Dear Staring Lady,
I was the woman sitting next to you in the fast food place that will remain unnamed, in the somewhat snooty suburb that will remain also unnamed. We were both with our husbands and one daughter. Your daughter was about three, a very cute and obviously bright little thing. My daughter was 13. She was the one you were staring at.
You know, you forced me to admit I've been lying, to myself and others. I have been saying that staring doesn't bother me any more, that I don't even notice it. But I guess what I really meant was some kinds of staring don't bother me. Little kids staring? No problem. The kind of staring that also includes a smile, a look that says "Your daughter is beautiful and interesting. I see she might also have some kind of disability. I'm pleased to see her, and kind of fascinated" That kind is okay too. But your kind of staring? Just plain old gaping, openly and for long, long moments? No, I'm not okay with that.
The thing is, we don't often eat in public. But we decided to try it, today. And we were thrilled at how well Janey did. She was wonderful. No screaming, no running around, no outbursts or tantrums. She was happy. She sat eating her food with joy. In line, before that, she was so happy she jumped a bit, but not in a way that would affect anyone else. As we told her over and over, we were very, very proud of her.
But you stared. You kept looking at us, and not with a nice look. It was a look that seemed to say "Why are weird kids allowed to be out here when I'm trying to have a meal with my perfect family?" Maybe that isn't what you were thinking. But you sure fooled me.
You know, I can judge too. I didn't stare, but I listened. I listened when your little girl got upset because you got her grilled nuggets, not ones with breading. She wasn't used to that. She said "These aren't nuggets! They are CHICKEN!" I thought that was pretty cute. But you insisted she eat them. She got upset. I was thinking "What's the big deal? Who cares? You have a daughter that can talk, that can express opinions. Enjoy that! Get her some regular nuggets if that's what she wants! Or at least say something to her to let her know you understand change can be tough. Don't you get that it's amazing, it's a small miracle, it's something to treasure, that you have a child who talks so easily?"
I could understand your staring a little more if Janey could possibly have been bothering you in any way. But she couldn't have been. She sat there and ate, much more nicely than your little girl. Okay, it was obvious we had to help her with a few things. It was obvious, probably, that she was developmentally not where most 13 year olds would be. But is that something that is so bizarre, so creepy, that you need to STARE ALL DURING OUR MEAL?
It's funny. The rudest people, the people most prone to staring, seem to be the ones that have lives that on the outside look enviable. We don't get stares much in the convenience store near our house, the one frequented by an eclectic mix of folks, few of them looking like your suburban ideals. In fact, there and in the stores in our section of the city, Janey gets mostly smiles, sometimes hugs, sometimes high fives. Or she gets no notice at all, which is fine too.
You could have smiled at us, even once. You could have talked to Janey. You could have glimpsed at her subtly, if you had to. You could have ignored her completely. You had a lot of options. But the one you chose sent a pretty powerful message.
As your child whined about her nuggets, Tony and I tried to ignore you and talk. Our conversation ambled to somehow talking about how in cartoons, if you get on a scale and you are very heavy, the pointer on the dial of the scale pops off and spins around in the air. I said something like "whoa-whoa-whoa-whoa", imitating a spin, and spun my hands around. Janey loved that. She started saying it too and spinning her hands---not loudly, but hilariously. We all had a good laugh. We enjoyed that moment a lot. I dare say, we enjoyed it a lot more than you were enjoying lecturing your three year old on healthy eating. I hope you never have a child like Janey. You might think that's a kind wish. It isn't. You'd be lucky to have a child as much fun, as fascinating, as beautiful and as special as Janey. Stare at that, lady.
Sincerely, A Proud Mother
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Showing posts with label staring. Show all posts
Showing posts with label staring. Show all posts
Saturday, March 24, 2018
Monday, March 27, 2017
Screaming, Shopping and Sleeping (or not)
On Saturday morning when Janey woke up, Tony was working on our state tax returns. Therefore, he wasn't available for the regular Saturday morning routine. We hadn't really been aware of how much Janey counted on that routine, but she let us know, that's for sure.
Usually, on Saturday morning, Tony makes Janey bacon. Then he has his coffee and she "steals" it---a game they've played for years. He says "I hope Janey doesn't steal my coffee!" and then sets it down, with a little black stirrer straw in it, and she does indeed grab it and steals it. Then he cries, a huge exaggerated cry. This goes on for a long time. We've had her her own coffee (hey, she's twelve, that's pretty late for an Italian to start on a lifelong coffee addiction), but she prefers the stealing method. She and Tony can make a full morning of coffee, bacon, and then cooking whatever else she asks for---"soup" (which is boiled greens), toast, home fries, whatever.
