{"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":"ambasadoret","status":"publish","type":"page","link":"https:\/\/www.globaldownsyndrome.org\/sq\/news-community\/ambassadors\/","title":{"rendered":"Ambasador\u00ebt e Fondacionit Global Down Syndrome"},"content":{"rendered":"
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\"\"<\/a>

2011 Ambasadori i Sindrom\u00ebs Down Global DeOndra Dixon me Rep. Patrick Kennedy<\/p><\/div>\n

P\u00ebrve\u00e7 nderimit t\u00eb njer\u00ebzve me sindrom\u00ebn Down me \u00c7mimi i Jasht\u00ebzakonsh\u00ebm i Avokimit Quincy Jones<\/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

Ambasador\u00ebt dhe familjet e tyre vazhdojn\u00eb t\u00eb mb\u00ebshtesin pun\u00ebn e Fondacionit duke p\u00ebrfaq\u00ebsuar fondacionin n\u00eb konferenca dhe konventa, duke mbledhur fonde p\u00ebr programe dhe seminare, duke marr\u00eb pjes\u00eb n\u00eb intervista p\u00ebr shtyp dhe duke avokuar p\u00ebr barazi dhe mb\u00ebshtetjen e qeveris\u00eb.<\/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

Lexo m\u00eb shum\u00eb<\/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

Lexo m\u00eb shum\u00eb<\/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

Lexo m\u00eb shum\u00eb<\/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

Lexo m\u00eb shum\u00eb<\/a> about Tucker Emry<\/p>\n

\n

Njihuni me Zaya Biel \u2013 Ambasadore e Fondacionit Global Down Syndrome 2024<\/b><\/a>\"Portreti<\/p>\n

P\u00ebrsh\u00ebndetje! Un\u00eb jam Zaya Rose, nj\u00eb 5-vje\u00e7are e vog\u00ebl e zjarrt\u00eb, e cila tashm\u00eb ka pasur nj\u00eb mori p\u00ebrvojash t\u00eb jasht\u00ebzakonshme. N\u00eb nat\u00ebn e Vitit t\u00eb Ri 2018, nd\u00ebrsa prind\u00ebrit e mi po festonin, un\u00eb i befasova t\u00eb gjith\u00eb duke mb\u00ebrritur 4 jav\u00eb m\u00eb her\u00ebt gjat\u00eb nj\u00eb stuhie t\u00eb madhe n\u00eb Kolorado.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> n\u00eb lidhje me Zaya Biel<\/p>\n

\n

Njihuni me Isla Eager \u2013 Ambasadoren e Fondacionit Global Down Syndrome 2024<\/b><\/a>
\n\"Portret<\/p>\n

\u00cbsht\u00eb me t\u00eb v\u00ebrtet\u00eb nj\u00eb nder p\u00ebr ne q\u00eb t\u00eb prezantojm\u00eb Isla-n si ambasadoren e GLOBAL p\u00ebr vitin 2024. Kur Isla ec\u00ebn n\u00eb nj\u00eb dhom\u00eb ju e dini k\u00ebt\u00eb. Dikush koh\u00ebt e fundit na e p\u00ebrshkroi Isl\u00ebn si nj\u00eb "bomb\u00eb g\u00ebzimi". \u00cbsht\u00eb e v\u00ebrtet\u00eb. Ajo \u00ebsht\u00eb nj\u00eb tornado aktiviteti dhe l\u00ebvizjeje pa pushim, por hedh drit\u00eb n\u00eb \u00e7do drejtim q\u00eb l\u00ebviz. M\u00ebsuesit e quajn\u00eb \u201ckryetarja\u201d e shkoll\u00ebs. Por e nj\u00ebjta gj\u00eb mund t\u00eb thuhet kur ajo \u00ebsht\u00eb n\u00eb zyr\u00ebn e mjekut, shesh loj\u00ebrash ose dyqan ushqimesh. Ajo nuk ka takuar kurr\u00eb nj\u00eb t\u00eb huaj dhe \u00ebsht\u00eb e shpejt\u00eb me nj\u00eb "P\u00ebrsh\u00ebndetje!", ve\u00e7an\u00ebrisht n\u00ebse personi n\u00eb fund nuk e ka v\u00ebn\u00eb re ende.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Isla Eager<\/p>\n

