{"id":73536,"date":"2023-06-05T11:51:54","date_gmt":"2023-06-05T15:51:54","guid":{"rendered":"https:\/\/wfh.org\/article\/speaker\/baiba-ziemele\/"},"modified":"2023-09-28T09:04:50","modified_gmt":"2023-09-28T13:04:50","slug":"baiba-ziemele","status":"publish","type":"speaker","link":"https:\/\/wfh.org\/fr\/article\/speaker\/baiba-ziemele\/","title":{"rendered":"Baiba Ziemele"},"content":{"rendered":"<p>President<br \/>\nLatvia Hemophilia Society<br \/>\nLatvia<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Baiba Ziemele is a passionate patient advocate from Latvia. Living with inherited bleeding disorder, von Willebrand disease (VWD), she has been heavily involved in patient advocacy, becoming president of Latvia Hemophilia Society in 2009, representing European community with bleeding disorders as ePAG in EuroBloodNet, European Reference Network for rare haematological diseases, engaging in Women\u2019s and Girls with Bleeding Disorders Committee and VWD and Rare Bleeding Disorders committee at World Federation of Hemophilia and VWD Committee at European Haemophilia Consortium. She has helped shaping rare disease field nationally and internationally. Since 2018, Baiba is also building Latvian Network of Patient Organizations to bring united patient voice and represent patient interests at various tables. In 2022, Baiba received Human Development award for outstanding contribution to health from Civic Alliance Latvia and US Embassy in Latvia.<\/p>\n","protected":false},"featured_media":73151,"template":"","meta":{"inline_featured_image":false},"speaker-type":[267,271,269],"class_list":["post-73536","speaker","type-speaker","status-publish","has-post-thumbnail","hentry","speaker-type-all-speakers-fr","speaker-type-program-committee-fr","speaker-type-speakers-fr"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.2 (Yoast SEO v27.2) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Baiba Ziemele | FMH - F\u00e9d\u00e9ration mondiale de l\u2019h\u00e9mophilie<\/title>\n<meta name=\"robots\" content=\"noindex, follow\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Baiba Ziemele\" \/>\n<meta property=\"og:description\" content=\"Baiba Ziemele is a passionate patient advocate from Latvia. Living with inherited bleeding disorder, von Willebrand disease (VWD), she has been heavily involved in patient advocacy, becoming president of Latvia Hemophilia Society in 2009, representing European community with bleeding disorders as ePAG in EuroBloodNet, European Reference Network for rare haematological diseases, engaging in Women\u2019s and Girls with Bleeding Disorders Committee and VWD and Rare Bleeding Disorders committee at World Federation of Hemophilia and VWD Committee at European Haemophilia Consortium. She has helped shaping rare disease field nationally and internationally. Since 2018, Baiba is also building Latvian Network of Patient Organizations to bring united patient voice and represent patient interests at various tables. 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