Showing posts with label Down Syndrome. Show all posts
Showing posts with label Down Syndrome. Show all posts

Monday, July 31, 2017

9-Year-Old With Down Syndrome Belts Out Whitney Houston Song in Viral Video

Source: www.yahoo.com

By Maya Chung


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A 9-year-old boy with Down syndrome has gone viral after his heartwarming version of one of Whitney Houston’s hit songs was posted online.

Dane Miller, of Texas, belted out Houston’s “I Have Nothing” while riding in the car with his dad on Monday, but his mother, Danna Miller, said it’s something her son does often.

“He’s been musical since around 2 years old,” Miller told InsideEdition.com. “He’s been playing the drums. He sings. He loves music. He puts his whole heart into everything he does.”

See video.

Friday, June 2, 2017

STONEWARE WITH THE CHARM OF THINGS IMPERFECT AND SIMPLE by Christian Royal

Source: https://www.christianroyalpottery.com

home_welcome_image_grandeTHE POTTERY – Christian Royal Pottery is high-fired stoneware that is handmade using slab-building techniques. The stoneware incorporates the natural splendor of leaves or the artistry of beautiful laces, which are shaped into flowing designs and functional forms. The making of stoneware involves numerous steps over several days. Each piece involves Christian and his assistants in a collaborative effort, following many sequential steps. While some of the pieces may be similar, none are identical due to the process. Handcrafting produces variations in size, shape, color saturation, depth of impression, and minor imperfections that give each piece part of its appeal. Thus, the studio adage: Stoneware With The Charm of Things Imperfect and Simple

THE POTTER – Christian Royal is a young man with Down syndrome who struggles with single words and has yet to grasp basic addition or time.  However, since his teen years, Christian has shown an interest in, and aptitude for, working with clay. Christian was unable to “do” school as other students did and began making pottery as part of his homeschooling program.  Since his first lesson with Kris Neal of Fire And Earth Pottery, pottery has increasingly become the  focus of his life.  Over the years, through many providential happenings, kind-hearted people have offered their expertise and help at just the right time for each step of what is now Christian Royal Pottery. Foremost are John and Jan Myers, professional potters, who inexplicably offered to teach Christian the methods and techniques they had developed over thirty years. They made this offer the first time we ever met them. A week later we had unpacked our bags in their home and were sitting in their studio as John began to instruct Christian.  John and Jan’s teaching of Christian enabled him to produce a style of pottery that captures simplicity and charm in its essence.

Continue reading.

Model With Down Syndrome Challenges Beauty Stereotypes: BORN DIFFERENT

Source: https://www.yahoo.com

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THE first model with Down Syndrome to front a beauty campaign is hoping to shake up the industry and prove that “beauty belongs to everybody.” Katie Meade is the first to admit that people with Down Syndrome, as well as other disabilities, are largely absent from the beauty and fashion industries – and she’s determined to change it. The 33-year-old made history last year when she became the first ever model with Down Syndrome to be the face of a beauty brand and her career – both as a model and as an ambassador for people with learning disabilities – continues to grow.

See video.

Monday, March 13, 2017

Sunday, May 8, 2016

News From Armenia: A loving son, a fun brother – a fulfilling life.

Source: http://digital.olivesoftware.com

By Katie Martin

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Some events in life are priceless such as weddings, graduations or births.

But for Christie Orta, an important life moment was a simple trip to the beach a couple of weeks ago.

“That one moment was worth more than every penny we paid and every tear that I cried, just to see him sitting in the ocean,” Christie said as she showed a video of her newly adopted son, Edgar, 4, playing in the surf.

“He was so excited he didn’t know what to do with himself,” she said. “He was flapping his arms so hard I’m surprised he didn’t fly away, he was just so excited.”

Since 2013 Christie and her husband, Raymundo Orta, have been working through the adoption process to bring Edgar, who has Down syndrome, home from Armenia. In February, they, along with their biological daughter, Laura, 9, officially became a family of four, bringing Edgar home to Savannah.

“I think he has completed our family in ways that we never thought he would. He’s made us a better family,” Christie said. “People have said he’s so blessed to be in a family now, but I think the opposite. We’re so blessed to have him.”

Read more.

Thursday, April 21, 2016

News from Armenia: WELCOME HOME SAM!!!!

Source: http://www.mlive.com

By Angie Jackson


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GRAND RAPIDS, MI – Smiling and laughing through tears, Sam Bode’s new extended family erupted into cheers as they spotted the 4-year-old and his adoptive parents at Gerald R. Ford International Airport.

Moments before, the huddle of grandparents, aunts, an uncle and cousins had grown quiet from nervousness and excitement. Over the past two years, they’ve only been able to communicate with the cheerful boy via Facetime while his parents, Erica and Jeff Bode, went through the lengthy process to adopt him from Armenia. On Wednesday night, he was officially welcomed into the tight-knit West Michigan family.

Sam, who has Down syndrome, arrived at the airport with the Bodes and their son Jack, 8, after the last leg of their trip home from Armenia. He has spent his entire life in an orphanage.

Read more.

