{"id":3239,"date":"2012-04-16T18:24:18","date_gmt":"2012-04-16T18:24:18","guid":{"rendered":"http:\/\/216.185.159.195\/?page_id=3239"},"modified":"2026-03-24T10:02:04","modified_gmt":"2026-03-24T16:02:04","slug":"embajadores","status":"publish","type":"page","link":"https:\/\/www.globaldownsyndrome.org\/es_mx\/news-community\/ambassadors\/","title":{"rendered":"Embajadores de la Fundaci\u00f3n Mundial del S\u00edndrome de Down"},"content":{"rendered":"
\n\t
\n\t\t
\n\t\t\t
\"\"<\/a>

DeOndra Dixon, embajadora mundial del s\u00edndrome de Down 2011, con el representante Patrick Kennedy<\/p><\/div>\n

Adem\u00e1s de homenajear a las personas con s\u00edndrome de Down con el Premio Quincy Jones a la Defensa Excepcional<\/a>, Global Down Syndrome Foundation is proud to honor individuals with Down syndrome each year as official Ambassadors for Foundation. Ambassadors and their families work hard to raise awareness for the Foundation\u2019s mission of significantly improving the lives of people with Down syndrome through research, medical care, education and advocacy.  Each Ambassador graces the cover of our Be Beautiful Be Yourself gala invitation and writes his or her own personal story.  The story is featured in the local press and as part of the invitation.  The Ambassador is also featured in a special video our Foundation produces for the marquee fundraising event and depending on the Ambassador\u2019s age, the Ambassador participates as a model in the fashion show.<\/p>\n

Los embajadores y sus familias siguen apoyando la labor de la Fundaci\u00f3n represent\u00e1ndola en conferencias y convenciones, recaudando fondos para programas y talleres, participando en entrevistas de prensa y abogando por la igualdad y el apoyo gubernamental.<\/p>\n

 <\/p>\n

Meet Letizia Napoleone\u2013 2026 Global Down Syndrome Foundation Ambassador<\/b><\/a>\"\"<\/p>\n

Letizia is a vibrant 23-year-old woman with Down syndrome who lives and works in New York City. She is actively pursuing her acting education at Epic Players, New York. In June 2024, she graduated from the Cooke School Transition Program Downtown. She radiates boundless energy and enthusiasm, earning her admiration among peers and friends at school. She is a cherished community member known for her outstanding self-confidence and exceptional social skills. Originally from a family of Italian descent, she is fluent in Italian and English.<\/p>\n

Seguir leyendo<\/a> about Letizia Napoleone<\/p>\n

\n

Meet Crystal Muro\u2013 2026 Global Down Syndrome Foundation Ambassador<\/b><\/a>\"\"<\/p>\n

Crystal Muro lives in Orange County, California with her mom, thanks to a very important decision her parents made when she was born.
\nWhile California’s Lanterman Act of 1969 ensured the rights of individuals with developmental disabilities to community-based care, Steve and Pia Muro were encouraged to consider committing Crystal to a state hospital when she was born. They knew immediately that their only option
\nwas to bring home their newborn and fully embrace her as a member of their loving family.<\/p>\n

Seguir leyendo<\/a> about Crystal Muro<\/p>\n

\n

Meet Guion Macsovits \u2013 2025 Global Down Syndrome Foundation Ambassador<\/b><\/a>\"\"<\/p>\n

Guion Macsovits is a fun-loving 19-year-old with a heart as big as his smile. He recently graduated from Cherry Creek High School where he was known for his kindness, thoughtfulness, and the way he naturally makes people feel valued. Whether holding the door between bells, checking in on a friend, or offering a word of encouragement, Guion has a way of making the world a little brighter. His emotional intelligence is off the charts, and he leads with                empathy in everything he does.<\/p>\n

Seguir leyendo<\/a> about Guion Mascovits<\/p>\n

\n

Meet Tucker Emry \u2013 2025 Global Down Syndrome Foundation Ambassador<\/b><\/a>\"\"<\/p>\n

