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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.
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…
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 ..
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.
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.
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.
Tommy fell on his snowboard over the weekend. He bruised his ribs, and twisted his knee. Although scared and scary, he will live to snowboard again. This necessitated Tom going home early, with me taking him. Alex was with her team practicing, so I [...]
Georgia commented on the blog post Bus Ride 15 hours, 4 minutes ago
I am a grandparent of a child who has chromosone 21, but I also am a bus attendent, The bus attendent should be able to connect with this child, and keep an eye on her, He should of taken classes on how to work with special needs children, But i’m afraid to say that all [...]
Alex’s Mom wrote on kart’s wire: 15 hours, 56 minutes ago
Hi – we have lots of experience with sports. My daughter is 16 and we’ve tried them all. She really does not need any adaptions, just a bit more time. Her reflexes are a bit slow, so the coaches in soccer and basketball worked with her teammates to make sure the ball is passed a [...]
Alex’s Mom commented on the blog post Life is not a bed of roses, unless you count the thorns 16 hours, 1 minute ago
Thanks for reading about us….It certainly has been an interesting and exciting journey. Best of luck with your granddaughter..
irene c. rodriguez wrote on Veronica Perez’s wire: 1 day, 9 hours ago
HI VERONICA, FIRST GIVE JONATON A BIG BIRTHDAY HUG FROM ME. I AM SORRY THAT JONATHON HAS BEEN HAVING A HARD TIME BUT THANK GOD THAT THERE IS ALWAYS A TREATMENT FOR WHAT EVER HE DEVELOPES. BELIEVE ME IT MAY SEEM LIKE THERE IS NO END TO THE TUNNEL OF WORRIES BUT THERE IS. I [...]
Harvey and heathermurray are now friends 1 day, 12 hours ago
Alex’s Mom wrote a new blog post: Sneaky or sincere? 1 day, 17 hours ago
Tommy fell on his snowboard over the weekend. He bruised his ribs, and twisted his knee. Although scared and scary, he will live to snowboard again.
This necessitated Tom going home early, with me taking him. Alex was with her team practicing, so I [...]
kart wrote on their own wire: 1 day, 22 hours ago
please advise: what sports can I teach to children with down syndrome and what are the materials…..thanks…
Veronica Perez wrote on irene c. rodriguez’s wire: 2 days, 3 hours ago
Jonathan celebrated his first birthday on March 2nd I posted a picture in the album.
Veronica Perez wrote on irene c. rodriguez’s wire: 2 days, 3 hours ago
Hi Irene, everything with the move to Georgia went well. We became residents of Georgia on December 31st. Jonathan was starting to do better with his sleeping patterns until he caught a virus mid-January. First the doctors said it was (RAD) Reactive Airway Disease along with a pneumonia but he has had several little [...]
bugsmom wrote on their own wire: 2 days, 4 hours ago
Hello fellow parents! I just wanted to say that I’m excited to join you all. My daughter is 20 months and is everything I asked for in a child – healthy and happy.
My husband and I are so proud of her for the things she accomplishes on a daily basis that so many parents [...]

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