Miss Devine is Tripp's new teacher. He loves her! This is his third week in the PPCD class. When we pulled up at his school today he said "See Miss Devine!" and when he saw Ms. Alice, the aide in his class, he said "Hey Ms. Alice." He is talking more than ever and has finally begun regaining the potty training ground we lost over the Chirstmas break. He has even started having "rest time" in his undies as he is very much opposed to wearing a "pull 'em up" for any reason. He does not object to "Mickey sleeping" (his overnight diaper) at bedtime though so I'd say we are in a very good place when it comes to the potty!
The other day in the car he said "Hey Mommy. Guess what." Shocked and amazed that he just initiated verbal interaction with me I said "What bubba?" What followed was a bunch of stuff I couldn't understand but he clearly wanted to tell me something and was satisfied that I listened even though I haven't a clue what he said. Good stuff!!
I think the only "down" news I have is what we saw over the weekend. Tripp didn't go to school Friday - Paris had a fever and Tripp was "iffy" (99.7) so we all stayed home. Saturday I was home with the kids all morning and when Easy got home about 1:00 I left and was gone until nearly 9:00. So, two days - no structure. Result? Sunday was awful! He tantrumed, he screamed, he cried, he tippy toed, he flicked his fingers, he made weird noises, he carried belts around all day to make numbers with, and he koala-beared so tightly to me that I didn't even have to hold him. It was probably the most "autistic" day we've had in over a month. Tell me this.....if two days of no structure did that, what would an entire summer at home do?!?!? I'm planning to write an email to his teacher and copy the diag on it letting them know what we saw this weekend. I know they won't have time between now and summer to document much since spring break is the only holiday in there so I figure my documentation is all I'm gonna have to get him services through the summer. For Easy and me it was crystal clear what was going on - I hope the district will see it as clearly.
So that's what things look like as we keep Monkey Dancin' forward. I still haven't started the "working sessions" with him here at home, but I will do that this week. I intended to start last week, but since we were roating the fever (we includes me!) it didn't happen. Sometimes I think I'm not doing near enough for him, and sometimes I think I couldn't possibly do any more. It is my prayer this week that I really see what things are important and make them the priority for my time - that goes for my whole family, not just Tripp. Since we are one family, we all do the Monkey Dance so I need to think of us overall and not just as individuals. Your prayers for discernment and wisdom are greatly appreciated.
Monday, February 25, 2008
Tuesday, February 5, 2008
Want to play E?
That is what Tripp says when he sees me anywhere near a computer. Translation? "Mommy, would you please click on Internet Explorer and go to Nick Jr. so that I can sit in your lap while you play a game and I cheer you on with shouts of "Good Job," "Watchout!" and "Keep Going?""
OK, I'm sure I didn't use those quotation marks correctly because it looks kind of silly to me but I think you know what I mean. He's so stinkin' cute!!
So it's been crazy since my last post. Last week I went and observed several classrooms. I saw the ABC class - this is the district class for kids with autism. I saw two PPCD (preschool program for children with disabilities) classes as well. I knew which one the diag wanted to place Tripp in so I went back for a second observation. After many conversations and LOTS of prayer we decided to agree with Molley's (the diag) recommendation and place Tripp in the PPCD class. He will stay at Sonshine school on TTH and go to the PPCD class MWF. Next year he will be with the school district 5 days a week.
The ARD was scheduled quickly - we had it yesterday afternoon. I think it went well. I liked everyone in attendance (I REALLY like Dr. Wehrly!!!), I liked the atmosphere at the school, I liked having my mom with me! I think Tripp's new teacher will be a good fit for him. She fits his preferred dark hair/petite/pale complexion profile to a T. Her personality is a bit more mellow than mine (shocking, I know) so I had to really step back and look at her and her classroom as not something that I would like, but rather how Tripp would fit there? It is going to be good.
I think I'm feeling overall very good about the district and Tripp's placement and what he'll be able to do there. I feel kind like I've been in a tornado for, well, a long time and now we're going to stop going in circles and get on the highway. I'm sure the drive won't be straight and smooth but at least we're on a road and I have lots of friends and a faithful Father that will guide us as we move forward.
