Rockingmyextrachromosome Photos & Videos on Instagram

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adan_theman

Had an amazing time in Xcaret. I love traveling and seeing new places. #Xcaret #lovemexico❤🇲🇽 #downsyndrome #downsyndromelove #downsyndromeawareness #rockingmyextrachromosome

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punkyandthechicks

Another Punky flashback from about 5 years ago! "When in Rome...", eat as the chickens eat! 😂 . #punkyandthechicks #wheninrome #chickenboy #rockingmyextrachromosome #t21 #chickenwhisperer #differentlyabled #theluckyfew

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fer.downtheroad

Fuimos a una zona de juegos y habia muchas máquinas con luces y canciones divertidas, en todos los juegos el objetivo era hacer el mayor número de puntos así es que yo pensé: “¿por que no en vez de lanzar pelotas me subo yo y me aseguro de derribar todos los globos?” 🤔🤣😎 ——————— We went to a playground and there were many machines with lights and funny songs. In all the games the objective was to make as many points as you could so I thought:”why not instead of throwing the balls I climb and I assure myself to knock down all the balloons?” #ferdowntheroad #havingfun #cuteboy #rockingmyextrachromosome #amorsindromededown

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fer.downtheroad

Hora de dormir! Buenas noches a todos 😴😘 —————— Time to sleep! Good night everyone 😴😘 #ferdowntheroad #cuteboy #handsomebaby #nite #downsyndrome #sindromededown #theluckyfew #downrightperfect #nothingdownaboutit #rockingmyextrachromosome

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fer.downtheroad

Cuando tu hermana y tus primas deciden abandonarte y tienes que buscar la manera de entretenerte solo 🙄🤔😜 —————— when your sister and your cousins ​​decide to leave you and you have to find a way to entertain yourself #ferdowntheroad #downsyndrome #sindromededown #theluckyfew #downrightperfect #rockingmyextrachromosome

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chroma_cutetees

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fer.downtheroad

Lentes de sol para tener actitud de fin de semana 😎☀️, pero con mameluco porque hace frío 😨❄️🙈 —————— Sunglasses to have a weekend attitude, but with a romper because it's cold 🙈 #ferdowntheroad #rockingmyextrachromosome #fridayattitude #downsyndrome #sindromededown #theluckyfew #nothingdownaboutit

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punkyandthechicks

Punky sporting his #punkyandthechicks official tee, and playing with his "Angel Bricky" - made by a friend after he lost his Bricky chickie. Sweet boy keeps this gift with his toys and "happy cries" when he thinks of Bricky. What a beautiful, positive outlook he has had after losing her. 💙🐔💛 . #aboyandhischicken #rockingmyextrachromosome #rockinthedowns #cfob

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punkyandthechicks

What's that you say Freddy? You love me too? Of course you do; you let me hug and kiss and snuggle you like a puppy! 😊💛🐔 . #punkyandthechicks #chickenpup #chickenwhisperer #downsyndromelove #careanimals #specialneedshomeschool

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still_always_dancing

Ufff! The shoulder!!

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fer.downtheroad

Hoy mami y yo nos divertimos jugando a las escondidas 🤫 Pero cuando vi que me había encontrado mejor decidí disimular y seguir caminando como si nada hubiera pasado 🙄😬😆 —————- Today mom and I had fun playing hide and seek 🤫 But when I saw that she had found me, I decided to disguise and keep walking as if nothing had happened 🙄😬😆 #ferdowntheroad #havingfun #cutebaby #downsyndrome #rockingmyextrachromosome #sindromededown #downsinmitos #amorsindromededown #theluckyfew #downrightperfect

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fer.downtheroad

Bonito lunes!! 🙌🏻 Yo estoy aquí empezando la semana con esta canción que me pone de muy buen humor 🐶😆 Besos a todos. 😗💙 ————— Nice Monday! 🙌🏻 I am here starting the week with this song that puts me in a very good mood 🐶😆 Kisses to everyone. 😗 #ferdowntheroad #niceweek #sindromededown #amorsindromededown #rockingmyextrachromosome #t21 #love #cutiebaby #downsinmitos

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still_always_dancing

Qeis leading his dance party on one of his first favourite Bollywood tracks :)

