Written on
April 23, 2011 by
Tammie
Learning…I’ve not written about homeschooling yet so I thought maybe this would be a good time. Homeschooling isn’t so typical for us, we have many challenges to get over. We do use therapies as part of our daily routine (even if we are still on sabbatical from professional therapies at our local hospital). We do…
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in
Assitive Technology,
Cerebral Palsy,
Communication,
Day In And Day Out,
Developmentally Delayed,
Education,
Epilepsy,
Family Life,
Feeding,
Fine Motor,
Gross Motor,
Homeschool,
Laughing Through The Tears,
Learning Disabilities,
Occupational Therapy,
Physical Therapy,
Problem Solving,
Sensory Processing Dysfunction,
Skill Development,
Speech Language Pathology,
Support,
Therapy,
Vision Therapy
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Written on
April 21, 2011 by
Debbie
Sometimes I wish I wasn’t so tuned in to the special needs community. Sometimes I wish I could just get on Facebook and see what goofy things people are doing, even if it’s so mundane as “I’m getting a haircut this afternoon.” But, in my group of friends, that’s not always possible. I have many…
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I arrived a few minutes before the bell that ends the school day. I realized that one of my friends was trying to get my attention and directing my gaze down the outdoor corridor outside my daughter’s classroom. I saw my daughter walking toward me with another friend of mine – fortunately one that has…
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Written on
April 19, 2011 by
Gina
She wailed that B had her popcorn. Popcorn being used loosely as the container that once held popcorn kernels, gladly accepted by her at its end as an addition to her kitchen belongings….this thing that B was handling in front of her (the nerve) with an item of his already stuffed inside. To keep my…
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Written on
April 18, 2011 by
Cheryl
I’ve mentioned before how absolutely thrilled we are that Jillian’s language is ahead of her actual age. Although, I must keep reminding my husband that she IS still 2.5 and that she will still have temper tantrums. Just as she feels she needs to be ahead of the times (except walking, I mean geez, what…
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Written on
April 17, 2011 by
Beth
DH and I met a lovely woman at the support group we attended last fall. Her son is similar in age to Precious and has a similar diagnosis; mild developmental disability. I emailed Steph a month or so ago and she, her husband and her son came over and hung out with our family for…
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Written on
April 16, 2011 by
Maggie
Am I the only one who can’t seem to find any time to take care of me in my life? OMG, for all the child-rearing and special needs advocating and work I’m doing, there doesn’t seem to be a moment left for me! I’m not talking about luxuries like taking a bubble bath, a night out…
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Written on
April 16, 2011 by
Tammie
My son had his Botox treatment this week. I knew about 2 weeks ago it was needed. It’s funny how that works. At first you think, is it worth it? Am I doing it for him or for me? Actually, both. I do it for him. His spasticity is so severe, he could curl into a…
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in
Cerebral Palsy,
Day In And Day Out,
Dealing With Public Perceptions,
Family Life,
Fine Motor,
Gross Motor,
Laughing Through The Tears,
Medications and Treatment Options,
Problem Solving,
Raising Awareness,
Skill Development,
Therapy
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Written on
April 14, 2011 by
Debbie
Life’s been crazy lately. Today especially. Add to that my lack of sleep from last night due to a certain visitor who dropped by almost every hour on the hour. Needless to say, I don’t really feel like writing and if I did, it would either be pretty much a pity party or a gripe…
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I’ve just about decided I don’t like the word mild – except as it relates to cheddar cheese and salsa. Mild should come with a warning label… I believe I recognized the signs of “mild” cognitive decline due to dementia in my mother-in-law a couple of years ago. Although I did what I could to…
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