We also had our first session with Dr. Montogmery (SW Autism Team) on Monday. Can we say overwhelmed? On top of starting a whole new schedule with school somewhere every day, I'm supposed to start having "working sessions" with Tripp daily at home. I'm praying about this - mostly that Vivie will take a stinking nap so I can actually accomplish it. It may take me a bit to get the swing of what Dr. Montgomery taught and modeled for me, but I'm commited to doing everything possible to help my Monkey.
If I had blogged yesterday it would have been through tears. Today I'm much better. I guess it's all just so very real now. It's been another one of those weeks where I am forced to acknowledge that this isn't going to go away. There is still this part of me that wants to beleive that if we do absolutely everything possible that the ASD will become imperceptible. (SP?) I don't know if that's possible or even if it's something I should hope for. The truth is, he's only three. His differences right now don't look all that strange. At age 9 I have no idea what he will look like or how different he will be from his peers. There so much changing in the world of autism I don't even really know what this process of treatment/therapy is going to look like. Now that the district and our private sector people agree that he fits the criteria for Apserger Syndrome does that mean anything different really than just saying he has an ASD? Dr. Montgomery even pointed out that the criteria fo Asperger's is changing so he may not meet it in another 2 years. So many unknowns, so many changes........but one thing does not change. Well, two things really.
1. God is faithful.
2. I love my son.
For now I'm going to hold on tightly to those two truths and embrace the new structure that will become our life for the rest of the school year. Who knows, it may even be good for all of us to have a more scheduled day - I just for the life of me can't figure out where to fit in cleaning my house.
OK, I'm sure I didn't use those quotation marks correctly because it looks kind of silly to me but I think you know what I mean. He's so stinkin' cute!!
So it's been crazy since my last post. Last week I went and observed several classrooms. I saw the ABC class - this is the district class for kids with autism. I saw two PPCD (preschool program for children with disabilities) classes as well. I knew which one the diag wanted to place Tripp in so I went back for a second observation. After many conversations and LOTS of prayer we decided to agree with Molley's (the diag) recommendation and place Tripp in the PPCD class. He will stay at Sonshine school on TTH and go to the PPCD class MWF. Next year he will be with the school district 5 days a week.
The ARD was scheduled quickly - we had it yesterday afternoon. I think it went well. I liked everyone in attendance (I REALLY like Dr. Wehrly!!!), I liked the atmosphere at the school, I liked having my mom with me! I think Tripp's new teacher will be a good fit for him. She fits his preferred dark hair/petite/pale complexion profile to a T. Her personality is a bit more mellow than mine (shocking, I know) so I had to really step back and look at her and her classroom as not something that I would like, but rather how Tripp would fit there? It is going to be good.
I think I'm feeling overall very good about the district and Tripp's placement and what he'll be able to do there. I feel kind like I've been in a tornado for, well, a long time and now we're going to stop going in circles and get on the highway. I'm sure the drive won't be straight and smooth but at least we're on a road and I have lots of friends and a faithful Father that will guide us as we move forward.
We also had our first session with Dr. Montogmery (SW Autism Team) on Monday. Can we say overwhelmed? On top of starting a whole new schedule with school somewhere every day, I'm supposed to start having "working sessions" with Tripp daily at home. I'm praying about this - mostly that Vivie will take a stinking nap so I can actually accomplish it. It may take me a bit to get the swing of what Dr. Montgomery taught and modeled for me, but I'm commited to doing everything possible to help my Monkey.
If I had blogged yesterday it would have been through tears. Today I'm much better. I guess it's all just so very real now. It's been another one of those weeks where I am forced to acknowledge that this isn't going to go away. There is still this part of me that wants to beleive that if we do absolutely everything possible that the ASD will become imperceptible. (SP?) I don't know if that's possible or even if it's something I should hope for. The truth is, he's only three. His differences right now don't look all that strange. At age 9 I have no idea what he will look like or how different he will be from his peers. There so much changing in the world of autism I don't even really know what this process of treatment/therapy is going to look like. Now that the district and our private sector people agree that he fits the criteria for Apserger Syndrome does that mean anything different really than just saying he has an ASD? Dr. Montgomery even pointed out that the criteria fo Asperger's is changing so he may not meet it in another 2 years. So many unknowns, so many changes........but one thing does not change. Well, two things really.
