I doubt it would surprise anybody who knows me that Hermione Granger is the character with whom I most relate. I was even a bit jealous when she got to take extra classes in The Prisoner of Azkaban, because I would have done that when I was back in school. (And sort of did since in my junior year I took a 0-hour class--a period that ran before the official day began--followed by a full day of academic courses, ending with an independent study after school. Eight courses in a normally six-period day.)
I could use a Time-Turner right about now. Not for academic over-achievement, but for simple achievement.
I am officially back on the clock for my doctoral program. I have set up a work area, read some secondary literature, figured out a direction for some immediate writing. But the time I have set aside on paper has a tendency to shrink and disappear.
Part of it is spent multi-tasking. Pumping so that J. can have a bottle (that he won't drink) at daycare. Grabbing some lunch. Making coffee. And yes, checking in on Twitter and the like since I have no opportunity to do that until after I finish teaching.
Part of it gets eaten up by the pull of my other identities. I tutor a couple hours a week--math right now--in my role as public-school teacher and small-town resident. I've been doing daycare pick-up for J., something that takes about an hour total. On occasion, I time it so that I can get J. early enough to then pick up E.
I have been trying to figure out how to shift some of my work to the evening, after both boys are in bed. But J. still sleeps inconsistently. At bedtime, I never know how long I will have before I'm needed back in the bedroom. And it takes me a while to get settled back into my planned task, to get my head back into that realm.
I should have done a little work just now. There's a section of my paper that I can envision and for which I have the foundation laid. I just need to turn it into academic-speak with appropriate footnotes and formatting. I have some citations to throw in, marked out in my notes. I want to do this soon, as a follow up to my latest correspondence with my supervisor, as proof to us both that I can still do this.
I figure just a few turns and I could have those pages in no time. Those pages and a good nap too!
Monday, January 10, 2011
Sunday, January 02, 2011
Resolved, 2011
I'm not even going to look back at what I wrote last year. That would be one sure way to pop the optimism I've mustered for this new year.
As always, there are plenty of goals I have as we hand a new calendar on the wall. This year, it's not simply inspired by the Earth's turning. Instead, we have a few changes here--J. is starting daycare, my grad-school maternity leave is up--which are inspiring some new-leaf-turning.
My goals and their reasons:
Household:
As always, there are plenty of goals I have as we hand a new calendar on the wall. This year, it's not simply inspired by the Earth's turning. Instead, we have a few changes here--J. is starting daycare, my grad-school maternity leave is up--which are inspiring some new-leaf-turning.
My goals and their reasons:
Household:
- We will finish rearranging our house. We've been moving furniture and going through our things to create space for everybody. Currently J. and all of his stuff are in our bedroom. We're about halfway through effecting the following: J.'s stuff into the third bedroom (plus switch some of E.'s furniture to J. and move other things into his room), office furniture (and A.'s workspace) into back of living room, M.'s stuff into corner of sunroom, all toys into boys' bedrooms. After all that, I hope to get started on the garden.
- We will be more organized during the school week. Now that all of us will need to get out of the house in the morning, we absolutely must follow through on things like packing lunches the night before and picking out clothes. I'm also going to return to meal-planning so we don't waste time every night debating what we feel like making or eating.
- I will work on E.'s accepted foods. We know better than to think this will be easy or quick, but I have a few ideas for this and a few more resources to consult. The meal-planning and family dinners are part of this. I will put a little bit of all we're eating on E.'s plate, in addition to his usual chicken nuggets or grilled cheese sandwich, not forcing him to eat any of it, but sort of desensitizing him. We are also not above bribery.
- I'm getting back on track for my PhD. I will be taking as much advantage of J.'s time in daycare as I can to make sure I keep things rolling. I expect to finish my comps in May or June, although the actual date of my exams will depend somewhat on my committee.
- I will do my best to pick up another 1 or 2 sections of teaching for next year (i.e. the 2011-12 school year). This will get me over the magical number that makes me eligible for insurance through the school district here and help us pump up our savings, all of which will give us some breathing room (and help us prepare for the eventuality in which A. goes down to part-time or returns to contract work).