This Saturday, I tried to hold Janey off until Tony could finish. I wasn't even able to get started before the screaming started. I was determined to give Tony the time he needed---he was on a roll. It was a hellish hour or so. The screaming...wow. I write so often about Janey's screaming here, but unless you have heard it, I don't think anyone can quite picture it. It's truly ear-piercing. I do think both Tony and I have lost some of our hearing from it. And despite many, many different methods I've tried to reduce it, nothing works consistently. It's Janey way of saying that the situation is just plain unacceptable, and it really doesn't stop until the situation improves in her eyes. I finally got through the time by her taking an extended shower---she screamed right up to getting in and screamed as soon as she was out. Once Tony was done, they did their routine, and Janey was quite happy. It's times like that that result in us usually just doing what Janey needs done. We are all happier that way. But we can't always, always do that.
On Sunday afternoon, after a decent enough weekend when the screaming was past, we took Janey out shopping. That is something we almost never do, except for quick grocery shops. She has learned to do very well in the grocery store, as long as she knows she'll soon be eating the food she picks out. But this was a shop to A.C. Moore (a craft type store) and Five Below (a store where everything costs five dollars or below). We weren't shopping for any real reason---we just both had the urge to browse around. And lo and behold, it went quite well!
In the ACMoore, I walked around with Janey for a while so Tony could look around, and it was actually fun---not something I've never really found when shopping with Janey much. She was interested in a lot of things in the store---some decorative feathers, some plastic models of animals, a wooden heart, a letter "J" to decorate----quite a few things. I asked her a couple times if she wanted to buy things, but I don't think that's a concept she truly gets except in the grocery store. It makes her cheap to shop with! She sees the store as a museum of sorts---a place to look at and sometimes touch things, but not take them home.
While we walked around, I thought to myself "You know, I don't think people are staring like they usually do" So I started taking note, and yes, they still were staring. The thing is---I don't notice it much any more. That's a huge change. I used to be very bothered by staring, and now, I'm so used to it I don't even see it. I think that goes along with a general shift in our thinking about Janey. I'm comfortable enough with her just being who she is that I don't really much care most of the time if other people find her stare-worthy. If I do notice them, I think I often assume (without really thinking, just letting my mind wander about) that they are thinking she is cool, because that is how I am seeing her. Or I think "it's great she is educating them about the existence of people like her, autistic older kids and adults" (because she looks fairly close to an adult now) Whatever it is, I'm glad it happened. We all live in a world partly made up of our own perceptions, and I like living in the one that doesn't notice or mind the staring.
Janey wasn't too interested in the Five Below, but I bought a few things there, including some ChocoTreasures eggs. I love Kinder Eggs, chocolate eggs with toys inside, but they are illegal in the US, so I'm happy to have discovered there are similar eggs that are now legal. I bought a few, ad in the car on the way home I did something stupid---I opened one of them. It was stupid because Janey and chocolate, after noon, don't mix. She saw the chocolate right away and asked for it, and instead of saying no, I gave her a little, little piece---about the size of my thumbnail.
And then we re-learned a lesson we should have learned long ago----if Janey has chocolate after noon, she doesn't sleep. I think it's so hard for me to grasp because it just seems not to make sense. How could that little an amount of chocolate keep her up? I think it's especially dark chocolate, which this was. Usually, Janey is asleep by about seven. Last night, although she was cheery and happy and willing to stay in her bed, she didn't get to sleep until about 11:30. Which meant, of course, one of us had to be up too. Tony has to work in the morning, I don't, and it was also me who gave her the chocolate, so I did most of the duty. Janey watched her iPad and sang to herself and asked me for cheese and generally just did her thing while I lay next to her, fighting sleep until she finally drifted off.
In thinking about the weekend, a fairly normal weekend, I am struck by something. So much of how Janey does depends on what we do---whether we follow routines, whether we let starers bother us, whether we stick to rules we've made ourselves about chocolate. We are all happier if we make Janey's life predictable, relaxed and sleep-at-night promoting. It's a feedback loop---the more we can do that, the happier she is, and the easier it is to enjoy her and keep her happy. We can't always get it right, because we are human, and we aren't completely in control of all aspects of life, but we can do our best, and when we do that, instead of expecting Janey to be something she isn't, life with our girl is better for all of us.
This Saturday, I tried to hold Janey off until Tony could finish. I wasn't even able to get started before the screaming started. I was determined to give Tony the time he needed---he was on a roll. It was a hellish hour or so. The screaming...wow. I write so often about Janey's screaming here, but unless you have heard it, I don't think anyone can quite picture it. It's truly ear-piercing. I do think both Tony and I have lost some of our hearing from it. And despite many, many different methods I've tried to reduce it, nothing works consistently. It's Janey way of saying that the situation is just plain unacceptable, and it really doesn't stop until the situation improves in her eyes. I finally got through the time by her taking an extended shower---she screamed right up to getting in and screamed as soon as she was out. Once Tony was done, they did their routine, and Janey was quite happy. It's times like that that result in us usually just doing what Janey needs done. We are all happier that way. But we can't always, always do that.