1. God is faithful.
2. I love my son.
For now I'm going to hold on tightly to those two truths and embrace the new structure that will become our life for the rest of the school year. Who knows, it may even be good for all of us to have a more scheduled day - I just for the life of me can't figure out where to fit in cleaning my house.
Monday, January 28, 2008
Monkey Business
So, my last few posts have been all about process. I thought it time to post some actual Monkey business instead! Here are some fun & funny things going on with my sweet Monkey!
As we have made our transition into a gluten-free diet things have been, well challenging in some ways and surprisingly easy in others. The lack of crackers has been very hard on our little Bug. About a week into our no-cracker house we were up at Sonshine School early. I had dressed the kids and we were just killing time until school started. Vivie was doing the incessant cracker asking. Then I heard it. Tripp, in his typical no eye contact or any visible sign that he was communicating with his sister, says "No moh cackers!" I cracked up laughing! How ironic that my sweet repetitive boy seemed annoyed by Viv's constant cracker asking! It was funny. It did not, however, stop her from asking again.
Monkey has also added several new words to his vocab. Most of them have to do with food - no doubt again dur to the dietary changes we've made. He has spontaneously asked for things ranging from "pedut pudder and jewy samich" to "nacchos." The things that have mad me smile most are his request to "open du pantwy?" and the fact that he usualy makes his request in the following format: "Do you want a chip today?" Hello, pantry and today? Great words!!
Also in the food department I'm very happy to say that he has added a new food to his will-eat list! He started asking for a hot dog on Saturday. He's never asked for a hot dog. He's never eaten a hot dog. After an entire afternoon of asking for a "hot dog today?" I gave him one - cold - straight out of the fridge. AND HE ATE IT! He even added "Mmmmmmmmmm, yummy hot dog!" LOVE IT!!! Packing lunch just got a lot easier!
As we have made our transition into a gluten-free diet things have been, well challenging in some ways and surprisingly easy in others. The lack of crackers has been very hard on our little Bug. About a week into our no-cracker house we were up at Sonshine School early. I had dressed the kids and we were just killing time until school started. Vivie was doing the incessant cracker asking. Then I heard it. Tripp, in his typical no eye contact or any visible sign that he was communicating with his sister, says "No moh cackers!" I cracked up laughing! How ironic that my sweet repetitive boy seemed annoyed by Viv's constant cracker asking! It was funny. It did not, however, stop her from asking again.
Monkey has also added several new words to his vocab. Most of them have to do with food - no doubt again dur to the dietary changes we've made. He has spontaneously asked for things ranging from "pedut pudder and jewy samich" to "nacchos." The things that have mad me smile most are his request to "open du pantwy?" and the fact that he usualy makes his request in the following format: "Do you want a chip today?" Hello, pantry and today? Great words!!
Also in the food department I'm very happy to say that he has added a new food to his will-eat list! He started asking for a hot dog on Saturday. He's never asked for a hot dog. He's never eaten a hot dog. After an entire afternoon of asking for a "hot dog today?" I gave him one - cold - straight out of the fridge. AND HE ATE IT! He even added "Mmmmmmmmmm, yummy hot dog!" LOVE IT!!! Packing lunch just got a lot easier!