This is the best thing that\u2019s ever happened to you \u2013 you just don\u2019t know it yet,\u201d was the message we received from a friend upon Tucker\u2019s birth. We hadn\u2019t expected him to be born with a little \u201csomething extra,\u201d but if we were privy to even a short preview of his future, we would have known not to worry. He lives life to the fullest and it\u2019s our privilege to be along for the ride<\/p>\n

Seguir leyendo<\/a> about Tucker Emry<\/p>\n

\n

Conozca a Zaya Biel - Embajadora 2024 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/b><\/a>\"Retrato<\/p>\n

\u00a1Hola! Soy Zaya Rose, una peque\u00f1a y fogosa ni\u00f1a de 5 a\u00f1os que ya ha vivido un sinf\u00edn de experiencias extraordinarias. En Nochevieja de 2018, mientras mis padres estaban de celebraci\u00f3n, sorprend\u00ed a todos llegando 4 semanas antes durante una gran ventisca en Colorado.<\/p>\n

Seguir leyendo<\/a> sobre Zaya Biel<\/p>\n

\n

Conoce a Isla Eager - Embajadora 2024 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/b><\/a>
\n\"Retrato<\/p>\n

Es un verdadero honor para nosotros presentar a Isla como Embajadora de GLOBAL 2024. Cuando Isla entra en una habitaci\u00f3n lo sabes. Alguien nos describi\u00f3 recientemente a Isla como una \"bomba de alegr\u00eda\". Y es verdad. Es un tornado de actividad y movimiento sin parar, pero derrama luz en todas las direcciones en las que se mueve. Sus profesores la llaman la \"alcaldesa\" del colegio. Pero lo mismo puede decirse cuando est\u00e1 en la consulta del m\u00e9dico, en el parque infantil o en el supermercado. Nunca conoce a un extra\u00f1o y no tarda en decir \"\u00a1Hola!\", sobre todo si la persona que la recibe a\u00fan no se ha fijado en ella.<\/p>\n

Seguir leyendo<\/a> sobre Isla Eager<\/p>\n

\n

Conozca a Grace Brennan - Embajadora 2023 de la Fundaci\u00f3n Mundial del S\u00edndrome de Down<\/b><\/a>\"\"<\/p>\n

Hola, me llamo Grace Brennan y este a\u00f1o cumplir\u00e9 9 a\u00f1os en septiembre. Estoy en segundo grado y me encanta caminar a la escuela con mis dos hermanas mayores, Audrey y Ava. Estoy incluida en el aula de educaci\u00f3n general del colegio de mi barrio desde T-K, y me encanta estar en el mismo colegio que mis hermanas. Incluso se podr\u00eda decir que soy m\u00e1s popular en nuestra escuela que ellas.<\/p>\n

Seguir leyendo<\/a> sobre Grace Brennan<\/p>\n

\n

Conozca a Abby Ashbrook - Embajadora 2023 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/b><\/a>\"\"<\/p>\n

Es un verdadero honor para nosotros presentar a Abby como Embajadora de este a\u00f1o de la Fundaci\u00f3n Global S\u00edndrome de Down. Abby es el regalo que nuestra familia no sab\u00eda que necesitaba, y nos hace mucha ilusi\u00f3n que la conozc\u00e1is.<\/p>\n

Seguir leyendo<\/a> sobre Abby Ashbrook<\/p>\n

\n

Conozca a Micah Quinones - Embajador de la Fundaci\u00f3n Global S\u00edndrome de Down 2022<\/b><\/a>\"\"<\/p>\n

Hola, soy Micah Quinones. Tengo ocho a\u00f1os y acabo de empezar segundo de primaria. Mi apodo es \"chi\", que es una versi\u00f3n abreviada de la palabra que mejor me describe: \u00a1descarado! Mis padres saben perfectamente lo mucho que me gusta llamar la atenci\u00f3n, \u00a1y har\u00e9 cualquier cosa para conseguirlo!<\/p>\n

