{"id":362,"date":"2025-04-14T14:46:23","date_gmt":"2025-04-14T14:46:23","guid":{"rendered":"https:\/\/spina-bifida.cz\/?p=362"},"modified":"2025-04-14T15:23:07","modified_gmt":"2025-04-14T15:23:07","slug":"adoptovane-devcatko","status":"publish","type":"post","link":"https:\/\/spina-bifida.cz\/index.php\/2025\/04\/14\/adoptovane-devcatko\/","title":{"rendered":"Adoptovan\u00e9 d\u011bv\u010d\u00e1tko"},"content":{"rendered":"\n<p>Unik\u00e1tn\u00ed kr\u00e1sn\u00fd p\u0159\u00edb\u011bh adopce p\u0159ekr\u00e1sn\u00e9ho americk\u00e9ho d\u011bv\u010d\u00e1tka s roz\u0161t\u011bpem vypr\u00e1v\u00ed Spina Bifida Association na sv\u00e9m <a href=\"https:\/\/www.spinabifidaassociation.org\/blog\/an-adoption-story\/\" data-type=\"link\" data-id=\"https:\/\/www.spinabifidaassociation.org\/blog\/an-adoption-story\/\" target=\"_blank\" rel=\"noreferrer noopener\">serveru<\/a>. <\/p>\n\n\n\n<p>Larry a Kelly Petersonovi jsou man\u017eel\u00e9 z Indiany, kte\u0159\u00ed oba \u017eij\u00ed s diagn\u00f3zou roz\u0161t\u011bpu p\u00e1te\u0159e. V roce 2019 se rozhodli adoptovat si d\u011b\u0165\u00e1tko. B\u011bhem procesu adopce Larry a Kelly spolupracovali se t\u0159emi agenturami a adopce miminka se speci\u00e1ln\u00edmi pot\u0159ebami jim tak n\u011bjak spadla do kl\u00edna. Kdy\u017e objevili v adop\u010dn\u00ed agentu\u0159e slo\u017eku sv\u00e9 hol\u010di\u010dky, \u0159ekli si, kdo by mohl b\u00fdt lep\u0161\u00edm rodi\u010dem tohoto d\u00edt\u011bte ne\u017e dva lid\u00e9, kte\u0159\u00ed hluboce rozum\u00ed v\u0161em p\u0159ek\u00e1\u017ek\u00e1m, kter\u00e9 ji v budoucnu \u010dekaj\u00ed.<\/p>\n\n\n\n<p>Pro Kelly a Larryho bylo rodi\u010dovstv\u00ed doposud radostn\u00e9 i n\u00e1ro\u010dn\u00e9. Radovali se, \u017ee mohou svou hol\u010di\u010dku neust\u00e1le dr\u017eet a p\u0159itulit, vid\u011bt, jak se jej\u00ed osobnost vyv\u00edj\u00ed, a sledovat, jak dos\u00e1hla d\u016fle\u017eit\u00fdch miln\u00edk\u016f, jako je prvn\u00ed \u00fasm\u011bv. Rodi\u010dovstv\u00ed samoz\u0159ejm\u011b p\u0159in\u00e1\u0161\u00ed tak\u00e9 starosti. I kdy\u017e m\u00e1 Kelly bohat\u00e9 zku\u0161enosti s d\u011btmi s posti\u017een\u00edm, proto\u017ee posledn\u00edch 18 let pracovala jako speci\u00e1ln\u00ed pedagog, b\u00fdt rodi\u010dem je \u00fapln\u011b jin\u00e1 liga. <\/p>\n\n\n\n<p>Co se p\u00e9\u010de o dceru t\u00fd\u010de, Larry a Kelly se u\u010d\u00ed svou novou rodi\u010dovskou roli ze sv\u00fdch invalidn\u00edch voz\u00edk\u016f. Kelly nepou\u017e\u00edv\u00e1 nohy a Larry dok\u00e1\u017ee chodit, kdy\u017e se p\u0159idr\u017euje v\u011bc\u00ed, tak\u017ee vym\u00fd\u0161lej\u00ed zp\u016fsoby, jak se o svou dceru postarat, ani\u017e by p\u0159ekro\u010dili sv\u00e9 fyzick\u00e9 limity. P\u0159\u00edklady \u00fakol\u016f, kter\u00e9 se museli p\u0159izp\u016fsobit, jsou koup\u00e1n\u00ed a bezpe\u010dn\u00e9 nalo\u017een\u00ed dcery do auta. Krom\u011b spiny bifidy se jejich dcera narodila s vrozenou srde\u010dn\u00ed vadou, co\u017e vy\u017eadovalo