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<title>Congenital Heart Defects &amp; acquired heart disease - Congenital Heart Defects &amp; acquired heart disease</title>
<description>Heart and Coeur is an organization that provides reliable information, support services, assistance to families of children with congenital heart defects and acquired heart disease, adults with congenital heart defects, and the professionals who work with them.</description><link>http://www.heartandcoeur.com/~forumEnglish/list.php?1</link><lastBuildDate>Thu, 17 May 2012 08:52:10 +0200</lastBuildDate>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,27,27#msg-27</guid>
<title>Information regarding correction of CHD</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,27,27#msg-27</link><description><![CDATA[ Dear Sir,<br /><br />MY son, 8 years, is having Dextrocardia, Pulmonary Atresia, Corrected Transposition of Great Arteries, Large VSD<br /><br />He undervent BDG Shunt Operation during 2004 August and was living normal.<br /><br />Now for some monthe he si becoming too tired on little exertion itself.<br /><br />Docters are confused about whether to proceed with Fonton or any other operation., Please advice.<br /><br />As per Echo report his earlier corrections of the heart is working fine]]></description>
<dc:creator>Mathew</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 02 May 2012 11:56:51 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,26#msg-26</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,26#msg-26</link><description><![CDATA[ please i will like to exchange with you. my baby will be born soon with HLSH. please can you explain to me how you are doing and how to manage the situation. thanks alot.<br /><a href="mailto:chelsiera@yahoo.fr">chelsiera@yahoo.fr</a>]]></description>
<dc:creator>chelsea</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sat, 21 Apr 2012 01:14:13 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,25#msg-25</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,25#msg-25</link><description><![CDATA[ hello and Thank you.<br />My Name is Svea and i have a heart fail- ( HLHS) Im 16 years old.<br />I was in 1996 by dr. Norwood op and been accepted, would like to contact him.<br /><br />Sorry my english is not so good.... :(<br /><br />love svea]]></description>
<dc:creator>&lt;3_Svea_ T. &lt;3</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 11 Apr 2012 10:39:58 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,24#msg-24</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,24#msg-24</link><description><![CDATA[ hello Friends i am here to let you know about my heart issue. I was having a slight pain in my hear, i thaught as if i have hole in my heart, but all thing was normal, i was nonly have some gas issue. It is really hillarious.]]></description>
<dc:creator>cbhattarai</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 28 Mar 2012 08:44:51 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,23#msg-23</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,23#msg-23</link><description><![CDATA[ bonjours, ma fille de 13 ans doit se faire operer a coeur ouvert .j ai tres peur.pouriez vous m indiquer quelque renseignement:elle a une CIA large 25mn, la prothese n a pas pu etre mise,donc elle sera operer pour lui mettre un patch de son pericarde...j ai plusieurs questions: quand son coeur sera arreter pour operer , vas t il repartir a coup sur apres, lors d une cec peut elle faire une hemoragie? j ai tres tres peur de la perdre a cause de cette operation , je suis perdue!!!! j ai peur qu elle meur sur la table d operation.tout ce processuce pour l opererer me terrifie!!! une thoracotomie laterale sera pratiquée , mais comment vont il acceder au coeur? a ce trou entre les 2 oreilletes??? merci de me repondre....]]></description>
<dc:creator>isa2bcorse</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Fri, 09 Mar 2012 19:55:47 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,22#msg-22</guid>
<title>Congenital Heart Disease</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,22#msg-22</link><description><![CDATA[ Congenital heart defects/disease are problems with the heart's structure that are present at birth. They change the normal flow of blood through the heart.<br /><br />Epilepsy Society]]></description>
<dc:creator>Alen</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 03 Aug 2011 16:01:12 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,21#msg-21</guid>
<title>Re: We kindly ask for your advice</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,21#msg-21</link><description><![CDATA[ You raise an interesting issue.<br />FOR MORE INFORMATION: cardiologyland.com<br />thank you.]]></description>
<dc:creator>SARA ANDERSON</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sun, 24 Jul 2011 06:16:32 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,20#msg-20</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,20#msg-20</link><description><![CDATA[ When you use exact medicine, It works by lowering the blood pressure levels, Generic for Aprovel (Irbesartan) is used to treat patients with high blood pressure and reducing the risk of a stroke. You can get info at Internationaldrugmart.com]]></description>
<dc:creator>Ammy</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Fri, 22 Jul 2011 12:35:35 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,15,19#msg-19</guid>
<title>Re: baby has a transposition of the great vessels</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,15,19#msg-19</link><description><![CDATA[ Dear<br />if you could go to china, the cost will not so much as you think!<br />But firstly, I must know the detailed TGA informaions, such as cardiac echo and especially needed the cardioangiography. You can send them to<br />My e_mail <a href="mailto:hjf2006111@163.com">hjf2006111@163.com</a>.<br />sincerely<br />Jianfeng Hou M.D.&amp;Ph.D.<br />Department of surgery, Fuwai hospital PUMC&amp;CAMS]]></description>
