Share something special
This website is for you and we want your story, videos, and pictures on the front page. This is a place to share, ask questions, make friendships and sometimes to vent and cry. More than anything, I want this to be a website where you brag, boast, take pride, and yes … even gloat (ooooh ) … I want you to tell the world how wonderful your children, grandchildren, friends, and family are.. Send me a picture (justin.jilg@gmail.com) and shoot me a note about an accomplishment, birthday, piece of art …you name it – we all want to see it (I promise we do!)
I have had the unique opportunity to be able to put my son Teddy on the front of this website several times .. Now, its your turn … Let’s see your photos and videos and let’s hear something that you want to tell the thousands of people that come to this site every day.
You can either send to my email address (above) or post something on your own blog and let me know on my wire that you would like it to go on the front of the website…
Remember…this is your site as much as it is mine . I can’t wait to see and hear the wonderful things you want to share with the World.

Hi all,
Would you consider adding my son Jacob’s website to yours? The website was set up by the Gulf Shores, Alabama Kiwanis Club.
http://www.JacobHalpin.com
Jacob is the only high school varsity athlete with Down syndrome to have earned All-State honors, this was from within a 402 school category. He is also the first athlete from the United States to hold world records through the Down Syndrome International Swimming Organization.
Jacob earned 4 varsity letters in swimming, All-State & All-County honors, participated in 4 High School State Championship Swim Meets, received the Alabama High School Sports Magazine’s Humanitarian Award and was a co-captain for his high school swim team in his senior year.
Jacob is a Trisomy 21 and began his competitive swimming career rather late during the summer between 7th and 8th grade when he joined the local age group swim team.
Mike Halpin (Jacob’s dad)
Mike,
Thanks for the request…Give me a few days.
Justin
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Articles »
That which we do today will echo throughout the generations to come
One of our wonderful visitors wrote in asking for activities to do with a group of people to help them get an understanding of what it might be like to have Down syndrome. The activities included are great for parents to present to their child’s class, a teacher to present to their class, or even a student to present to their class as a project. We appreciate this educator’s commitment to making the world a better and more accommodating. Thank you for everything that you do.
Blogs »
Featured Blogs – The Ordinary Life of an Extraordinary Girl
I finally did it — I hid the gross, disgusting, ugly ,worn-out, fake crocs that Alex has been wearing every day for 2 1/2 years. It took a lot of guts – but I am proud of myself (at least for now).
When my kids were little, I thought it was sort of cute if they wanted to wear the same pair of jeans or shirt for more than two days in a row. However, Alex is 16 and these dreadful blue shoes have got to go. She should not have even worn them for two weeks in a row.
Many people I know with down syndrome have flat, wide feet. I am not sure exactly why that is – but as a result Alex has a funny step and walks with her feet pointed outwards. As with everything in her life, Alex has learned to compensate, and walking or even running – as evidenced by the fact we are going to participate in track and field at the National Olympic Games – is not a problem for her…
Books and Videos »
My Son Teddy
Hello everyone..I wanted to post a video of my son Teddy. It has a song that I love that makes me tear up every time. I wanted to kick this multimedia experience off by posting something of my own. I absolutely encourage you all to post your own pictures and videos. As the site grows it will become easier. Please enjoy ..
Education »
That which we do today will echo throughout the generations to come
One of our wonderful visitors wrote in asking for activities to do with a group of people to help them get an understanding of what it might be like to have Down syndrome. The activities included are great for parents to present to their child’s class, a teacher to present to their class, or even a student to present to their class as a project. We appreciate this educator’s commitment to making the world a better and more accommodating. Thank you for everything that you do.
Support Groups »
Long Island Buddy Walk – Alexander’s Angels – Down Syndrome Research and Treatment Foundation
Let’s welcome the latest addition to the DownSyndrome.com team, Laura Suer. Laura has accepted a position as a participating volunteer and editorial staff member who will focus on partner outreach and strategy. She has been active on the site since its inception blogging at the URL tri21.downsyndrome.com. One of Laura’s first coups (I’m sure one of many) is to establish a relationship with Alexander’s Angels who runs the Long Island Buddy Walk and has a great future of providing much needed services to the constituents of Long Island.
Thank you Laura for bridging the relationship with such a wonderful organization. If you live in the Long Island area or if you have the inclination to help their wonderful support group, please consider providing assistance in the form of either volunteerism or financial support. Additionally, the Down Syndrome Research and Treatment Fund has an online store that further supports important DS research that hopefully will benefit all of our loved ones in the future. Support for DSRTF can be in the form of purchasing items from the Down Syndrome Store.
What is Down Syndrome? »
What is Down Syndrome?
Down syndrome is a genetic disorder that delays in physical and intellectual development. The condition varies in severity, so developmental problems may range from mild to serious.
Down syndrome is the most common genetic cause of severe learning disabilities in children, occurring in one in every 800 infants. Every year, as many as 6,000 babies are born with Down syndrome in the United States. The condition is named after John Langdon Down, the doctor who first identified the syndrome.
There’s no medical cure for this condition. But increased understanding of Down syndrome and early interventions make a big difference in the lives of both children and adults with Down syndrome.
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