On Sunday afternoon, after a decent enough weekend when the screaming was past, we took Janey out shopping. That is something we almost never do, except for quick grocery shops. She has learned to do very well in the grocery store, as long as she knows she'll soon be eating the food she picks out. But this was a shop to A.C. Moore (a craft type store) and Five Below (a store where everything costs five dollars or below). We weren't shopping for any real reason---we just both had the urge to browse around. And lo and behold, it went quite well!
In the ACMoore, I walked around with Janey for a while so Tony could look around, and it was actually fun---not something I've never really found when shopping with Janey much. She was interested in a lot of things in the store---some decorative feathers, some plastic models of animals, a wooden heart, a letter "J" to decorate----quite a few things. I asked her a couple times if she wanted to buy things, but I don't think that's a concept she truly gets except in the grocery store. It makes her cheap to shop with! She sees the store as a museum of sorts---a place to look at and sometimes touch things, but not take them home.
While we walked around, I thought to myself "You know, I don't think people are staring like they usually do" So I started taking note, and yes, they still were staring. The thing is---I don't notice it much any more. That's a huge change. I used to be very bothered by staring, and now, I'm so used to it I don't even see it. I think that goes along with a general shift in our thinking about Janey. I'm comfortable enough with her just being who she is that I don't really much care most of the time if other people find her stare-worthy. If I do notice them, I think I often assume (without really thinking, just letting my mind wander about) that they are thinking she is cool, because that is how I am seeing her. Or I think "it's great she is educating them about the existence of people like her, autistic older kids and adults" (because she looks fairly close to an adult now) Whatever it is, I'm glad it happened. We all live in a world partly made up of our own perceptions, and I like living in the one that doesn't notice or mind the staring.

And then we re-learned a lesson we should have learned long ago----if Janey has chocolate after noon, she doesn't sleep. I think it's so hard for me to grasp because it just seems not to make sense. How could that little an amount of chocolate keep her up? I think it's especially dark chocolate, which this was. Usually, Janey is asleep by about seven. Last night, although she was cheery and happy and willing to stay in her bed, she didn't get to sleep until about 11:30. Which meant, of course, one of us had to be up too. Tony has to work in the morning, I don't, and it was also me who gave her the chocolate, so I did most of the duty. Janey watched her iPad and sang to herself and asked me for cheese and generally just did her thing while I lay next to her, fighting sleep until she finally drifted off.
In thinking about the weekend, a fairly normal weekend, I am struck by something. So much of how Janey does depends on what we do---whether we follow routines, whether we let starers bother us, whether we stick to rules we've made ourselves about chocolate. We are all happier if we make Janey's life predictable, relaxed and sleep-at-night promoting. It's a feedback loop---the more we can do that, the happier she is, and the easier it is to enjoy her and keep her happy. We can't always get it right, because we are human, and we aren't completely in control of all aspects of life, but we can do our best, and when we do that, instead of expecting Janey to be something she isn't, life with our girl is better for all of us.
Labels:
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coffee,
Five Below,
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Kinder Eggs,
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showers,
sleep,
staring,
strangers staring,
taxes
Wednesday, November 16, 2016
Annual physical and a surprise sentence
Janey had her annual physical yesterday. She's had a fairly healthy year, so we hadn't seen her pediatrician since last January.
The tough part of the visit was the wait. We were in the waiting room for about 45 minutes. That's quite unusual, but I guess they were very busy. In the past, this would have been a recipe for extreme disaster. As it was, it was hard but not impossible. Several times, Tony took Janey for a little walk, staying near enough so I could call him right back if we were called. As the room cleared out, and we kept thinking surely we would be called any second, we stayed in the room and entertained Janey as best we could. It struck me that although part of what's different than the past is that Janey has matured, part of it is that Tony and I just do what we have to do now, without caring how it looks. For a long time, we sang and danced with her. I sang Christmas songs, quietly but not silently, and I didn't care if people stared. And people did stare---especially kids. I don't like the stares, but they don't stop me any more. I know Janey confuses kids sometimes. It's hard for them to figure her out. I less like the stares of the parents. I want to say to them "Have you never seen a child with disabilities before? Is is really that shocking to you? You know, she's a lot more interesting than your little snobby brats!" Not nice thoughts, but when you've been trying to hold it all together for as long as that wait seemed, you get nasty sometimes in your mind.
Once we got into a room, it was much easier. We really like our pediatrician a lot. I'm glad we made the change about a year ago. The pediatrician that saw the boys was right for them, but I don't think he ever felt comfortable with Janey. I am pretty sure he saw her as a tragedy. That is not the attitude I want in someone treating her. The new pediatrician seems to delight in her, while still understanding the challenges she presents. She listens well, and she talks directly to Janey. She did a good exam, and Janey looks healthy. At the end of the appointment, Janey got a flu shot, which we were not sure how she'd take, but she took it extremely well---not a single protest or scream. You never know with her. Hopefully, she won't get the flu this winter as she did last winter.
