Stunning photo collection celebrates beauty of children with down syndrome
“I’m really hoping that through my photos, we can change the way some people perceive Down syndrome.”
Julie Willson, a New Jersey photographer, is making headlines as of late due to her stunning photo series that celebrates the beauty of children with down syndrome.
In October of 2015, Willson brought 11 children with down syndrome and their families together in order to capture the amazing collection. The kids range in age from 0 to 5-years-old, and the results of the photoshoot are nothing short of sheer beauty.
Willson is not unfamiliar with down syndrome. Her sister, Dina, was born with down syndrome and was partly the inspiration for the album. “Dina was born in 1975 with Down syndrome and was the absolute light of our family,” she told The Huffington Post in a recent interview. Tragically, Dina passed in 2011 due to congestive heart failure.
“Photographing these 11 kids brought back so many great memories of my sister,” Willson explained in her interview. “I’m really hoping that through my photos, we can change the way some people perceive Down syndrome.”
The positive feedback and support from netizens and parents around the world led Wilson to co-found Nothing Down — a non-profit organization dedicated to raising awareness about Down syndrome.
Willson on her non-profit and its goals: “Unfortunately, we’ve learned that not much has changed since my sister was born 40 years ago. My parents were offered and recommended to put my sister in a ‘home. Today, parents receiving their child’s diagnosis during pregnancy are often offered to terminate their pregnancy due to Down syndrome and those receiving the diagnosis after birth are told of all the negatives of their child’s future instead of the positives.”
“Through Nothing Down, we are hoping to show the world all of the positives of kids with Down syndrome through photo and video projects,” she added.
You can check out some of the amazing photos from the series accompanied by detailed descriptions from each kid’s parents here. Be sure to check out Nothing Down’s website for more info!
“Our Finnegan has such a tender, sweet heart. He takes in everything around him with such a zest for every moment. I think one of our favorite things about Finnegan is when we watch him play; he smiles and laughs without prompting, just enjoying himself so much in the moment. He has a purity about him and a certain wisdom in his eyes. He loves with his whole heart, full force, completely and tirelessly.”
See more from the stunning photo series by clicking next!
“Alexa is full of energy, running around with her brothers like any other 5-year-old. We admire her for her strength and her determination. She doesn’t listen to what she can’t do and she makes everything seem possible. Her smile alone is one that brings you joy in an instant. We continue to be amazed at what she has overcome and how she has beaten such great odds. No one looks at her and sees Down syndrome. They look at her as a beautiful little girl who is ready to take on the world.”
“Tristan has rocked our world in ways we never knew were possible! Tristan is intelligent, persistent, strong willed, and knows what he wants. He loves to eat and dance! He also is very healthy and capable of anything he sets his mind to. He never gives up and he is fearless. His favorite person is his 5-year-old brother, Jael, who is his protector, playmate, and best friend. The love between the two of them is the most beautiful and special love that I have ever seen. He is loved by so many people, and he has brought our family closer.”
“When Carly was first born, our family mourned the loss of ‘the normal child’ we were planning on, however we quickly realized that Carly was exactly the normal that we needed. She lights up a room, has a contagious smile, and amazes everyone around her day in and day out. Carly teaches us all to be more compassionate and more inspired. She never gives up, always tries her best and is determined to keep learning new things.”
“Michael is 2 years old and is the best thing that has ever happened to me and my family. From the moment he wakes up to the moment he goes to bed at night, he has a constant smile on his face. He loves Mickey Mouse and loves to dance and play ball! Every time he hears music, he dances. Even in his car seat, in the car, he’s constantly moving to whatever comes on the radio!”
See more from the stunning photo series by clicking next!
“Olivia is a crazy, trouble-making, opinionated, smart, funny and beautiful toddler. She is more active than her brothers ever were and keeps me on my toes every minute. Her brothers love her and thank me for giving them a baby sister. Early intervention services started as soon as she came home from the hospital and I believe have made a huge difference in her. We have two wonderful support groups that have activities for the children and siblings, parent events that we enjoy going to where we spend time with other families helping us learn what else we can do to help Olivia reach her full potential.”
“Zach is a fighter. He wasn’t expected to make it through the pregnancy, yet he did. He is not even remotely the child that the doctors predicted he would be. He is happy, engaging and so loving. He’s always ready with a hug or snuggle.”
“There is so much about Aiden that has brought our family joy and it’s hard to put it into words. His smile alone is enough to melt your heart. The constant love that he shows us is beyond words. Watching him achieve each milestone is amazing knowing that he has to work harder to get there.”
This story was first covered by The Huffington Post
If you have any insights, questions or comments regarding the article, please share them in our Comment box below. Like us on Facebook and follow us on Google+ and Twitter to stay up-to-date on the latest from theIndusparent.com