\n

Njihuni me Grace Brennan \u2013 Ambasadoren e Fondacionit Global Down Syndrome 2023<\/b><\/a>\"\"<\/p>\n

P\u00ebrsh\u00ebndetje, emri im \u00ebsht\u00eb Grace Brennan dhe do t\u00eb b\u00ebhem 9 vje\u00e7 k\u00ebt\u00eb vit n\u00eb shtator. Un\u00eb jam n\u00eb klas\u00ebn e dyt\u00eb dhe m\u00eb p\u00eblqen t\u00eb eci n\u00eb shkoll\u00eb me dy motrat e mia t\u00eb m\u00ebdha, Audrey dhe Ava. Un\u00eb jam p\u00ebrfshir\u00eb n\u00eb klas\u00ebn e arsimit t\u00eb p\u00ebrgjithsh\u00ebm n\u00eb shkoll\u00ebn e lagjes sime q\u00eb nga TK dhe m\u00eb p\u00eblqen t\u00eb jem n\u00eb t\u00eb nj\u00ebjt\u00ebn shkoll\u00eb me motrat e mia. Ju madje mund t\u00eb thoni se un\u00eb jam m\u00eb popullor n\u00eb shkoll\u00ebn ton\u00eb sesa ata!<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Grace Brennan<\/p>\n

\n

Njihuni me Abby Ashbrook \u2013 Ambasadorja e Fondacionit Global Down Syndrome 2023<\/b><\/a>\"\"<\/p>\n

\u00cbsht\u00eb me t\u00eb v\u00ebrtet\u00eb nj\u00eb nder p\u00ebr ne t\u00eb prezantojm\u00eb Abby si Ambasadoren e k\u00ebtij viti p\u00ebr Fondacionin Global Down Syndrome. Abby \u00ebsht\u00eb dhurata q\u00eb familja jon\u00eb nuk e dinte se kishim nevoj\u00eb, dhe ne jemi shum\u00eb t\u00eb emocionuar q\u00eb ju ta takoni at\u00eb.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Abby Ashbrook<\/p>\n

\n

Njihuni me Micah Quinones \u2013 Ambasadori i Fondacionit Global Down Syndrome 2022<\/b><\/a>\"\"<\/p>\n

P\u00ebrsh\u00ebndetje, Micah Quinones k\u00ebtu! Un\u00eb jam aktualisht tet\u00eb vje\u00e7 dhe sapo kam filluar klas\u00ebn e dyt\u00eb! Pseudonimi im \u00ebsht\u00eb "chi" q\u00eb \u00ebsht\u00eb nj\u00eb version i shkurt\u00ebr i fjal\u00ebs q\u00eb m\u00eb p\u00ebrshkruan m\u00eb mir\u00eb - i pafytyr\u00eb! Prind\u00ebrit e mi e din\u00eb plot\u00ebsisht se sa shum\u00eb e dua v\u00ebmendjen dhe do t\u00eb b\u00ebj gjith\u00e7ka p\u00ebr ta marr\u00eb at\u00eb!<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Micah Quinones.<\/p>\n

\n

Njihuni me Jonah Berger \u2013 Sindroma Global Down 2022<\/strong>Ambasadori i Fondacionit<\/strong><\/a>\"2022<\/p>\n

Ky \u00ebsht\u00eb Jonah Berger. Ai \u00ebsht\u00eb djali, v\u00ebllai, nipi, kush\u00ebriri, nipi, shoku, fqinji, nx\u00ebn\u00ebsi dhe mbi t\u00eb gjitha \u00ebsht\u00eb m\u00ebsuesi yn\u00eb. Kur Jonah lindi dhjet\u00eb vjet m\u00eb par\u00eb, ne nuk e dinim se ai do t\u00eb kishte sindrom\u00ebn Down.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> p\u00ebr Jonah Berger.<\/em><\/p>\n

\n

Njihuni me Archie dhe Sevy Eicher \u2013 Ambasador\u00ebt e Fondacionit Global Down Syndrome 2021<\/strong><\/a><\/p>\n