After the shot, as we were putting on Janey's coat, she said, plain as day, "Can we go home now?" Tony and I looked at each other in amazement. That might not seem like a remarkable sentence, but it's the type that is extremely rare with Janey. Her speech is rarely that direct. The usual thing she'd say in that situation would be "Want to take the big girl for a car ride?" or "Listen to music in the car?" or "Do you want salami?" or something else that means basically the same thing, but doesn't come out and say it. A sentence like the one we heard, direct and grammatical and appropriate and succinct, is very, very unusual for her. It was wonderful to hear.
As the years go by, we measure success with Janey on a scale that isn't the same as most parents might use. It's her own scale. We headed home feeling that we are indeed making progress. And by we, I do include Tony and me. We are making progress in being Janey's parents. And she is making progress in being herself. And that is a good feeling, something to be thankful for.
The tough part of the visit was the wait. We were in the waiting room for about 45 minutes. That's quite unusual, but I guess they were very busy. In the past, this would have been a recipe for extreme disaster. As it was, it was hard but not impossible. Several times, Tony took Janey for a little walk, staying near enough so I could call him right back if we were called. As the room cleared out, and we kept thinking surely we would be called any second, we stayed in the room and entertained Janey as best we could. It struck me that although part of what's different than the past is that Janey has matured, part of it is that Tony and I just do what we have to do now, without caring how it looks. For a long time, we sang and danced with her. I sang Christmas songs, quietly but not silently, and I didn't care if people stared. And people did stare---especially kids. I don't like the stares, but they don't stop me any more. I know Janey confuses kids sometimes. It's hard for them to figure her out. I less like the stares of the parents. I want to say to them "Have you never seen a child with disabilities before? Is is really that shocking to you? You know, she's a lot more interesting than your little snobby brats!" Not nice thoughts, but when you've been trying to hold it all together for as long as that wait seemed, you get nasty sometimes in your mind.

After the shot, as we were putting on Janey's coat, she said, plain as day, "Can we go home now?" Tony and I looked at each other in amazement. That might not seem like a remarkable sentence, but it's the type that is extremely rare with Janey. Her speech is rarely that direct. The usual thing she'd say in that situation would be "Want to take the big girl for a car ride?" or "Listen to music in the car?" or "Do you want salami?" or something else that means basically the same thing, but doesn't come out and say it. A sentence like the one we heard, direct and grammatical and appropriate and succinct, is very, very unusual for her. It was wonderful to hear.
As the years go by, we measure success with Janey on a scale that isn't the same as most parents might use. It's her own scale. We headed home feeling that we are indeed making progress. And by we, I do include Tony and me. We are making progress in being Janey's parents. And she is making progress in being herself. And that is a good feeling, something to be thankful for.
Labels:
autism,
Christmas music,
doctors,
flu,
other kids,
pediatrician,
physical,
sentences,
sickness,
staring,
surprises,
talking,
waiting room
Monday, January 25, 2016
Road Trip
This past weekend, we took Freddy back to college in Saratoga Springs, NY. We were going to make it a one night trip, but with the early week reports of the blizzard possibly hitting Boston, we added Friday night on. The blizzard didn't hit, but the two nights away made for a good little getaway.
Janey did extremely well with the trip overall. There were many great moments. She loves hotel rooms, and we stayed in two different ones (as it was too late to add a second night to the first one we booked). She literally danced around with joy at her first sight of each one. I've heard a few other parents of kids like Janey say that their kids love hotels, too. I'm not sure why. Part of it with Janey is that hotel rooms tend to have lots of mirrors, and she very much enjoys mirrors, but I think part of it is just having a new little pocket world to explore. She can go anywhere she wants within the room, and that gives her something new to explore on her own---something she doesn't get a lot of.

When we ate in public on the trip---one trip to Wendys and one to the hotel breakfast buffet, and when we went to the Target to get Freddy some last minute things, I realized something interesting. It doesn't bother me when Janey gets stared at anymore, not really at all. She was stared at plenty, but although I noticed it, I was able to pretty much ignore it. Or else I thought "Yeah, here's one of those kids with autism you hear so much about in the press, live and in person! Feast your eyes!" It was a bit of an in your face attitude I felt, and believe me, that is not an attitude that comes easily to me. But as Janey gets bigger, she stands out more and more, and unless we keep her out of sight at all times, she's going to be stared at. And...so be it. Especially in the Target, there were plenty of odd people that I think warranted more staring than Janey, but that's life.