Thursday, January 24, 2008
Decisions, Decisions
Well, our February 5th deadline for our first ARD is nearing. I've been in contact with the district diagnostician and we need to make some decisions about placement so we know which campus to have the ARD on. It seems that the district isn't sure that the ABC class (that's the one just for kids on the spectrum) is the best fit for Tripp. She presented me with three options, 2 of which I have vetoed already. One was to keep him at SSS and have the district consult with them. Nope - they are doing all they can at SSS and since I know some of the administrative dynamics going on I veto this option. I simply don't think they have the resources to do any more than they already do and I think Tripp needs something more than two days a week. Another option was to keep him at SSS and have him receive speech/language therapy. I didn't think this would be enough, and Dr. Montgomery (Scott & White Autism Team) concurred that he needs more than that. So that leaves us with option three which is to keep him at SSS two days a week (per my request so he can have that social time with typical peers) and place him in the regular PPCD class the other days. So, after conferring with my mom, Dr. Montgomery, my good friend Irene (who has experience with the district here) I have asked to:
#1 - get my hands on the district's official report on Tripp
#2 - go observe the ABC class they don't want to put him in
#3 - go observe the PPCD class
I have about a week to get that all done. The only part of this that has me uneasy is that the diagnostician told me on the phone she had hoped to hire another pre-school teacher and create another class that Tripp would have been well suited for - targeting high functiong kids on the spectrum. Apparently the hire is not getting approved by her superiors so I'm left with the options listed above. To me it sounds like if she got to pick he would be in a more specialized class than the regular PPCD. All that leaves me feeling like we might be settling and that is, well, uncomfortable. I'm going to go observe next week - please pray that I'm able to see both classes and that God will make the choices clear and the path available.
#1 - get my hands on the district's official report on Tripp
#2 - go observe the ABC class they don't want to put him in
#3 - go observe the PPCD class
I have about a week to get that all done. The only part of this that has me uneasy is that the diagnostician told me on the phone she had hoped to hire another pre-school teacher and create another class that Tripp would have been well suited for - targeting high functiong kids on the spectrum. Apparently the hire is not getting approved by her superiors so I'm left with the options listed above. To me it sounds like if she got to pick he would be in a more specialized class than the regular PPCD. All that leaves me feeling like we might be settling and that is, well, uncomfortable. I'm going to go observe next week - please pray that I'm able to see both classes and that God will make the choices clear and the path available.
Thursday, January 17, 2008
8 Random Things About Me - by Tripp, the Monkey
My friend Jacob tagged me, so here are 8 random things about me. My mom is helping since language isn't my strongest skill.
1. I LOVE NUMBERS!!!!!!!!!!! That's right, numbers. I carry and sleep with a calculator all the time. I count everything imaginable (including my poo-poos) and sometimes even things that are only imagined by me. Mommy just shrugs here shoulders and smiles alot when she doesn't understand what I'm counting.
2. I can form numbers with my fingers - 1-9. I made Mommy do it with me once, but she said her hand hurt when we were done. Sowwy mommy.
3. I love my big sister Paris. I used to call her Diggadauh just to irritate her. Now I call her Pawis and my favortie part of the day is when we go in Pawis from school. (that's go get Paris from school for those not fluent in Monkey speak)
4. My mom calls me her Monkey. I don't get it.
5. Every Friday I play with my friend Jacob at Miss Temaphie's house. (That would be Miss Stephanie!) Even though I usually just play by myself when I'm there I really like going and I try to play with Jacob - he makes me laugh sometimes. And sometimes Mister Ewic is there and I watch him on the puter. (computer)
6. I love to be outside. I think running on my tip toes in cirles in the backyard is really cool. I also like to play ball with Daddy. He throws it and I go get it. I saw them do this with Cowboy, that dog that tries to lick my face, and it looked like fun.
7. I don't like Cowboy to lick me. His breath is yucky.
8. My mommy doesn't know that I know this, but every night before she goes to bed she comes in and lays down on my bed. She puts her hand on my head and she talks to God. She loves me a lot. I don't always wake up, but most of the time I smile while she's talking to God.
I'm not sure what it means to tag someone else, and mommy syas most of my firends have already been tagged so I think I'll just go to bed now. Night night.
1. I LOVE NUMBERS!!!!!!!!!!! That's right, numbers. I carry and sleep with a calculator all the time. I count everything imaginable (including my poo-poos) and sometimes even things that are only imagined by me. Mommy just shrugs here shoulders and smiles alot when she doesn't understand what I'm counting.
2. I can form numbers with my fingers - 1-9. I made Mommy do it with me once, but she said her hand hurt when we were done. Sowwy mommy.
