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Sensory Processing Disorder

 

Most days I am home with my three youngest and Eby spends much of his time playing outdoors.  With his Sensory Processing issues, he needs plenty of room to move, lots of stimulation, and not too many people.  The downside of being one of the youngest is that Eby and Little Man don’t get out much and lately I’ve been thinking that I need to start taking them along with me more often.  Our town has a nice Farmers Market on Saturday mornings, so this weekend Mimi, Sweet Pea and I decided to take the girls. It seemed like a good opportunity to include the little boys, so we took them along.

Thanks for the great comments on my post about Eby andVBS.  Beth left a comment that I would like to share,

Lisa, Thanks for sharing your story! You said a thank you to Karyn Purvis when you prompted eye contact with Eby. I am curious to know what this interaction may have looked like before Empowered to Connect and TBRI training. Are you willing to share that with readers?

Absolutely – I only wish we could sit down and I could talk with all of you for a few hours.  There is so much to learn and I feel passionately about it!  Anybody have a big living room and a huge pot of coffee?

Prior to learning from Karyn Purvis, Empowered to Connect, and understanding Sensory Processing Disorder, I would have been very embarrassed by Eby’s behavior.

The kids are going to vacation Bible school at a local church and it seems to be providing us with lots of opportunities to think about Sensory Processing Disorder.

The first day when I arrived to pick them up, the director took me aside to tell me that during the closing music Eby and a new friend had gotten a little rowdy and were jostling each other while doing the motions to songs.  Eventually Eby pushed the other boy who fell, hitting his head on the pew and getting a small cut.  I knew this was going to be a big deal for Eby to process and I wanted to get him home quickly.  She suggested that I might want to take Eby to see the boy before we left and tell him he was sorry, but I explained that it probably wouldn’t go well and I would talk with him at home.

If you have kids with Sensory Processing issues, or suspect that you might, take a moment to watch the trailer for a new instructional DVD by Dr. Karyn Purvis:

A Sensory World: Making Sense of Sensory Disorders

You can also read more about it on the Empowered to Connect website.

I was so impressed that I ordered a copy today. At $30 for over 90 minutes of instruction, I am confident that it is a worthwhile purchase.  I can’t read the stack of books by my bed in 90 minutes and I am guessing I’ll quickly learn lots of good information and new techniques by watching this DVD.

I’m excited to tell you all about it.  Maybe we’ll have to mail it around the country to each other.

~Lisa

Do you remember last March when I wrote a post about weighted blankets being used for children with Sensory Processing Disorder? A wonderful thing happened as a result. Two readers emailed me and offered to make blankets for my children — can you believe it?

A new reader, Shannon, recently left a comment about using weighted blankets with children who have sensory issues and/or a history of trauma.  Weighted blankets are expensive to purchase, but  her family was given weighted blankets by an organization called Project Linus.  According to the Project Linus website:

First, it is our mission to provide love, a sense of security, warmth and comfort to children who are seriously ill, traumatized, or otherwise in need through the gifts of new, handmade blankets and afghans, lovingly created by volunteer “blanketeers.”

After looking at their website, I contacted Project Linus and asked about weighted blankets.   Mary referred me to a page on their site for blanket patterns and particularly a weighted blanket called Lili’s Hug. She suggested that I make one (not likely to happen) or find somebody who sews and will make one for me.  She also said it would be worthwhile to contact a local chapter to see if they make Lili’s Hug blankets.  I may give that a try.

Does somebody want to whip up one of these blankets and let us know what you think?

Shannon also said,

Our son is “Mr. Muscle,” he is45 pounds, but he can lift my 65 pound son easily. SO, our therapist recommended that we make his blanket a pound heavier than normal (typically 10% of body weight + 1 pound for blankets). This is the BEST thing to settle him down. We also use the blanket when we are going to talk about Ethiopia during therapy, it settles him and he puts the blanket over everything but his head.

Sounds interesting and hopeful to me. Does anybody else have experience with weighted blankets?  I would love to hear from you.

~Lisa

I finally got a bin, put rice in it, and added a few toys.  The boys love it!  An old red bedspread tossed on the floor works well to define the space for play and catch the rice that inevitably spills out.  The bin is large enough for two boys to play at a time.  They dig in it, pour the rice into cups, and shove it around with their hands.   I had to make rules such as, “Only hands in the bin,” when they squeezed into it and sat down; the rice got in their clothes and made a big mess.

My friend, Jillian, wrote a great post yesterday featuring photos of her son in his Lycra Spacial Body Bag.  The pictures will make you smile – I can almost guarantee it. You can see it yourself at Rooted in Love.

Like Eby, her son is a “sensory seeker” who likes deep pressure. His school recommended this Bag as a calming tool…

My Eby is a Sensory Seeker.  He can’t get enough of jumping on the trampoline, banging on surfaces, or making excessive noise.  When he watches a movie, he laughs loudly, calls out to the characters, and makes lots of comments.  He lives life at a higher level of excitement than most of us.

Dr. Miller, author of Sensational Kids, compares this intense craving for sensation…

I have a little tip that has been very helpful with Eby.  He has extreme reactions to disappointments, mild injuries, correction, etc.  Deborah taught us to use our hands