hier<\/a> een artikelvan CAICT over de uitreiking.<\/p>\n","protected":false},"excerpt":{"rendered":"Op dinsdag 30 september 2014 vond de Avond van de Digitale Economie plaats, waarbij de Mens & ICT Award uitgereikt werd. Ik was gevraagd om zitting te nemen in de jury.<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[4],"tags":[],"jetpack_featured_media_url":"","yoast_head":"\n
Jurylid Mens & ICT Award - Wilma Westenberg<\/title>\n<meta name=\"description\" content=\"Facial Infiltrating Lipomatosis (FIL), is een ultra zeldzame aandoening in de wang en de helft van het gezicht met slechts een handjevol pati\u00ebnten wereldwijd. Lees meer over mijn leven met FIL.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/wilmawestenberg.nl\/jurylid-mens-ict-award\/\" \/>\n<meta property=\"og:locale\" content=\"nl_NL\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Jurylid Mens & ICT Award - Wilma Westenberg\" \/>\n<meta property=\"og:description\" content=\"Facial Infiltrating Lipomatosis (FIL), is een ultra zeldzame aandoening in de wang en de helft van het gezicht met slechts een handjevol pati\u00ebnten wereldwijd. 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Lees meer over mijn leven met FIL.\",\"inLanguage\":\"nl\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/wilmawestenberg.nl\/jurylid-mens-ict-award\/\"]}]},{\"@type\":\"Person\",\"@id\":\"https:\/\/wilmawestenberg.nl\/#\/schema\/person\/1bc71ed07a5faae412a0cd84cdc69c3c\",\"name\":\"Wilma\",\"image\":{\"@type\":\"ImageObject\",\"@id\":\"https:\/\/wilmawestenberg.nl\/#personlogo\",\"inLanguage\":\"nl\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/76c81b4022e72ad8d4700b3c9e4cebf1?s=96&d=identicon&r=g\",\"caption\":\"Wilma\"},\"description\":\"I'm Wilma (26) and I was born with a benign tumor in my face. For 22 years I did not know what it was. In 2017 I did a second opinion and got diagnosed with Facial Infiltrating Lipomatosis; an ultra rare condition with only a few people affected world wide. 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<\/p>\n