Sometimes I don't know what to do with this blog. I started it because I read my Grandmother's journals and it gave me a whole new understanding of her. I wanted to leave something like that for my family. Also? My mother and I have issues with memory. We can forget the things that did happen and remember things that didn't. It's a gift. I try to leave written accounts of things so that I have a record of the life I actually lived, as opposed to the fun house mirror version I remember. Lastly, I have found that reading about other people's lives on the internet comforts me. I feel less singular. Most of my day is spent without the company of other adults, so this is not trivial. Writing in my blog is my way of paying it back. Maybe some other mother sees herself mirrored here and finds her way to having some compassion for herself. I hope so.
The problem I find myself having is that I don't blog as much of my daily living as I'd like, because I've wanted this to be a blog I wouldn't have to be ashamed of my family finding. I don't want them to stumble across this, recognize my life, then be hurt by the things I've said. I have a lot to say, however, and I don't see how I can serve the purpose of this blog by not saying them. This is the problem inherent in putting your diary on the internet, and I haven't solved it yet. Ideas and suggestions from the peanut gallery are most welcome:)
So.
Anyway.
In the interest of having this blog adhere to its purpose, I will fill you in on what's been up this winter. I've been sick. I get these spells where my legs don't work too good, I'm tingly in spots and unbelievably tired. It comes and goes, now and then. Right now my Doctor says that since my lab results are normal it must be in my head, and has written me up a script for SSRIs. I know they won't work, because I've done this several times around. However, I do think he is a good Doctor, and I will try anything, because if it worked I would be very very glad. Also? Whatever it is isn't going to kill me. It's just life alteringly annoying. And another also? I want to be the willing patient so that he will work with me to figure this out. And the last also? I have been depressed this winter. Not the teenage kind of depression, where being alive=anguish. More of a middle-aged depression, where everything fucking annoys the piss out of me, it's all a bit too much, and really, why even bother anyway. So. SSRIs it is.
My Mom is in the states for a while and is staying with my Aunt. My mom is attempting to finish my Aunt's basement. Mom has the time to do this, and no one else does. It is good for all concerned. Auntie M saved up some time off and they came out here for a visit, also good for all concerned. They got to stay for a week and play with babies. The first day they were here they played with the Bean so much she pooped out and went to bed two hours early. Her favorite game was to get somebody, usually Auntie M, to walk around the house on a loop from the kitchen through the foyer through the living room through the dining room and back to the kitchen. If the Bug could be convinced to join, all the better. And for an extra special touch, all the girls would put on their snow boots and march and yell on their way around the circuit. This came to be known as the "Pink Boot Parade". Other options including singing various songs, counting steps and jumping on ten, and occasionally playing chase. By the time the visit was over, the Bean was finally saying "Four" after "three", instead of "nine", or perhaps "two" again.
My Mothers also bought me a cabinet and some table legs so I could put up a counter in my kitchen. The kitchen here is good sized, but strangely lacking in cabinetry. MyFarmer had given me a butcher block when she moved, and with the stuff they bought me we had all the parts necessary to remedy the situation.
It was interesting putting it all together. My woodworking skill set is weak. Simon's job entails many of the skills needed, and when he came home to find me working on the legs and things he let me know how he would have done things differently. I had spent all day working on the damn things, and was feeling pretty proud that I had managed to get them attached, seeing as how my past wood working projects had ended up in pieces or flames before I finished them. Simon was looking at the legs and feeling pretty certain they wouldn't hold up, although I still think he was doing the mental calculations based on whether what I'd done would keep an airplane together at 20000 feet.* I let Simon know that he had hurt my feelings, and he said sorry, and I believe there were some physical apologies all around. The next day I took the legs off and had another go. This time things went much better.** Even he was impressed. Then we proceeded to throw a new set of hissy fits at each other over getting the counter on the cabinets. It's deuced awkward to land a two ton counter and its holes smack onto the screws sticking up from the cabinet. And no, we couldn't just screw the screws up into the counter because it's made of maple and maple is HARD. In the end, Simon came up with the genius idea of using the kid's building blocks as shims, which we put under the legs and on top of the cabinet, which let us see what we were doing, and then we smacked the shims out and tada! We did it! The end result may not be aesthetically pleasing, but it is much better than the three legged card table I had been using. Srsly.
Let's see. What else. The Bean's birthday means that her therapies are going to be provided by the school district instead of the county. There was a round of testing, followed by the recommendation that she see a speech therapist 3 times a week, a physical therapist 2 times a week, and a special education teacher two hours a week. Currently she sees a speech therapist twice a week, and physical therapist once a month. Since her test scores were the same for the school district as they had been for the county, Simon and I are left wondering whether she hasn't needed more services all along. The therapists themselves are of differing opinions.
I think it's a matter of who typically receives services. The county usually sees kids who were born with a syndrome or illness that is so severe they don't have to be tested in order to get put into the system, or the Doctor decides that something is wrong and asks for an evaluation. Given that the Doctor usually spends 10 minutes with a kid, said kid has to be pretty off for the typical Doctor to notice. I suspect that there is a large group of kids who would qualify for services if they were tested, but they don't get tested because their parents either don't know enough about child development or don't know that services are available. The upshot of all this is that the county spends most of its time with very, very messed up kids. The school district, on the other hand, sees all the kids in the district once they start school. This means they see all the kids that slipped through the cracks and didn't get seen as toddlers. They end up providing services to many kids who have issues but mostly function. It's a matter of degree. The county's speech therapist is teaching kids to swallow, the school district's speech therapist is teaching kids to pronounce their "l"s. So when the county looks at the Bean they say "She's getting along fine", and the school district says "This girl needs a lot of catching up.". Of course, this is just my theory. She's getting more services now, so it doesn't matter why, I guess.
She's still being served by the county, but based on the school district's recommendations they're sending out a special ed teacher, upping her physical therapy to once a week and sending her to a play group with other special needs kids. For my part, I've signed her up for story time at the library and am getting together with a couple of moms who have 3/4 yos. Last week she went to story time on Weds, playgroup on Thurs, our friend's on Fri, and came down with a bad cold on Sat. Since then we've missed two therapy sessions, one playgroup and story time. Oh, and lots of sleep. Now the Bug is coming down with it, so more fun will be had by all, I'm sure.
On a happier note, the house is clean right now. It was clean yesterday too. Yay us! We're celebrating Simon's birthday tonight with a good dinner and presents, which will be fun. Yay again!
Suppose I better go get working on that, because I sure loves me some Simon.
I'll be back soon,
ephelba
*His day job is airplane mechanic. Since you can't pull an airplane over to the side of the sky, the mechanics are making things very tight and strong. Can't fault them for that.
**Can I hear it for JB Weld?
Saturday, February 07, 2009
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1 comment:
There's a lot I don't say, for the reasons you describe. And yet I'm pretty truthful. On the whole, respectful to friends' and family's feelings, I hope. Having told them (family, a couple of friends) about the blog quite early on makes me careful, but they also understand that I'll express myself as I wish to.
I wonder, in all your busy life, if you've ever had time to really get over the fact that the Bean has problems. It's a big thing, and usually we just get on and cope, especially when another baby comes along. But any setbacks with beloved and darling children take their toll and your body can let you down in an unexpected way. If your doctor is right and there isn't a physical reason, and you're both right and depression comes into it, how will masking that, without doing anything to recover from it, help?
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