Archie dhe Sevy pat\u00ebn fillime t\u00eb padrejta t\u00eb jet\u00ebs - kur konsideroheshin t\u00eb padenj\u00eb p\u00ebr familjen ose p\u00ebr t\u00eb qen\u00eb pjes\u00eb e shoq\u00ebris\u00eb. Dhe tani, \u00e7do dit\u00eb, ata po e v\u00ebrtetojn\u00eb at\u00eb bot\u00ebkuptim t\u00eb gabuar.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Archie dhe Sevy Eicher.<\/em><\/p>\n

\n

Njihuni me Caroline Cardenas \u2013 Ambasadoren e Fondacionit Global Down Syndrome 2021<\/strong><\/a><\/p>\n

Emri im \u00ebsht\u00eb Caroline Cardenas dhe jam 17 vje\u00e7. Un\u00eb jetoj n\u00eb Dallas, Teksas me mamin, babin, tre motrat dhe qenin tim, Luka. Motrat e mia jan\u00eb shoqet e mia m\u00eb t\u00eb mira: Grace \u00ebsht\u00eb n\u00eb kolegj, Emily do t\u00eb shkoj\u00eb n\u00eb kolegj k\u00ebt\u00eb vit dhe Claire \u00ebsht\u00eb n\u00eb shkoll\u00eb t\u00eb mesme. Ata gjithmon\u00eb gjejn\u00eb koh\u00eb p\u00ebr t\u00eb kaluar me mua. E gjith\u00eb familja p\u00eblqen t\u00eb luaj\u00eb loj\u00ebra n\u00eb tavolin\u00eb, t\u00eb luaj\u00eb sporte Wii, t\u00eb shikoj\u00eb filma dhe t\u00eb haj\u00eb akullore s\u00eb bashku!<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Caroline Cardenas.<\/em><\/p>\n

\n

Njihuni me Walt Snodgrass \u2013 Ambasadorin e Fondacionit Global Down 2020<\/strong><\/a><\/p>\n

P\u00ebrsh\u00ebndetje, emri im \u00ebsht\u00eb Thomas Walter Snodgrass. Un\u00eb jam 16 vje\u00e7 dhe jam student n\u00eb shkoll\u00ebn e mesme. T\u00eb gjith\u00eb m\u00eb th\u00ebrrasin "Walt". Kjo \u00ebsht\u00eb e p\u00ebrshtatshme sepse m\u00eb p\u00eblqen t\u00eb shkoj n\u00eb Walt Disney World.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Walt Snodgrass.<\/em><\/p>\n

\n

Njihuni me Charlotte Fonfara-LaRose \u2013 Ambasadore e Fondacionit Global Down 2019<\/strong><\/a><\/p>\n

Emri im \u00ebsht\u00eb Charlotte Fonfara-LaRose, por miqt\u00eb e mi m\u00eb quajn\u00eb Charley. Un\u00eb jam nj\u00eb 16-vje\u00e7are studente e dyt\u00eb e shkoll\u00ebs s\u00eb mesme nga Annapolis, Maryland!<\/p>\n

Un\u00eb kam nj\u00eb mot\u00ebr Noelle dhe nj\u00eb familje t\u00eb madhe t\u00eb zgjeruar! Prind\u00ebrit e mi, Cathy dhe Scott, jan\u00eb v\u00ebrtet me fat q\u00eb m\u00eb kan\u00eb. Kur linda, i befasova t\u00eb gjith\u00eb me nj\u00eb kromozom shtes\u00eb. Pavar\u00ebsisht tonit t\u00eb zymt\u00eb n\u00eb spital, u largova prej andej i lumtur dhe i sh\u00ebndetsh\u00ebm, gati p\u00ebr t\u00eb filluar jet\u00ebn time t\u00eb mrekullueshme.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Charlotte Fonfara-LaRose.<\/em><\/p>\n

\n

\"Njihuni me CC Mullen \u2013 Ambasadorin e Fondacionit Global Down 2019<\/strong><\/a><\/p>\n

Emri im \u00ebsht\u00eb Caroline "CC" Mullen. Un\u00eb jam nj\u00eb tornado e vog\u00ebl e ndritur, e lumtur dhe e vendosur, e cila thjesht ka sindrom\u00ebn Down! Un\u00eb jetoj n\u00eb Virxhinia me mamin, babin dhe motr\u00ebn e madhe Amelia. M\u00eb p\u00eblqen t\u00eb kaloj koh\u00eb me familjen time dhe jam me fat q\u00eb kam shum\u00eb prej tyre rreth meje! M\u00eb p\u00eblqen gjithashtu t\u00eb k\u00ebrcej, t\u00eb lexoj libra me n\u00ebn\u00ebn time dhe t\u00eb ha!<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth CC Mullen.<\/em><\/p>\n

