{"id":160188,"date":"2023-02-22T09:22:21","date_gmt":"2023-02-22T08:22:21","guid":{"rendered":"https:\/\/novice.si\/page\/?p=160188"},"modified":"2023-02-22T10:09:01","modified_gmt":"2023-02-22T09:09:01","slug":"triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila","status":"publish","type":"post","link":"https:\/\/novice.si\/page\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\/","title":{"rendered":"Triletna Karolina je hudo bolna: v dru\u0161tvu Viljem Julijan zbirajo denar za razvoj zdravila"},"content":{"rendered":"<p><strong>Triletna Karolina iz okolice Ljubljane ima kruto in smrtonosno prirojeno redko bolezen, za katero \u017eal ni nobenega zdravila. V Dru\u0161tvu Viljem Julijan so spro\u017eili dobrodelno akcijo, s katero \u017eelijo zbrati dva milijona evrov, ki so potrebni za razvoj genskega zdravljenja za njeno bolezen. S tem zdravilom bi lahko zaustavili napredovanje bolezni in Karolini re\u0161ili \u017eivljenje, so sporo\u010dili iz dru\u0161tva.<\/strong><\/p>\n<p><a href=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-scaled.jpg\" data-gallery><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-160189 alignleft\" src=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-200x300.jpg\" alt=\"\" width=\"200\" height=\"300\" srcset=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-200x300.jpg 200w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-683x1024.jpg 683w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-768x1152.jpg 768w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-1024x1536.jpg 1024w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-1365x2048.jpg 1365w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-696x1044.jpg 696w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-1068x1602.jpg 1068w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-280x420.jpg 280w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-16x24.jpg 16w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-24x36.jpg 24w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-32x48.jpg 32w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina7-scaled.jpg 1707w\" sizes=\"auto, (max-width: 200px) 100vw, 200px\" \/><\/a>Karolina je triletna deklica, ki so ji lani, malo pred Bo\u017ei\u010dem, odkrili uni\u010dujo\u010do in smrtonosno prirojeno redko bolezen, ki se imenuje Cockayne sindrom &#8211; tip B, oziroma \u00bbbolezen hitrega staranja\u00ab.<br \/>\nZa njeno bolezen \u017eal ni nobenega zdravila ali zdravljenja, vendar pa za Karolino vendarle obstaja re\u0161itev in upanje. V Dru\u0161tvu Viljem Julijan so na pro\u0161njo star\u0161ev proti vsem mo\u017enostim namre\u010d uspeli najti znanstvenike, ki so pripravljeni razviti zdravilo za to bolezen in so \u017ee uspe\u0161no naredili nekaj za\u010detnih raziskav v tej smeri. Zato so v Dru\u0161tvu Viljem Julijan za\u010deli z veliko zbiralno akcijo za Karolino, s katero morajo zbrati vsaj 2 milijona evrov za razvoj genskega zdravljenja za Cockayne sindrom \u2013 tip B.<br \/>\n&#8220;Razvoj genskega zdravljenja je za Karolino edino upanje. V situaciji njene krute bolezni, za katero ni nobenega zdravila ali zdravljenja, je to edini svetli \u017earek, na katerega se lahko opreva in ki pomeni mo\u017enost, da najini h\u010derki re\u0161imo \u017eivljenje. Zato iz srca prosiva vse, ki ste pripravljeni donirati za razvoj zdravila za njeno bolezen, da nam pomagate,&#8221; se na javnost s pro\u0161njo obra\u010data Karolinina star\u0161a, Borut in Sabina.<\/p>\n<p><strong>Za razvoj zdravila \u2013 genskega zdravljenja \u2013 za Karolino lahko prispevate SMS s klju\u010dno besedo KAROLINA5 ali KAROLINA10 na 1919 ali z nakazilom donacije na TRR Dru\u0161tva Viljem Julijan SI56 0400 0027 7357 570, sklic SI00 111888, namen \u00bbZa Karolino\u00ab.<\/strong><\/p>\n<p>Predsednik Dru\u0161tva Viljem Julijan <strong>dr.<\/strong> <strong>Nejc Jelen<\/strong> je za Radio Rogla povedal:<\/p>\n<audio class=\"wp-audio-shortcode\" id=\"audio-160188-1\" preload=\"none\" style=\"width: 100%;\" controls=\"controls\"><source type=\"audio\/mpeg\" src=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/nejc-jelen.mp3?