Friday, December 24, 2010
Santa Claus is coming to town
My parents didn't want me to believe in Santa Claus. So, of course, I did.
It's not even that they didn't do anything to reinforce the myth. They straight out told me that Santa didn't exist. I would argue with them. Magic explained it all. It didn't matter that I knew my parents bought the presents and filled the stockings. Somehow Santa was still a part of it all.
I think I needed that magic in my life. Still do, although it manifests now as my love of reading science fiction and fantasy.
The year that my parents had nearly convinced me of Santa's non-existence, I received a present with a "From: Santa" gift-tag. I waved that around as the very proof I had been lacking for so many years. Even though the gift wrap and handwriting matched the other gifts from a certain aunt.
I suspect that my parents' original decision, not to indulge a belief in Santa, came from my father and matched his decision to raise us knowing about both Christianity and Judaism without encouraging blind belief in either. It's something I never thought to ask my dad before he died, but I can imagine it as a topic we might have discussed over coffee when E. was a baby. (My mother is something of an "unreliable narrator," so conversations like this just don't happen very often for us.)
A. and I are letting E. believe in Santa. The story is everywhere anyway, and E. just loves the various Christmas movies and stories, fed by A.'s love of them and habit of playing them during the fall, starting with The Nightmare Before Christmas shortly before Halloween. After seeing The Polar Express a few years ago, he found a jingle bell in our house and carried it around with great reverence.
I can reconcile our encouragement of all this with our desire to raise E. to be a critical thinker thanks to an essay written by Dale McGowan. He's run it during a couple Christmas seasons and it appears in his book Parenting Beyond Belief. The short version is that Santa provides kids with an opportunity to reason through something that they are originally told just to believe.
E. is not ready to stop believing yet. He has accepted, without question, Santa's budgetary limits and deadlines for wishlists. He does not care to notice that the gift-tags are the same as on some of our presents, that the handwriting is mine, that Santa uses different wrapping paper at our house and at his grandparents'. He does not dwell on the logisitics of Santa making it around the world in one night. All of it still just is.
And I'm happy for it to stay that way for just a bit longer.
It's not even that they didn't do anything to reinforce the myth. They straight out told me that Santa didn't exist. I would argue with them. Magic explained it all. It didn't matter that I knew my parents bought the presents and filled the stockings. Somehow Santa was still a part of it all.
I think I needed that magic in my life. Still do, although it manifests now as my love of reading science fiction and fantasy.
The year that my parents had nearly convinced me of Santa's non-existence, I received a present with a "From: Santa" gift-tag. I waved that around as the very proof I had been lacking for so many years. Even though the gift wrap and handwriting matched the other gifts from a certain aunt.
I suspect that my parents' original decision, not to indulge a belief in Santa, came from my father and matched his decision to raise us knowing about both Christianity and Judaism without encouraging blind belief in either. It's something I never thought to ask my dad before he died, but I can imagine it as a topic we might have discussed over coffee when E. was a baby. (My mother is something of an "unreliable narrator," so conversations like this just don't happen very often for us.)
A. and I are letting E. believe in Santa. The story is everywhere anyway, and E. just loves the various Christmas movies and stories, fed by A.'s love of them and habit of playing them during the fall, starting with The Nightmare Before Christmas shortly before Halloween. After seeing The Polar Express a few years ago, he found a jingle bell in our house and carried it around with great reverence.
I can reconcile our encouragement of all this with our desire to raise E. to be a critical thinker thanks to an essay written by Dale McGowan. He's run it during a couple Christmas seasons and it appears in his book Parenting Beyond Belief. The short version is that Santa provides kids with an opportunity to reason through something that they are originally told just to believe.