\n

\"Njihuni me Sam Levin \u2013 Ambasadorin e Fondacionit Global Down 2018<\/strong><\/a><\/p>\n

Kushdo q\u00eb e njeh Semin e di se ai \u00ebsht\u00eb i vet\u00ebm n\u00eb llojin e tij. Ai merr pjes\u00eb n\u00eb kampet e GLOBAL's Dare to Play Football me Ed McCaffrey, luan n\u00eb ekipet e basketbollit, futbollit, lakros dhe pista Cherry Creek High School Unified. Tani ai \u00ebsht\u00eb ambasadori i vitit 2018 Beautiful Be Yourself.
\nLexo m\u00eb shum\u00eb<\/a> n\u00eb lidhje me Sam Levin.<\/em><\/p>\n

\n

\"\"Njihuni me Frank Stephens \u2013 Ambasadori i Fondacionit Global Down 2018<\/strong><\/a><\/p>\n

Frank Stephens \u00ebsht\u00eb nj\u00eb z\u00ebdh\u00ebn\u00ebs aktiv i Fondacionit Global Down Syndrome dhe an\u00ebtar i Bordit t\u00eb Drejtor\u00ebve t\u00eb Olimpiad\u00ebs Speciale t\u00eb Virxhinias. Frank shpesh flet se sa me fat ndihet q\u00eb jeton n\u00eb nj\u00eb brez ku t\u00eb gjitha arritjet e tij jan\u00eb t\u00eb mundshme p\u00ebr nj\u00eb burr\u00eb me sindrom\u00ebn Down.
\nLexo m\u00eb shum\u00eb<\/a> rreth Frank Stephens.<\/em><\/p>\n

\n

\"MarcusNjihuni me Marcus Sikora \u2013 Ambasadori i Fondacionit Global Down 2017<\/strong><\/a><\/p>\n

Si autor, k\u00ebng\u00ebtar, aktor dhe vet\u00eb-avokat, Marcus Sikora tashm\u00eb ka arritur m\u00eb shum\u00eb n\u00eb jet\u00ebn e tij se shumica e 26-vje\u00e7ar\u00ebve t\u00eb tjer\u00eb. Tani ai po mbledh nj\u00eb tjet\u00ebr arritje si ambasadori i vitit 2017 B\u00ebhu i Bukur B\u00ebhu vet\u00eb.
\nLexo m\u00eb shum\u00eb<\/a> p\u00ebr Marcus Sikora.<\/em><\/p>\n

\n

Njihuni me Louis Rotella IV \u2013 Ambasadori i Fondacionit Global Down Syndrome 2016<\/strong><\/a><\/p>\n

\"Louis\"Louis "Louie" Rotella IV - djali simpatik q\u00eb frym\u00ebzoi baban\u00eb e tij p\u00ebr t\u00eb krijuar historin\u00eb e famshme t\u00eb pranimitMbreti i Vog\u00ebl dhe Mbret\u00ebria e tij Marshmallow<\/a><\/em>\u2014do t\u00eb frym\u00ebzoj\u00eb nj\u00eb audienc\u00eb prej 1200 vetash kur t\u00eb dal\u00eb n\u00eb pist\u00eb si Ambasador i 2016-\u00ebs n\u00eb shfaqjen e mod\u00ebs t\u00eb Global Beautiful Beautiful Be Yourself t\u00eb shtun\u00ebn, m\u00eb 12 n\u00ebntor.
\nLexo m\u00eb shum\u00eb<\/a> p\u00ebr Louis Rotella.<\/em><\/p>\n

\n

\"ClarissaNjihuni me Clarissa Capuano \u2013 Ambasadorja e Fondacionit Global Down 2015<\/strong><\/a><\/p>\n