3. I love my big sister Paris. I used to call her Diggadauh just to irritate her. Now I call her Pawis and my favortie part of the day is when we go in Pawis from school. (that's go get Paris from school for those not fluent in Monkey speak)
4. My mom calls me her Monkey. I don't get it.
5. Every Friday I play with my friend Jacob at Miss Temaphie's house. (That would be Miss Stephanie!) Even though I usually just play by myself when I'm there I really like going and I try to play with Jacob - he makes me laugh sometimes. And sometimes Mister Ewic is there and I watch him on the puter. (computer)
6. I love to be outside. I think running on my tip toes in cirles in the backyard is really cool. I also like to play ball with Daddy. He throws it and I go get it. I saw them do this with Cowboy, that dog that tries to lick my face, and it looked like fun.
7. I don't like Cowboy to lick me. His breath is yucky.
8. My mommy doesn't know that I know this, but every night before she goes to bed she comes in and lays down on my bed. She puts her hand on my head and she talks to God. She loves me a lot. I don't always wake up, but most of the time I smile while she's talking to God.
I'm not sure what it means to tag someone else, and mommy syas most of my firends have already been tagged so I think I'll just go to bed now. Night night.
Wednesday, January 2, 2008
A bit overdue
Sorry for the delay in posting. We could call it a holiday hiatus, or maybe Christmas crazy - regardless I haven't posted in a while and I apologize. So in an effort to catch up..................
Tripp had his assessments with the school district done on the 19th. Everyone there is also in agreement that he's on the spectrum. They just need to score all their little testing tools to see where to place him. He absolutely entertained the diag and speech pathologist while they did their stuff with him. He started the whole deal off by spontaneously counting by 7's. Yes, by 7's. We were all a bit amazed. I went to do my interview with the psychologist while they did all there stuff and when I came back they were all having fun. Apparently they got further in one of the testing tools than they ever had before. The diag said shell be interested to see all the "results" because he struggled with the lower level stuff and then all of the sudden they hit a point and he blew the rest out of the water. Clearly he is missing some basic components in his development, but once they got to a section he "got" he was on fire! So, the aboslute latest we will have our ARD is February 5th, but it could be before then. That's when we will find out what services they are going to provide. Keep praying over all of that.
Since that week I've been distracted a bit by the busyness of the holidays. I have these moments of reality where I think about what life will be like when our Monkey is 8 or 12. I mean, at this point lots of what he does could easliy be chalked up to just being a silly three year old. I sense, however, that the older he gets the more different he will look from his peers. I have some saddness when I think of the future at times. I just want all good things for him and reality is that it isn't going to be all good. But I guess that's true for all kids. Maybe it's just that I see it coming, or that I feel like it should be different for him because he's special. Then again, my girls are special too and I want all good things for them, and the first boy that breaks their heart deserves to be smooshed into nothingness.
I've had other reality check moments - the ones that just blow me away because Tripp is just so amazing. I mean, hello, he counted by 7's. I have to think hard after 35! And for all his disconnect and quirkiness, he has a tremendous amount of love to share. So, yeah, he's kinda picky about who he shares it with, but when your the recipient of a hug that he initiates the rest of the world just seems to melt away. I like those moments better than the ones where I worry about his future.
One things is for sure - this holiday break with no routine, no schedule, no structure has taken a toll. I've seen a lot of tippy toes this week in particular. He's not sleeping well. He's not eating well. And no, he's not pottying well. He actually peed a puddle in my kitchen floor on Monday. He hasn't done that in months! I'm ready to get back into our routine for pee patrol alone. I am so tired of wet undies!!! (of course, about the time we get things rolling again I'll start potty trainging Viv and have went panties as well!)
SSS starts back next Tuesday though, so we only have a little more chaos to endure. It's really driven home how important it's going to be to find something for the summer. I don't know if the district does any kind of summer program. If not, I'm going to have to find somehwere for him to go so we don't go spirally backwards. Who knew relaxation could be so stressful?!?!?!?
Tripp had his assessments with the school district done on the 19th. Everyone there is also in agreement that he's on the spectrum. They just need to score all their little testing tools to see where to place him. He absolutely entertained the diag and speech pathologist while they did their stuff with him. He started the whole deal off by spontaneously counting by 7's. Yes, by 7's. We were all a bit amazed. I went to do my interview with the psychologist while they did all there stuff and when I came back they were all having fun. Apparently they got further in one of the testing tools than they ever had before. The diag said shell be interested to see all the "results" because he struggled with the lower level stuff and then all of the sudden they hit a point and he blew the rest out of the water. Clearly he is missing some basic components in his development, but once they got to a section he "got" he was on fire! So, the aboslute latest we will have our ARD is February 5th, but it could be before then. That's when we will find out what services they are going to provide. Keep praying over all of that.