E. is not ready to stop believing yet. He has accepted, without question, Santa's budgetary limits and deadlines for wishlists. He does not care to notice that the gift-tags are the same as on some of our presents, that the handwriting is mine, that Santa uses different wrapping paper at our house and at his grandparents'. He does not dwell on the logisitics of Santa making it around the world in one night. All of it still just is.
And I'm happy for it to stay that way for just a bit longer.
Monday, December 20, 2010
On sneezer and wheezer and cougher and...
Less than a week until Christmas. This holiday season has been more fraught than others, with E. on a bit of a trigger. It probably didn't help that we started out December with a rush of presents. E. has two advent calendars this year: a Lego one, which has become something of a tradition, and the more common chocolate calendar, courtesy of his grandma. On top of that, Hanukkah began December 1st, so there were gifts associated with that. The tears began immediately when he had some trouble putting together the Lego Star Wars set on that very first night.
Finally, we realized that he's probably been fighting illness since Thanksgiving. None of us has been at our best since he came down with some 24-hour bug the night before Thanksgiving. For the past two weeks, I've had a particularly bad sore throat. Through several doctors' visits, at least one for each of us, we've determined the following: our household is suffering from a combination of strep throat, stomach flu, and a virus (or 3). E. stayed home from school on Thursday and Friday, extending his winter break by a couple days, but he's still coughing up a storm. We should have realized, even before the sore throat and coughing began, that he was not feeling well, as an inexplicable increase in meltdowns is almost always a sign he's ill. We'd attributed it to the holiday season, but it's been even more intense than usual.
After two days of antibiotics, I'm starting to feel functional again. For the virus E. has, it's likely to take another 3-5 days for recovery. Just in time for the Christmas festivities. I sure hope that works out since I'd rather avoid continuous Lego meltdown next Saturday.
Finally, we realized that he's probably been fighting illness since Thanksgiving. None of us has been at our best since he came down with some 24-hour bug the night before Thanksgiving. For the past two weeks, I've had a particularly bad sore throat. Through several doctors' visits, at least one for each of us, we've determined the following: our household is suffering from a combination of strep throat, stomach flu, and a virus (or 3). E. stayed home from school on Thursday and Friday, extending his winter break by a couple days, but he's still coughing up a storm. We should have realized, even before the sore throat and coughing began, that he was not feeling well, as an inexplicable increase in meltdowns is almost always a sign he's ill. We'd attributed it to the holiday season, but it's been even more intense than usual.
After two days of antibiotics, I'm starting to feel functional again. For the virus E. has, it's likely to take another 3-5 days for recovery. Just in time for the Christmas festivities. I sure hope that works out since I'd rather avoid continuous Lego meltdown next Saturday.
Wednesday, December 08, 2010
Can I get that in writing?
Back when E. was in kindergarten, A. and I borrowed a DVD from the school district's autism team (not an unusual act). Three hours of Tony Attwood discussing Asperger's. Both of us found it riveting. And one thing I definitely have to give him is that it's possible to listen to him talk about the challenges posed and the work that needs to go into supporting Aspies and still come away feeling optimistic. He clearly appreciates Aspies' strengths and quirks and is one of the few NTs I've come across who really seems to get it.
A. has read even more of Attwood's work than I have at this point, and getting to hear him talk in person was a definite highlight of the conference we attended this summer.
As I mentioned before, J. was with us for the conference. A. and I had our spots on the far aisle, just a few tables in from the door. When he would fuss beyond being hungry, I would take him just out of the auditorium, catching as much as I could from the chairs on the other side of the door. I had both the stroller and sling, so we walked a lot too.
At one of the breaks, I was back in the auditorium with A. Attwood was striding out, trying, I'm sure, to get a few minutes downtime before continuing his presentation. But when he saw us off to the side passing J. back and forth between us, he came over and expressed his surprise to see the baby. He'd had no idea there was one in the crowd. I explained that we'd been in and out, depending on J.'s mood (and felt better knowing that he had not been disruptive). Attwood bent down a little and looked J. in the eyes for a few seconds, taking his measure, smiling, engaging him. He looked back at us and pronounced, "He's just fine. No autism here."
