had it off and on, sometimes for days in a row. No doctor seemed particularly concerned. This fall the pain has become a daily constant. Recently I&#039;ve had a feeling like something heavy in my throat -lame description . . . it&#039;s like it hurts to swallow as if the area just gets stiff. I frequently have discomfort after eating-sore throat and mild pain. Does that make any sense to anyone? Can the portal hypertension cause pain that severe? Could I have the beginning of varices that, while not bleeding, is causing a lot of discomfort? My family doc, here where we live in a rural area, says there are NO symptoms of varices except bleeding and so when I have bleeding I should let them know! Searching the internet for symptoms of varices is not much better-there too bleeding seems to be the only symptom worth noting. 
My doc suggested something else was causing the pain, but prescribed nexium, which my insurance did not cover so that was the end of that. I already take prilosec, buy zantac over the counter and get little relief when the pain is particularly bad . . .  then nothing helps.
Rachel</description>
		<content:encoded><![CDATA[<p>Hi, I hope I&#8217;m not crashing your party but yours is the most hopeful source of information I have found in searching for help with symptoms of portal hypertension. I&#8217;ve been reading through your blog for a while and haven&#8217;t come across anyone with a Hepatitis C diagnosis. In 2004 I was diagnosed with HepC, did 11 months of chemo+antiviral treatment that did nothing helpful. In 2006 I was diagnosed with portal hypertension. I&#8217;ve had no more treatment than medication to control acid reflux. In the last year I&#8217;ve developed an excruciating chest pain that is always in the same spot. I&#8217;ve had it off and on, sometimes for days in a row. No doctor seemed particularly concerned. This fall the pain has become a daily constant. Recently I&#8217;ve had a feeling like something heavy in my throat -lame description . . . it&#8217;s like it hurts to swallow as if the area just gets stiff. I frequently have discomfort after eating-sore throat and mild pain. Does that make any sense to anyone? Can the portal hypertension cause pain that severe? Could I have the beginning of varices that, while not bleeding, is causing a lot of discomfort? My family doc, here where we live in a rural area, says there are NO symptoms of varices except bleeding and so when I have bleeding I should let them know! Searching the internet for symptoms of varices is not much better-there too bleeding seems to be the only symptom worth noting.<br />
My doc suggested something else was causing the pain, but prescribed nexium, which my insurance did not cover so that was the end of that. I already take prilosec, buy zantac over the counter and get little relief when the pain is particularly bad . . .  then nothing helps.<br />
Rachel</p>
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		<title>By: Clint</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-922</link>
		<dc:creator>Clint</dc:creator>
		<pubDate>Fri, 29 Jul 2011 20:22:56 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-922</guid>
		<description>Hi Anna,

I am sorry for such a delayed response to your message, but I am having difficulties with my server for this blog and it will not allow me to directly approve comments as it should, but if I reply it is working just fine - which is always what I aim for.  

I have a contact in the Ukraine who herself is a medical doctor, and coincidentally has a little girl with PH.   In speaking with her and hospital personnel from Childrens Memorial Hospital in Chicago they mentioned that Chernobyl explosion is likely the cause of many people illness not only in the Ukraine, but countries that surround it.  The doctor from the US (Chicago) was over in the Ukraine a few years ago, and he noted that many of the kids who had PH were born prematurely and had some sort of infection in their umbilical cords to begin with.  At one hospital that this doctor visited, there were over 40 children with PH and most of them had the same symptoms at birth.  

All being said and I have said this before, I am always saddened to hear that kids are having to deal with this disease and not only that but any kind of condition that may be life threatening.  I will I could do more for these kids especially, but I am only one person and the only thing I can do is to say what I say and pray for them.  If you haven&#039;t yet noticed I am a person of faith, and I believe part of my calling is to offer support to people who are perplexed about this disease, and of course put them in touch with others so that they do not feel so all alone.  

If you try to post here again and I don&#039;t reply right away, I am working to resolve this server issue and will do my best to get back to you when things are working properly.  