Since that week I've been distracted a bit by the busyness of the holidays. I have these moments of reality where I think about what life will be like when our Monkey is 8 or 12. I mean, at this point lots of what he does could easliy be chalked up to just being a silly three year old. I sense, however, that the older he gets the more different he will look from his peers. I have some saddness when I think of the future at times. I just want all good things for him and reality is that it isn't going to be all good. But I guess that's true for all kids. Maybe it's just that I see it coming, or that I feel like it should be different for him because he's special. Then again, my girls are special too and I want all good things for them, and the first boy that breaks their heart deserves to be smooshed into nothingness.
I've had other reality check moments - the ones that just blow me away because Tripp is just so amazing. I mean, hello, he counted by 7's. I have to think hard after 35! And for all his disconnect and quirkiness, he has a tremendous amount of love to share. So, yeah, he's kinda picky about who he shares it with, but when your the recipient of a hug that he initiates the rest of the world just seems to melt away. I like those moments better than the ones where I worry about his future.
One things is for sure - this holiday break with no routine, no schedule, no structure has taken a toll. I've seen a lot of tippy toes this week in particular. He's not sleeping well. He's not eating well. And no, he's not pottying well. He actually peed a puddle in my kitchen floor on Monday. He hasn't done that in months! I'm ready to get back into our routine for pee patrol alone. I am so tired of wet undies!!! (of course, about the time we get things rolling again I'll start potty trainging Viv and have went panties as well!)
SSS starts back next Tuesday though, so we only have a little more chaos to endure. It's really driven home how important it's going to be to find something for the summer. I don't know if the district does any kind of summer program. If not, I'm going to have to find somehwere for him to go so we don't go spirally backwards. Who knew relaxation could be so stressful?!?!?!?
Monday, December 17, 2007
I Really Don't Know
what to title this post.
At this moment my gut wants to post the short, just the facts version of how our visit to Temple went today. In an effort to be a little more authentic however - here's how the last 26+ hours have gone.
Saturday night I had trouble going to sleep. All I could think was "what do I pack?" I mean seriously, what do you wear to this appointment?!? I'd love to go comfy and pack sweats, but I'm afraid that would send the "I don't really care and I'm over-extended so I won't be much help for my son" message. I also don't want to go too put together because that could send an "I run a tight ship, have it all together at all times and accept nothing less - so I won't be much help for my son" message. Not a lot of sleep happened. ( I ended up packing jeanes, sneakers, and a button down collared shirt.)
We got all packed and ready to leave yesterday afternoon. Tripp was kind of wild all day, but we figured he'd zonk out in the car. I had gone in to "quiet mode." That's what I do when I'm facing a reality that is hard. (like the day my mom left to go home each time after I had a baby) It's a combination of fear, sadness, and a host of other emotions. I walked around to where my dad was sitting and gave him a wave good bye. He grabbed my hand and said "I'll be prayin' for you." I cried as I walked out the door.
We get all loaded and head out. Tripp seemed overjoyed to have Mommy & Daddy to himself. In fact, he was pretty much in Tripp heaven. Mommy, Daddy, Elmo, Blanket, and the Video Now Jr - does it get any better? The trip was uneventful itself. Our Monkey did NOT take a nap in the car. We picked up fast-food dinner and checked into our motel. We went cheap (like we had a choice!) since it was just one night. The Econolodge was, well, an Econolodge. It was clean.
Tripp thought it was the coolest place ever. He was pinging off the walls. There was more tippy-toe monkey dancin' than I've seen in quite some time. He even kept running into the closet and back out like he'd found a secret hiding place or something. My genius husband had packed his laptop and Tripp's favorite movies so that helped us calm him down enough to eat his dinner and then go to bed. He wasn't too happy that Mommy & Daddy were sleeping in the big bed and he was sleeping in his Winnie the Pooh bed, but he got over it and went to sleep by 9:00.