Saturday, March 19, 2016

She Inspired Those With Down Syndrome As Unstoppable

Source: www.washingtonpost.com
By Theresa Vargas

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Laura Lee took pride in her résumé. On it, separated by bold lettering and bullet points, she listed one achievement after another: She graduated from George Mason University. She worked at the World Bank. She volunteered at a food bank. She spoke at national conventions.

Not mentioned: She was born with Down syndrome.

For the 400,000 Americans like her who are often characterized by their limitations, Lee changed what they and their families viewed as possible. She was the first person with Down syndrome many people saw participate on panels. Or go to college. Or work in a professional setting. At the World Bank, where she was an office assistant earning $12.24 an hour, her name was on her office door. If the cruelest part of Down syndrome comes from the walls it erects, the ultimate joy for many people in the intellectual-disabilities community came in watching Lee leap over those walls, time and again. In many ways, she seemed unstoppable — until she wasn’t.

Read more.

Thursday, January 21, 2016

Parents Speak Out a Year After Dad ‘Chose’ Son With Down Syndrome Over Wife

A year ago Samuel Forrest’s life abruptly changed forever. In the span of just a few days he gained a son, began divorce proceedings with his wife and found himself the focus of a lot of media attention.


(Photo: Samuel Forrest)

Now, a year later, Forrest and his wife have reconciled.

Leo Forrest was born with Down syndrome on January 21, 2015 in Yerevan, Armenia. After he was diagnosed, his mother, Ruzan Forrest, gave his dad, Samuel Forrest, an ultimatum: if he decided to keep the baby, she’d file for divorce.

Samuel Forrest decided not to have Leo placed for adoption.

“They took me in to see him and I looked at this guy and I said, he’s beautiful, he’s perfect,” Forrest told ABC News last year. “I’m absolutely keeping him.”

Forrest decided he and Leo would move back to Auckland, New Zealand, where he is from, and his wife remained in Armenia and began divorce proceedings.

Read more.

Friday, August 14, 2015

Madeline Stuart, 18-Year-Old Model With Down Syndrome, Will Walk In NYFW

Source: http://www.huffingtonpost.com

By Carly Ledbetter

11850016_1099023933458652_694340305_n In just one year, Madeline Stuart, an 18-year-old with Down syndrome, has become the face of two fashion campaigns. Now the Australia native is set to walk in New York Fashion Week on September 13.

"When we were asked to do New York Fashion Week, it didn't surprise me," said her mother, Rosanne Stuart, in an interview with Cosmopolitan. "I don't think anything really surprises me anymore. She's been asked to do a lot of stuff and I was hoping to she'd get asked to do NYFW but I assumed it would happen. I hope that doesn't sound too pretentious."

Read more.

Tuesday, February 17, 2015

Mothers of children with Down syndrome Survey

Taylor%20 Hello!

My name is Amanda Smith. I am conducting a survey of biological and adoptive mothers of children with Down syndrome for my dissertation. I have been more successful in receiving responses from biological mothers. I am trying to now reach more mothers who have adopted.

Overall, the purpose of this research is to understand the feelings and experiences of being a mother in general and being a mother to a child with Down syndrome. The survey will take no longer than 5 minutes. The first page of the survey is a welcome letter that will inform those who click on the link that their information is confidential and the survey is anonymous.  If you would forward on this link to my survey to any support groups or parent groups you may have, I would be incredibly grateful. If anyone completes the survey and would like more information  or would like to share about their experiences, please don't hesitate to send them my email address.

https://www.surveymonkey.com/s/mothers_of_children_with_DS

Mothers of children with Down syndrome Survey

Hello! As a caregiver of a child with Down syndrome you know firsthand the trials and successes you feel as a parent and for your child. Being a mother gives you experiences that are identical to no one else.

Read more...

Thank you for your time!

Amanda A Smith, Ed.S.

Friday, February 6, 2015

Here's To Leo and His Dad. Changing The World For The Better!

Source: http://abcnews.go.com

By Nicole Pelletiere

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When Samuel Forrest of Armenia heard a baby crying from outside his wife's hospital room, he knew his life would change forever.

Not only had he become a father, but he would soon receive some unexpected news about his newborn son.

"This pediatrician walks out of the room with a little bundle -- that was Leo," Forrest said. "She had his face covered up and hospital authorities wouldn't let me see him or my wife. When the doctor came out, he said 'there’s a real problem with your son.'

Read more.

Wednesday, January 7, 2015

Traveling Abroad and the Child With Special Needs: Do The Right Thing

Read more: https://www.yahoo.com/travel/unitedwithivy-mom-was-so-wrong-107267702627.html

By Hallie Levine

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Levine and her adorable daughter, Jo Jo, who's 6. (Hallie Levine)

As a mom of three kids, two of whom have special needs (one has Down Syndrome and one is legally blind), I’m well aware that vacation traveling with small children — especially those with disabilities — is no walk in the park. But the attention mongering schemes of Elit Kirschenbaum, who took to Twitter last week lambasting a United Airways flight attendant for refusing to allow her to hold her disabled three year old daughter on her lap during take off, make me want to puke.