Now I get that this is not a formal evaluation and that we will have no recourse should we find ourselves with a diagnosis down the line, but really Attwood was giving weight to an opinion A. and I have already expressed: J. is neurotypical.
Some of our reasons are subtle and hard to pin down. It's been seven years since E. was this age, so the memories are not fresh. Yet while we did not have concerns at this point in E.'s life, we were able to recognize some of the earlier signs once we began reading about Asperger's.
It's not that E. did not make eye contact, but it wasn't his focus. J., on the other hand, craves our attention and draws it out of us by catching our eye. Whereas E. could spend a long time studying geometric patterns, J. will only look at them as long as there's no face or other interactive opportunity available.
There's a huge difference in how our two boys play(ed) at this age. E. has always loved toys with wheels. We would later find out that staring at spinning wheels is a common trait of kids on the spectrum. J. enjoys his buses, but generally propels them along so that he can pursue. He varies how he plays with his toys and explores them with all of his senses. Everything goes into his mouth or is used to bang into something else. We joke that his use of toys as tools illustrates the human link with the apes.
The differences extend to all of J.'s interactions with the world, his movement, his interests, the way he eats. I know that this is not a "Get out of jail free" card and that we have a high chance of some sensory issue and/or other quirks, but it's clear to us that J. is on a far different trajectory than E. ever was. It's not necessarily better--I have moments of wondering, "What am I going to do with an NT?"--just new ground.
A. has read even more of Attwood's work than I have at this point, and getting to hear him talk in person was a definite highlight of the conference we attended this summer.
As I mentioned before, J. was with us for the conference. A. and I had our spots on the far aisle, just a few tables in from the door. When he would fuss beyond being hungry, I would take him just out of the auditorium, catching as much as I could from the chairs on the other side of the door. I had both the stroller and sling, so we walked a lot too.
At one of the breaks, I was back in the auditorium with A. Attwood was striding out, trying, I'm sure, to get a few minutes downtime before continuing his presentation. But when he saw us off to the side passing J. back and forth between us, he came over and expressed his surprise to see the baby. He'd had no idea there was one in the crowd. I explained that we'd been in and out, depending on J.'s mood (and felt better knowing that he had not been disruptive). Attwood bent down a little and looked J. in the eyes for a few seconds, taking his measure, smiling, engaging him. He looked back at us and pronounced, "He's just fine. No autism here."
Now I get that this is not a formal evaluation and that we will have no recourse should we find ourselves with a diagnosis down the line, but really Attwood was giving weight to an opinion A. and I have already expressed: J. is neurotypical.
Some of our reasons are subtle and hard to pin down. It's been seven years since E. was this age, so the memories are not fresh. Yet while we did not have concerns at this point in E.'s life, we were able to recognize some of the earlier signs once we began reading about Asperger's.
It's not that E. did not make eye contact, but it wasn't his focus. J., on the other hand, craves our attention and draws it out of us by catching our eye. Whereas E. could spend a long time studying geometric patterns, J. will only look at them as long as there's no face or other interactive opportunity available.
There's a huge difference in how our two boys play(ed) at this age. E. has always loved toys with wheels. We would later find out that staring at spinning wheels is a common trait of kids on the spectrum. J. enjoys his buses, but generally propels them along so that he can pursue. He varies how he plays with his toys and explores them with all of his senses. Everything goes into his mouth or is used to bang into something else. We joke that his use of toys as tools illustrates the human link with the apes.
The differences extend to all of J.'s interactions with the world, his movement, his interests, the way he eats. I know that this is not a "Get out of jail free" card and that we have a high chance of some sensory issue and/or other quirks, but it's clear to us that J. is on a far different trajectory than E. ever was. It's not necessarily better--I have moments of wondering, "What am I going to do with an NT?"--just new ground.
Monday, November 08, 2010
What I did on summer vacation
In the middle of a week during the summer, A. and I dropped E. and Z. at the grandparents' and headed one state over to an autism conference. J. came along with us, mostly because he had no choice.
