down syndrome awareness

I know a girl whose smile lights up the world, whose frown tugs at the heart strings, and whose tears can melt the hardest of hearts. This little girl has Down Syndrome.
With the attention focused on the Presidential election, it is easy to forget that there are committed professionals working
When disability is a storyline, a rare feat in itself, it's often a tragic plot point or sensationalized heroism. Even more troublesome, the character is usually portrayed by an actor without a disability.
"[I]t’s not OK to leave someone out because of their disability, race, or gender."
"We can change the way some people perceive Down syndrome."
While it is important to celebrate all the things that people with Down syndrome can do and how similar they are to others, I would argue it is equally important to acknowledge the ongoing fight against discrimination that their differences evoke.
• Don't be so timid. My niece has never met a stranger. Wherever she is, no matter how large the crowd, she's liable to be
This has been my dilemma as Marcus and I have met each new group. Should we talk about Down syndrome? And to what extent? It is, after all, Down Syndrome Awareness Month, and Marcus does happen to have Down syndrome.
"They have been wonderful witnesses of love to me."
As the world cheers on Madeline Stuart, the Australian model with Down syndrome who just announced she'll walk the runway at New York Fashion Week, I'm cheering too. Yet I'm also feeling uneasy, because negative perceptions of people with disability are rearing their heads.
She is my daughter. Louise. She is four months old, has two arms, two legs, two great chubby cheeks, and one extra chromosome.
These unique photos are Alan's heartfelt contribution to the world in an effort to draw attention to the reality that raising a child with Down syndrome, though difficult at times, is not a burden but a joy to him and his family.
What's the best thing about being Ariana and Kiki's mom? And what's the hardest thing? The best thing about being their mom
I know I am supposed to be the teacher, the mother. But the truth is, you have taught me more than I'm sure I have managed to teach you.
It's impossible to pay it forward and not feel better about the day. This March 21st, on World Down Syndrome Day (WDSD), many in the Down syndrome community will put this idea into action.
I wondered if I would lay claim to those words -- not just string them together, but lay claim to their meaning. Lay claim not just to my daughter, but to her extra chromosome. Because cognitive disability was hard for me. Very, very hard.
Wright's new venture, Dye Creek Capital, would function differently than most other companies. The first thing the businessman