therighttoliveajoyfullife.blogspot.com
the right to live a joyful life: KICK A$$ BLOGGER AWARD
http://therighttoliveajoyfullife.blogspot.com/2008/09/kick-blogger-award.html
The right to live a joyful life. Tuesday, September 23, 2008. KICK A$ BLOGGER AWARD. Kelly over at Where There’s A Will. Has passed on The Kick A$ Blogger award to me. Thank you Kelly, I am fully aware that with only 8 blog entries over the course of the past 9 months the award that I really deserve is The Lazy A$ Blogger award but you are a nice lady and you have passed this on to me. I am honored. OK now. Let’s see if I can follow the rules. I am to mention MammaDawg. Tricia at Unringing The Bell.
therighttoliveajoyfullife.blogspot.com
the right to live a joyful life: Two Horse Crazy Girls Live Here
http://therighttoliveajoyfullife.blogspot.com/2009/07/two-horse-crazy-girls-live-here.html
The right to live a joyful life. Tuesday, July 7, 2009. Two Horse Crazy Girls Live Here. The girls love to ride. Each girl rides twice a week. Check out this link for a great video featuring The Rascal riding at The Champlain Adaptive Mounted Program (CHAMP). The Rascal is in the picture in the upper right corner. She's wearing the light blue fleece with yellow sleeves. Cursor over her picture and then click on "watch our story" Vermont Matters. This is Jim. He lives in The Rascal's room. Seat Of My Pants.
theupsideofdownsyndromethatis.blogspot.com
the Upside of Down (syndrome, that is): February 2009
http://theupsideofdownsyndromethatis.blogspot.com/2009_02_01_archive.html
The Upside of Down (syndrome, that is). Come meet Lauren: a girl with 47 chromosomes and 47,000 ways to make us smile. Saturday, February 14, 2009. On being an older Mom. I have to admit that after I found out Lauren would have Down syndrome, I felt like such a cliche'. There I was, the woman of 'advanced maternal age. Pressing the envelope of natural events by becoming pregnant. If I had just stopped with Gabe, everything would have been okay. And now look at the mess you have made. The statistics say t...
theupsideofdownsyndromethatis.blogspot.com
the Upside of Down (syndrome, that is): some kids take a whole lifetime to raise aka. i'm still learning how to be a mom....
http://theupsideofdownsyndromethatis.blogspot.com/2010/02/some-kids-take-whole-lifetime-to-raise.html
The Upside of Down (syndrome, that is). Come meet Lauren: a girl with 47 chromosomes and 47,000 ways to make us smile. Monday, February 8, 2010. Some kids take a whole lifetime to raise aka. i'm still learning how to be a mom. He's my son and, yet, he's a stranger. All children are a mystery to be solved, but none moreso for me than Nolan. Not only is he my first son but he has the IQ of a gifted person, mad skills in music and math, huge hair that I call the 8th wonder of the world, a snowboarder (w...
gearytime.blogspot.com
Sheena Time: November 2009
http://gearytime.blogspot.com/2009_11_01_archive.html
This blog is dedicated to my little girl, Sheena Tara - a gorgeous little girl born in January 2006. Sheena has Down Syndrome and had some major health problems in her first 18 months of life, the most significant being West Syndrome or Infantile Spasms. She's now recovered from that, and well and truly making up for lost time. Welcome to Sheena Time! Sunday, November 08, 2009. Subscribe to: Posts (Atom). T21 Blogs and Other Blogs of Interest. My Sister's Blog 1709Christy. Prince Vince Meets the World.
gearytime.blogspot.com
Sheena Time: November News
http://gearytime.blogspot.com/2009/11/november-news.html
This blog is dedicated to my little girl, Sheena Tara - a gorgeous little girl born in January 2006. Sheena has Down Syndrome and had some major health problems in her first 18 months of life, the most significant being West Syndrome or Infantile Spasms. She's now recovered from that, and well and truly making up for lost time. Welcome to Sheena Time! Sunday, November 08, 2009. Have you had her tested for that condition where kids dont sweat properly? Good luck with the potty training!
theupsideofdownsyndromethatis.blogspot.com
the Upside of Down (syndrome, that is): July 2009
http://theupsideofdownsyndromethatis.blogspot.com/2009_07_01_archive.html
The Upside of Down (syndrome, that is). Come meet Lauren: a girl with 47 chromosomes and 47,000 ways to make us smile. Wednesday, July 29, 2009. Zoo Trip - LoLo style. Today, I went to the Toledo Zoo with Gabe, Lauren and Ada - it was a spur of the m. Oment excursion; you know, those outings that usually turn out the best because the lack of planning means that nothing could go wrong. Gabe was in charge of the camera for most of the day - so the pictures, if they didn't include him. Definitely a good egg.
theupsideofdownsyndromethatis.blogspot.com
the Upside of Down (syndrome, that is): November 2009
http://theupsideofdownsyndromethatis.blogspot.com/2009_11_01_archive.html
The Upside of Down (syndrome, that is). Come meet Lauren: a girl with 47 chromosomes and 47,000 ways to make us smile. Monday, November 30, 2009. Motherhood: it's like Deja Vu, all over again. So, a couple of weeks ago I was with Chaz and Lauren at the children's hospital at University of Michigan waiting for Lauren to get her hearing tested. This had been a much longer than necessary amount of time spent at the hospital - who knew that a 2 year old could go 9 hours during the day without eating? So, as ...
theupsideofdownsyndromethatis.blogspot.com
the Upside of Down (syndrome, that is): Having Lauren
http://theupsideofdownsyndromethatis.blogspot.com/2010/03/having-lauren.html
The Upside of Down (syndrome, that is). Come meet Lauren: a girl with 47 chromosomes and 47,000 ways to make us smile. Tuesday, March 16, 2010. Having Lauren is like sitting on the shore of the ocean and the waves just keep washing over you.over and over.surrounding you, drowning you, smoothing out the rough edges and sometimes scaring you. Waves of joy and peace and sorrow and hope. It's being surprised and expecting the unexpected. She is all that I could want in a child and more.she stretches me i...
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