Brainstorming 101: Fixing the Garage Door

After Sam finished fixing problems that came with the Lion upgrade, he suggested that we tackle the garage door. We have an automatic door opener that works when it wants to.

And it doesn’t want to very often.

It’s been a great chance to brainstorm solutions. We’ve watched videos on YouTube. We’ve called Uncle Matt. We’ve taken turns trying things and watching the trouble spots to come up with ideas.

And because it’s primarily a mechanical system, it seems that each thing we try brings a small reward, whether it’s knocking down wasp nests to remove a blocked pathway or lubricating parts to lessen the drag on the motor. Each step brings progress.

Sam has decided that we still have some kind of electrical problem, though. He says because we have to hold the button down for it to open there must be some kind of wear in the wires. I told him I’d like to replace the sensors — they look like they’ve just about had the life kicked out of them, they’ve been bumped and bustled so much — and he’s agreed.

And if that doesn’t do the trick, he’s going after the wiring.

Reading Assignment

Before my writing partner, Shahla Alai-Rosales, headed out of town for a few weeks, she left me with a reading assignment. (Once a professor, always a professor, she gave me more than I think I can consume in the time period allotted.)

We are looking for books that could be competition or complementary to the book we are planning to propose to a few specialty publishers — a book about decision-making for parents and caregivers.

For those of us loving and supporting someone with a disability, those decisions can feel pretty high stakes sometimes. Our kids aren’t as resilient if those decisions end up being mistakes. Most of us expect to have some role throughout our child’s life in that decision-making, but it’s easy to get in the habit of doing more than you should.

(Brief digression: Some years ago, my husband wanted me to take over driving while he tended to some other task in the truck. For some reason, he kept barking out directions and reminders to me — something he did not normally do. I drove past the on-ramp to the freeway and he asked me why on earth did I miss that. I told him that for the past several minutes he had bossed me around so much he just took my brain away. I wish I could say we laughed then, but I can’t, and that is the end of this digression, since I hope my point has been made.)

One of the books is by the Turnbulls, et al., from the University of Kansas. Heavy hitters in the world of disability studies and powerful voices when it comes to parenting and advocating. It’s title “Disability and the family: a guide to decisions for adulthood.” (1990: Paul H. Brookes Publishing)

The layout looked like other books I had to consume in grad school (unbearably dense), but it belied it’s content. It’s readable and full of terrific information.

It didn’t take long for me to get hung up on a page that spelled out the steps of a decision-making process. And they are:

Defining the problem or need
Brainstorming
Evaluating and choosing alternatives
Communicating the decision to others
Taking action
Evaluating the outcome of the action

It’s pretty easy for me to imagine Sam being able to define a problem or need in many situations. But there are scores of situations where brainstorming and evaluating alternatives would vex him.

For example, Sam wants to move into an apartment. But we have done some computer searches and I can tell he has no idea how to find a place that’s safe, appropriate and economical.

My first apartment choice was an unqualified disaster. My roommate moved in three months earlier than me, enough time to set up patterns for her cats to urinate on the carpet (the odor made your eyes water) and to leave dirty dishes long enough that the roaches swarmed as soon as the lights were turned out.

I complained. She made some changes, but ultimately I couldn’t get out of there fast enough.

The next place wasn’t much better. A firetrap on the second floor, with a neighbor who cooked on his hibachi at the top of the stairs every evening.

The next place after that was a house I shared with two other girls. It was a lot better, but not without its inequities. I allowed them in order to get along.

It helps to know what to think about. He’ll need more help than the admonition I could get away with making to my other kids, “don’t make the mistakes I made.”

Out Like a Lion

Sam got sidetracked with his plans to write an app for iPhone that restores some contact-sorting features he used to have on his Nokia.

Sam works on an old Dell a dear friend gave us, so any app work is going to happen on my Mac. He started amassing the resources he needed and then came to me to say the final step was this: we need to upgrade to Lion OS.

I consented to this upgrade without asking probing questions — completely, utterly stupid on my part.

Ever since I got my first Mac in 1988 and we made the leap to System 7, I’ve known it’s never simple. System upgrades are like taking off down the autobahn without tying down a bunch of your stuff in the back of the pick-up.

(My mind is in funny loop just now, imagining pick-up trucks on the autobahn racing past Benzes and Beemers.)

What flew out of the Wolfe family pick-up, you ask?

All my financial records (yes, Intuit let the weenies rule over Quicken). Sam’s amazing fixes for our family computer network — including a peripheral switch for our printer and our portable back-up drive. The entire Microsoft Office suite.

I sooooo knew better.

Major backtracking today.

But I’m proud of Sam. He downloaded Open Office. That’s fixed. And knowing Sam, we’ll be true contributors to the community.

Then, we pulled the Quicken data off portable back-up and he’s going to use Paige’s laptop to help me convert to iBank. That should be fixed tomorrow.

Right now, he’s writing the manufacturers of that peripheral equipment and asking for patches.

See Sam Go.

Anesthesia and the Incredible Likeness of Your Being

I just brought Paige home from the dentist where she had all four of her wisdom teeth extracted. I’ve been through this enough — with Mark and the boys and myself — to know what to expect.

Paige, always thinking, rarely speaking, has yet to say a word, but we’re communicating. That includes her throwing a hand signal to make sure I didn’t forget about the construction detour on the way home. (I almost did.)

Michael, always questioning, came out of anesthesia with a 10-second loop of memory. He looked at me and asked, “Is it over? That wasn’t too bad. How do I look?” Before I could answer the second question, he came again. “Is it over? That wasn’t too bad. How do I look?” I squeezed his arm and tried to get to that second question again when he looked up at me the same way for the third time. “Is it over? That wasn’t too bad. How do I look?”

The nurse said, “That’s pretty common. He’ll get his memory back.”

Mark had a tougher time of it. Like most of his life, everything came with complications. When I’ve been under, all I do is sleep and puke. I have to purge before I can get on with my life. But when I do, it’s a brand new day.

Sam becomes his essential self, too. When he wakes up from anesthesia, his big brown eyes turn into holes of the universe, just like when he was a baby, and if you let yourself fall in, it’s love and terror all in one.

Expert Consultation Coming

I hope.

The ARC sent me a link to a website that is supposed provide self-help for adults with autism in the work force, called JobTIPS.

I asked Sam to take a look at it. Some of the pages are about interacting with the supervisor and how to keep a job, so it applies.

I think it looks good and the information is helpful, and clearly presented.

He said he’d take a look at it this weekend and let me know what he thought — I’m hoping to blog it.

Stay tuned.