_=1\" \/><a href=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/nejc-jelen.mp3\">https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/nejc-jelen.mp3<\/a><\/audio>\n<p><strong>Te\u017eave so opazili pri letu in pol<\/strong><\/p>\n<p><a href=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-scaled.jpg\" data-gallery><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-160192 alignleft\" src=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-175x300.jpg\" alt=\"\" width=\"175\" height=\"300\" srcset=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-175x300.jpg 175w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-596x1024.jpg 596w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-768x1319.jpg 768w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-894x1536.jpg 894w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-1193x2048.jpg 1193w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-696x1195.jpg 696w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-1068x1834.jpg 1068w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-245x420.jpg 245w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-14x24.jpg 14w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-21x36.jpg 21w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-28x48.jpg 28w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina2-scaled.jpg 1491w\" sizes=\"auto, (max-width: 175px) 100vw, 175px\" \/><\/a>Karolina z dru\u017eino \u017eivi v okolici Ljubljane in bo \u017ee \u010dez nekaj dni, konec februarja dopolnila 4 leta, so sporo\u010dili iz dru\u0161tva Viljem Julijan.<br \/>\n\u010ce bi jo vpra\u0161ali po njenem najbolj\u0161em prijatelju, bi bil to zagotovo njen ku\u017ea Ari. Malo pred njenim drugim letom je dobila \u0161e sestrico Tinkaro, s katero se imata zelo radi in sta nerazdru\u017eljivi.<br \/>\nKarolina se je rodila kot popolnoma zdrav otrok in je \u017ee prvo leto zelo napredovala. Zelo je bila aktivna, kmalu se je sama usedla in pri 13-ih mesecih tudi shodila. Pri letu in pol pa sta njena star\u0161a opazila, da ima nekoliko slab\u0161e ravnote\u017eje, pri dveh letih se ji je pri dolo\u010denih gibih tudi zatresla rokica. Zato sta h\u010derko iz previdnosti odpeljala na preiskave.<br \/>\nLanskega decembra, en teden pred Bo\u017ei\u010dem, sta od zdravnikov dobila pretresljivo novico, ki si je ne \u017eeli sli\u0161ati noben star\u0161. Genetske preiskave so pokazale, da ima Karolina izjemno redko genetsko bolezen, ki je posledica drobne spremembe v njenem genetskem zapisu.<br \/>\nBolezen se imenuje Cockayne sindrom, tipa B (CSB, okvara v genu ERCC6) in Karolina je edini otrok s to boleznijo v Sloveniji.<br \/>\nBolezen je zelo kruta in povzro\u010da hude zdravstvene posledice ter okvare v telesu, ki spominjajo na prehitro staranje, zato ji pravijo tudi \u00bbbolezen hitrega staranja\u00ab. Povzro\u010da te\u017eke okvare po celotnem telesu, v jetrih, ledvicah, mo\u017eganih, ko\u017ei in drugih organih. Povzro\u010di tudi po\u0161kodbe vida in sluha ter ve\u010dinoma vodi v slepoto in gluhost pri zgodnji starosti. Bolezen je napredujo\u010da in povpre\u010dna \u017eivljenjska doba bolnikov je zgolj 12 let. \u010ce za Karolino v najkraj\u0161em mo\u017enem ne bo razvito gensko zdravljenje, ji bo v naslednjih nekaj letih bolezen po\u010dasi odvzela vse sposobnosti in na koncu veliko prezgodaj tudi \u017eivljenje.<\/p>\n<p><strong>Razviti \u017eelijo zdravilo<\/strong><\/p>\n<p><a href=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-scaled.jpg\" data-gallery><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-160191 alignleft\" src=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-300x242.jpg\" alt=\"\" width=\"300\" height=\"242\" srcset=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-300x242.jpg 300w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-1024x826.jpg 1024w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-768x620.jpg 768w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-1536x1239.jpg 1536w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-2048x1653.jpg 2048w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-696x562.jpg 