I also noticed during the trip that we are better able than we used to be to set aside tough moments and remember times as positive. There were certainly screaming moments on the trip, times that Janey for no reason we could see just lost it and screamed and bit her arm, times that she was quite unhappy. But we know now that usually, unless something big is going on, these times pass if she's in a generally good mood. She said one of her longest sentences in a while when looking in the mirror---"I have one blue eye and one big eye" She actually has two blue eyes that look the same size to me, but it was a cool moment to hear her thoughts while looking at herself. She also did a lot of singing and dancing---always fun to watch.
As the years go by, I think we are learning to meet Janey in the middle. For someone with typical kids only, this trip might have seemed like not much fun. We did little outside the hotel rooms or the car. We drove around a lot, as Janey loves that. We did get out to dinner, just Tony and me, on Saturday night---thanks, big brother Fred! We dealt with a few meltdowns, but we also laughed a lot. Our lives with Janey are never going to be mainstream. She's going to be stared at, she's going to scream at times, we aren't going to be able to do typical getaway things. But we will also have the fun of watching her joy at little things, and the freedom, in a way, that comes from having a preteen that still gets a thrill out of being with her parents doing not much. We'll keep on going, and take our fun where we can get it.
When we ate in public on the trip---one trip to Wendys and one to the hotel breakfast buffet, and when we went to the Target to get Freddy some last minute things, I realized something interesting. It doesn't bother me when Janey gets stared at anymore, not really at all. She was stared at plenty, but although I noticed it, I was able to pretty much ignore it. Or else I thought "Yeah, here's one of those kids with autism you hear so much about in the press, live and in person! Feast your eyes!" It was a bit of an in your face attitude I felt, and believe me, that is not an attitude that comes easily to me. But as Janey gets bigger, she stands out more and more, and unless we keep her out of sight at all times, she's going to be stared at. And...so be it. Especially in the Target, there were plenty of odd people that I think warranted more staring than Janey, but that's life.
As the years go by, I think we are learning to meet Janey in the middle. For someone with typical kids only, this trip might have seemed like not much fun. We did little outside the hotel rooms or the car. We drove around a lot, as Janey loves that. We did get out to dinner, just Tony and me, on Saturday night---thanks, big brother Fred! We dealt with a few meltdowns, but we also laughed a lot. Our lives with Janey are never going to be mainstream. She's going to be stared at, she's going to scream at times, we aren't going to be able to do typical getaway things. But we will also have the fun of watching her joy at little things, and the freedom, in a way, that comes from having a preteen that still gets a thrill out of being with her parents doing not much. We'll keep on going, and take our fun where we can get it.
Tuesday, July 7, 2015
Mining for Positives
After I wrote that title, I pictured Minecraft, a game Freddy used to be into, and how you can mine and find gems. I pictured a gem called Positive, a sparkly and bright one, that is very hard to find, so you have to look hard for it, but it's also very useful to find. That is how it's been looking for positives with Janey the past few days.
We were so hopeful a few weeks ago. Janey was off all medication, and we really saw no change from when she was on it. She was smiling a lot, and recovering slowly from her surgery and hospitalization. But starting about a week ago, things went quite strongly downhill.
The screaming has been the toughest thing. Janey has always screamed off and on, but lately, it's a different kind of setup. Things will seem calm for a few minutes, then she will ask for something she wants. If I can't give it to her that very instant, she screams---a loud, piercing, hysterical scream. Then she bites her arm, badly. Then, sometimes, she tries to hit me, or anyone else who is around.
In looking for positives, I must say these episodes are pretty quick. They are super intense, but fast. They start too quickly for me to start giving positive reinforcement for not getting upset---sometimes she starts screaming as soon as she asks the question, if she knows the answer is no. And if the fits go on very long, it's been working lately to say "Can you try to calm down?" and just waiting. She does try, and she does calm down. For a few minutes. Until the next fit.
The screaming has essentially trapped us in the house. We can't take Janey anyplace at all. Tonight, Tony tried taking her to the grocery store, someplace he's taken her for many years. It was always a positive routine for the two of them. However, after they had picked out just a few items, Janey did her extreme screaming and arm biting. They had to leave. If you are thinking "Oh, lots of kids have tantrums in stores. You just have to wait them out!" then you have never seen Janey's screams. They are the screams of nightmares, and the arm biting is an added touch of horror. Every single eye in anyplace we are turns to us, and if we stay, it will only happen again a few minutes later.
Yesterday was one of the longest days I've ever had. Tony and both boys were at work. Janey was not happy. I would say she had a screaming episode about every 10 minutes, all day long. I tried everything. I tried reading to her, coloring with her, singing to her, giving her a shower, playing toys with her, sitting with her watching TV, cuddling her, listening to music with her---nothing pleased her. She wanted to "Go to Maryellen's house!" She loves Maryellen, but if we actually go there, she is happy for about 5 minutes. And then, when we leave, on the way home, she again says "Go to Maryellen's house!" It's just something to ask for. It's not really what she wants.
