By Anne Thompson and Amber Payne
NBC News
Ryan Langston has everything a casting director would want in a child model: charisma, a hip haircut and a knockout smile. This 6-year-old also has Down syndrome -- and it is that fact that has daytime talk shows, international newspapers and news networks all wanting to tell Ryan's story.
His appearance in a Nordstrom catalog this summer, and a Target ad this month created the kind of buzz marketing directors dream of -- because of what the ads do not do. They don't emphasize or point out that Ryan has special needs. He's just a good looking kid in an ad, appearing alongside other good looking kids about the same age.
On the Internet, parents of other special needs children are praising the ads -- and Ryan -- an outpouring that's surprised and overwhelmed his parents, Amanda and Jim Langston.
In the Langstons' first broadcast interview, which aired on Jan. 16 on NBC Nightly News, Ryan's mother Amanda Langston said they are "thrilled" that their son has become an inspiration to so many others.
"He's a beautiful little boy and he does shine, he has a beautiful little light and I think that's what people are seeing," Ryan's mother Amanda said, when she spoke to NBC's Anne Thompson at the Langstons' home in Garwood, N.J.
Ryan is every bit a 6-year-old boy: riding his bike in the back yard, climbing the rock wall on his playground set, and using all sorts of trucks to dig up his mother's garden. He's a bundle of energy who had a very difficult start. Ryan was born with a hole in his heart and had open heart surgery when he was just 3 months old. That hurdle cleared, his parents began early intervention to help Ryan develop muscle tone and communication skills.
Fast forward a few years, and Ryan is a happy, engaged child. A cute kid with blonde hair and blue eyes, he has been modeling ever since he was 3 years old. The now famous Target ad shows Ryan posing next to four other children. He's the only child with Down syndrome, but he blends right in -- and Target didn't attempt to highlight his difference.
"The fact that they are not making a big deal - it's ironic," Ryan's father Jim said. "It's a big deal because they are not making a big deal about it."

Courtesy Amanda and Jim Langston
Ryan Langston.
The Langstons' decision to involve Ryan in modeling was never about the money, Amanda said. "This has just become his own thing," she said. And it's also turned into a confidence booster.
"There are times where his speech is unbelievable, he's speaking full sentences," Amanda said. At other times, the stress of being unable to communicate can have a snowball effect.
"A lot of people with Down syndrome have anxiety, and he does," Jim said. "You see him rubbing his hands in nervousness, or he takes a step back and says, 'OK, OK' because he is trying to reset his mind to thinking what to say."
But when Ryan is on set, surrounded by his family and hamming it up for the photographer, his anxiety seemingly disappears.
"Ryan loves doing it, and when I say this I don't think people understand that he knows it's his thing!" Amanda said. "I joke all the time that after the shoot is over he does not want to leave, I almost have to drag him out from wherever we are."
Despite the attention generated by Ryan's Target spread, ads that feature children with disabilities are not new. According to Target spokesperson Jessica Carlson, the company has included people with disabilities in ads since the early 1990s. And Nordstrom catalogs, where Ryan has also appeared, have been including child models with Down syndrome since 1997.
Most of these print ads have come and gone with little fanfare. Ryan's Target ad might not have been any different if it wasn't for so-called "daddy blogger" Rick Smith, who wrote about Ryan's Target ad on Jan. 2. That posting, and the accompanying ad picture, went viral.
"The response has been overwhelming," Smith said. "Hopefully stories like Ryan, and Noah and the community that is building online will help keep this story going strong." Smith writes about his 11-month-old son Noah on NoahsDad.com. Smith's son also has Down syndrome, and his blog is a platform for the world to see that their life is much more normal then "un-normal."

Courtesy Amanda and Jim Langston
Twins Ryan and Ian Langston.
Every day Smith posts a one-minute video called "Noah's Minute." These short videos are a glimpse into their everyday life, and range from Noah playing on the swingset to his physical therapy sessions.
"For so many years people assumed our story was a sad one. We hope that our son can sort of open the book for them, so to speak," Smith said. "We don't live in a sad story. We live in a good one."
The Smiths traveled from Dallas to New York City for a vacation over the weekend and were thrilled to meet Ryan and the Langston family in person for the first time on Monday.
Ellen Narucki, Ryan's special needs teacher at The Arc of Essex County Stepping Stones School in Roseland, N.J., said the clothing ads are sending a positive message for people with Down syndrome, and show how they can also be accepted as part of society.