For two days, we had a chance to listen to some amazing experts in the field of autism. This was for us, in many ways, our music festival stocked with revered celebrities. We had watched and/or read presentations by all of the speakers who would be there, but we wanted to see them in person anyway. Going into the event, we were both excited for the day with Tony Attwood and Temple Grandin.
Since J. was with us, I spent a large part of several sessions outside of the auditorium. Whenever he started fussing, I headed to the door. If he wasn't too worked up, I discovered that I could still hear the presenter while sitting in the chairs just outside the doors. When that would fail, we would walk around the hotel lobby. We got to know some of the vendors pretty well. A. took him for one session each day, so I had some uninterrupted time. And we also received a booklet with many of the slides from the presentations, so I was able to fill in the gaps.
We purchased a few books and a kit, although we haven't done nearly as much with them as I would like. (Everything's getting pushed to another time. Lots of "once the baby's sleeping better." Which still hasn't happened.) But we walked away with a lot of good material and high spirits.
A. and I also got to eat out a couple times and stroll around a shopping center (with the all-important stop at the Lego Store). Sure we had J. with us, but he was mostly content to hang out with us.
I had three interactions with presenters which made the whole trip worthwhile. Each one deserves its own post; I hope to give them space in the next week or two.
For two days, we had a chance to listen to some amazing experts in the field of autism. This was for us, in many ways, our music festival stocked with revered celebrities. We had watched and/or read presentations by all of the speakers who would be there, but we wanted to see them in person anyway. Going into the event, we were both excited for the day with Tony Attwood and Temple Grandin.
Since J. was with us, I spent a large part of several sessions outside of the auditorium. Whenever he started fussing, I headed to the door. If he wasn't too worked up, I discovered that I could still hear the presenter while sitting in the chairs just outside the doors. When that would fail, we would walk around the hotel lobby. We got to know some of the vendors pretty well. A. took him for one session each day, so I had some uninterrupted time. And we also received a booklet with many of the slides from the presentations, so I was able to fill in the gaps.
We purchased a few books and a kit, although we haven't done nearly as much with them as I would like. (Everything's getting pushed to another time. Lots of "once the baby's sleeping better." Which still hasn't happened.) But we walked away with a lot of good material and high spirits.
A. and I also got to eat out a couple times and stroll around a shopping center (with the all-important stop at the Lego Store). Sure we had J. with us, but he was mostly content to hang out with us.
I had three interactions with presenters which made the whole trip worthwhile. Each one deserves its own post; I hope to give them space in the next week or two.
Monday, November 01, 2010
This Aspie speaks
I'd sort of seen some talk about today's Communication Shutdown, which encourages people to stay off of Facebook, Twitter, and social networking in general in support of autism. With J. not sleeping and a build up on my "to do" list--plus my mind had registered that this was all taking place "next month"--I hadn't really paid it any attention. But now it's next month and my Twitter is awash in #ASDay and #AutismShoutOut hash tags.
As it turns out, much has already been said of what I'm thinking, but I'll add my thoughts anyway.
The idea behind not using social media for a day is to experience the frustration of a social disconnect. Yet this is almost backwards, as many people with autism have found that social media provide them with ways to connect much more successfully than in real life. I prefer email and internet research to phone calls. Facebook is how I keep in touch with many family members and friends. I was late to join Twitter, but mostly because I have always known that it would suck me in too much (I'm trying very hard to balance that, and working has helped limit my time). Online conversations play to my strengths and smooth over some of the weaknesses. I get more time to process what has been said and think through my response. My correspondent's words are available to read and re-read; I don't have to rely on a memory that's being bombarded with lots of simultaneous pieces of information.
The flip side is that Asperger's has not led to anything resembling silence for me. I am frequently a chatterbug in real life. In fact, I had to learn to be quiet and really listen and comprehend what's being said to me. My experience of real-time conversations is probably different from most of yours, but I didn't know that for the longest time and have never known a different experience. I didn't think to feel this set me apart until I was told that it did.