Seguir leyendo<\/a> sobre Micah Quinones.<\/p>\n

\n

Conozca a Jonah Berger - 2022 Global Down Syndrome<\/strong>Embajador de la Fundaci\u00f3n<\/strong><\/a>\"2022<\/p>\n

Este es Jonah Berger. Es nuestro hijo, hermano, nieto, primo, sobrino, amigo, vecino, alumno y, sobre todo, es nuestro maestro. Cuando Jonah naci\u00f3 hace diez a\u00f1os, no sab\u00edamos que tendr\u00eda s\u00edndrome de Down.<\/p>\n

Seguir leyendo<\/a> sobre Jonah Berger.<\/em><\/p>\n

\n

Conozca a Archie y Sevy Eicher - Embajadores de la Fundaci\u00f3n Global S\u00edndrome de Down 2021<\/strong><\/a><\/p>\n

Archie y Sevy tuvieron unos comienzos de vida injustos, en los que se les consideraba indignos de formar parte de una familia o de la sociedad. Y ahora, cada d\u00eda, demuestran que esa visi\u00f3n del mundo era err\u00f3nea.<\/p>\n

Seguir leyendo<\/a> sobre Archie y Sevy Eicher.<\/em><\/p>\n

\n

Conozca a Caroline Cardenas - Embajadora 2021 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Me llamo Caroline Cardenas y tengo 17 a\u00f1os. Vivo en Dallas, Texas, con mi madre, mi padre, mis tres hermanas y mi perro, Luka. Mis hermanas son mis mejores amigas: Grace est\u00e1 en la universidad, Emily va a ir a la universidad este a\u00f1o, y Claire est\u00e1 en la escuela secundaria. Siempre sacan tiempo para estar conmigo. A toda la familia le encanta jugar a juegos de mesa, practicar deportes con la Wii, ver pel\u00edculas y comer helados juntos.<\/p>\n

Seguir leyendo<\/a> sobre Caroline Cardenas.<\/em><\/p>\n

\n

Conozca a Walt Snodgrass - Embajador 2020 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Hola, me llamo Thomas Walter Snodgrass. Tengo 16 a\u00f1os y estoy en segundo de bachillerato. Todo el mundo me llama \"Walt\". Es apropiado porque me encanta ir a Walt Disney World.<\/p>\n

Seguir leyendo<\/a> sobre Walt Snodgrass.<\/em><\/p>\n

\n

Conoce a Charlotte Fonfara-LaRose - Embajadora 2019 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Me llamo Charlotte Fonfara-LaRose, pero mis amigos me llaman Charley. Tengo 16 a\u00f1os y soy estudiante de segundo de bachillerato en Annapolis, Maryland.<\/p>\n

Tengo una hermana, Noelle, y una gran familia. Mis padres, Cathy y Scott, son muy afortunados de tenerme. Cuando nac\u00ed, sorprend\u00ed a todos con un cromosoma de m\u00e1s. A pesar del tono sombr\u00edo del hospital, sal\u00ed de all\u00ed feliz y sana, lista para empezar mi gran vida.<\/p>\n

Seguir leyendo<\/a> sobre Charlotte Fonfara-LaRose.<\/em><\/p>\n

\n

\"Conoce a CC Mullen - Embajador 2019 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Me llamo Caroline \"CC\" Mullen. Soy un peque\u00f1o tornado brillante, alegre y decidido que casualmente tiene s\u00edndrome de Down. Vivo en Virginia con mi madre, mi padre y mi hermana mayor Amelia. Me encanta pasar tiempo con mi familia y tengo la suerte de tener a muchos de ellos a mi alrededor. Tambi\u00e9n me gusta bailar, leer libros con mi madre y comer.<\/p>\n

