{"id":2618,"date":"2014-10-12T12:49:00","date_gmt":"2014-10-12T12:49:00","guid":{"rendered":"https:\/\/designedin.org\/?post_type=projects&#038;p=2618"},"modified":"2025-09-11T13:19:54","modified_gmt":"2025-09-11T13:19:54","slug":"heroes-are-rare-as-kids-with-nf","status":"publish","type":"projects","link":"https:\/\/designedin.org\/pt-pt\/projects\/heroes-are-rare-as-kids-with-nf\/","title":{"rendered":"Heroes are rare as kids with NF"},"content":{"rendered":"\n<p>Neurofibromatosis (NF) is a rare genetic disease. Claas R\u00f6hl,&nbsp;the founder and chairman of NF Kinder, is a good friend who has a child diagnosed with Neurofibromatosis (NF). When she was a baby he started this non-profit organisation in Austria, based in Vienna dedicated to supporting individuals and their families, affected by NF. They provide resources, information, and support for those living with NF, aiming to improve their quality of life. NF Kinder is actively involved in fundraising efforts to further research and raise awareness about NF, collaborating with some hospitals such as the Medical University of Vienna, Kepler University Hospital, and Ordensklinikum Linz Barmherzige Schwestern. NF Kinder&#8217;s initiatives include fundraisers and other campaigns to support people with NF, demonstrating a commitment to making a difference in the lives of individuals affected by NF.<\/p>\n\n\n\n<p>In 2013 Claas asked me for help and, with my studio Claan, I developed a campaign to raise funding. This was the first of our collaboration, through out the years we have been supporting NF with campaigns, web-development and a digital platform.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"722\" height=\"1024\" src=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-722x1024.png\" alt=\"\" class=\"wp-image-2621\" srcset=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-722x1024.png 722w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-212x300.png 212w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-768x1089.png 768w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-1084x1536.png 1084w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-1445x2048.png 1445w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-141x200.png 141w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05-600x851.png 600w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.05.png 1820w\" sizes=\"auto, (max-width: 722px) 100vw, 722px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"722\" height=\"1024\" src=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-722x1024.png\" alt=\"\" class=\"wp-image-2623\" srcset=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-722x1024.png 722w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-212x300.png 212w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-768x1089.png 768w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-1084x1536.png 1084w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-1445x2048.png 1445w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-141x200.png 141w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29-600x851.png 600w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.55.29.png 1820w\" sizes=\"auto, (max-width: 722px) 100vw, 722px\" \/><\/figure>\n\n\n\n<p>This series of posters with the slogan &#8220;Heroes are rare&#8221; (<em>Helden Sind Selten<\/em>) were intended to communicate with children and families affected by NF. I&#8217;ve worked on this concept using a little stuffed monkey with NF (characterised by the visible nodules) so that kids would empathise and identify themselves with this superhero. I designed the prop by adapting the stuffed animal, made the photo-shooting and the graphic design. <\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"722\" height=\"1024\" src=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-722x1024.png\" alt=\"\" class=\"wp-image-2619\" srcset=\"https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-722x1024.png 722w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-212x300.png 212w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-768x1089.png 768w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-1084x1536.png 1084w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-1445x2048.png 1445w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-141x200.png 141w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51-600x851.png 600w, https:\/\/designedin.org\/wp-content\/uploads\/2024\/05\/Screenshot-2024-05-12-at-12.54.51.png 1820w\" sizes=\"auto, (max-width: 722px) 100vw, 722px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Neurofibromatosis (NF) is a rare genetic disease. Claas R\u00f6hl,&nbsp;the founder and chairman of NF Kinder, is a good friend who has a child diagnosed with Neurofibromatosis (NF). When she was a baby he started this non-profit organisation in Austria, based in Vienna dedicated to supporting individuals and their families, affected by NF. They provide resources, information, and support for those living with NF, aiming to improve their quality of life. NF Kinder is actively involved in fundraising efforts to further research and raise awareness about NF, collaborating with some hospitals such as the Medical University of Vienna, Kepler University Hospital,\u2026<\/p>\n","protected":false},"featured_media":2621,"template":"","meta":{"_acf_changed":true},"categories":[53],"tags":[],"class_list":["post-2618","projects","type-projects","status-publish","has-post-thumbnail","hentry","category-graphic-design-photography"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Heroes are rare as kids with NF - DesignedIn<\/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:\/\/designedin.org\/projects\/heroes-are-rare-as-kids-with-nf\/\" \/>\n<meta property=\"og:locale\" content=\"pt_PT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Heroes are rare as kids with NF - DesignedIn\" \/>\n<meta property=\"og:description\" content=\"Neurofibromatosis (NF) is a rare genetic disease. Claas R\u00f6hl,&nbsp;the founder and chairman of NF Kinder, is a good friend who has a child diagnosed with Neurofibromatosis (NF). When she was a baby he started this non-profit organisation in Austria, based in Vienna dedicated to supporting individuals and their families, affected by NF. They provide resources, information, and support for those living with NF, aiming to improve their quality of life. 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