{"id":974,"date":"2015-08-07T09:25:46","date_gmt":"2015-08-07T14:25:46","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=974"},"modified":"2015-08-07T09:25:46","modified_gmt":"2015-08-07T14:25:46","slug":"samantha","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/it\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/","title":{"rendered":"INDIVIDUO CON LGMD: Samantha"},"content":{"rendered":"<p>08\/07\/2015:<\/p>\n<p><strong>Nome<\/strong>:  Samantha\u00a0 <strong>ET\u00c0<\/strong>: 7 anni<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/08\/LGMD2i-Samantha.png\"><img decoding=\"async\" class=\"lazyload  size-medium wp-image-975 alignright\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27169%27%20viewBox%3D%270%200%20300%20169%27%3E%3Crect%20width%3D%27300%27%20height%3D%27169%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2015\/08\/LGMD2i-Samantha-300x169.png\" alt=\"LGMD2i - Samantha\" width=\"300\" height=\"169\" \/><\/a><\/p>\n<p>PAESE: USA<\/p>\n<p>Sottotipo LGMD: LGMD2i<\/p>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong>A che et\u00e0 \u00e8 stata fatta la diagnosi<\/strong>:<\/p>\n<p>Mi \u00e8 stata diagnosticata all'et\u00e0 di 2 anni.<\/p>\n<p><strong>Quali sono stati i primi sintomi<\/strong>:<\/p>\n<p>Mia madre e mio padre mi hanno visto cadere spesso e ho avuto difficolt\u00e0 a tenere il passo con i miei amici.<\/p>\n<p><strong>Avete altri familiari affetti da LGMD:<\/strong><\/p>\n<p>No, sono l'unica persona della mia famiglia affetta da LGMD.<\/p>\n<p><strong>Quali sono, secondo lei, le sfide pi\u00f9 grandi da affrontare nella convivenza con la LGMD?<\/strong>:<\/p>\n<p>Non mi piace non poter correre come i miei amici a scuola.  \u00c8 difficile fare ginnastica, ma mi diverto comunque a provarci.  Mia madre e mio padre mi fanno prendere una vitamina chiamata \"CoQ10\" e non mi piace il suo sapore.  Non mi piace nemmeno indossare gli stivali da stretching di notte.   Non mi piace molto che la gente sappia che ho la LGMD perch\u00e9 \u00e8 un po' imbarazzante.<\/p>\n<p><strong>Qual \u00e8 il suo pi\u00f9 grande risultato<\/strong>:<\/p>\n<p>Sono orgoglioso di saper leggere i libri a capitoli e di saper andare a cavallo.  Sono anche entusiasta di poter scendere dal trampolino e di poter nuotare nella parte profonda della piscina.   Colpisco bene la palla quando gioco a softball e mi emoziono quando arrivo in base.<\/p>\n<p><strong>In che modo la LGMD l'ha influenzata nel diventare la persona che \u00e8 oggi:<\/strong><\/p>\n<p>Posso fare bancarelle di limonate e vendere braccialetti con i miei cugini per raccogliere fondi per la LGMD.   Sono fortunata perch\u00e9 ho conosciuto altre persone affette da LGMD quando sono andata a una conferenza in Iowa.  Ora sono miei amici.<\/p>\n<p><strong>Cosa volete che il mondo sappia della LGMD?<\/strong>:<\/p>\n<p>\u00c8 difficile avere la LGMD, ma a volte incontro altre persone con disabilit\u00e0 peggiori della mia e mi rendo conto che la LGMD non \u00e8 poi cos\u00ec grave.<\/p>\n<p><strong>Se la vostra LGMD potesse essere \"curata\" domani, quale sarebbe la prima cosa che vorreste fare?<\/strong>:<\/p>\n<p>Getterei i miei stivali da stretching fuori dalla finestra e andrei all'Hershey Park per festeggiare!<\/p>","protected":false},"excerpt":{"rendered":"<p>08\/07\/2015: Name:\u00a0 Samantha\u00a0 AGE: 7 yrs. old COUNTRY: USA LGMD [&hellip;]<\/p>","protected":false},"author":1,"featured_media":975,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[13,35],"tags":[36,16],"class_list":["post-974","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-individuals-with-lgmd-interviews","category-lgmd2i","tag-lgmd2i","tag-united-states"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>LGMD Spotlight Interview - Samantha<\/title>\n<meta name=\"description\" content=\"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.lgmd-info.org\/it\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"LGMD Spotlight Interview - Samantha\" \/>\n<meta property=\"og:description\" content=\"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.lgmd-info.org\/it\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\" \/>\n<meta property=\"og:site_name\" content=\"LGMD Awareness Foundation\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/LGMDawareness\/\" \/>\n<meta property=\"article:published_time\" content=\"2015-08-07T14:25:46+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2021\/06\/LGMD-Logo_1200X630.