rozs\u00e1hl\u00e9 sledov\u00e1n\u00ed a operaci v ran\u00fdch f\u00e1z\u00edch \u017eivota. Pro Larryho a Kelly to bylo t\u011b\u017ek\u00e9, proto\u017ee na rozd\u00edl od roz\u0161t\u011bpu p\u00e1te\u0159e nebyli obezn\u00e1meni s probl\u00e9my, kter\u00e9 p\u0159in\u00e1\u0161\u00ed \u017eivot s vrozenou srde\u010dn\u00ed vadou. Oba se v\u0161ak od t\u00e9 doby vr\u00e1tili do pr\u00e1ce a b\u011bhem v\u0161edn\u00edch dn\u016f maj\u00ed bl\u00edzko k rodin\u011b.<\/p>\n\n\n\n<p>Larry a Kelly cht\u011bj\u00ed b\u00fdt zdrojem odvahy pro dosp\u011bl\u00e9 s roz\u0161t\u011bpem, kte\u0159\u00ed doufaj\u00ed, \u017ee se stanou rodi\u010di, aby pomohli zm\u00edrnit stigmata a negativn\u00ed stereotypy, kter\u00e9 si spole\u010dnost vytvo\u0159ila v souvislosti s posti\u017een\u00edm a rodi\u010dovstv\u00edm. Cht\u011bj\u00ed b\u00fdt tak\u00e9 k dispozici nov\u00fdm rodi\u010d\u016fm, kte\u0159\u00ed se ned\u00e1vno diagn\u00f3zu ro\u0161t\u011bpu dozv\u011bd\u011bli. Ned\u00e1vno zalo\u017eili na Facebooku str\u00e1nku s n\u00e1zvem <a href=\"https:\/\/www.facebook.com\/journeydownacountryroad\" target=\"_blank\" rel=\"noreferrer noopener\">Journey Down a Country Road: Spina Bifida + Adoption= Our Family<\/a>, aby lid\u00e9 mohli sledovat jejich cestu, kl\u00e1st ot\u00e1zky a hledat oporu p\u0159i \u0159e\u0161en\u00ed t\u00e9mat adopce a rodi\u010dovstv\u00ed. \u201eChceme, aby spole\u010dnost vid\u011bla, \u017ee lid\u00e9 s roz\u0161t\u011bpem p\u00e1te\u0159e \u017eij\u00ed \u017eivot stejn\u011b jako jejich neposti\u017een\u00ed vrstevn\u00edci. Nen\u00ed to nic \u0161okuj\u00edc\u00edho nebo \u00fa\u017easn\u00e9ho&#8221;, \u200b\u200b\u0159ekla Kelly.<\/p>\n\n\n\n<p>Kr\u00e1tce pot\u00e9, co se Kelly s Larrym stali rodi\u010di, kontaktovali fotografku Angelu Forkerovou, kter\u00e1 se specializuje na focen\u00ed d\u011bt\u00ed s posti\u017een\u00edm prost\u0159ednictv\u00edm sv\u00e9ho projektu <em>Precious Baby Project<\/em>. Projekt se sest\u00e1v\u00e1 z fotografov\u00e1n\u00ed zdravotn\u011b posti\u017een\u00fdch d\u011bt\u00ed um\u00edst\u011bn\u00fdch do propracovan\u00fdch sc\u00e9n inspirovan\u00fdch d\u00edlem Adele Enerson. Mnoh\u00e9 z jej\u00edch fotek maj\u00ed za sebou skv\u011bl\u00e9 p\u0159\u00edb\u011bhy. &#8220;Tyto d\u011bti a j\u00e1 m\u00e1me misi uk\u00e1zat, \u017ee v\u0161ichni lid\u00e9 jsou kr\u00e1sn\u00ed a cenn\u00ed,&#8221; \u0159ekla Angela.<\/p>\n\n\n\n<p>Fotka, kterou Angela rodin\u011b nakonec po\u0159\u00eddila, spo\u010d\u00edvala v tom, \u017ee v\u0161ichni t\u0159i le\u017eeli na b\u0159i\u0161e a uk\u00e1zali sv\u00e9 jizvy fotoapar\u00e1tu. To symbolizovalo, \u017ee i kdy\u017e Larry a Kelly nesd\u00edlej\u00ed se svou dcerou stejnou DNA, maj\u00ed stejn\u00e9 jizvy.