Emri im \u00ebsht\u00eb Clarissa Joann Capuano. Un\u00eb jam shtat\u00eb vje\u00e7 dhe jetoj me mamin dhe babin tim. Un\u00eb kam dy v\u00ebllez\u00ebr m\u00eb t\u00eb m\u00ebdhenj Alec & Jesse, t\u00eb cil\u00ebt jan\u00eb t\u00eb dy n\u00eb kolegj. M\u00eb p\u00eblqen t\u00eb k\u00ebndoj, t\u00eb k\u00ebrcej, t\u00eb kal\u00ebroj kuaj, t\u00eb notoj, t\u00eb eci dhe t\u00eb luaj me veshje.
\nLexo m\u00eb shum\u00eb<\/a> p\u00ebr Clarissa Capuano.<\/em><\/p>\n

\n

Njihuni me Steven Dulcie \u2013 Ambasadori i Fondacionit Global Down Syndrome 2014<\/strong><\/a>
\n\"Steven<\/p>\n

Steven i sjell kujtdo q\u00eb e njeh G\u00ebzimin me shkronj\u00ebn "J" t\u00eb madhe, Ai e do futbollin dhe bejsbollin dhe \u00ebsht\u00eb ekspert n\u00eb filma dhe p\u00eblqen muzik\u00ebn dhe k\u00ebrcimin.
\nLexo m\u00eb shum\u00eb<\/a> p\u00ebr Steven Dulcie.<\/em><\/p>\n

\n

Njihuni me Katherine Felicia Norton \u2013 Ambasadore e Fondacionit Global Down Syndrome 2014<\/strong>
\n\"Katherine<\/p>\n

Emri im \u00ebsht\u00eb Katherine Felicia Norton. Un\u00eb jam 43 vje\u00e7 dhe jetoj n\u00eb Uashington, DC, ku n\u00ebna ime, Eleanor Holmes Norton, p\u00ebrfaq\u00ebson Distriktin e Kolumbis\u00eb n\u00eb Kongres. M\u00eb p\u00eblqen t\u00eb k\u00ebrcej, t\u00eb b\u00ebj enigma dhe t\u00eb performoj n\u00eb pantomim\u00eb n\u00eb Institutin e Terapis\u00eb s\u00eb Artit dhe Dram\u00ebs dhe t'u tregoj t\u00eb gjith\u00ebve se sa i aft\u00eb dhe arg\u00ebtues jam.<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Katherine Felicia Norton.<\/em><\/p>\n

\n

Njihuni me Cole Rodgers \u2013 Ambasadori i Fondacionit Global Down Syndrome 2013<\/strong><\/p>\n

\"Cole<\/p>\n

Emri im \u00ebsht\u00eb Cole Rodgers. Un\u00eb jam 6 vje\u00e7. Un\u00eb e dua muzik\u00ebn, shkoll\u00ebn dhe gjalpin e kikirikut. Familja ime \u00ebsht\u00eb nga shteti i Uashingtonit Lindor, por shumic\u00ebn e koh\u00ebs, ne jetojm\u00eb n\u00eb Uashington, DC<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Cole.<\/em><\/p>\n

\n

Njihuni me Samantha Marcia Stevens \u2013 Ambasadore e Fondacionit Global Down Syndrome 2012<\/strong><\/p>\n

\"\"<\/p>\n

Emri im \u00ebsht\u00eb Samantha Marcia Stevens dhe jetoj jasht\u00eb Bostonit me mamin dhe babin tim. Edhe pse jam vet\u00ebm 6 vje\u00e7, e kam mbushur jet\u00ebn time dhe t\u00eb gjith\u00ebve q\u00eb takoj me buz\u00ebqeshje dhe lumturi.<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Samant\u00ebs.<\/em><\/p>\n

\n

Njihuni me DeOndra Dixon \u2013 Ambasadore e Fondacionit Global Down Syndrome 2011<\/strong><\/p>\n

\"\"<\/p>\n

Nj\u00eb nderim i dashur p\u00ebr Ambasadoren GLOBAL DeOndra Dixon<\/a><\/strong><\/p>\n