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"630\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"dooley\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@LgmdAwareness\" \/>\n<meta name=\"twitter:site\" content=\"@LgmdAwareness\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"dooley\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\"},\"author\":{\"name\":\"dooley\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/007755074875959ad5503c1c969678c7\"},\"headline\":\"INDIVIDUAL WITH LGMD: Samantha\",\"datePublished\":\"2015-08-07T14:25:46+00:00\",\"dateModified\":\"2015-08-07T14:25:46+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\"},\"wordCount\":351,\"publisher\":{\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#organization\"},\"image\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage\"},\"thumbnailUrl\":\"\",\"keywords\":[\"LGMD2i\",\"United States\"],\"articleSection\":[\"Individuals with LGMD - Interviews\",\"LGMD2I\"],\"inLanguage\":\"it-IT\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\",\"url\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\",\"name\":\"LGMD Spotlight Interview - Samantha\",\"isPartOf\":{\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage\"},\"image\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage\"},\"thumbnailUrl\":\"\",\"datePublished\":\"2015-08-07T14:25:46+00:00\",\"dateModified\":\"2015-08-07T14:25:46+00:00\",\"description\":\"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#breadcrumb\"},\"inLanguage\":\"it-IT\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"it-IT\",\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage\",\"url\":\"\",\"contentUrl\":\"\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/www.lgmd-info.org\/de\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"INDIVIDUAL WITH LGMD: Samantha\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#website\",\"url\":\"https:\/\/www.lgmd-info.org\/de\/\",\"name\":\"LGMD Awareness Foundation\",\"description\":\"Information Hub for the LGMD community\",\"publisher\":{\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.lgmd-info.org\/de\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"it-IT\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#organization\",\"name\":\"LGMD Awareness Foundation, Inc.\",\"url\":\"https:\/\/www.lgmd-info.org\/de\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"it-IT\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#\/schema\/logo\/image\/\",\"url\":\"https:\/\/lgmd-info.org\/wp-content\/uploads\/2021\/02\/LGMD_Logo.png\",\"contentUrl\":\"https:\/\/lgmd-info.org\/wp-content\/uploads\/2021\/02\/LGMD_Logo.png\",\"width\":208,\"height\":61,\"caption\":\"LGMD Awareness Foundation, Inc.\"},\"image\":{\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#\/schema\/logo\/image\/\"},\"sameAs\":[\"https:\/\/www.facebook.com\/LGMDawareness\/\",\"https:\/\/x.com\/LgmdAwareness\",\"https:\/\/www.instagram.com\/lgmdawareness\/\"]},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/007755074875959ad5503c1c969678c7\",\"name\":\"dooley\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"it-IT\",\"@id\":\"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/c87b3b784fd4c1975884b6c3eab282b5?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/secure.gravatar.com\/avatar\/c87b3b784fd4c1975884b6c3eab282b5?s=96&d=mm&r=g\",\"caption\":\"dooley\"},\"sameAs\":[\"https:\/\/live-lgmd-2021.pantheonsite.io\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"LGMD Spotlight Interview - Samantha","description":"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.lgmd-info.org\/it\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/","og_locale":"it_IT","og_type":"article","og_title":"LGMD Spotlight Interview - Samantha","og_description":"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.","og_url":"https:\/\/www.lgmd-info.org\/it\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/","og_site_name":"LGMD Awareness Foundation","article_publisher":"https:\/\/www.facebook.com\/LGMDawareness\/","article_published_time":"2015-08-07T14:25:46+00:00","og_image":[{"width":1200,"height":630,"url":"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2021\/06\/LGMD-Logo_1200X630.png","type":"image\/png"}],"author":"dooley","twitter_card":"summary_large_image","twitter_creator":"@LgmdAwareness","twitter_site":"@LgmdAwareness","twitter_misc":{"Written