<dc:creator>Jianfeng Hou</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sat, 05 Mar 2011 17:19:27 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,18#msg-18</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,18#msg-18</link><description><![CDATA[ hi helen yes im peters mom please contact me on this numer ++4407503908254 if you dont get through just send me a message on here and give me your number. Peter is doing fine hope everythink is ok. xx]]></description>
<dc:creator>lorraine</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Mon, 28 Feb 2011 00:04:26 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,15,15#msg-15</guid>
<title>baby has a transposition of the great vessels</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,15,15#msg-15</link><description><![CDATA[ Good afternoon,<br /><br />Our names are Didimo Martrus and Katty Cervantes Martrus parents of Piero Martrus 29 days old, we are desperate, our baby has a transposition of the great vessels of the heart, this condition is not operable in our country, we have tried to get help but we made it difficult to this way, we come to you in desperation, we know this is costly (do not have many resources), so we ask you to give us a special price on the cost of this intervention, here I will move heaven and earth to get this money, please help us, I know that you have many cases, but our baby has only few weeks if he does not get the surgery.<br /><br />Our son only has a life of couple of months expectancy without operation, that is why We are desesperate.<br /><br />Hopefully God will hear this message and you, and is to convey to the people who can help us with this case.<br /><br />Regards,<br /><br />Didimo Martrus<br /><a href="mailto:dmartrus@siglo21.net">dmartrus@siglo21.net</a>]]></description>
<dc:creator>Didimo Martrus</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Thu, 26 Aug 2010 18:14:32 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,14,14#msg-14</guid>
<title>thrombolie pulmonaire</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,14,14#msg-14</link><description><![CDATA[ my wife has the chrons desease and she is taking injection adelimumab(HUMIRA) .SINCE 5MONTH SHE HAD a thrombolie pulmonaire.<br />does the chrons desease or the adelimumab is the reason. the INR is about 2-2.3 is good? she is taking anticoagulant cintrum one tablet per day.]]></description>
<dc:creator>elie</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Thu, 05 Aug 2010 22:14:24 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,13#msg-13</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,13#msg-13</link><description><![CDATA[ Lorraine ... is your son Peter ?]]></description>
<dc:creator>Helen</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 05 May 2010 13:09:04 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,12#msg-12</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,12#msg-12</link><description><![CDATA[ webmaster Wrote:Hi - Mya daughter has just been diagnosed with a 7mm ASD heart defect - She is not gaining much weight and has continual colds/blocked nose/cough - The doctor has recommended surgery closure as she is now 16 months old - but when would this happen and at what age?<br />-<br />&gt; NEW FORUM FOR C.H.D<br />&gt; This new forum is the forum for children,parents,<br />&gt; adults with CHD, and family members of children<br />&gt; who have Congenital Heart Defects in the world .<br />&gt; Interested health professionals are also invited<br />&gt; to participate in discussions.<br />&gt; Have all a great day<br />&gt; DAUMAL Christian dad of Gaelle (single-ventricle)<br />&gt;<br />&gt; President and webmaster of the &quot;heart and coeur&quot;<br />&gt; website<br />&gt; [<a href="http://www.heartandcoeur.com" target="_blank" rel="nofollow" >www.heartandcoeur.com</a>]]]></description>
<dc:creator>rosemais</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Tue, 02 Mar 2010 21:45:26 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,11#msg-11</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,11#msg-11</link><description><![CDATA[ not sure if i am the lorraine you need to speak to. but i may be,<br />kind regards lorraine]]></description>
<dc:creator>lorraine</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sat, 12 Dec 2009 20:31:35 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,10#msg-10</guid>
<title>Re: invitation for the upcoming conference</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,10#msg-10</link><description><![CDATA[ For Innovations in Cardiovascular Interventions - ICI Meeting<br />this is the web address:<br />www.congress.co.il/ici2009]]></description>
<dc:creator>The Doc</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 21 Oct 2009 12:56:57 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,9#msg-9</guid>
<title>Re: invitation for the upcoming conference</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,9#msg-9</link><description><![CDATA[ what is the URL?]]></description>
<dc:creator>Res</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Wed, 21 Oct 2009 12:53:19 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,8#msg-8</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,8#msg-8</link><description><![CDATA[ Dear Sir,<br /><br />my freinds son is 6 month old and he has AP window 7.8 mm , what is his treatment and prognosis about this congental defect<br /><br />regards<br /><br />Dr.rajesh kumar]]></description>
<dc:creator>drrajesh</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sun, 18 Oct 2009 08:17:47 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,7#msg-7</guid>
<title>invitation for the upcoming conference</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,7,7#msg-7</link><description><![CDATA[ Dear Colleagues,<br /><br />We would like to invite you to take part in the meeting “Innovations in Cardiovascular Interventions” (ICI) that will be held on December 6-8, 2009 in Tel-Aviv, Israel. Among the topics that will highlight: new devices for trancatheter therapeutics, drug eluting stents, novel molecular therapeutics, vascular molecular biology, restenosis solutions, adjunctive drug therapy and many more.<br /><br />The conference is applying clinical cardiologist, scientists and engineers as well as to financial investors and medical companies, do not miss this event!<br /><br />We look forward to the pleasure of greeting you at what promises to be an exciting and fruitful meeting with a high scientific standard.]]></description>