Janey hasn't been to school for a long time, since late May. That's probably one of her longest stretches in years without school. Summer school starts Monday. I am hopeful it will help, but not confident, really.
We started the medication again today. We didn't want to, but the intensity of Janey's unhappiness told us that what we wanted wasn't really the issue here.
It is getting harder and harder lately. I have to admit it. I sometimes truly feel scared, and I know I feel depressed. I do see a therapist, but I haven't been able to go since Janey got sick---there is no-one to watch her. However, although I certainly like having someone to talk to, it isn't going to change the situation any. I am more and more aware there is not any help but school. It doesn't exist, not for kids like Janey.
I will mine for positive at the end here. I cut Janey's hair out of desperation the other day, because after the long hospital stay it was quite tangled and she wasn't happy with brushing. I think it came out not badly for a completely non-professional haircut. Now a quick brush is all she needs. It's little tiny things like that that are all we can really do to make our lives easier. So here's a picture of Janey's new 'do!
Labels:
autism,
biting self,
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feeling trapped,
friends,
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minecraft,
negative thoughts,
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staring,
stores
Wednesday, March 25, 2015
A thankfully rare memory of rude people!
Janey's brother Freddy has been attending an after-school support group for siblings of children with special needs, run by a fellow student. I am so happy he's getting a chance to talk with other kids who truly understand what life is like for families like ours. The leader of the group asked him to write about a memory that stood out from his childhood involving Janey. He wrote about a time I remember vividly. Here's what he wrote...
Going out to public places has always been one of the most difficult things to do with my younger sister. When she was around 6 and I was 13, we went to a fast food place simply because my sister doesn't do well with long waits. My sister was just being herself, quoting the TV shows she likes, repeating nursery rhymes, and occasionally joyful outbursts. She wasn't bothering anyone, or so we thought. At the table next to us, there was a family of people from another part of the country with two children, a boy and a girl, under 10. I'll never forget the way they looked at my sister. They stared at her and exchanged whispers, as if she were some sort of alien. Instantly, I felt extreme hatred towards them. Jane is my sister, how dare they even look at her like that. Of course, they may have just never seen an autistic child before, and they were "interested" or something, but I couldn't take it. I had to get us out of there, because I couldn't take another minute of their stares. When we got into the car, my brother and mother felt the exact same way I did. We had just as much right to eat at that place as they did, and they were staring at us like our hair was on fire.
Don't get me wrong, this didn't stop us from eating out. Luckily, most people in Boston are quite tolerant of special needs children, but I have no tolerance for those who don't.
I remember so much about that awful meal. The family was talking loudly at first, before they noticed Janey, and we heard all about how they were vacationing here. Janey was being so good, I was thinking at the time. She was sitting nicely, eating, and talking away. We loved then and love now when she gets into one of her fairly rare talkative moods. As Freddy said, she was quoting all kinds of shows, singing a bit and perhaps now and then making a happy noise. The family suddenly got very quiet. They all started staring at Janey. This wasn't any subtle stare. It was an all-out stare, like, as Freddy said, they were watching an alien being. Then they started the whispering---taking a look at her, whispering to each other and then taking another long look.
What upset me most was that the adults (what looked like a mother and grandmother) were fully involved in this staring and whispering, just as much so if not more so than the kids. I remembering hoping against hope that the boys were not noticing what was going on. However, before we finished eating, they both asked to go. I was happy to. We gathered up our food and went to the car, Janey happily holding our hands. For once, I was very glad she was oblivious to all that was going on.
In the car, both boys burst out in anger. They were furious at the family. And I found myself completely unable to disagree.
What strikes me is how unusual this scene was. I've had people say something nasty to me about Janey maybe three times ever. I've had people notice her and look sad somehow. I've had people ignore her. But I don't really think I can ever, ever think of another incident of people staring and whispering. And that is good. Maybe Freddy is onto something. Maybe the greater Boston area is a good place to have a child like Janey. Bostonians are fairly tolerant. They are also generally not whisperers, I'd say! If they have something to say, they say it. Maybe this family felt it was more polite to stare and whisper than to smile at us, to let us know that they saw Janey was unusual and to talk to us about it.
I'm thinking in contrast of something that happened this weekend. Tony and I were at a Dunkin Donuts with Janey, and she ran away from us and went to a table where a man and woman were sitting. She reached for the woman's doughnut just as Tony grabbed her and stopped her. The woman gave us a big smile as Tony said he was sorry. She asked Janey her name, and Tony said Janey was autistic and wasn't much of a talker, and asked Janey to say her name, which she did. Later, when taking Janey to the bathroom, we passed them again, and they smiled and waved to Janey. That was a case where the people obviously realized Janey had special needs, but they acted in such a way that we left feeling happy and included. It takes so little to do that, and I must say, most people are great in that way.