"That's a very important point, I think, that in the long term our goal is to have our children be profitable and to be part of society," Narucki said.
As long as Ryan continues to enjoy modeling, the family will continue to support him -- especially his fraternal twin brother.
Amanda says Ian, who does not have Down syndrome, "has probably been the largest part of Ryan's success."
The two boys still sleep in the same room, although they'll eventually be separated. For now, Amanda said, "we feel it's important that bonding is there."
"Ian is his big brother, even though they [were born] one minute apart," Amanda said. "Ian is the big brother, and Ian is taking on that role, and he has that personality. It's just who he is."
His brother's affection is just one of the many ways Ryan knows he's important.
"He looks at the Target ad and goes, 'That's me!'" Jim said. "The fact that Ryan, how he is, can enlighten people and gives his life value, he can be an ambassador in some way, we were thrilled about that."
Additional reporting by msnbc.com's Christina Caron.


This is an awesome article!! Thank you so much for having positive and inspirational stories every night in your news broadcast.
I love how happy he is. That is enough for me. I love happy children...they make you feel good.
Amen!
I am so happy to see this article. Finally People is realizing that those with different attitudes towards life, are as important as those of us who are just average! I am the PROUD mother of a child with special needs to, and Nick as well as Ryan loves and follows on the foot steps of his twin brother. My son has had already 7 brain surgeries, GO RYAN!!! you are a star!!!!!!!!
Wonderful story! Thank you for airing it. It would be great if NBC News would adopt people first language throughout the broadcast. It was mentioned on air tonight that Ryan goes to school with other down syndrome kids. It would better to say that Ryan goes to school with other children who have down syndrome. It's a small change in word order that shows NBC News has respect for their guests and subject matter.
Thank you for that comment! I actually just logged in to say the same thing. I am an exceptional education teacher and the school where I used to work recently posted this as their Facebook status:
"An individual's disability does not define who they are, so always put the person first!" I think Ryan proves that! Fantastic story, though. It brought tears to my eyes!
Totally agree ............. I heard that line too & it made me cringe.
now that you pointed it out, I can see why you would prefer that comment to be reworded, but COME ON. I get so angry that you expect perfection in EVERYTHING you hear. It is exhausting to hear others ridiculed for the slightest error.
Fantastic story, thank you Ryan....
Models really aren't known for their brains.
True, but that's because most who don't model don't realize how much work - and thought - goes into it. This kid's got talent, and he's learning how to use it.
Just remember on thing when you have child with special needs "It's not what they can't do but what they can do" with this... many doors will open for them. How do i know this i have 2 children with special needs
Bless you and your family AK 1961 !!!
Wonderful story about Ryan. My granddaughter has Down Syndrome and while she had a rough beginning, every day she amazes us with what she's accomplished. She's such a happy child, one can't help but smile when she enters the room. God blessed our family with our little RayRay.
Another thanks for covering this piece of incredibly positive news.
Just one little thing.
Toward the bottom of the story, you start a paragraph: "Everyday Smith posts a one-minute video...." FAIL!
It should be "Every day Smith posts a one-minute video..." because the compound word you used is an adjective.
Unless, of course, the guy's name is Everyday Smith, which is ridiculous, but so are "Anfernee" and "D'Brickashaw," so I can't really judge.
But I do think the editor was sleeping on the job. Stay in School!!!
Run on sentences and sentence fragments are far worse than not putting a space between two words. School might help you. The editor is fine.
This article is inspirational and uplifting! It was wonderful to read about this special child and his supportive family.
I do, however, agree with Warren noting the error. I also do not believe fragments are far worse. Sentence fragments are quite useful when making a point. Language and literature are filled with them.
Another error that I'm surprised wasn't caught is: "Smith's son also has Down syndrome, and his blog is a platform for the world to see that their life is much more normal then 'un-normal.'"
The "then" should be "than," unless the journalist was making a reference to a time sequence.
Wonderful that in this world there can be this joy. Ryan is a joy and blessing. Target should also be praised for doing ads like this.
As a mother of a child with Down syndrome, the story tonight feels like a triumph for those of us who live in the disability world. We know to use people first language and would love to get the word out to the general public that a person is not defined by their disabilty, they are a person first. It should be stated that Ryan goes to a school with other children with Down syndrome...not Down syndrome children. Please share this information with your viewers. Thanks!
