I made it down to the heel flap on Patriotic Betsy Sock #1 and was a few inches down the leg of sock #2 when I put my knitting down this morning and came downstairs to check the computer. About 30 minutes later, I hear my husband ask S “S what are you doing with mommy’s knitting? Did you unravel that?”
*sigh*
I ran upstairs to a pile of unraveled yarn and my dpns scattered around the living room floor. :( It had to happen sometime – I think it does to everyone who knits with small kids in the house. At least it wasn’t the other sock that is about 7″ long….
I’ve also been working on cotton dishcloths that I’m planning on putting up in my etsy store once I crochet up a big enough selection to be interesting to anyone. Here is one of the patterns I’ve been playing with that I really like:

After swearing off kit-of-the-month clubs in scrapbooking, I found myself lured into theknitter.com’s sock of the month club. There is something so seductive about yarn and a pattern carefully selected by a sock expert showing up at my door every month for such a reasonable price!
I’ve got April and May’s kits waiting for me, but when I opened June’s kit last week, I couldn’t wait to get started, even though it meant going out of order. They are a wonderfully fun zig zaggy lace pattern with the cutest striped sock yarn by Regia. Here is one of them a couple of days into the process:

These are definitely going to take a bit longer than the toe-up socks, because I’m back down to 2.5mm needles. I’m enjoying the pattern, however. Happy knitting!
We have a unique situation with S that I thought I’d write about because so far I have yet to run across other families with autism that report this same issue.
S has had a high threshold for pain since birth. The normal bumps, bruises and falls of childhood that would send other kids howling rarely illicit much of a reaction. I think that it takes a higher level intensity for most kinds of stimulation, including taste for him. Unlike many kids on the autism spectrum who like bland foods, S craves things like vinegar (loves salt and vinegar chips) and hot sauce of all varieties. He loves hard boiled eggs, but they need to have a coating of tabasco. When we go for chicken, he prefers it shredded and then dips it into whatever hot sauce is on the table.
Lately, when he is bored, he appears to be using Tabasco as a way to self stim. We have a bottle sitting out on our kitchen table along with the salt, pepper, and napkins. He will sit there with a cup of lemon water (his favorite drink is water with a hefty dose of plain lemon juice in it – no sugar, just lemon) and place a dollop of Tabasco on his hand, lick it off, wait a couple of seconds (until the burn sets in, I’m guessing), and then take a swig of water and repeat the whole process. He will sit there and do this for 30 minutes at a time and become very upset if you take the Tabasco away (I’ve hidden it in our locked pantry for now).
I’d be interested to hear from any other parents of kids on the spectrum if you see this type of behavior in your kids: this seeking stimulation through strong flavors and/or using them as self-stimming behaviors. So, please, if you see this, I’d love it if you would share.
E’s bus will pull up any minute now and we’ll go to meet S’s bus in 45 minutes. Even though I ran to Starbucks, Office Depot, Target, Costco and to the school office (to drop off my check for next year’s school supply packs through the PTA) in the two hours that the kids were gone this morning, I’m still not ready for school to be out for the summer.
E’s going through a phase where it is nearly impossible to take him out shopping without a meltdown, so we’re going to spend a lot of time at home this summer and I’ll go shopping at night after the kids go to sleep. I did buy a number of age-appropriate workbooks for the boys to work on at Office Depot – hopefully that will help alleviate the boredom.
Thank heavens we can start swimming again in another 2 weeks after E’s clavicle heals some more!