by":"dooley","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#article","isPartOf":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/"},"author":{"name":"dooley","@id":"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/007755074875959ad5503c1c969678c7"},"headline":"INDIVIDUAL WITH LGMD: Samantha","datePublished":"2015-08-07T14:25:46+00:00","dateModified":"2015-08-07T14:25:46+00:00","mainEntityOfPage":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/"},"wordCount":351,"publisher":{"@id":"https:\/\/www.lgmd-info.org\/de\/#organization"},"image":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage"},"thumbnailUrl":"","keywords":["LGMD2i","United States"],"articleSection":["Individuals with LGMD - Interviews","LGMD2I"],"inLanguage":"it-IT"},{"@type":"WebPage","@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/","url":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/","name":"LGMD Spotlight Interview - Samantha","isPartOf":{"@id":"https:\/\/www.lgmd-info.org\/de\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage"},"image":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage"},"thumbnailUrl":"","datePublished":"2015-08-07T14:25:46+00:00","dateModified":"2015-08-07T14:25:46+00:00","description":"Samantha, who is diagnosed with Limb Girdle Muscular Dystrophy (LGMD), shares her experience in living with this progressive neuro-muscular disease.","breadcrumb":{"@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#breadcrumb"},"inLanguage":"it-IT","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/"]}]},{"@type":"ImageObject","inLanguage":"it-IT","@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#primaryimage","url":"","contentUrl":""},{"@type":"BreadcrumbList","@id":"https:\/\/www.lgmd-info.org\/fr\/individuals-with-lgmd-interviews\/2015\/08\/07\/samantha\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.lgmd-info.org\/de\/"},{"@type":"ListItem","position":2,"name":"INDIVIDUAL WITH LGMD: Samantha"}]},{"@type":"WebSite","@id":"https:\/\/www.lgmd-info.org\/de\/#website","url":"https:\/\/www.lgmd-info.org\/de\/","name":"LGMD Awareness Foundation","description":"Information Hub for the LGMD community","publisher":{"@id":"https:\/\/www.lgmd-info.org\/de\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.lgmd-info.org\/de\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"it-IT"},{"@type":"Organization","@id":"https:\/\/www.lgmd-info.org\/de\/#organization","name":"LGMD Awareness Foundation, Inc.","url":"https:\/\/www.lgmd-info.org\/de\/","logo":{"@type":"ImageObject","inLanguage":"it-IT","@id":"https:\/\/www.lgmd-info.org\/de\/#\/schema\/logo\/image\/","url":"https:\/\/lgmd-info.org\/wp-content\/uploads\/2021\/02\/LGMD_Logo.png","contentUrl":"https:\/\/lgmd-info.org\/wp-content\/uploads\/2021\/02\/LGMD_Logo.png","width":208,"height":61,"caption":"LGMD Awareness Foundation, Inc."},"image":{"@id":"https:\/\/www.lgmd-info.org\/de\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.facebook.com\/LGMDawareness\/","https:\/\/x.com\/LgmdAwareness","https:\/\/www.instagram.com\/lgmdawareness\/"]},{"@type":"Person","@id":"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/007755074875959ad5503c1c969678c7","name":"dooley","image":{"@type":"ImageObject","inLanguage":"it-IT","@id":"https:\/\/www.lgmd-info.org\/de\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/c87b3b784fd4c1975884b6c3eab282b5?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/c87b3b784fd4c1975884b6c3eab282b5?s=96&d=mm&r=g","caption":"dooley"},"sameAs":["https:\/\/live-lgmd-2021.pantheonsite.io"]}]}},"_links":{"self":[{"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/posts\/974","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/comments?post=974"}],"version-history":[{"count":0,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/posts\/974\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/"}],"wp:attachment":[{"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/media?parent=974"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/categories?post=974"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.lgmd-info.org\/it\/wp-json\/wp\/v2\/tags?post=974"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}