{"id":12535,"date":"2026-03-09T09:53:37","date_gmt":"2026-03-09T07:53:37","guid":{"rendered":"https:\/\/www.afadoc.it\/wp22\/?p=12535"},"modified":"2026-03-09T09:54:36","modified_gmt":"2026-03-09T07:54:36","slug":"a-fa-d-o-c-aps-associazione-famiglie-deficit-ormone-della-crescita-ed-altre-patologie-rare","status":"publish","type":"post","link":"https:\/\/www.afadoc.it\/wp22\/?p=12535","title":{"rendered":"A.Fa.D.O.C. aps: Associazione Famiglie Deficit Ormone della Crescita ed altre patologie rare"},"content":{"rendered":"<h6><em><img decoding=\"async\" loading=\"lazy\" class=\"aligncenter wp-image-12536\" src=\"https:\/\/www.afadoc.it\/wp22\/wp-content\/uploads\/2026\/03\/as.jpg\" alt=\"\" width=\"461\" height=\"306\" srcset=\"https:\/\/www.afadoc.it\/wp22\/wp-content\/uploads\/2026\/03\/as.jpg 916w, https:\/\/www.afadoc.it\/wp22\/wp-content\/uploads\/2026\/03\/as-300x199.jpg 300w, https:\/\/www.afadoc.it\/wp22\/wp-content\/uploads\/2026\/03\/as-768x510.jpg 768w\" sizes=\"(max-width: 461px) 100vw, 461px\" \/><\/em><\/h6>\n<h6><em>Quando si parla di malattie rare i pazienti e le loro famiglie si sentono spesso abbandonate. Chi soffre del deficit dell\u2019ormone della crescita pu\u00f2 per\u00f2 contare sull\u2019aiuto concreto e psicologico di A.Fa.D.O.C.<\/em><\/h6>\n<p style=\"text-align: justify;\">A.Fa.D.O.C. ovvero Associazione Famiglie Deficit Ormone della Crescita ed altre patologie rare. Un acronimo che svela il ruolo importante di questa organizzazione di volontariato costituita nel 1993 grazie a un gruppo di mamme e pap\u00e0 di bambini affetti da questa patologia ai quali si sono uniti successivamente i genitori delle bambine con sindrome di Turner e altre malattie ancora pi\u00f9 rare, sempre legate dalla terapia con questo ormone. L\u2019Associazione, che ha sede a Vicenza, ma \u00e8 presente anche a Roma e a Palermo, ha un duplice obiettivo: sia assistere i pazienti e i loro cari dal punto di vista pratico e psicologico sia supportare i medici di base e i pediatri di famiglia per favorire la diagnosi precoce. A.Fa.D.O.C. si rivolge anche al personale paramedico, per creare contatti e rapporti migliori con chi \u00e8 in cura, e alla scuola cos\u00ec da permettere un maggior inserimento dei bambini nell\u2019ambito educativo. Plus Magazine ha incontrato la Presidente Cinzia Sacchetti.<\/p>\n<p><a href=\"https:\/\/www.plusmagazine.news\/a-fa-d-o-c-aps-associazione-famiglie-deficit-ormone-della-crescita-ed-altre-patologie-rare\/\"><strong>Leggi l&#8217;intervista<\/strong><\/a><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"Plus Magazine ha incontrato la Presidente di A.Fa.D.O.C. Cinzia Sacchetti.","protected":false},"author":1,"featured_media":12536,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[1,244],"tags":[536,344],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO 5.0.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Plus Magazine ha incontrato la Presidente di A.Fa.D.O.C. 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