We do know that Down Syndrome kids are not the majority....they go to what ever schools are in their vicinity. Private schools take them as well at 15K per year like the rest of the kids. They are not expected to excel but they are good PR for the school.
Oh my Gosh! Is that boy not adorable?
I have 2 "normal" kids and my bet is that they were/are as challenging/funny/annoying/lovable as this child. He makes me smile in the same way that my 2 kids do.
Kids. Ya gotta love em.
A child in my elementary school wrote the following poem about a little girl in his class with Down syndrome:
"Katy is so beautiful.
I think she's part Chinese.
Her voice is very low and soft.
It's like the morning breeze!"
That's sweet Molly Cruz !!
I live in the Twin Citities (home of Target) and this precious little dude is the toast of the town here. Go get'm Ryan, here's hoping you don't have to thwart the assasination of the prime minister of Malaysia. in your future.
This inspires me. . . to make sure and have extensive fetal screening.
Wow! You are one callous person!
Nah - I get mani-pedis!
Too bad your mother wasn't so inspired. You left the door open...
mrdifficult
you are one shallow ignoramus pig. Karma will find you..
mrd...you are a Jack a$$ and I hope you do not have any offspring! Yes no one hopes for a child that has disabiltiy or problems, but everyone should love every child in this world, and make sure they have a chance at life and also live to their fullest ability.
I think it is great that Target has stepped up to the plate and are using everyday children, this boy is beautiful inside and out and God Bless Ryan and his family!
Ah mr. You're an awful troll.
Now, remember: Finish school, do what your mom says and make sure you eat your veggies.
First, I must note that further down in the comments, sbpb said to MrDifficult: "The human race is NOT bettered by the continuation of individuals like Mrdifficult. You, sir, are truly defective.", and SQ77 said to MrDifficult: "DS is one of the easier birth defects to live with. Besides it sure as hell beats the one you have. You can't fix stupid.".
I find it hilarious how people such as SQ77 pathologically attribute rival beliefs which are more logical than their own, to stupidity. I have a tested IQ of over 130, yet I have been called 'stupid' many times by my political rivals.
Anyway, that makes at least four people- sbpb, SQ77, kat-1762684, and AmericaFirst-500386, who have expressed or implied a desire to murder MrDifficult and/or his offspring, just because he supports the freedom to abort fetuses with severe defects, thus saving oneself from such an impractical burden, and saving the child from a life of disability.
Notice how people who are militantly opposed to the right to breed eugenicly, rarely fail to hypocritically use the language of eugenics, in reference to the person who supports such rights ("You, sir, are truly defective", "it sure as hell beats the [birth defect] you have.", "I hope you do not have any offspring", "Too bad your mother wasn't so inspired [to screen fetuses]"). That is because their opposition to the right of eugenic breeding is not rooted in any genuine belief that the genes are not decisive, but rather it is due to their fanatical desire to force everyone to take on symbolic burdens (and imposing such tyranny requires removing from the gene pool those people who would refuse that burden, such as MrDifficult). Such fanatics possess the perverse desire to take on symbolic burdens (which I am okay with, as I respect personal freedom of choice in all things), but they realize, perhaps even on an instinctive level, that such burdens put themselves at a competitive disadvantage to others, so the only solution is to impose tyranny which forces everyone to engage in such perverse self-burdenning behavior, and kill off any people who refuse. The ultimate purpose of such fanatical tyranny is thus to proliferate the genes which cause such pathological symbolic self-burdenning behavior- genes which would otherwise be selected out of the gene pool due to being out-competed. There is therefore no genetic trait that is more harmful to the genetic progress of the human species than that innate pathological desire to force symbolic burdens onto everyone, and to kill off anyone who says otherwise- a genetic trait which several people here clearly possess.
MrDifficult, I have written this post in large part for the sake of advancing your own understanding, though any other rational people who gain this knowledge are a bonus. I ask that you in turn spread this knowledge to others. We must defeat fanatical dysgenic tyranny, by making and supporting as many [non-defective] offspring as we can, offspring which do not possess such heritable fanaticism. I have long known this, so I have already made many excellent children.
Ms. Eugenic, your willingness to spend so much effort to reply to an obvious trolling comment casts a shadow over your claimed IQ of 130+
I have a son with down syndrome. He is now 24yrs old graduated from high school and works at a warehouse full time. He pays taxes and contributes to society. His mother and I never worried about he wasn't able to do... But focused on what he could. Beautiful article....I forgot to mention he was a honor student as well....