Memory is funny. I am not sure why Freddy and I, and William too, so vividly remember that awful family. I wish memory saved instead the many, many times people have been kind to Janey, have delighted with us in her uniqueness. They are the people I want to have occupying my memory.
Going out to public places has always been one of the most difficult things to do with my younger sister. When she was around 6 and I was 13, we went to a fast food place simply because my sister doesn't do well with long waits. My sister was just being herself, quoting the TV shows she likes, repeating nursery rhymes, and occasionally joyful outbursts. She wasn't bothering anyone, or so we thought. At the table next to us, there was a family of people from another part of the country with two children, a boy and a girl, under 10. I'll never forget the way they looked at my sister. They stared at her and exchanged whispers, as if she were some sort of alien. Instantly, I felt extreme hatred towards them. Jane is my sister, how dare they even look at her like that. Of course, they may have just never seen an autistic child before, and they were "interested" or something, but I couldn't take it. I had to get us out of there, because I couldn't take another minute of their stares. When we got into the car, my brother and mother felt the exact same way I did. We had just as much right to eat at that place as they did, and they were staring at us like our hair was on fire.
Don't get me wrong, this didn't stop us from eating out. Luckily, most people in Boston are quite tolerant of special needs children, but I have no tolerance for those who don't.
I remember so much about that awful meal. The family was talking loudly at first, before they noticed Janey, and we heard all about how they were vacationing here. Janey was being so good, I was thinking at the time. She was sitting nicely, eating, and talking away. We loved then and love now when she gets into one of her fairly rare talkative moods. As Freddy said, she was quoting all kinds of shows, singing a bit and perhaps now and then making a happy noise. The family suddenly got very quiet. They all started staring at Janey. This wasn't any subtle stare. It was an all-out stare, like, as Freddy said, they were watching an alien being. Then they started the whispering---taking a look at her, whispering to each other and then taking another long look.
What upset me most was that the adults (what looked like a mother and grandmother) were fully involved in this staring and whispering, just as much so if not more so than the kids. I remembering hoping against hope that the boys were not noticing what was going on. However, before we finished eating, they both asked to go. I was happy to. We gathered up our food and went to the car, Janey happily holding our hands. For once, I was very glad she was oblivious to all that was going on.
In the car, both boys burst out in anger. They were furious at the family. And I found myself completely unable to disagree.
What strikes me is how unusual this scene was. I've had people say something nasty to me about Janey maybe three times ever. I've had people notice her and look sad somehow. I've had people ignore her. But I don't really think I can ever, ever think of another incident of people staring and whispering. And that is good. Maybe Freddy is onto something. Maybe the greater Boston area is a good place to have a child like Janey. Bostonians are fairly tolerant. They are also generally not whisperers, I'd say! If they have something to say, they say it. Maybe this family felt it was more polite to stare and whisper than to smile at us, to let us know that they saw Janey was unusual and to talk to us about it.
I'm thinking in contrast of something that happened this weekend. Tony and I were at a Dunkin Donuts with Janey, and she ran away from us and went to a table where a man and woman were sitting. She reached for the woman's doughnut just as Tony grabbed her and stopped her. The woman gave us a big smile as Tony said he was sorry. She asked Janey her name, and Tony said Janey was autistic and wasn't much of a talker, and asked Janey to say her name, which she did. Later, when taking Janey to the bathroom, we passed them again, and they smiled and waved to Janey. That was a case where the people obviously realized Janey had special needs, but they acted in such a way that we left feeling happy and included. It takes so little to do that, and I must say, most people are great in that way.
Memory is funny. I am not sure why Freddy and I, and William too, so vividly remember that awful family. I wish memory saved instead the many, many times people have been kind to Janey, have delighted with us in her uniqueness. They are the people I want to have occupying my memory.
Labels:
autism,
echolalia,
fast food,
kind people,
memories,
restaurants,
rude people,
school,
siblings,
singing,
staring,
whispering
Sunday, September 7, 2014
Yet Another Screaming Post
If you read this blog regularly, you might be thinking "She's writing about screaming AGAIN?" Well, yes, because right now, it's the very toughest issue we are facing. You might ask, "Why would screaming be tougher than all the other issues? She's got plenty to choose from--severe intellectual disability, lack of toilet training, self-injury, sleep issues..." Yeah, I do have a few. But none of them affect our life quite like the screaming.
I'll use yesterday as an example of how the screaming affects and limits Janey's life and our own. Janey was in rare form yesterday, with a huge amount of screaming. It started early, very early, like 5 am. We were awakened to screaming, not for the first time that night, of course, but this time we were up for good. We tried to figure it out, as we generally uselessly always do. She was wet, she was hungry, she hadn't had her medication yet. We run through the list, and it helps, or it doesn't. By around 8, we were totally burnt out. Imagine someone repeatedly screaming absolutely as loud as they can, at random intervals, and there being no reason we can possibly figure as to why. We resorted to ignoring. That is very hard to do, but it works as well as anything, not better, not worse.
