Written on
October 4, 2011 by
Emily
I originally posted this on my own blog six months ago. I’ve gotten such a great response online and have had people asking me about our low-tech PECS so often that I thought I would post here as well. Picture Exchange Communication System (PECS) is something we’ve been working on with Chewy. Since he’s non-verbal…
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Written on
October 4, 2011 by
Laurie
“They don’t want to play with me!” She yells, stomping up the stairs and throwing her book bag down the hall. As is my daily habit, I wait until she blows off steam and it’s calm in her room again. Then I walk in, plop on the floor next to her where she’s creating an…
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I have a few issues, just like everyone else. However, my current giant flaw is my inability to be mean. Seriously, I’m totally a “tell it like it is” kinda girl, but I can usually say it with as much grace as I can muster. I don’t like to hurt people’s feelings or make them…
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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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I’ve been thinking a lot about how being a special needs parent has changed my life. Sure, there are sleepless nights, giant messes, and financial worries. Even typical parents have those problems! Yet, I have learned priceless lessons—some about me, some about the world. These…are the secrets that make this journey worth it all. 1….
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Written on
August 14, 2011 by
Suzanne
…”The hard part is trying to answer the questions Walker raises in my mind every time I pick him up, What is the value of a life like his — a life lived in the twilight and often in pain? What is the cost of his life to those around him? … If Walker is…
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in
Adoption,
Advocacy,
Autism Spectrum,
Cerebral Palsy,
Day In And Day Out,
Dealing With Public Perceptions,
Developmentally Delayed,
Epilepsy,
Laughing Through The Tears,
Learning Disabilities,
Me Time,
Medications and Treatment Options,
Mental Health,
Raising Awareness,
Resources,
Sensory Processing Dysfunction
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Written on
August 9, 2011 by
Laurie
Anyone else living in a trashed house? I do. It’s the kind where rays of sunshine pour over beautifully painted walls – well, mostly, except for the place where our 8 year old kicked a hole through one in a rage months ago. Or where doors are missing from being slammed through frames. Or where…
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Written on
July 30, 2011 by
Tammie
Ok, maybe it dates me that I can remember that tune that played out on television…”My buddy, my BUDdy, My buddy and me can climb up a tree, my buddy and me are the best friends we can be~~ My buddy and me” I wish I could turn the picture for you…but editing isn’t letting me. Anyway,…
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Written on
July 19, 2011 by
Gina
Connection with another is the most natural occurrence in a human life. From the instant a child is born, we talk about ways to connect, laying upon his mother’s bosom for skin to skin contact, for the mother-to-child bond that is so crucial. When we’re sad or elated, even going about the normal routine of…
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Written on
July 17, 2011 by
Suzanne
I am not sure when it was exactly, that I stopped planning ahead. It could have been when Zoe was little and ill all the time. Maybe when her big sister Olivia was still catching every virus too- but somewhere along the years with appointments, kids school stuff, daily care and flu seasons- and trying…
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