Does he live alone and has a drivers license ?
And why do you ask Alumette? Sounds like these parents are proud of their son's accomplishments, and why shouldn't they be?
How fantastic. :)
We have a young man with Downs in our neighborhood and he volunteers at the local food bank, rides the bus everywhere (or his bike) and works at a diner part time. He's a very sweet boy.
You're obviously parents who cared about their son and his welfare just beyond the standard 18 years.
Alumette- what this man does is not any of your business. Nosy wench.
So relieved to see only one snarky comment so far. I am angered so frequently by the vile comments people make anytime news stories cover issues about exceptional children and families. Kudos to Ryan!
Congratulations Mr Difficult, you win the prize for the first thoughtless comment! And, your name suits you...
It's called trolling. Better to ignore it.
FINALLY, a correct media headline identifying the person BEFORE the disability. Cheers!!! to the author for the effort to recognize the PERSON who inspires us.
a "child model with Down's Syndrome"
instead of the usual sloppy "Down's Syndrome child model"
Target was a leader during the 1991 Intl Special Olympics Summer Games and continue 21 years later.
You go Ryan...WooHoo!!
Auditioned my daughter for Tommy Hilgifer years ago, but he missed his chance. Macy's had a DS baby back when my daughter tried out. Hats off to those that see their own "it factor." What a ray of sunshine!
Great to see NBC run this story. I"m Noah's Dad (the site on shown on the story)....I hope more media outlets will run stories like this! Thanks again NBC.
Rick
I am very glad to read this story and love getting the Facebook updates from Noahsdad! I too am very lucky to have a 6 yr old with Down Syndrome, he is the light of my life.
I don't like reading some peoples comments, but then there is Kharma!!
I am proud of both of my childrens accomplishments, I want them both to be all they can be and that is my only wish! and if you don't wish those things, remember what your Mother said " if you don't have something nice to say, keep your mouth shut!"
My condolences for your potential loss Mr. Difficult. My child was one of the best things that ever happened. Challenged and changed my life; she made all of us, even cantankerous old souls, better people.
Get real. . . you go poll 100 currently pregnant women and see how many 'don't care.' You will get 90 that pray their child is NOT DS, and 10 politically correct liars. No species is bettered by the continuation of defective (TRULY DEFECTIVE) chromosomal structure.
If that's what it takes for you to be a better person, then my condolences to YOU.
Mr Difficult, what guarantees do you have in life......other than your death? How do you know that YOU have perfect DNA, nothing lurking there to present itself in the future.........?
I guess you can count me in the 10% that doesn't care. Obviously everyone wants a healthy baby but nothing is guaranteed. Raising a down syndrome child is a rewarding experience. DS is one of the easier birth defects to live with. Besides it sure as hell beats the one you have. You can't fix stupid.
The human race is NOT bettered by the continuation of individuals like Mrdifficult. You, sir, are truly defective.
*woops...Hilfiger.
I have known two people with Down's Syndrome. They were both very good natured, affectionate, and a pleasure to be around. I am nearing retirement age, and one of the things I would like to do after I retire is volunteer with Special Olympics
Hopefully this article inspires women to stop aborting their downs syndrome children....all kids are gifts from God and this article showcases the blessings of all children.
Kids are not a gift from God. They are the results of unprotected sex between a man and a woman. It is a huge difference......not to confuse it with divine events. We control our reproductive system or at least, we have the science and the brains to do so.....unfortunately, some primitive people do not seem to get it. There is nothing like education to fix that myth.
Of course they should abort a known defective fetus. Don't try to guilt people from making a logical decision.
I hate that everytime I read the comments on these articles there has to be "somebody" that has to criticize or put down people with disabilities and their parents for choosing to move forward with a pregnancy. My husband and I chose to move forward with a pregnancy knowing that there was a slight risk that our child would be born with Down syndrome. We opted not have any testing done because we believe in the sanctitiy of life. I guess I am just one of those primitive people, Alumette, who don't get it. I "logically" opted not to use science to eliminate what it says is not perfect. By doing so I can be assured that my children will never be posting comments like yours and for that I already immensely proud. Maybe I am just too underschooled and could correct those myths that you talk about by getting more educated. But as I already having a jurisdoctorate I think I will skip that step.
Beautiful child :) He really made me smile!
agreed:)
Thank you soooo much for telling this story! More people need to know what our kids can do. Our kids/adults are more alike than different!!!