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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 08:52:33 +0200</lastBuildDate>
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<title>Information regarding correction of CHD (no replies)</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?1,15,15#msg-15</guid>
<title>baby has a transposition of the great vessels (1 reply)</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>Sat, 05 Mar 2011 17:19:27 +0100</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,14,14#msg-14</guid>
<title>thrombolie pulmonaire (no replies)</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?1,7,7#msg-7</guid>
<title>invitation for the upcoming conference (2 replies)</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>Wed, 21 Oct 2009 12:56:57 +0200</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 (-1 replies)</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>Mon, 28 Jul 2003 07:43:16 +0200</pubDate></item>
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<guid>http://www.heartandcoeur.com/~forumEnglish/read.php?1,2,2#msg-2</guid>
<title>situs invertus (no replies)</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 (15 replies)</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>Sat, 21 Apr 2012 01:14:13 +0200</pubDate></item>
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