Last weekend, we paused briefly in our home renovating/DIY journey and watched the movie ‘Temple Grandin‘. It is a wonderful film, but that wasn’t the most interesting part of the experience. That is reserved for learning about the different ways people think and process information. Particularly sensory information.
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Keeping Balanced: Promoting Health and Wellness in the Gifted/2E Child
This topic is close to my heart, because it is something we deal with in this house everyday. As I have talked about before, both my kids have LDs. My son has SPD and ideopathic toe walking (plus another unknown disability we’re going through the wringer to get diagnosed). My daughter has anxiety disorder – she gets stressed and then is unable to feel pain – which causes her to be a sensory seeker – she likes throwing herself onto the floor for the bump. I cried the first time she complained about a minor injury. Because it was a big deal – it meant that she was able to feel it, and therapy was working.
So today I’m going to talk about how we incorporate strategies into our day to keep everyone on an even keel. Some of these are for the disabilities, some for the OEs. They all help.
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My Kid is NOT Average, and Pride Has Nothing to Do With It.
What can I say about the post, ‘My kid is average and I am oh so proud‘ ?
I can say that it makes me feel deeply uncomfortable. Maybe it’s the passive aggressive tone, maybe it’s the conflation of their child’s achievements and their own ego. I’m not sure.
What I think is damaging and breath-takingly dangerous about this post, is that it reinforces stereotypes that encourage discrimination and prejudice. Even if the opposite was the author’s intent. Which I’m not sure is the case.
Continue reading “My Kid is NOT Average, and Pride Has Nothing to Do With It.”
Homeschooling My Gifted Kid, Part 3: The Twice Exceptional Wrinkle
In this third part on our convoluted journey to homeschooling, I’d like to talk about what twice exceptional means – and a bit about what it feels like to parent such kids!
This is not meant to be a definitive guide for people trying to discover more about twice exceptional kids. This is just our personal journey, and a few of the curious signposts along the way.
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Dealing with Diagnosis Soup
It’s been a while since my last post. Mainly because we’ve been busy with what I like to call the ‘diagnosis soup’ – seeing all the specialists who have a stake in helping C with his disabilities. As well as learning how to integrate all the home therapy into our daily routine. With all of C’s and J’s diagnoses, if we did all that each Dr recommended – there would be no time for eating, sleeping …or living!
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