696w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-1068x862.jpg 1068w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-521x420.jpg 521w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-24x19.jpg 24w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-36x29.jpg 36w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina3-48x39.jpg 48w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a>V Dru\u0161tvu Viljem Julijan so zato nedavno ustanovili projekt \u00bbZdravilo za Karolino \u2013 zdravilo za Cockayne sindrom, tipa B\u00ab in za\u010deli po celotnem svetu iskati znanstvenike, ki bi bili sposobni in pripravljeni razviti gensko zdravljenje za to stra\u0161no smrtonosno bolezen.<br \/>\nUspelo jim je najti dve raziskovalni ekipi, na Portugalskem in v ZDA, ki so \u017ee naredili za\u010detne raziskave za razvoj genskega zdravljenja za to bolezen. Uspe\u0161no so se povezali s temi znanstveniki, ki so na pro\u0161njo dru\u0161tva in Karolininih star\u0161ev sedaj pripravljeni nadaljevati z razvojem zdravila, pri \u010demer pa je za to potrebno zagotoviti potrebna sredstva. Zato so v Dru\u0161tvu Viljem Julijan\u00a0 za\u010deli z veliko zbiralno akcijo, s katero morajo za pred-klini\u010dno stopnjo raziskav zbrati vsaj 2 milijona \u20ac, ki so potrebni za za\u010detno financiranje razvoja genskega zdravljenja.<br \/>\nZaradi ve\u010dje mo\u017enosti za uspeh bodo v dru\u0161tvu tudi financirali raziskave obeh skupin. Ker je Cockayne sindrom napredujo\u010da bolezen je za Karolino \u010das zelo pomemben dejavnik, zato si \u017eelijo v Dru\u0161tvu Viljem Julijan \u010dim prej zbrati potrebno vsoto, 2 milijona \u20ac, da bo lahko razvoj zdravila potekal brez presledkov in zaustavitev. V prvem koraku je tako klju\u010dno, da konca meseca marca zberejo vsaj 400.000\u20ac, da bodo lahko krili stro\u0161ke prvega nadaljnjega sklopa raziskav.<br \/>\n<a href=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-scaled.jpg\" data-gallery><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-160193 alignleft\" src=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-201x300.jpg\" alt=\"\" width=\"201\" height=\"300\" srcset=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-201x300.jpg 201w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-687x1024.jpg 687w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-768x1144.jpg 768w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-1031x1536.jpg 1031w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-1375x2048.jpg 1375w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-696x1037.jpg 696w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-1068x1591.jpg 1068w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-282x420.jpg 282w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-16x24.jpg 16w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-24x36.jpg 24w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-32x48.jpg 32w, https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-scaled.jpg 1718w\" sizes=\"auto, (max-width: 201px) 100vw, 201px\" \/><\/a>\u010ce bo razvoj genskega zdravljenja potekal uspe\u0161no in po predvidenem na\u010drtu, bi po optimisti\u010dnem scenariju Karolina zdravilo v okviru klini\u010dnega preizku\u0161anja lahko prejela \u017ee mogo\u010de v drugi polovici naslednjega leta. V Dru\u0161tvu Viljem Julijan se ob tem skupaj s Karolininimi star\u0161i zavedajo, da je razvoj novega genskega zdravila kompleksen in zahteven postopek, ki lahko potencialno traja tudi ve\u010d let.<br \/>\n\u00bbVse na\u0161e \u017eelje in upi so uprti v to, da bo razvoj zdravila potekal uspe\u0161no in da bo imel sre\u010den razplet, ob tem pa se zavedamo, da je razvoj nove genske terapije znanstveno zahteven proces in da stopamo v obse\u017een projekt, kjer ti nih\u010de ne more podati dokon\u010dnega zagotovila za uspeh in razplet, kot si ga \u017eelimo. Vendar pa je ta pot za Karolino edino upanje, druge re\u0161itve zanjo ni. Ker v tej tragi\u010dni zgodbi obstaja tak\u0161no svetlo upanje, potem nikakor ne moremo stati kri\u017eem rok in deklico prepustiti kruti usodi njene bolezni. Moramo poskusiti narediti vse, kar je v na\u0161i mo\u010di,\u00ab pravi <strong>dr. Nejc Jelen,<\/strong> predsednik Dru\u0161tva Viljem Julijan.