Seguir leyendo<\/a> sobre CC Mullen.<\/em><\/p>\n

\n

\"Conoce a Sam Levin - Embajador 2018 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Cualquiera que conozca a Sam sabe que es \u00fanico en su clase. Participa en los campamentos de f\u00fatbol americano Dare to Play de GLOBAL con Ed McCaffrey, juega en los equipos de baloncesto, f\u00fatbol americano, lacrosse y atletismo de Cherry Creek High School Unified. Ahora es el Embajador Be Beautiful Be Yourself de 2018.
\nSeguir leyendo<\/a> sobre Sam Levin.<\/em><\/p>\n

\n

\"\"Conoce a Frank Stephens - Embajador 2018 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Frank Stephens es un activo portavoz de la Global Down Syndrome Foundation y miembro del Consejo de Administraci\u00f3n de Special Olympics Virginia. Frank habla a menudo de lo afortunado que se siente por vivir en una generaci\u00f3n en la que todos sus logros son posibles para un hombre con s\u00edndrome de Down.
\nSeguir leyendo<\/a> sobre Frank Stephens.<\/em><\/p>\n

\n

\"MarcusConoce a Marcus Sikora - Embajador 2017 de la Fundaci\u00f3n Global S\u00edndrome de Down.<\/strong><\/a><\/p>\n

Como autor, cantante, actor y defensor de s\u00ed mismo, Marcus Sikora ya ha conseguido m\u00e1s cosas en su vida que la mayor\u00eda de los j\u00f3venes de 26 a\u00f1os. Ahora re\u00fane otro logro m\u00e1s como Embajador Be Beautiful Be Yourself 2017.
\nSeguir leyendo<\/a> sobre Marcus Sikora.<\/em><\/p>\n

\n

Conoce a Louis Rotella IV - Embajador 2016 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

\"louis\"Louis \"Louie\" Rotella IV, el encantador ni\u00f1o que inspir\u00f3 a su padre para crear la c\u00e9lebre historia de la aceptaci\u00f3nEl peque\u00f1o rey y su reino de malvavisco<\/a><\/em>-inspirar\u00e1 a un p\u00fablico de 1.200 personas cuando se suba a la pasarela como embajador de 2016 en el desfile de moda Be Beautiful Be Yourself de Global el s\u00e1bado 12 de noviembre.
\nSeguir leyendo<\/a> sobre Louis Rotella.<\/em><\/p>\n

\n

\"ClarissaConoce a Clarissa Capuano - Embajadora 2015 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a><\/p>\n

Me llamo Clarissa Joann Capuano. Tengo siete a\u00f1os y vivo con mi madre y mi padre. Tengo dos hermanos mayores, Alec y Jesse, que van a la universidad. Me encanta cantar, bailar, montar a caballo, nadar, ir de excursi\u00f3n y jugar a disfrazarme.
\nSeguir leyendo<\/a> sobre Clarissa Capuano.<\/em><\/p>\n

\n

Conoce a Steven Dulcie - Embajador 2014 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/a>
\n\"Steven<\/p>\n

Steven aporta a cualquiera que le conozca Alegr\u00eda con may\u00fasculas. Le encantan el f\u00fatbol y el b\u00e9isbol, es un experto en cine y le encanta la m\u00fasica y bailar.
\nSeguir leyendo<\/a> sobre Steven Dulcie.<\/em><\/p>\n

\n

Conoce a Katherine Felicia Norton - Embajadora 2014 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong>
\n\"Katherine<\/p>\n

Me llamo Katherine Felicia Norton. Tengo 43 a\u00f1os y vivo en Washington, DC, donde mi madre, Eleanor Holmes Norton, representa al Distrito de Columbia en el Congreso. Me encanta bailar, hacer puzzles y actuar en pantomimas en el Instituto de Arte y Terapia Dram\u00e1tica y demostrar a todo el mundo lo capaz y divertida que soy.<\/a><\/p>\n

Seguir leyendo<\/a> sobre Katherine Felicia Norton.<\/em><\/p>\n

\n

Conoce a Cole Rodgers - Embajador 2013 de la Fundaci\u00f3n Global S\u00edndrome de Down.<\/strong><\/p>\n

