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	<title>Team &#8211; PH Austria</title>
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	<description>Lungenkinder Forschungsverein</description>
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	<title>Team &#8211; PH Austria</title>
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		<title>Gerald Fischer</title>
		<link>https://lungenhochdruck.at/en/team/gerald-fischer/</link>
		
		<dc:creator><![CDATA[AlphaHosting]]></dc:creator>
		<pubDate>Thu, 28 Nov 2024 14:03:15 +0000</pubDate>
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					<description><![CDATA[Gerry Fischer, Chairman of PH Austria &#8211; Initiative Lungenhochdruck. Er hat zudem 1999 den Lungenkinder Forschungsverein ins Leben gerufen Gerry Fischer is chairman of PH Austria &#8211; Initiative Lungenhochdruck. He also set up the Lungenkinder Forschungsverein in 1999: I foundet the Lungenkinder Forschungsverein because my family and I are personally affected. Both associations are very [&#8230;]]]></description>
										<content:encoded><![CDATA[<p style="text-align: justify;">Gerry Fischer, Chairman of PH Austria &#8211; Initiative Lungenhochdruck. Er hat zudem 1999 den Lungenkinder Forschungsverein ins Leben gerufen<br />
<span id="more-1053"></span>Gerry Fischer is chairman of PH Austria &#8211; Initiative Lungenhochdruck. He also set up the Lungenkinder Forschungsverein in 1999: I foundet the Lungenkinder Forschungsverein because my family and I are personally affected. Both associations are very close to my heart! The life-threatening disease pulmonary hypertension occurs very rarely, and the general economic interest in research into the desease and appropriate therapies and drugs is unfortunately very low. There are only a few specalist centers that deal with the disease in both, research and treatment &#8211; mainly there is a lack of financial resources. In addition, the population´s willingnes to donate is also very reserved. The aim is to make the rare disease better known, to create compassion and solidarity for those affected through information and to advance important research.<span id="more-364"></span></p>
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		<title>Jacqueline Salopek</title>
		<link>https://lungenhochdruck.at/en/team/jacqueline-salopek/</link>
		
		<dc:creator><![CDATA[Freshfox]]></dc:creator>
		<pubDate>Thu, 28 Nov 2024 13:39:42 +0000</pubDate>
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					<description><![CDATA[Ehrenamtliche Unterstützung für PHA Europe]]></description>
										<content:encoded><![CDATA[<p>Ehrenamtliche Unterstützung für PHA Europe</p>
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		<title>Eva Otter</title>
		<link>https://lungenhochdruck.at/en/team/eva-otter/</link>
		
		<dc:creator><![CDATA[AlphaHosting]]></dc:creator>
		<pubDate>Tue, 28 Sep 2021 22:36:44 +0000</pubDate>
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					<description><![CDATA[Support for PH-Patients Eva lives in St. Pölten in Lower Austria and worked as a doctor´s assistant in a nuclear medicine laboratory. She had to quit her job in 2008, five years after she was diagnosed with PAH. To help other PH Patients cope their illness, social cases and other matters, she started working at [&#8230;]]]></description>
										<content:encoded><![CDATA[<p style="text-align: justify;">Support for PH-Patients<br />
<span id="more-1054"></span> <span id="more-364"></span>Eva lives in St. Pölten in Lower Austria and worked as a doctor´s assistant in a nuclear medicine laboratory. She had to quit her job in 2008, five years after she was diagnosed with PAH. To help other PH Patients cope their illness, social cases and other matters, she started working at PH Austria. She has been trained as a person of trust for people with reduced mobility and is also part of the board of PHA Europe.</p>
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