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extra_cute_cayson

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fer.downtheroad

Desde hace 2 años, octubre significa para nosotros mucho más que disfraces de Halloween 🎃👻y fiestas. Significa gritar al mundo el valor de todas aquellas personas que tienen síndrome de Down. ☺️ Terminó el mes de concientización sobre esta condición, pero la lucha por abrirnos paso y generar empatía, entendimiento e inclusión debe continuar, no importando el día ni el mes. ☝🏻 Los invitamos a seguir compartiendo con nosotros este recorrido lleno de matices y aprendizajes, pero sobre todo lleno de amor💙😋🙌🏻 Buen fin de semana a todos 😘 ————- Since 2 years ago, October means much more to us than Halloween costumes and parties. It means shouting to the world the value of all those people who have Down syndrome. ☺️ The awareness month on this condition ended, but the struggle to open up and generate empathy, understanding and inclusion must continue, no matter the day or the month. ☝🏻 We invite you to continue sharing with us this journey, full of nuances and learning, but above all full of love💙😋🙌🏻 Good weekend to everyone 😘 #ferdowntheroad #aprendiendojuntos #sindromededown #downsyndrome #rockingmyextrachromosome #trisomia21 #downsinmitos #amordown

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fer.downtheroad

Hoy empezamos el día trabajando un poco la motricidad fina con mi laberinto que mami compró en @diakoabc ☺️☺️ me encantó porque además tiene muchas formas y colores! 🔵🔴🔶⚪️ Sin duda puedo pasar mucho tiempo jugando a esto. 🙌🏻 —————— Today we start the day working a little fine motor skills with my labyrinth that mom bought in @diakoabc ☺️☺️ I loved it because it also has many shapes and colors! 🔵🔴🔶⚪️ I can certainly spend a lot of time playing this. #ferdowntheroad #aprendiendo #undíaalavez #downsyndromerocks #sindromededown #downsyndrome #rockingmyextrachromosome

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fer.downtheroad

La mejor compañera de juego 👧🏻👦🏻💙 ————— The best playmate 💙💓 #ferdowntheroad #playmates #brotherandsister #purelove #purehappiness #downsyndrome #sindromededown #rockingmyextrachromosome #downrightperfect

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joy.dasher

As we are now nearing the end of October, I wanted to focus my last Down Syndrome Awareness Month post on the story that is closest to my heart at this time. Two years ago I had the life changing opportunity to go and volunteer in China at a foster home who houses children with a disability called Journey of a Joyful Life. Over the last year though China has changed a significant number of laws that pertain to foster homes and adoption within their country. Part of that being that they are no longer allowing foreigners to run foster homes within China. With that change, came an almost complete shut down of Journey, which means that the orphans who were inside of it have now been sent back to their home orphanages. I don’t say these things lightly, I’ve had many sleepless nights breaking down in tears and arguing with God over this. Knowing that He is faithful, and that He loves these kids even more than I do is something that I am trying to hold on to and understand in this but it is also insanely difficult to believe in times like this. Here’s why I say this, these children are not well cared for in their orphanages or institutions. The majority of these children were originally sent to Journey malnourished, and having been left in their cribs never once feeling the love of another human being caring for them before Journey. I say all of this to not only bring awareness to the situation and what is going on in other countries, but to also stress the importance of adoption. Orphans all around the world need our prayer and they need to be adopted more than ever. I cannot stress enough the need for these children to have forever families. Once these children hit a certain age they are removed from the adoption system and put inside of an institution with no hope of a normal life. I put in my bio a link to an advocacy page for children in China. Even if you haven’t thought about adopting, go look at this link. Pray for these children. Pray for the foster homes that they have been taken from because those moms all have broken hearts right now from seeing their children ripped from their homes. And adopt. adopt. adopt.

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its.me.kierra

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joy.dasher

Meet Janna. This girl has more wisdom inside of her than most adults do. Her strength and resilience to move forward in life is matched by none. While it has been a few years since I have seen her I still think of her and miss her almost every day. With it being Down Syndrome Awareness month though, I thought it important to speak about every person who  has a diagnosis of Down Syndrome who has changed my life whether I have seen them in a while or not. —————————————————————————— Today I want to highlight specifically the importance of using “Person First” language. Person first language is an alternative way to talk about children's disabilities that places the focus on the person and not the disability. For instance, “My sister’s name is Janna, she has Down Syndrome.” At the end of the day it is not a diagnosis that defines a person, it is their character and who they are as a person that defines them. Why does this matter some might ask? It changes our outlook on a person who has a disability. It helps us realize their potential as a human being knowing that they can do the same things that we can do and more. Having a disability doesn’t change that. So let’s focus on the person and not the disability. It goes back to not letting what other people say about us or letting what we do become the definition of us. At the end of the day only the Lord can define us. So why not adopt this language into our every day lives? ——————————————————————————— Hi. My name is Joy Dasher, and I am a Millennial, but that isn’t what defines me. Only the Lord can define me.