Slight aside: It irks me to be told that Aspies can't multitask. The truth is that we are champion multitaskers; we just fill up our queues with items that might be considered a single task, or no task at all, by others. When I'm talking to a person, I'm consciously processing what I hear, actively filtering out other noises, judging facial expressions and their relevance, scanning my databases for appropriate responses or anecdotes, weighing the quantity and quality of eye contact, and monitoring my own expressions and body language. When I'm tired, I know that there will be a decrease in my comprehension, a lag in putting on appropriate appearances, and markedly less eye contact.
But really, that starts to get at my main issue with things like this Communication Shutdown. So much of the conversation about autism is a description from the outside. And I can't tell you how many times I've read an article about autism or Asperger's where the outside perspective is presented as fact and I find myself frustrated since it falls so far from my experience or clearly misunderstands. I spent a long time convinced I couldn't have Asperger's because of these descriptions, because I am extremely sensitive and empathetic, because eye contact is difficult for me due to the overwhelming flood of information it provides. It was only through the process of E.'s diagnosis, the 3 1/2 years leading up to it with us knowing this is what we were dealing with, and the persistent research both A. and I undertook that I was able to realize that there is a disconnect between a large part of the literature and the actual experience.
And I guess that's why I've shifted my focus here. I want to correct some of those descriptions that share so little with my reality and give you a peek of the view from this side.
I can't do that if I shutdown communications. Likewise, you can't hear me if you turn off your social media.
As it turns out, much has already been said of what I'm thinking, but I'll add my thoughts anyway.
The idea behind not using social media for a day is to experience the frustration of a social disconnect. Yet this is almost backwards, as many people with autism have found that social media provide them with ways to connect much more successfully than in real life. I prefer email and internet research to phone calls. Facebook is how I keep in touch with many family members and friends. I was late to join Twitter, but mostly because I have always known that it would suck me in too much (I'm trying very hard to balance that, and working has helped limit my time). Online conversations play to my strengths and smooth over some of the weaknesses. I get more time to process what has been said and think through my response. My correspondent's words are available to read and re-read; I don't have to rely on a memory that's being bombarded with lots of simultaneous pieces of information.
The flip side is that Asperger's has not led to anything resembling silence for me. I am frequently a chatterbug in real life. In fact, I had to learn to be quiet and really listen and comprehend what's being said to me. My experience of real-time conversations is probably different from most of yours, but I didn't know that for the longest time and have never known a different experience. I didn't think to feel this set me apart until I was told that it did.
Slight aside: It irks me to be told that Aspies can't multitask. The truth is that we are champion multitaskers; we just fill up our queues with items that might be considered a single task, or no task at all, by others. When I'm talking to a person, I'm consciously processing what I hear, actively filtering out other noises, judging facial expressions and their relevance, scanning my databases for appropriate responses or anecdotes, weighing the quantity and quality of eye contact, and monitoring my own expressions and body language. When I'm tired, I know that there will be a decrease in my comprehension, a lag in putting on appropriate appearances, and markedly less eye contact.
But really, that starts to get at my main issue with things like this Communication Shutdown. So much of the conversation about autism is a description from the outside. And I can't tell you how many times I've read an article about autism or Asperger's where the outside perspective is presented as fact and I find myself frustrated since it falls so far from my experience or clearly misunderstands. I spent a long time convinced I couldn't have Asperger's because of these descriptions, because I am extremely sensitive and empathetic, because eye contact is difficult for me due to the overwhelming flood of information it provides. It was only through the process of E.'s diagnosis, the 3 1/2 years leading up to it with us knowing this is what we were dealing with, and the persistent research both A. and I undertook that I was able to realize that there is a disconnect between a large part of the literature and the actual experience.
And I guess that's why I've shifted my focus here. I want to correct some of those descriptions that share so little with my reality and give you a peek of the view from this side.
I can't do that if I shutdown communications. Likewise, you can't hear me if you turn off your social media.
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