<br \/>\n(Vir: Dru\u0161tvo Viljem Julijan)<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Triletna Karolina iz okolice Ljubljane ima kruto in smrtonosno prirojeno redko bolezen, za katero \u017eal ni nobenega zdravila. V Dru\u0161tvu Viljem Julijan so spro\u017eili dobrodelno akcijo, s katero \u017eelijo zbrati dva milijona evrov, ki so potrebni za razvoj genskega zdravljenja za njeno bolezen. S tem zdravilom bi lahko zaustavili napredovanje bolezni in Karolini re\u0161ili \u017eivljenje, [&hellip;]<\/p>\n","protected":false},"author":12,"featured_media":160193,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[14,868,17,16,141,3108,693,57],"tags":[17154,17153,17155],"class_list":{"0":"post-160188","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-aktualno","8":"category-casopisi","9":"category-celjsko","10":"category-konjisko","11":"category-novice","12":"category-radio-rogla","13":"category-sentjurske-novice","14":"category-sentjursko","15":"tag-drustvo-viljem-julijan","16":"tag-karolina","17":"tag-redke-bolezni"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Triletna Karolina je hudo bolna: v dru\u0161tvu Viljem Julijan zbirajo denar za razvoj zdravila - Novice.si<\/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:\/\/novice.si\/page\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\/\" \/>\n<meta property=\"og:locale\" content=\"sl_SI\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Triletna Karolina je hudo bolna: v dru\u0161tvu Viljem Julijan zbirajo denar za razvoj zdravila - Novice.si\" \/>\n<meta property=\"og:description\" content=\"Triletna Karolina iz okolice Ljubljane ima kruto in smrtonosno prirojeno redko bolezen, za katero \u017eal ni nobenega zdravila. V Dru\u0161tvu Viljem Julijan so spro\u017eili dobrodelno akcijo, s katero \u017eelijo zbrati dva milijona evrov, ki so potrebni za razvoj genskega zdravljenja za njeno bolezen. S tem zdravilom bi lahko zaustavili napredovanje bolezni in Karolini re\u0161ili \u017eivljenje, [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/novice.si\/page\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\/\" \/>\n<meta property=\"og:site_name\" content=\"Novice.si\" \/>\n<meta property=\"article:published_time\" content=\"2023-02-22T08:22:21+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2023-02-22T09:09:01+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/novice.si\/page\/wp-content\/uploads\/2023\/02\/Karolina1-scaled.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1718\" \/>\n\t<meta property=\"og:image:height\" content=\"2560\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Uredni\u0161tvo Celjana\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Uredni\u0161tvo Celjana\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"7 minut\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/\"},\"author\":{\"name\":\"Uredni\u0161tvo Celjana\",\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/#\\\/schema\\\/person\\\/51903923b50fefb075bc1cd24fe4d065\"},\"headline\":\"Triletna Karolina je hudo bolna: v dru\u0161tvu Viljem Julijan zbirajo denar za razvoj zdravila\",\"datePublished\":\"2023-02-22T08:22:21+00:00\",\"dateModified\":\"2023-02-22T09:09:01+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/\"},\"wordCount\":1062,\"publisher\":{\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/novice.si\\\/page\\\/wp-content\\\/uploads\\\/2023\\\/02\\\/Karolina1-scaled.jpg\",\"keywords\":[\"dru\u0161tvo viljem julijan\",\"karolina\",\"redke bolezni\"],\"articleSection\":[\"Aktualno\",\"\u010casopisi\",\"Celjsko\",\"Konji\u0161ko\",\"Novice\",\"Radio Rogla\",\"\u0160entjurske Novice\",\"\u0160entjursko\"],\"inLanguage\":\"sl-SI\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/\",\"url\":\"https:\\\/\\\/novice.si\\\/page\\\/triletna-karolina-je-hudo-bolna-v-drustvu-viljem-julijan-zbirajo-denar-za-razvoj-zdravila\\\/\",\"name\":\"Triletna Karolina je hudo bolna: v dru\u0161tvu Viljem Julijan zbirajo denar za razvoj zdravila - 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