Written on
January 11, 2015 by
SusanC
Jennifer Donovan is here to share about a home organizational system aimed to help kids become more independent and self-reliant. This is a sponsored post, but her opinions are her own. I’ve outlined some of the features about the M.O.M. Method that I love, over in my post at 5 Minutes for Mom about how…
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Written on
February 4, 2013 by
Suzanne
When Zoe was little I spent a lot of time thinking ( and writing) about about how different she was. Then she grew, and through her grade school years blossomed with the encouragement to try and do her best as I made sure she was always included, and treated just like everyone else. Zoe will be starting…
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in
Advocacy,
Autism Spectrum,
Cerebral Palsy,
Day In And Day Out,
Dealing With Public Perceptions,
Developmentally Delayed,
Down Syndrome,
Epilepsy,
Laughing Through The Tears,
Me Time,
Resources,
Sensory Processing Dysfunction
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Written on
December 29, 2012 by
Maggie
This year, like the past seven, we’d been telling my live-in-the-moment Boys (identical twins with Down syndrome) for weeks that Santa Claus would soon be paying us a visit and leaving toys under Christmas trees all around the world for good little girls and boys in honor of Jesus’ birthday. “Why?” Because Jesus is all…
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Happy November, Friends! (How did this happen? Wasn’t it just January?) The past few months have been sort of rough for us. For some reason, it seems like everything we’ve done, or tried to do, went horribly wrong. When things don’t go the way I envision them, I tend to get–shall we say–moody? Maybe not…
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Hi you guys! This is basically my week again…only different surgery on the stomach…I’ll update you later… **************************************************************************** I get tired–the kind of tired that makes your bones ache. Sometimes, I get grumpy too. Hey, don’t we all? In this ever-winding road of special needs parenting, I find myself often in a…
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Written on
September 23, 2012 by
Maggie
Need a little help here, PLEASE: My Big Little Man (who is smaller by 5 lbs now than My Little Man) got that back-to-school cold going around. For us, that means an imminent sinus infection as his compressed sinus cavities — a trait common to those with Down syndrome — makes him prone to this…
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Hi there! Remember me? (don’t answer that…I’m beginning to feel a foreigner in my own land!) So, here’s the current score. School District: 5, Jack: 3. It’s looking rough out there. His IEP was completed a few weeks ago. Because he turned 6, he has to be “transitioned” from the developmental delay label to…
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I sat in the developmental psychologist’s waiting room just simply observing the behavior of the parents. Some were busy filling out paperwork, one was reading a book, another was totally in to playing Angry Birds. Not a single one was watching their child. I watched these children, who were obviously there for a reason, as…
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School. It’s happening around here. Some of the counties near where we live have already returned to recess, brown bag lunch, and smiling teachers. We…start Monday. Well, my daughter starts Monday. My friend’s children start Monday. Jack. Not so much. See, we qualified for Hospital Homebound (HH). Basically, this is a school within a school….
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in
Adoption,
Cerebral Palsy,
Day In And Day Out,
Developmentally Delayed,
Education,
Individual Educational Plans,
Learning Disabilities,
PDD,
Physical Therapy,
Speech Language Pathology,
Support,
Therapy
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The child reminded me of a poignant moment from her babyhood the other day. She was maybe three years old at the time, and still very much a baby with her speech and social delays. I was with her at our church for some reason – going to a meeting or something and she was…
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