Last Friday I reached a limit of frustration trying to get my daughter out the door to school. Three days a week I juggle all three kids in the morning, to get everyone fed, dressed, packed and dropped off at their respective schools. On Friday Daddy had to leave early for a meeting in the…
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Written on
March 15, 2011 by
Lee
I have witnesses a worrisome trend—couples divorcing after their special needs child reaches age 18. When the mom retains custody of the child, what is the continuing responsibility of the father? Will he remain involved in the life of the child? Will he continue providing financial support? Will he take the High Road?
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Written on
March 15, 2011 by
Gina
I know it’s not perfect, the medication J is on. But it’s doing something. It’s helping to quiet the activity in his brain…sometimes. It’s helping him to find more words, helping the words to find their place within a sentence, to communicate. I talk about watching our children’s achievements, however small, but sometimes these achievements…
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Written on
March 15, 2011 by
Laurie
As special needs parents, we give up a lot. Our time. Our energy. Some of our relationships. Our vision of what might have been our lives as a family. With all the things we give up, it would be really darned nice if we didn’t fall under the same rules of slowing middle-aged metabolism, so…
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Written on
March 14, 2011 by
Cheryl
I’m finally on the mend after the weirdest virus/cold I’ve never had! Thankfully, I learned well from my girls and I decided to share with them. In all honesty, I really need to teach them what IS appropriate to share and what isn’t. And I should probably take that lesson myself. Since Jillian was born,…
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Written on
March 13, 2011 by
Suzanne
It’s a typical school day morning, and I am in the kitchen double checking Zoe’s lunch bag, snack bag, toiletry bag- loading her backpack . I glance up, over the kitchen counter, just in time to see Zoe, who is hovering nearby in her walker. She is smiling and elaborately shaking her groove thing to…
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Written on
March 12, 2011 by
Maggie
We are in the process of formalizing a diagnosis of Attention Deficit Disorder with secondary Anxiety Disorder (at-risk for depression) for my “gifted” 9-year-old daughter. For me, this process began more than 2 years ago, brought to light by the abusive treatment she suffered at the hands of her 2nd grade teacher who drove her to tears…
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Written on
March 12, 2011 by
Tammie
This week my husband’s grandmother passed away. She was 93 year old, never took more than a multi-vitamin in her life. She did however, several years back, begin her journey with Alzheimer’s Disease. It was a long journey, spending 10 years in a nursing home. She had 5 children, 12 grandchildren…and so many great grand…
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in
Advocacy,
Cerebral Palsy,
Communication,
Conditions and Diseases,
Day In And Day Out,
Dealing With Public Perceptions,
Developmentally Delayed,
Education,
Epilepsy,
Family Life,
Fine Motor,
Gross Motor,
Medications and Treatment Options,
Problem Solving,
Raising Awareness,
Resources,
Self Care,
Social Skills,
Support,
Therapy
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Being the mom of a Super Hero isn’t easy! There are the people who see you coming, and run to the other side of the street avoid you so as to not get in your way. Others give their unsolicited opinions… The third group ask questions…brutal, hurtful, sometimes ridiculous, questions. My favorite this week: “I…
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Written on
March 11, 2011 by
MarjH
Well, our little Houdini is at it again. We try to keep it safe and locked down around here, but the truth is he is getting older and bigger and smarter and he’s figuring it all out. See, most devices and locks and whatnot are for BABY PROOFING. Not IAN PROOFING. Even autism-specific products. We…
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