Kindest regards,

Clint</description>
		<content:encoded><![CDATA[<p>Hi Anna,</p>
<p>I am sorry for such a delayed response to your message, but I am having difficulties with my server for this blog and it will not allow me to directly approve comments as it should, but if I reply it is working just fine &#8211; which is always what I aim for.  </p>
<p>I have a contact in the Ukraine who herself is a medical doctor, and coincidentally has a little girl with PH.   In speaking with her and hospital personnel from Childrens Memorial Hospital in Chicago they mentioned that Chernobyl explosion is likely the cause of many people illness not only in the Ukraine, but countries that surround it.  The doctor from the US (Chicago) was over in the Ukraine a few years ago, and he noted that many of the kids who had PH were born prematurely and had some sort of infection in their umbilical cords to begin with.  At one hospital that this doctor visited, there were over 40 children with PH and most of them had the same symptoms at birth.  </p>
<p>All being said and I have said this before, I am always saddened to hear that kids are having to deal with this disease and not only that but any kind of condition that may be life threatening.  I will I could do more for these kids especially, but I am only one person and the only thing I can do is to say what I say and pray for them.  If you haven&#8217;t yet noticed I am a person of faith, and I believe part of my calling is to offer support to people who are perplexed about this disease, and of course put them in touch with others so that they do not feel so all alone.  </p>
<p>If you try to post here again and I don&#8217;t reply right away, I am working to resolve this server issue and will do my best to get back to you when things are working properly.  </p>
<p>Kindest regards,</p>
<p>Clint</p>
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		<title>By: Aurea</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-890</link>
		<dc:creator>Aurea</dc:creator>
		<pubDate>Mon, 25 Jul 2011 00:23:52 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-890</guid>
		<description>Hi, Clint. It was very interesting to find a site like yours to share with people that has similar experiences. 
I would like to share with everyone about my brother&#039;s condition. He was diagnose to have liver cirrhosis where his esophageal and gastric varices started from. As of this time, he is fortunate to not have bleeding, although he has low platelet count coming from his spleenomegaly. The good thing about his condition is that it was found out before any bleeding started and that he is now placed on propanolol, hctz and inderal. 
Couple of weeks ago, he complained of stomach ache which prompted his gastroenterologist to order an endoscopy. That is when he found out that my brother has the varices. 
Unfortunately, my brother is in the, Philippines, where interventions can be limited. Wish he is with us here in the U.S.
His doctor told him that he can never fly ever. Unseemingly, this may not be true because as you have shared you are able to travel even with your present condition. This is something that I might ask his doctor. 
I will be including you in my prayers, and so with everyone who&#039;s suffering the same condition. I hope that you all retain a better condition.</description>
		<content:encoded><![CDATA[<p>Hi, Clint. It was very interesting to find a site like yours to share with people that has similar experiences.<br />
I would like to share with everyone about my brother&#8217;s condition. He was diagnose to have liver cirrhosis where his esophageal and gastric varices started from. As of this time, he is fortunate to not have bleeding, although he has low platelet count coming from his spleenomegaly. The good thing about his condition is that it was found out before any bleeding started and that he is now placed on propanolol, hctz and inderal.<br />
Couple of weeks ago, he complained of stomach ache which prompted his gastroenterologist to order an endoscopy. That is when he found out that my brother has the varices.<br />
Unfortunately, my brother is in the, Philippines, where interventions can be limited. Wish he is with us here in the U.S.<br />
His doctor told him that he can never fly ever. Unseemingly, this may not be true because as you have shared you are able to travel even with your present condition. This is something that I might ask his doctor.<br />
I will be including you in my prayers, and so with everyone who&#8217;s suffering the same condition. I hope that you all retain a better condition.</p>
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		<title>By: Audra</title>
		<link>http://www.portal-hypertension.com/my-own-portal-hypertension-journey/comment-page-1/#comment-842</link>
		<dc:creator>Audra</dc:creator>
		<pubDate>Thu, 14 Jul 2011 02:50:15 +0000</pubDate>
		<guid isPermaLink="false">http://www.portal-hypertension.com/my-own-portal-hypertension-journey/#comment-842</guid>
		<description>Hi
I am responding to Anna question.  I was diagnosed with PVT and portal hypertension 3 years ago (see previous posts).  I live in British Columbia, Canada and in the last 2 years I have travelled by plane several times.  In January 2010, I flew to Arizona and in the summer of 2010, I flew to Toronto.  This March I went to Palm Springs and in May to New Orleans.  My doctor told be I was fine to fly because I am on Warfarin which should prevent clotting.  I have also taken a few long car trips, making sure to stop every couple of hours to walk around.  I hope this helps.  

Take Care,

Audra</description>
		<content:encoded><![CDATA[<p>Hi<br />
I am responding to Anna question.  I was diagnosed with PVT and portal hypertension 3 years ago (see previous posts).  I live in British Columbia, Canada and in the last 2 years I have travelled by plane several times.  In January 2010, I flew to Arizona and in the summer of 2010, I flew to Toronto.  This March I went to Palm Springs and in May to New Orleans.  My doctor told be I was fine to fly because I am on Warfarin which should prevent clotting.  I have also taken a few long car trips, making sure to stop every couple of hours to walk around.  I hope this helps.  </p>
<p>Take Care,</p>
<p>Audra</p>
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