“She told us that we had to make her sit. And I said to her, ‘I would give my left arm to make her sit, of course I want to have her sit but she just can’t do it,” Kirschenbaum recently told CBS news. 

Read more.

Friday, September 26, 2014

Check Out This Video

This video is dedicated to MattyB's little sister Sarah Grace who was born with Down Syndrome. Sarah is the most beautiful girl in the world and she is an absolute joy to everyone's life she has impacted.

See Video.

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Tuesday, January 14, 2014

How Smudge Came

by Nan Gregory

173dab77991394bfaa910ca4933d511c “You respond to the universal pet story before the illustrations show that Cindy is a young woman with Down’s syndrome. [This book] is remarkable in telling it as Cindy sees it. Lightburn’s realistic pictures in soft-tone colored pencil have the same beautiful sense of fragility, steadfastness, and connection.”—Booklist (starred review) 

This happens to be one of our very favorite books. Learn more.

Tuesday, September 24, 2013

Partnership with NDSA

Hopscotch Adoptions, is happy to announce our new partnership with the National Down Syndrome Adoption Network!  We appreciate their passionate advocacy for all children with Down Syndrome in need of a permanent family.  Be sure to check out their website and visit their waiting child page.  Like them on their Facebook and follow them on Twitter too.

Thursday, August 8, 2013

Would A 'Cure' Change The Love?

By Beverly Beckham |  Globe Correspondent     August 04, 2013

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Lucy loves to share online songs and videos with her grandmother.

It was the middle of the heat wave and we were inside sitting on the floor, Lucy using my iPad, looking at Disney characters on YouTube. “Not that. Not that. Not that. This one, Mimi!”

Then she clicked and Mulan sang.

“Who is that girl I see

Staring straight back at me?

When will my reflection show

Who I am inside?”

Then she clicked on “Pocahontas.”

“You think the only people who are people

Are the people who look and think like you.

But if you walk the footsteps of a stranger

You’ll learn things you never knew you never knew.”

Then she chose a clip from the Disney movie “Tarzan.” A mother ape walks out of the woods holding a human baby and the other apes gasp and the dialogue went like this:

“Freaky looking.”

“What the heck is it anyway?”

“He’s a baby,” the mother explained.

And the other apes looked again and said, “You know he’s not so bad, once you get used to him.”

And I looked at Lucy and thought, as I have since the day my granddaughter was born, there is so much going on inside this child.

She turned 10 in June. Double digits. “You’re a big girl now,” we told her. And she is.

But she is not like most girls her age.

Lucy has Down syndrome and that makes her different. She was born with an extra chromosome that’s in each cell of her body. We human beings have 100 trillions cells. With that one extra chromosome present in all those cells, there’s a lot more substance to Lucy than to most people.

But substance is not what people see.

Lucy was born with a heart problem that required surgery. People saw this. She walked and talked later than typical kids. They saw this, too. She has trouble forming sentences. She has to work hard to speak clearly. She has low muscle tone. And she is intellectually delayed.

These are the things that most people see.

Her essence?

Lucy wanting me to hear words that have meaning to her. Lucy, knowing when someone needs a hug. Lucy, walking up to an elderly woman in a wheelchair, leaning close and asking, “Are you OK, Grandma?”

People don’t see these things.

When Mason, my goddaughter’s son, was born in the spring, Lucy, her mom, and I raced to the hospital to meet him. Lucy took off her shoes and climbed onto the bed and plunked herself between Sarah and her husband, Kyle. And draping one arm over Sarah’s shoulder and the other over Kyle’s she declared with a huge smile, “My family.”

Lucy knows things.

Her extra chromosome gets a rap for all of her disabilities. But could it be responsible for this, too, for her ability to love and empathize, for her insight, her honesty, and her genuine goodness?

Last month, Jeanne Lawrence, a researcher at University of Massachusetts Medical School, wrote in the science journal Nature that she and her team had figured out a way to switch off the extra chromosome linked to Down syndrome in human cells in a laboratory.

This is a huge discovery, a potential cure for Down syndrome.

But what does cure mean? What more, besides medical and intellectual issues, is that one extra chromosome responsible for?

Lucy tries so hard. When she was a baby, we would watch her practicing her words, holding her toy mirror and studying the shape of her mouth. She still practices words and phrases. “How are you?” “May I please have?” Is this Down syndrome? Or did she get this doggedness from my father? He couldn’t spell. But he never stopped trying.

Lucy likes musicals and show tunes. Is this Down syndrome? Or does she like them because her mother and Aunt Julie and I do?

The other day she sang a duet with me. She was brushing her teeth and I was beside her and she put down her toothbrush, brought her head close to mine, and grinning in the mirror, began.

“Together at last. Together forever.

We’re tying a knot, they never can sever!

I don’t need sunshine now, to turn my skies to blue.

I don’t need anything but you!”

Is this Down syndrome? Maybe. Maybe not. But if it is, why would we ever want to change it?


Beverly Beckham can be reached at beverlybeckham@me.com.