<dc:creator>M. Dinar</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Thu, 08 Oct 2009 11:09:32 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,6#msg-6</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,6#msg-6</link><description><![CDATA[ I'm trying to contact Lorraine. I'm from South Australia &amp; have spoken to her on the phone several times &amp; also had a discussion with her lawyer. We lost contact when I moved house<br />Please can you direct me how to contact her?<br /><br />Thanks<br />Helen]]></description>
<dc:creator>Helen Hamilton</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Thu, 04 Jun 2009 16:09:50 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,5#msg-5</guid>
<title>We kindly ask for your advice</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,5#msg-5</link><description><![CDATA[ We are a young family of doctors and have a 2.4 years old son who was born with critical isthmic coarctation of aorta, secondary pulmonary hypertension, tricuspidal insuffiency III degree and aortal bicuspidy.<br /><br />He was operated and the coarctation was corrected in the first 12 days of life in Cluj Napoca at the Cardiovascular Institute through an head-to-head anastomosis.<br /><br />The post-operatory evolution was very good, and by the 6, 12, 18, 24 months controlls an progressive aortal stenosis was observed.<br /><br />At this time, the gradient is 110 mm HG at the highest level and at 70 mm Hg at the medium level.<br />The ejection fractio is 70%. The left ventricle is not dilatated, but with a concentric hypertrophy.<br />The ascending aorta is constricted at the sino-tubular level.<br />Pulmonary insufficiency I degree was noted.<br /><br />The child is very well clinically, the effort capacity is very good, he doesn’t have any sign of illness, and is very smart.<br /><br />We are proposed now to operate him because of the gradient of the aortal stenosis, who involves the 3 levels, below, middle add upper in the form of a clepsydra but the riscs of needing a pace-maker was told to us is very very big.<br /><br />Our concerning is about these high risks, and we would like to ask if there are other options or techniques with lower risks in this situation.<br /><br />For your kindness, thank you<br /><br />Cristian and Mihaela Chirila, Oradea]]></description>
<dc:creator>Cristian Chirila</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Mon, 09 Mar 2009 14:58:27 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,4#msg-4</guid>
<title>Re: NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,4#msg-4</link><description><![CDATA[ Thank you sir.. I have a question.. What could be the possible risks why some infants are born with congenital heart defects? [<a href="http://doctorfinders.com/coherex.php" target="_blank" rel="nofollow" >doctorfinders.com</a>]]]></description>
<dc:creator>jollivee</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sat, 31 Jan 2009 06:56:45 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,3,3#msg-3</guid>
<title>Re: Ebstein s Anomaly Valve replacement</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,3,3#msg-3</link><description><![CDATA[ Dear Alison Nice to meet you on this forum, Like your son Ben Gaelle our daugter has a Single Ventricule - just left ventricle without right ventricle - Situs solitus-Transposition of the great vessels-Atrial septal defect- Atresia valve atrium - ventricle - Coarctation of the Aorta-Hypoplastic aortic - Today Gaelle is 13 and a beautiful girl,but gaelle had five important surgery to repair her heart and maybe another in the future I would like never but ... The last surgery was from a TOTAL exclusion of the right heart by interposition of a tube core-tex between the IVC Inferior Vena Cava and the pulmonary junction after plastie of the junction. Now Gaelle is pink with a saturation near 95per cent and she is brimming with life,she does bicycle with her brother Adrien, swimming, dance etc... We Gaelle's parents are happiest... we live in Paris France. For me it is important for all to be able to help itself between us in the world, to exchange ideas,and to compare impressions. How old is your son? I look forward to hearing from you. Christian-Maryvonne-Gaelle-Adrien]]></description>
<dc:creator>Wes</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sun, 02 Nov 2008 12:47:51 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,2,2#msg-2</guid>
<title>situs invertus</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,2,2#msg-2</link><description><![CDATA[ In 2001 our daughter was almost two when our son was born and required surgery,Our newborn's heart defect was not detected in the hospital when he was born. He had a sistus invertus. Now I would like to seek another parent with same disease.]]></description>
<dc:creator>cdaumal</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sun, 30 Nov 2008 16:41:36 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,1#msg-1</guid>
<title>NEW FORUM for congenital heart defects</title><link>http://www.heartandcoeur.com/~forumEnglish/read.php?1,1,1#msg-1</link><description><![CDATA[ NEW FORUM FOR C.H.D<br />This new forum is the forum for children,parents, adults with CHD, and family members of children who have Congenital Heart Defects in the world .<br />Interested health professionals are also invited to participate in discussions.<br />Have all a great day<br />DAUMAL Christian dad of Gaelle (single-ventricle)<br />President and webmaster of the &quot;heart and coeur&quot; website<br />[<a href="http://www.heartandcoeur.com" target="_blank" rel="nofollow" >www.heartandcoeur.com</a>]]]></description>
<dc:creator>webmaster</dc:creator>
<category>Congenital Heart Defects &amp; acquired heart disease</category><pubDate>Sun, 23 Nov 2008 21:08:12 +0100</pubDate></item>
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