\"Cole<\/p>\n

Me llamo Cole Rodgers. Tengo 6 a\u00f1os. Me encanta la m\u00fasica, la escuela y la mantequilla de cacahuete. Mi familia es del este del estado de Washington, pero la mayor parte del tiempo vivimos en Washington, D.C.<\/a><\/p>\n

Seguir leyendo<\/a> sobre Cole.<\/em><\/p>\n

\n

Conozca a Samantha Marcia Stevens - Embajadora 2012 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"\"<\/p>\n

Me llamo Samantha Marcia Stevens y vivo en las afueras de Boston con mi mami y mi papi. Aunque s\u00f3lo tengo 6 a\u00f1os, he llenado mi vida y la de todos los que conozco de sonrisas y felicidad.<\/a><\/p>\n

Seguir leyendo<\/a> sobre Samantha.<\/em><\/p>\n

\n

Conoce a DeOndra Dixon - Embajadora 2011 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"\"<\/p>\n

Un cari\u00f1oso homenaje a la embajadora de GLOBAL DeOndra Dixon<\/a><\/strong><\/p>\n

DeOndra fue la primera galardonada con el Premio Quincy Jones a la Promoci\u00f3n Excepcional y Embajadora de Global desde 2011. DeOndra viv\u00eda en California con su hermano, Jamie Foxx, sus padres y su familia. DeOndra estaba muy agradecida a su familia por ayudarla a alcanzar su potencial y, a su vez, ayud\u00f3 a otras personas con s\u00edndrome de Down a hacer lo mismo.
\n<\/a><\/p>\n

Seguir leyendo<\/a> sobre DeOndra.<\/em><\/p>\n

\n

Conoce a Alex Sessions - Embajadora 2011 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"\"<\/p>\n

Me llamo Alexander Gregory Sessions y tengo 17 a\u00f1os. Nac\u00ed el 19 de enero de 1994 en Dallas, Texas. Nac\u00ed con s\u00edndrome de Down. Mis padres estaban muy contentos cuando nac\u00ed: mi hermano Bill ten\u00eda 4 a\u00f1os y siempre hab\u00edan querido tener dos varones. No sab\u00edan mucho sobre el s\u00edndrome de Down, pero pronto empezaron a informarse para asegurarse de que hac\u00edan todo lo posible por ayudarme a alcanzar mi potencial intelectual y f\u00edsico.<\/a><\/p>\n

Seguir leyendo<\/a> sobre Alex.<\/em><\/p>\n

\n

Conozca a Katherine Vollbracht Winfield - Embajadora 2010 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"\"<\/p>\n

Me llamo Katherine Vollbracht Winfield. Me gustan las luces brillantes y las risitas. Eso es porque s\u00f3lo tengo 15 meses. Vivo en Seattle con mi madre, mi padre y mi hermano mayor Kirby III. Sorprend\u00ed a todos llegando 3 semanas antes. Y tuve otra gran sorpresa: nac\u00ed con s\u00edndrome de Down.<\/a><\/p>\n

Seguir leyendo<\/a> sobre Katherine.<\/em><\/p>\n

\n

Conozca a Chase Turner Perry - Embajador 2009 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"\"<\/p>\n

Me llamo Chase Turner Perry. Tengo tres a\u00f1os y vivo en Colorado con mi mam\u00e1, mi pap\u00e1 y mi hermanito Cooper. He o\u00eddo muchas veces a mis padres contar la historia del d\u00eda en que nac\u00ed. Fui una gran sorpresa. Mis padres no sab\u00edan que era un ni\u00f1o ni que ten\u00eda un cromosoma de m\u00e1s.<\/p>\n

Seguir leyendo<\/a> sobre Chase.<\/em><\/p>\n

\n

Conozca a Sophia Whitten - Embajadora 2008 de la Fundaci\u00f3n Global S\u00edndrome de Down<\/strong><\/p>\n

