{"id":32350,"date":"2021-06-24T17:12:45","date_gmt":"2021-06-24T15:12:45","guid":{"rendered":"https:\/\/eufortrisomy21.eu\/?p=32350"},"modified":"2022-07-22T10:28:28","modified_gmt":"2022-07-22T08:28:28","slug":"online-conference-improving-the-visibility-of-people-with-down-syndrome-an-emergency-for-europe","status":"publish","type":"post","link":"https:\/\/eufortrisomy21.eu\/et\/online-conference-improving-the-visibility-of-people-with-down-syndrome-an-emergency-for-europe\/","title":{"rendered":"Veebikonverents - 8. juuli 2021 - Downi s\u00fcndroomiga inimeste n\u00e4htavuse parandamine"},"content":{"rendered":"<p style=\"text-align: right;\"><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-14470 alignleft\" src=\"https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7-300x120.jpg\" alt=\"\" width=\"300\" height=\"120\" srcset=\"https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7-300x120.jpg 300w, https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7-1024x410.jpg 1024w, https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7-768x307.jpg 768w, https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7-1536x614.jpg 1536w, https:\/\/eufortrisomy21.eu\/wp-content\/uploads\/2020\/02\/Banniere7.jpg 2000w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<h2 style=\"text-align: center;\">Downi s\u00fcndroomiga inimeste n\u00e4htavuse parandamine: h\u00e4daolukord Euroopale. Miks? Kuidas?<\/h2>\n<p>Downi s\u00fcndroomiga inimeste n\u00e4htavuse parandamine Euroopas peaks olema suur arutelu <a href=\"https:\/\/futureu.europa.eu\/\" target=\"_blank\" rel=\"noopener\">kodanike konsultatsioon Euroopa tuleviku nimel<\/a>.<\/p>\n<p><strong><a href=\"https:\/\/docs.google.com\/forms\/d\/e\/1FAIpQLSfcweCVPOG7YO_JwvF9NAbhpVdDDrUbxl59EM7JJ17kPaB95Q\/viewform\" target=\"_blank\" rel=\"noopener\">Registreeru siin<\/a> <\/strong>osaleda veebikonverentsil EUfortrisomy21 teemal <strong>8. juulil kell 18.00 (Br\u00fcsseli aja j\u00e4rgi)<\/strong> ning aidata kaasa Euroopa tuleviku teemalise kodanikukonsultatsiooni veebiaruteludele, et parandada Downi s\u00fcndroomiga inimeste n\u00e4htavust.<\/p>\n<p><strong>Keeled:<\/strong> Inglise, hispaania, prantsuse, saksa, saksa lihtsakeelne, t\u0161ehhi ja itaalia keel<\/p>\n<p>&nbsp;<\/p>\n<h2><u>Programm:<\/u><\/h2>\n<p><strong>Sissejuhatus: <\/strong>Hr Brando Benifei (Euroopa Parlamendi liige - Itaalia)<\/p>\n<p><strong>1. osa: Vastuolulised diskrimineerimise juhtumid Euroopas\u00a0<\/strong><\/p>\n<ul>\n<li>Kallis tulevane ema - Riccardo Bianchi - Coordown (IT)<\/li>\n<li>Kallis tulevane ema (tsensuur ja kohtuasi EI\u00d5K ees) - Lucie Pacherie - Fondation J\u00e9r\u00f4me Lejeune (Prantsusmaa)<\/li>\n<li>Arcadi Spada juhtum (SP) ja Richard Dawkinsi juhtum - Raquel del Barrio (Hispaania 21. Trisoomia referentvanem)<\/li>\n<\/ul>\n<p><strong>2. osa: Miks on see diskrimineeriv k\u00f5ne Euroopas endiselt olemas?<\/strong><\/p>\n<ul>\n<li>Filosoof: Danielle Moyse (Prantsusmaa)<\/li>\n<li>Tina Sander (\u00fchingu asutaja): #NoNIPT kampaania Saksamaal (GE)<\/li>\n<li>Enda eestk\u00f5neleja: Natalie Dedreux-blogija ja ajakirjanik (GE)<\/li>\n<\/ul>\n<p><strong>Osa 3: Kuidas tegutseda, et edendada 21. trisoomiaga inimeste v\u00e4\u00e4rikust ja soodustada nende n\u00e4htavust?<\/strong><\/p>\n<ul>\n<li>Enda eestk\u00f5neleja: Caterina Moretti (SP)<\/li>\n<li>Video Euroopa tuleviku konverentsi Euroopa Komisjoni esimehe pr Dubravka Suicast<\/li>\n<\/ul>\n<p><strong>K\u00fcsimused ja vastused<\/strong><\/p>\n<p><strong>J\u00e4reldus: <\/strong>Pr Radka Maxova (Euroopa Parlamendi liige - T\u0161ehhi Vabariik)<\/p>\n<p id=\"tw-target-text\" class=\"tw-data-text tw-text-large XcVN5d tw-ta\" data-placeholder=\"Traduction\">Meie veebikonverentsi kordusvideod on saadaval <a href=\"https:\/\/www.youtube.com\/channel\/UCFbORaGOrc9HBNBSK7DG-nQ?app=desktop&amp;pli=1\" target=\"_blank\" rel=\"noopener\">meie YouTube&#039;i kanalil<\/a>.<\/p>\n<p style=\"text-align: center;\"><span class=\"fontstyle0\">EUfortrisomy21 <\/span><span class=\"fontstyle2\">on Downi s\u00fcndroomiga laste vanemate kogukond,<br \/>\n\u00fchendatud Downi s\u00fcndroomiga inimeste \u00f5iguste edendamiseks neljas prioriteetses valdkonnas:<br \/>\nn\u00e4htavus, mittediskrimineerimine, tervis, autonoomia<\/span><\/p>\n<p style=\"text-align: center;\"><strong>V\u00f5ta \u00fchendust<\/strong> : contact@eufortrisomy21.eu<\/p>\n<p style=\"text-align: right;\">","protected":false},"excerpt":{"rendered":"<p>Improving the visibility of people with Down syndrome in Europe should be a major debate in the citizen\u2019s consultation for&hellip;<\/p>","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[45],"tags":[],"class_list":["post-32350","post","type-post","status-publish","format-standard","hentry","category-21-march-21"],"acf":[],"_links":{"self":[{"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/posts\/32350"}],"collection":[{"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/comments?post=32350"}],"version-history":[{"count":0,"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/posts\/32350\/revisions"}],"wp:attachment":[{"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/media?parent=32350"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/categories?post=32350"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/et\/wp-json\/wp\/v2\/tags?post=32350"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}