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"483\" src=\"https:\/\/spina-bifida.cz\/wp-content\/uploads\/2025\/04\/85O_4356abcdefrcabcopy-1050x495-c-1-1024x483.jpg\" alt=\"\" class=\"wp-image-368\" srcset=\"https:\/\/spina-bifida.cz\/wp-content\/uploads\/2025\/04\/85O_4356abcdefrcabcopy-1050x495-c-1-1024x483.jpg 1024w, https:\/\/spina-bifida.cz\/wp-content\/uploads\/2025\/04\/85O_4356abcdefrcabcopy-1050x495-c-1-300x141.jpg 300w, https:\/\/spina-bifida.cz\/wp-content\/uploads\/2025\/04\/85O_4356abcdefrcabcopy-1050x495-c-1-768x362.jpg 768w, https:\/\/spina-bifida.cz\/wp-content\/uploads\/2025\/04\/85O_4356abcdefrcabcopy-1050x495-c-1.jpg 1050w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<p>K velk\u00e9mu p\u0159ekvapen\u00ed v\u0161ech se fotka stala vir\u00e1ln\u00ed a b\u011bhem 14 hodin po zve\u0159ejn\u011bn\u00ed na Facebooku si z\u00edskala celon\u00e1rodn\u00ed pozornost. &#8220;<em>Kelly a Larry tvrd\u011b pracuj\u00ed. D\u00edky sv\u00e9mu odhodl\u00e1n\u00ed p\u0159ekon\u00e1vaj\u00ed v\u0161echny v\u00fdzvy. Pr\u00e1ce s nimi byla od za\u010d\u00e1tku do konce takov\u00e1 z\u00e1bava! Tento p\u00e1r m\u011b uchv\u00e1til,<\/em>&#8221; \u0159ekla Angela Forkerov\u00e1.<\/p>\n\n\n\n<p>Pro v\u00edce informac\u00ed o Precious Baby Project nav\u0161tivte Angely <a href=\"https:\/\/www.preciousbabyphotography.com\/\" target=\"_blank\" rel=\"noreferrer noopener\">webov\u00e9 str\u00e1nky<\/a>.<\/p>\n\n\n\n<p>Zdroj: <a href=\"https:\/\/www.spinabifidaassociation.org\/blog\/an-adoption-story\/\" target=\"_blank\" rel=\"noreferrer noopener\">www.spinabifidaassociation.org\/&#8230;<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Unik\u00e1tn\u00ed kr\u00e1sn\u00fd p\u0159\u00edb\u011bh adopce p\u0159ekr\u00e1sn\u00e9ho americk\u00e9ho d\u011bv\u010d\u00e1tka s roz\u0161t\u011bpem vypr\u00e1v\u00ed Spina Bifida Association na sv\u00e9m serveru. Larry a Kelly Petersonovi jsou man\u017eel\u00e9 z Indiany, kte\u0159\u00ed oba \u017eij\u00ed s diagn\u00f3zou roz\u0161t\u011bpu p\u00e1te\u0159e. V roce 2019 se rozhodli adoptovat si d\u011b\u0165\u00e1tko. B\u011bhem procesu adopce Larry a Kelly spolupracovali se t\u0159emi agenturami a adopce miminka se speci\u00e1ln\u00edmi pot\u0159ebami [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":363,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[6],"tags":[],"class_list":["post-362","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-pribehy"],"_links":{"self":[{"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/posts\/362","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/comments?post=362"}],"version-history":[{"count":5,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/posts\/362\/revisions"}],"predecessor-version":[{"id":369,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/posts\/362\/revisions\/369"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/media\/363"}],"wp:attachment":[{"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/media?parent=362"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/categories?post=362"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/spina-bifida.cz\/index.php\/wp-json\/wp\/v2\/tags?post=362"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}