\"Retrato<\/p>\n

Me llamo Sophia Kay Whitten. Tengo cinco a\u00f1os y vivo en Colorado con mi mam\u00e1, mi pap\u00e1 y mi hermanito Patrick.<\/p>\n

Seguir leyendo<\/a> sobre Sophia.<\/em><\/p>\n

\n

 <\/p>\n

 <\/p>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div>\n<\/div>","protected":false},"excerpt":{"rendered":"2011 Global Down Syndrome Ambassador DeOndra Dixon with Rep. Patrick Kennedy In addition to honoring people with Down syndrome with the Quincy Jones Exceptional Advocacy Award, Global Down Syndrome Foundation is proud to honor individuals with Down syndrome each year as official Ambassadors for Foundation. Ambassadors and their families work hard to raise awareness for [...]","protected":false},"author":3,"featured_media":0,"parent":28,"menu_order":50,"comment_status":"open","ping_status":"closed","template":"","meta":{"_acf_changed":false,"ngg_post_thumbnail":0,"footnotes":""},"class_list":["post-3239","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nGlobal Down Syndrome Foundation Ambassadors | Global Down Syndrome Foundation<\/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:\/\/www.globaldownsyndrome.org\/es_mx\/comunidad-de-noticias\/embajadores\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Global Down Syndrome Foundation Ambassadors | Global Down Syndrome Foundation\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.globaldownsyndrome.org\/es_mx\/comunidad-de-noticias\/embajadores\/\" \/>\n<meta property=\"og:site_name\" content=\"Global Down Syndrome Foundation\" \/>\n<meta property=\"article:modified_time\" content=\"2026-03-24T16:02:04+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2026\/03\/Letizia-Napoleone-300x300-1.png\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"11 minutos\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/\",\"url\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/\",\"name\":\"Global Down Syndrome Foundation Ambassadors | Global Down Syndrome Foundation\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/Letizia-Napoleone-300x300-1.png\",\"datePublished\":\"2012-04-16T18:24:18+00:00\",\"dateModified\":\"2026-03-24T16:02:04+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/#breadcrumb\"},\"inLanguage\":\"es\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"es\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/#primaryimage\",\"url\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/Letizia-Napoleone-300x300-1.png\",\"contentUrl\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/wp-content\\\/uploads\\\/2026\\\/03\\\/Letizia-Napoleone-300x300-1.png\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/ambassadors\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"GLOBAL In the News\",\"item\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/news-community\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Global Down Syndrome Foundation Ambassadors\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#website\",\"url\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/\",\"name\":\"Global Down Syndrome Foundation\",\"description\":\"Dedicated to significantly improving the lives of people with Down Syndrome through RESEARCH, MEDICAL CARE, EDUCATION AND ADVOCACY\",\"publisher\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"es\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#organization\",\"name\":\"Global Down Syndrome Foundation\",\"url\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"es\",\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/wp-content\\\/uploads\\\/2022\\\/11\\\/logo.jpg\",\"contentUrl\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/wp-content\\\/uploads\\\/2022\\\/11\\\/logo.jpg\",\"width\":2351,\"height\":896,\"caption\":\"Global Down Syndrome Foundation\"},\"image\":{\"@id\":\"https:\\\/\\\/www.globaldownsyndrome.org\\\/#\\\/schema\\\/logo\\\/image\\\/\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Embajadores de la Fundaci\u00f3n Global S\u00edndrome de Down | Fundaci\u00f3n Global S\u00edndrome de Down","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.globaldownsyndrome.org\/es_mx\/comunidad-de-noticias\/embajadores\/","og_locale":"es_MX","og_type":"article","og_title":"Global