{"id":3155,"date":"2023-01-12T10:38:51","date_gmt":"2023-01-12T08:38:51","guid":{"rendered":"https:\/\/rijetke-bolesti.com\/?page_id=3155"},"modified":"2025-04-29T12:46:40","modified_gmt":"2025-04-29T10:46:40","slug":"acf","status":"publish","type":"page","link":"https:\/\/rijetke-bolesti.com\/en\/projekti\/acf\/","title":{"rendered":"ACF"},"content":{"rendered":"<h1 class=\"wp-block-heading\">Active Citizens Fund &#8211; ACF<\/h1>\n\n\n\n<h2 class=\"wp-block-heading\">WOMEN'S VOICE FOR THE SYSTEM!\nComprehensive Support and Empowerment of Women Facing the Challenges of Rare Diseases<\/h2>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"359\" src=\"https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-1024x359.png\" alt=\"\" class=\"wp-image-2984\" style=\"width:679px;height:auto\" srcset=\"https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-1024x359.png 1024w, https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-300x105.png 300w, https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-768x270.png 768w, https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-1536x539.png 1536w, https:\/\/rijetke-bolesti.com\/wp-content\/uploads\/2022\/09\/Active-citizens-fund@4x-2048x719.png 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<p><strong>Project Description:<\/strong><\/p>\n\n\n\n<p>Rare diseases affect fewer than 5 in 10,000 people. They encompass a broad spectrum of conditions about which both medical professionals and the general public often lack sufficient knowledge. Consequently, psychosocial support and other necessary forms of assistance for affected individuals are not well-developed or organized, which significantly reduces their quality of life. The Croatian Alliance for Rare Diseases provides psychological support, counselling on legal rights, occupational therapy, and advocacy for the rights of people living with rare diseases.<\/p>\n\n\n\n<p>Through many years of work, we have observed that challenges are particularly pronounced for women living with rare diseases and mothers of children with developmental difficulties. The legal, psychological, and medical issues they face impact both their private and professional lives, and they often encounter systemic obstacles and societal stigma. To provide them with comprehensive support, the Croatian Alliance for Rare Diseases launched the project&nbsp;<strong>WOMEN'S VOICE FOR THE SYSTEM!<\/strong>&nbsp;<strong>Comprehensive support and empowerment of women facing the challenges of rare diseases,\u201d funded by the Active Citizens Fund.<\/strong><\/p>\n\n\n\n<p>The project introduces the&nbsp;<em>Case management&nbsp;<\/em>model\u2014a stable point of contact offering a comprehensive, holistic, continuous, and person-centered one-on-one approach. It involves a multidisciplinary team of professionals and volunteers who provide legal, psychological, and medical support, as well as information, education, and networking opportunities.\nThis model will also be implemented by the partner organization Inkluzivna ku\u0107a Zvono, thereby decentralizing services and support for women living with rare diseases or caring for children with disabilities, and making them more accessible in less developed regions.<\/p>\n\n\n\n<p>The project also includes research into the problems and needs of women living with rare diseases and mothers of children with developmental difficulties. This research will form the basis for a situation analysis, with preparatory support from partner organization CESI based on its extensive experience. In addition to the Croatian Alliance for Rare Diseases, the research will be conducted by the project partners Inclusive House \u201cZvono\u201d and the National Organization for Rare Diseases of Montenegro (NORBCG), providing insight into the issue across different regional contexts and creating a foundation for advocacy in public policy.&nbsp;<strong>CESI<\/strong>In addition to the Croatian Alliance for Rare Diseases, the research will be conducted by the project partners Inclusive House \u201cZvono\u201d and the National Organization for Rare Diseases of Montenegro (NORBCG)&nbsp;<strong>Inclusive House Zvono<\/strong>&nbsp;i&nbsp;<strong>National Organization for Rare Diseases of Montenegro (NORBCG)<\/strong>providing insight into the issue across different regional contexts and creating a foundation for advocacy in public policy.\n\nAdvocacy activities within the project will include an international conference involving the project coordinator and all partners, as well as a public awareness campaign. The campaign will benefit from the expertise and experience of the partner organizations FRAMBU (Norway) and CESI, aiming to raise public awareness and foster a more inclusive society that enables women empowered through the project to participate equally.&nbsp;<strong>FRAMBU<\/strong>&nbsp;(Norway) and&nbsp;<strong>CESI<\/strong>, s ciljem podizanja javne svijesti i stvaranja inkluzivnijeg dru\u0161tva koje \u0107e \u017eenama osna\u017eenima kroz projekt omogu\u0107iti ravnopravno sudjelovanje.<\/p>\n\n\n\n<p><strong>Project duration:<\/strong>&nbsp;15 months (September 1, 2022 \u2013 November 30, 2023)<\/p>\n\n\n\n<p><strong>Project value:<\/strong>&nbsp;86.044,53 EUR<\/p>\n\n\n\n<p><strong>Contact person:<\/strong>&nbsp;Suzana Saki\u0107, Project Manager&nbsp;<a href=\"mailto:projekti.hsrb@gmail.com\">projekti.hsrb@gmail.com<\/a><\/p>\n\n\n\n<p><strong>Web page:<\/strong>&nbsp;<a href=\"https:\/\/rijetke-bolesti.com\/en\/\">https:\/\/rijetke-bolesti.com\/<\/a><\/p>\n\n\n\n<p><strong>Project Partners:<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>CESI \u2013<\/strong>&nbsp;Centar za edukaciju i istra\u017eivanje <a href=\"http:\/\/www.cesi.hr\/\">http:\/\/www.cesi.hr\/<\/a><\/li>\n\n\n\n<li><strong>Inclusive House Zvono<\/strong>&nbsp;<a href=\"https:\/\/udrugazvono.hr\/\">https:\/\/udrugazvono.hr\/<\/a><\/li>\n\n\n\n<li><strong>NORBCG \u2013<\/strong>&nbsp;National Organization for Rare Diseases of Montenegro (NORBCG) <a href=\"https:\/\/rijetkebolesti.com\/\">https:\/\/rijetkebolesti.com\/<\/a><\/li>\n\n\n\n<li><strong>FRAMBU<\/strong>&nbsp;(Norway) <a href=\"https:\/\/frambu.no\/\">https:\/\/frambu.no\/<\/a><\/li>\n<\/ul>","protected":false},"excerpt":{"rendered":"<p>Active Citizens Fund &#8211; ACF \u017dENSKI STAV ZA SUSTAV!\u00a0Sveobuhvatna podr\u0161ka i osna\u017eivanje \u017eena s izazovima rijetkih bolesti Opis projekta: Rijetke bolesti javljaju se kod manje od 5 osoba na 10 000 ljudi. Radi se o \u0161irokom spektru bolesti o kojima \u010desto medicinska struka i javnost&#8230;<\/p>","protected":false},"author":3,"featured_media":0,"parent":1590,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"content-type":"","footnotes":""},"class_list":["post-3155","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>ACF - Hrvatski savez za rijetke bolesti<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/rijetke-bolesti.com\/en\/projekti\/acf\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ACF - Hrvatski savez za rijetke bolesti\" \/>\n<meta property=\"og:description\" content=\"Active Citizens Fund &#8211; ACF \u017dENSKI STAV ZA SUSTAV!\u00a0Sveobuhvatna podr\u0161ka i osna\u017eivanje \u017eena s izazovima rijetkih bolesti Opis projekta: Rijetke bolesti javljaju se kod manje od 5 osoba na 10 000 ljudi. 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