Later in the day, Tony took Janey to the grocery store. That is something she usually enjoys, and for most of the trip, she did yesterday too. But near the end of the shopping, she suddenly screamed as loud as she possibly could, over and over. The store was pretty empty, but a man around 50 yards away started holding his ears---Tony felt not to be nasty, but just because it was truly hurting his ears. Tony braced himself for what we always fear will happen---someone calling the cops, as it would reasonably sound like she was being tortured. But no-one did. She screamed until she was sick of screaming, and then fairly happily checked out and came home in a good mood. Tony, however, was shaken and burnt out. It's harder and harder and harder to take Janey anyplace. The sudden screaming outbursts make it at the least not fun, at the worse, frightening.
After a while with Janey being happy, she decided to start the screaming up again. We were at that point exhausted and completely done for. I tried giving Janey a shower, which sometimes calms her, but she was having no part of it. I lay down with her, trying to calm her. Finally, in desperation, I started doing a silly game of clapping her feet together (which she loves) and singing "Clap, Clap, Janey feels like screaming (3 times for that line) But We Aren't Going to Scream!" It worked, for then. I have no illusion it will work ever again. I have so many times felt I've had a breakthrough with an idea about controlling the screaming, only to have it completely not work the next time I try it.
I spent a good potion of the night trying to figure out what might make her scream. I was too tired to think very effectively. All I came up with is that screaming makes something happen. It makes us upset. Even when we ignore it, that's something happening---us being unresponsive. If we are in public, it creates a scene. It hurries us out.
But what good does knowing that do? If ignoring doesn't work (and it's completely impossible to ignore her in public---WE might be able to, but those around us can't), if the events that cause the screaming seem random---what are we to do? We have no idea. None at all. In my dramatic moments, I have been thinking that the screaming is ruining our lives, and Janey's life. It's that bad. And I have nothing positive to end with here. Just a silent scream of my own.
I'll use yesterday as an example of how the screaming affects and limits Janey's life and our own. Janey was in rare form yesterday, with a huge amount of screaming. It started early, very early, like 5 am. We were awakened to screaming, not for the first time that night, of course, but this time we were up for good. We tried to figure it out, as we generally uselessly always do. She was wet, she was hungry, she hadn't had her medication yet. We run through the list, and it helps, or it doesn't. By around 8, we were totally burnt out. Imagine someone repeatedly screaming absolutely as loud as they can, at random intervals, and there being no reason we can possibly figure as to why. We resorted to ignoring. That is very hard to do, but it works as well as anything, not better, not worse.
Later in the day, Tony took Janey to the grocery store. That is something she usually enjoys, and for most of the trip, she did yesterday too. But near the end of the shopping, she suddenly screamed as loud as she possibly could, over and over. The store was pretty empty, but a man around 50 yards away started holding his ears---Tony felt not to be nasty, but just because it was truly hurting his ears. Tony braced himself for what we always fear will happen---someone calling the cops, as it would reasonably sound like she was being tortured. But no-one did. She screamed until she was sick of screaming, and then fairly happily checked out and came home in a good mood. Tony, however, was shaken and burnt out. It's harder and harder and harder to take Janey anyplace. The sudden screaming outbursts make it at the least not fun, at the worse, frightening.
After a while with Janey being happy, she decided to start the screaming up again. We were at that point exhausted and completely done for. I tried giving Janey a shower, which sometimes calms her, but she was having no part of it. I lay down with her, trying to calm her. Finally, in desperation, I started doing a silly game of clapping her feet together (which she loves) and singing "Clap, Clap, Janey feels like screaming (3 times for that line) But We Aren't Going to Scream!" It worked, for then. I have no illusion it will work ever again. I have so many times felt I've had a breakthrough with an idea about controlling the screaming, only to have it completely not work the next time I try it.
I spent a good potion of the night trying to figure out what might make her scream. I was too tired to think very effectively. All I came up with is that screaming makes something happen. It makes us upset. Even when we ignore it, that's something happening---us being unresponsive. If we are in public, it creates a scene. It hurries us out.
But what good does knowing that do? If ignoring doesn't work (and it's completely impossible to ignore her in public---WE might be able to, but those around us can't), if the events that cause the screaming seem random---what are we to do? We have no idea. None at all. In my dramatic moments, I have been thinking that the screaming is ruining our lives, and Janey's life. It's that bad. And I have nothing positive to end with here. Just a silent scream of my own.
Labels:
autism,
despair,
out in public,
screaming,
singing,
staring,
stores,
strategies
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