Down Syndrome Foundation Ambassadors | Global Down Syndrome Foundation","og_url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/comunidad-de-noticias\/embajadores\/","og_site_name":"Global Down Syndrome Foundation","article_modified_time":"2026-03-24T16:02:04+00:00","og_image":[{"url":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2026\/03\/Letizia-Napoleone-300x300-1.png","type":"","width":"","height":""}],"twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"11 minutos"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/","url":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/","name":"Embajadores de la Fundaci\u00f3n Global S\u00edndrome de Down | Fundaci\u00f3n Global S\u00edndrome de Down","isPartOf":{"@id":"https:\/\/www.globaldownsyndrome.org\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/#primaryimage"},"image":{"@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2026\/03\/Letizia-Napoleone-300x300-1.png","datePublished":"2012-04-16T18:24:18+00:00","dateModified":"2026-03-24T16:02:04+00:00","breadcrumb":{"@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/#breadcrumb"},"inLanguage":"es","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/"]}]},{"@type":"ImageObject","inLanguage":"es","@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/#primaryimage","url":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2026\/03\/Letizia-Napoleone-300x300-1.png","contentUrl":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2026\/03\/Letizia-Napoleone-300x300-1.png"},{"@type":"BreadcrumbList","@id":"https:\/\/www.globaldownsyndrome.org\/news-community\/ambassadors\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.globaldownsyndrome.org\/"},{"@type":"ListItem","position":2,"name":"GLOBAL In the News","item":"https:\/\/www.globaldownsyndrome.org\/news-community\/"},{"@type":"ListItem","position":3,"name":"Global Down Syndrome Foundation Ambassadors"}]},{"@type":"WebSite","@id":"https:\/\/www.globaldownsyndrome.org\/#website","url":"https:\/\/www.globaldownsyndrome.org\/","name":"Fundaci\u00f3n Mundial del S\u00edndrome de Down","description":"Dedicada a mejorar significativamente la vida de las personas con s\u00edndrome de Down a trav\u00e9s de la INVESTIGACI\u00d3N, LA ATENCI\u00d3N M\u00c9DICA, LA EDUCACI\u00d3N Y LA DEFENSA.","publisher":{"@id":"https:\/\/www.globaldownsyndrome.org\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.globaldownsyndrome.org\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"es"},{"@type":"Organization","@id":"https:\/\/www.globaldownsyndrome.org\/#organization","name":"Fundaci\u00f3n Mundial del S\u00edndrome de Down","url":"https:\/\/www.globaldownsyndrome.org\/","logo":{"@type":"ImageObject","inLanguage":"es","@id":"https:\/\/www.globaldownsyndrome.org\/#\/schema\/logo\/image\/","url":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2022\/11\/logo.jpg","contentUrl":"https:\/\/www.globaldownsyndrome.org\/wp-content\/uploads\/2022\/11\/logo.jpg","width":2351,"height":896,"caption":"Global Down Syndrome Foundation"},"image":{"@id":"https:\/\/www.globaldownsyndrome.org\/#\/schema\/logo\/image\/"}}]}},"jetpack_shortlink":"https:\/\/wp.me\/P70gmm-Qf","jetpack-related-posts":[{"id":155417,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/deondra-dixon-include-project-act\/","url_meta":{"origin":3239,"position":0},"title":"Ley del Proyecto INCLUDE de DeOndra Dixon","author":"Wes Butler","date":"marzo 20, 2024","format":false,"excerpt":"","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":151153,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/employment-awards-recipients\/","url_meta":{"origin":3239,"position":1},"title":"Global Down Syndrome Foundation Provides $16,000 in Employment Awards to Down Syndrome Organizations Across the United States","author":"Global Down Syndrome Foundation","date":"abril 20, 2023","format":false,"excerpt":"\u00a0 In April, the Global Down Syndrome Foundation (GLOBAL) awarded $16,000 in Employment Awards to Down syndrome organizations across the United States. The GLOBAL Employment Awards are a distinguished benefit for GLOBAL