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justwhenyouthinkshesdown

#Repost @se7entees with @get_repost ・・・ Nothing, I repeat NOTHING in this world is “perfect”. All things are beautiful and worth it. Especially humans, just like this tiny one ❤️❤️❤️❤️ PC @justwhenyouthinkshesdown Use code DIVERSITY for 25% off . . . . . . . . . . . #Ilovesomeonewithdownsyndrome #downsyndromepride#homiewithanextrachromie#justlikeyou#lifeisbetterwithyou • • #myextrachromosomemakesmeextacute#normalizeddownsyndrome#nothingdownaboutit#notspecialneeds#notspecialneedshumanneeds#rockingmyextrachromosome#seetheability#t21#t21journey#theluckyfew#trisomy21#upsyndrome#weseetheabilty

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se7entees

Nothing, I repeat NOTHING in this world is “perfect”. All things are beautiful and worth it. Especially humans, just like this tiny one ❤️❤️❤️❤️ PC @justwhenyouthinkshesdown . . . . . . . . . . . . #Ilovesomeonewithdownsyndrome #downsyndromepride#homiewithanextrachromie#justlikeyou#lifeisbetterwithyou • • #myextrachromosomemakesmeextacute#normalizeddownsyndrome#nothingdownaboutit#notspecialneeds#notspecialneedshumanneeds#rockingmyextrachromosome#seetheability#t21#t21journey#theluckyfew#trisomy21#upsyndrome#weseetheabilty . . . , . . . .

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london.rose.co

Did you know October was Down syndrome awareness month?. . This October I’ve had the pleasure of talking with and sharing London Rose love with some amazing little girls, making them bows in downsyndrome awareness colors! i even got to meet sweet Emmy, finding out she lived so close to me!. . Did you know? . • Down syndrome is the most commonly occurring chromosomal condition. Approximately one in every 700 babies in the United States is born with Down syndrome – about 6,000 each year • All people with Down syndrome experience cognitive delays, but the effect is usually mild to moderate and is not indicative of the many strengths and talents that each individual possesses Love shows no boundaries. 💙💛 . . . #downsyndromeawarenessmonth #downsyndrome #rockingtheextrachromosome #bringawareness #beautiful #lovedoesntcountchromosomes #rockingmyextrachromosome #happy #beautiful #naturalbeauty #downsyndromebaby #dowmsyndromebeauty #downsyndromelove #downsyndromecutie #downsyndromemodel

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noemialveo

J´adore los weekends 😀😀😂😛 #rockingmyextrachromosome #downsyndrome #misamores

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joy.dasher

Jamie, Jamie, Jamie. Where do I even start with this girl? First of all, girl, those dimples. They’re the cutest. Her laugh? The best. Jamie dreams of being a mom and tries bossing her siblings around because of it. —————————————————————————— Jamie is a third grader at my family’s local elementary school. She has been able to thrive in the setting of a public school and has an incredible team to support. It has been incredible to watch her grow in that aspect! —————————————————————————— I’ve heard people ask how we handled the grief of learning that they had Down syndrome, or how we became ok with them never being able to have a normal life. Nothing has been less true than those comments. Everyone person who has a disability has the opportunity to have a normal life if they are given the chance to. For Down syndrome specifically, they can read, they can write, they can do everything we can do. It might just take them a bit longer to learn how to get there. That being said though, are we giving them the opportunity to learn these things? If we are not, how do we change that?

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extra_cute_cayson

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still_always_dancing

Pre-dinner dancing!

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noemialveo

Happy Birthday mi viejito hermoso. Que Dios te siga cuidando y bendiciendo ya son 4 años donde has llenado nuestras vidas con amor y nos has enseñado a Dar gracias y ser feliz cada dia con todo lo que Dios nos da . te amamos con todo el corazón Mamá, Tata, Nano, Lolo, keki, Ai. #rockingmyextrachromosome #downsyndrome. #misamores

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dasbuntezebra


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