{"id":1213,"date":"2025-12-11T08:58:18","date_gmt":"2025-12-11T08:58:18","guid":{"rendered":"https:\/\/www.weandmecfs.org\/?p=1213"},"modified":"2026-01-27T14:13:23","modified_gmt":"2026-01-27T13:13:23","slug":"brent-stirton-fotografiert-me-cfs-patienten-in-oesterreich-ausstellung-bei-der-art-antique-in-der-hofburg","status":"publish","type":"post","link":"https:\/\/www.weandmecfs.org\/de\/brent-stirton-fotografiert-me-cfs-patienten-in-oesterreich-ausstellung-bei-der-art-antique-in-der-hofburg\/","title":{"rendered":"Brent Stirton fotografiert ME\/CFS-Patienten in \u00d6sterreich \u2013 Ausstellung bei der Art &amp; Antique in der Hofburg"},"content":{"rendered":"\n<p>Mit gro\u00dfer Freude d\u00fcrfen wir verk\u00fcnden, dass der international renommierte und vielfach preisgekr\u00f6nte Fotograf Brent Stirton, bekannt f\u00fcr seine tief bewegenden Arbeiten zu humanit\u00e4ren Krisen, Umweltkatastrophen und verheerenden Krankheiten, in \u00d6sterreich eine au\u00dfergew\u00f6hnliche Fotoserie \u00fcber ME\/CFS-Patient*innen geschaffen hat. Stirton, dessen eindrucksvolle Bilder regelm\u00e4\u00dfig in \u201eNational Geographic\u201c und dem \u201eTime Magazine\u201c zu sehen sind, hat im August 2024 zehn Menschen portr\u00e4tiert, die an ME\/CFS leiden.<\/p>\n\n\n\n<p>Mit seinem unvergleichlichen Blick f\u00fcr menschliche Schicksale hat er die tiefen Herausforderungen und die stille Tragik, die das Leben der Betroffenen pr\u00e4gen, in ergreifenden Bildern eingefangen. Seine Fotografien zeigen auf eindr\u00fcckliche Weise, wie diese kaum erforschte Krankheit das Leben der Erkrankten und ihrer Angeh\u00f6rigen dominiert. Jede Aufnahme erz\u00e4hlt nicht nur die Geschichte des individuellen Leidens, sondern gibt den oft in Isolation lebenden Betroffenen eine Stimme, die geh\u00f6rt werden muss. Stirtons Serie tr\u00e4gt dazu bei, das Bewusstsein f\u00fcr ME\/CFS zu sch\u00e4rfen und das unsichtbare Leiden vieler Menschen ins Licht der \u00d6ffentlichkeit zu r\u00fccken.<\/p>\n\n\n\n<p>F\u00fcnf dieser tief bewegenden Fotografien werden vom 7. bis 11. November 2024 im Rahmen der Art &amp; Antique in der Wiener Hofburg erstmals der \u00d6ffentlichkeit pr\u00e4sentiert \u2013 ein besonderes Highlight, das Besucher*innen tief ber\u00fchren wird.<\/p>\n\n\n\n<p>Am 10. November um 15:00 Uhr wird zudem die Charity-Aktion \u201eKUNSTH\u00c4NDLER*INNEN HELFEN\u201c zugunsten der WE &amp; ME Stiftung stattfinden. Im Rahmen dieser Initiative werden f\u00fcnf hochkar\u00e4tige Kunstwerke, die von f\u00fchrenden Galerien gespendet wurden, verlost. Mit einem Los ab nur 20 Euro k\u00f6nnen Sie nicht nur die Chance auf ein Meisterwerk erhalten, sondern auch aktiv dazu beitragen, Menschen mit ME\/CFS zu unterst\u00fctzen.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Mit gro\u00dfer Freude d\u00fcrfen wir verk\u00fcnden, dass der international renommierte und vielfach preisgekr\u00f6nte Fotograf Brent Stirton, bekannt f\u00fcr seine tief bewegenden Arbeiten zu humanit\u00e4ren Krisen, Umweltkatastrophen und verheerenden Krankheiten, in \u00d6sterreich eine au\u00dfergew\u00f6hnliche Fotoserie \u00fcber ME\/CFS-Patient*innen geschaffen hat. Stirton, dessen eindrucksvolle Bilder regelm\u00e4\u00dfig in \u201eNational Geographic\u201c und dem \u201eTime Magazine\u201c zu sehen sind, hat im [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":1214,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[51,1],"tags":[],"class_list":["post-1213","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news","category-uncategorized"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Brent Stirton fotografiert ME\/CFS-Patienten in \u00d6sterreich \u2013 Ausstellung bei der Art &amp; Antique in der Hofburg &#8226; WE &amp; ME Stiftung<\/title>\n<meta name=\"description\" content=\"Mit gro\u00dfer Freude d\u00fcrfen wir verk\u00fcnden, dass der international renommierte und vielfach preisgekr\u00f6nte Fotograf Brent Stirton, bekannt f\u00fcr seine tief\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.weandmecfs.org\/de\/brent-stirton-fotografiert-me-cfs-patienten-in-oesterreich-ausstellung-bei-der-art-antique-in-der-hofburg\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Brent Stirton fotografiert ME\/CFS-Patienten in \u00d6sterreich \u2013 Ausstellung bei der Art &amp; 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Jan Equiluz had to give up his passion. He was studying trumpet and psychology when he fell ill. He wanted to become a professional musician. He was well on his way there. But a corona infection that led to ME\\\/CFS changed everything. Even listening to music is now far too stressful for Jan, let alone playing an instrument. Jan had to stop studying the trumpet and later also pause his psychology studies. \u201cIt's so frustrating,\u201d says Jan. His mother is a doctor. She soon suspects what is wrong with her son. As a result, Jan receives a diagnosis and the best possible treatment faster than most. The few doctors with ME\\\/CFS expertise in the country are almost all private practitioners - unlike many others, Jan is fortunate that his family can afford it. But Jan still loses almost everything - ME\\\/CFS destroys lives, no matter how privileged you are. Jan moves back in with his mother. Coping with everyday life alone is impossible. 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Jan Equiluz had to give up his passion. He was studying trumpet and psychology when he fell ill. He wanted to become a professional musician. He was well on his way there. But a corona infection that led to ME\/CFS changed everything. Even listening to music is now far too stressful for Jan, let alone playing an instrument. Jan had to stop studying the trumpet and later also pause his psychology studies. \u201cIt's so frustrating,\u201d says Jan. His mother is a doctor. She soon suspects what is wrong with her son. As a result, Jan receives a diagnosis and the best possible treatment faster than most. The few doctors with ME\/CFS expertise in the country are almost all private practitioners - unlike many others, Jan is fortunate that his family can afford it. But Jan still loses almost everything - ME\/CFS destroys lives, no matter how privileged you are. Jan moves back in with his mother. Coping with everyday life alone is impossible. In his room are many of his non-fiction books, which he can no longer read - and his instruments and CDs, which he no longer uses. Jan spends most of his time in bed. When his mother comes home, they spend the evening talking. On good days, Jan can go to the pharmacy around the corner. About once a month, he meets friends in a bar. \u201cI need to get out at least briefly and experience everyday life,\u201d says Jan. Even though he has more and stronger symptoms afterwards, Jan says the isolation is the worst thing. Sometimes anger boils up inside Jan. He is angry because so few people take ME\/CFS seriously. Because there isn't more intensive research into it. Because hardly anyone speaks out, even though the situation of those affected is so precarious. Jan tries to make the best of it. In the fall, he wants to resume his interrupted psychology studies and attend at least a few lectures from home. 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