Written on
October 20, 2011 by
Gina
At the end of our lives, we again become vulnerable. Charged to those with hands we hope are gentle, hearts we hope are warm. Family we wish…if all goes well. But what about our children? So many times we are focused on the now, as we should be, as we need to be…with the future…
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The first thing I noticed about Kayla is her big blueberry eyes. She has the biggest, bluest eyes I have ever seen. When she smiles, they just seem to light up. The fact that she has Down Syndrome just seems so secondary to who she is. Get to know Kayla more in her mom’s own…
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Written on
October 6, 2011 by
Gina
Our family floats upon a cloud that delivers us from one crisis to another, sometimes playing bumper cars with the these crisis’ making them all blend into an amazing storm. I’m currently taking Certified Nursing Assistant classes for 5 hours per night (5 pm to 10pm) four nights a week for four weeks…not to mention…
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To start off Down Syndrome Awareness Month, enjoy this video of a very special girl. Share what you managed to capture this week. Please spread the comment love around. Thank you, *originally posted here
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Written on
September 14, 2011 by
Kimberly
Each new school year I hand over a “parent report” to the child’s new teacher. I wrote a blog post about it at my personal site a couple of years ago. I still think it is one of the most powerful tools in my special needs mom arsenal. Our report is about five pages long, though I’ve also…
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Written on
September 6, 2011 by
Gina
The holiday has passed, the change of season seems to be upon us – something I am nothing short of thankful for. It’s this time of the year I get energized, my mood is much happier, the bounce is added to my step. If this morning is any indication, it’s a good thing it is….
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Written on
August 29, 2011 by
Cheryl
Happy Monday!! I thought we could do something a little bit different this week. I’m always thrilled to interact with readers, so hopefully we can get some great conversations going. On my personal blog, I wrote about being sucker punched. Obviously I was well aware that my girls would start asking questions about Jillian’s cerebral…
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Written on
August 28, 2011 by
Beth
Many of us ride the roller coaster of hope. Things are easier to manage when we have hope that everything’s going to turn out all right. When we’re going down the roller coaster, everything looks dismal and bleak. I’m happy to say that I’ve gotten off of the roller coaster for the time being. Things…
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Written on
August 23, 2011 by
Gina
I want to write to you to tell you all the positives that can come from special needs, or rather, what we learn and how we grow as individuals raising children with special needs. I want to give inspiration rather than sorrow, the promise of a rainbow after the clouds. But I can’t. Not because…
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Written on
August 9, 2011 by
Gina
The problem with diagnosis is…. It puts people, individuals with likes and dislikes, quirks, needs, abilities and disabilities in a box. Cutting out their very individuality that makes one person differ so entirely from another. The differences between them no longer seen. In essence treating one person with an ability within a diagnosis the same…
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