DeOndra ishte p\u00ebruruesja inauguruese e \u00c7mimit t\u00eb Avokimit t\u00eb Jasht\u00ebzakonsh\u00ebm t\u00eb Quincy Jones t\u00eb Global dhe nj\u00eb Ambasadore Globale q\u00eb nga viti 2011. DeOndra jetonte n\u00eb Kaliforni me v\u00ebllain e saj, Jamie Foxx, prind\u00ebrit e saj dhe familjen e gjer\u00eb. DeOndra ishte shum\u00eb mir\u00ebnjoh\u00ebse p\u00ebr familjen e saj q\u00eb e ndihmoi t\u00eb arrinte potencialin e saj dhe nga ana tjet\u00ebr ajo ndihmoi t\u00eb tjer\u00ebt me sindrom\u00ebn Down t\u00eb b\u00ebnin t\u00eb nj\u00ebjt\u00ebn gj\u00eb.
\n<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth DeOndra.<\/em><\/p>\n

\n

Njihuni me Alex Sessions \u2013 Ambasadori i Fondacionit Global Down Syndrome 2011<\/strong><\/p>\n

\"\"<\/p>\n

Emri im \u00ebsht\u00eb Alexander Gregory Sessions, jam 17 vje\u00e7. Un\u00eb kam lindur m\u00eb 19 janar 1994 n\u00eb Dallas, Teksas. Un\u00eb kam lindur me sindrom\u00ebn Down. Prind\u00ebrit e mi ishin shum\u00eb t\u00eb lumtur kur linda - v\u00ebllai im Bill ishte 4 vje\u00e7 dhe ata gjithmon\u00eb donin dy djem. Ata nuk dinin shum\u00eb p\u00ebr sindrom\u00ebn Down, por shpejt filluan t\u00eb edukoheshin p\u00ebr t'u siguruar q\u00eb b\u00ebnin gjith\u00e7ka q\u00eb mundeshin p\u00ebr t\u00eb m\u00eb ndihmuar t\u00eb arrij potencialin tim intelektual dhe fizik.<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Aleksit.<\/em><\/p>\n

\n

Njihuni me Katherine Vollbracht Winfield \u2013 Ambasadore e Fondacionit Global Down Syndrome 2010<\/strong><\/p>\n

\"\"<\/p>\n

Emri im \u00ebsht\u00eb Katherine Vollbracht Winfield. M\u00eb p\u00eblqejn\u00eb dritat e ndezura dhe qeshjet. Kjo sepse un\u00eb jam vet\u00ebm 15 muajsh! Un\u00eb jetoj n\u00eb Seattle me mamin, babin dhe v\u00ebllain e madh Kirby III. I befasova t\u00eb gjith\u00eb duke ardhur 3 jav\u00eb m\u00eb her\u00ebt. Dhe pata nj\u00eb tjet\u00ebr surpriz\u00eb t\u00eb madhe \u2013 kam lindur me sindrom\u00ebn Down.<\/a><\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Katerin\u00ebs.<\/em><\/p>\n

\n

Njihuni me Chase Turner Perry \u2013 Ambasadori i Fondacionit Global Down Syndrome 2009<\/strong><\/p>\n

\"\"<\/p>\n

Emri im \u00ebsht\u00eb Chase Turner Perry. Un\u00eb jam tre vje\u00e7 dhe jetoj n\u00eb Kolorado me maman\u00eb, babin dhe v\u00ebllain e vog\u00ebl Cooper. I kam d\u00ebgjuar prind\u00ebrit e mi t\u00eb tregojn\u00eb shum\u00eb her\u00eb historin\u00eb e dit\u00ebs kur linda. Isha nj\u00eb surpriz\u00eb e madhe. Prind\u00ebrit e mi nuk e dinin q\u00eb isha djal\u00eb dhe nuk e dinin q\u00eb kisha nj\u00eb kromozom shtes\u00eb.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> rreth Chase.<\/em><\/p>\n

\n

Njihuni me Sophia Whitten \u2013 Ambasadore e Fondacionit Global Down Syndrome 2008<\/strong><\/p>\n

\"Portret<\/p>\n

Emri im \u00ebsht\u00eb Sophia Kay Whitten. Un\u00eb jam pes\u00eb vje\u00e7 dhe jetoj n\u00eb Kolorado me mamin, babin dhe v\u00ebllain tim t\u00eb vog\u00ebl Patrick.<\/p>\n

Lexo m\u00eb shum\u00eb<\/a> n\u00eb lidhje me Sofin\u00eb.<\/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,"_monsterinsights_skip_tracking":false,"ngg_post_thumbnail":0,"footnotes":""},"class_list":["post-3239","page","type-page","status-publish","hentry"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t\n\t\n\t\n\t\n\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t