organization members. The awards create collaboration with local organizations and fund programs that have a direct and positive\u2026","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/www.globaldownsyndrome.org\/wp-content\/uploads\/2023\/04\/300x300.jpg?resize=350%2C200&ssl=1","width":350,"height":200},"classes":[]},{"id":150833,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/2023-ambassador-abby-ashbrook\/","url_meta":{"origin":3239,"position":2},"title":"2023 Ambassador Abby Ashbrook","author":"Global Down Syndrome Foundation","date":"marzo 27, 2023","format":false,"excerpt":"It is truly an honor for us to introduce Abby as this year\u2019s Ambassador for the Global Down Syndrome Foundation. Abby is the gift our family didn\u2019t know we needed, and we are so excited for you to meet her. From the moment Abby was born on January 10th, 2011,\u2026","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"2023 Ambassador Abby Ashbrook","src":"https:\/\/i0.wp.com\/www.globaldownsyndrome.org\/wp-content\/uploads\/2023\/03\/abbyresize231x223-1.jpg?resize=350%2C200&ssl=1","width":350,"height":200},"classes":[]},{"id":151288,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/photos-and-videos\/videos\/2020-ambassador-walt-snodgrass-tribute-video\/","url_meta":{"origin":3239,"position":3},"title":"2020 Ambassador Walt Snodgrass Tribute Video","author":"Global Down Syndrome Foundation","date":"mayo 11, 2023","format":false,"excerpt":"The Global Down Syndrome Foundation honored Ambassador Walt Snodgrass at the Be Beautiful Be Yourself Fashion Show\u00a0 https:\/\/www.youtube.com\/watch?v=LPiqUAugPis \u00a0","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/img.youtube.com\/vi\/LPiqUAugPis\/0.jpg?resize=350%2C200","width":350,"height":200},"classes":[]},{"id":157452,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/advocacy-center\/us-house-passed-deondra-dixon-include-project-act\/","url_meta":{"origin":3239,"position":4},"title":"The U.S. House Passed Our DeOndra Dixon INCLUDE Project Act","author":"Global Down Syndrome Foundation","date":"septiembre 18, 2024","format":false,"excerpt":"\u00a0 \u00a0 U.S. House of Representatives Vote on C-SPAN \u00a0 September 6, 1984 \u2013 October 19, 2020 DeOndra Dixon Tribute Video ALWAYS LOVED NEVER FORGOTTEN \u00a0 Global's Quincy Jones Exceptional Advocacy Award Winner Frank Stephens Gives Powerful Speech Contact Your U.S. Senator Today! DeOndra Dixon INCLUDE Project Act FAQ's \u00a0\u2026","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/www.globaldownsyndrome.org\/wp-content\/uploads\/2024\/12\/Thanks-To-Our-Congressional-Champions-1-600x318.png?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.globaldownsyndrome.org\/wp-content\/uploads\/2024\/12\/Thanks-To-Our-Congressional-Champions-1-600x318.png?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/www.globaldownsyndrome.org\/wp-content\/uploads\/2024\/12\/Thanks-To-Our-Congressional-Champions-1-600x318.png?resize=525%2C300&ssl=1 1.5x"},"classes":[]},{"id":151282,"url":"https:\/\/www.globaldownsyndrome.org\/es_mx\/photos-and-videos\/videos\/2021-ambassadors-archie-sevy-eicher-tribute-video\/","url_meta":{"origin":3239,"position":5},"title":"2021 Ambassadors Archie & Sevy Eicher Tribute Video","author":"Global Down Syndrome Foundation","date":"mayo 11, 2023","format":false,"excerpt":"The Global Down Syndrome Foundation honored Ambassador Archie & Sevy Eicher at the Be Beautiful Be Yourself Fashion Show on Saturday, November 13, 2019. https:\/\/youtu.be\/BKrI4PO52xI \u00a0","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/img.youtube.com\/vi\/BKrI4PO52xI\/0.jpg?resize=350%2C200","width":350,"height":200},"classes":[]}],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/pages\/3239","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/comments?post=3239"}],"version-history":[{"count":0,"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/pages\/3239\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/pages\/28"}],"wp:attachment":[{"href":"https:\/\/www.globaldownsyndrome.org\/es_mx\/wp-json\/wp\/v2\/media?parent=3239"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}