I turned the TV off at 10:00. I know I was still awake at 10:45. I slept for a while, but from about 3:00 on it was in 20 minutes spurts. There was no alarm clock in the room so we were relying on my watch and Easy's phone to wake us. I was terrified we'd over sleep. We didn't - everyone was up and ready to hit the road at 7:30 which gave us plenty of time to get there....so we thought.
We drove over to the address we had been given. Turns out the the ENTIRE Scott & White medical facility has one address. It also turns out that the valet at the hopsital gives incorrect directions to the pediatric clinic. As does the receptionist at the main clinic information desk. We got to our appointment after WAY too much walking in the cold about 15 minutes late. Fortunately no one complained about our tardiness - I may have blown a gasket if they had.
So, we check in, wait all of three minutes and meet Dr. Montogmery, the psychologist that is the first point of contact on the Autism Team. Our time with her was, well, anticlimatic. (not sure I spelled that right, but I assume you know what I mean) She did a lengthy background interview. There was no paperwork to fill out. The interview felt as much like a conversation as anything else. She choose to not do any testing since he has his appointment for testing through the school district on Wednesday.
So, here's the bottom line based on our interview...........he WILL clinically be on "the spectrum." As for exactly which box on the spectrum we don't know yet. Her inclination is that he will eventually be given the diagnosis of Asperger's. At the moment, however, he is a bit young to be given that label so as we continue throught this process we may be given "high-functioning autism" as our label. So, there you go. And there I sat, hearing the words I expected to hear, and still I found tears streaming down my face. I was surprised by them. It's not like I didn't know it was coming. I don't know if it was that last little part of me that had been hoping this was all a dream finally letting go, or maybe it was simply relief that I am not crazy and the things I've been concerned about are real. Regardless of where the tears came from, they were needed in that moment, and then they passed as we started making a plan.
Here's the really good news........Dr. Montgomery will be coming to College Station once a month starting in January!!! She is referring us to see Dr. Hall, the developmental pediatrician. She said we don't really NEED him at this point, but we will eventually so it's better to see him now and stay in touch as Tripp gets older so he will be "on board" from the beginning. I am supposed to email her after his assessments on Wednesday and let her know exactly what tests they did. If she feels the need to do any additional tests she will work us in on her January visit to CS. We have appointments already booked with her for February and March. She had VERY positive things to say about our school district. There are a lot of more technical things I could tell you about treatment approaches and recommendations and upcoming changes, but I'll save all that for another post.
At this moment I feel pretty good. I am releived that I'm not nuts. As I typed this I fought back tears more than once, and I'm sure that will continue throughout this process. That's just part of being mom. I'm tired, I'm hoping to go to bed early, maybe I'll even go to sleep. Keep those prayers going, we've got a long week and absolutely NONE of it is part of Tripp's normal routine. Pray for my patience, endurance, and please pray for peace in my precious son's mind as his world each day will simply not be what he is expecting.
At this moment my gut wants to post the short, just the facts version of how our visit to Temple went today. In an effort to be a little more authentic however - here's how the last 26+ hours have gone.
Saturday night I had trouble going to sleep. All I could think was "what do I pack?" I mean seriously, what do you wear to this appointment?!? I'd love to go comfy and pack sweats, but I'm afraid that would send the "I don't really care and I'm over-extended so I won't be much help for my son" message. I also don't want to go too put together because that could send an "I run a tight ship, have it all together at all times and accept nothing less - so I won't be much help for my son" message. Not a lot of sleep happened. ( I ended up packing jeanes, sneakers, and a button down collared shirt.)
We got all packed and ready to leave yesterday afternoon. Tripp was kind of wild all day, but we figured he'd zonk out in the car. I had gone in to "quiet mode." That's what I do when I'm facing a reality that is hard. (like the day my mom left to go home each time after I had a baby) It's a combination of fear, sadness, and a host of other emotions. I walked around to where my dad was sitting and gave him a wave good bye. He grabbed my hand and said "I'll be prayin' for you." I cried as I walked out the door.
We get all loaded and head out. Tripp seemed overjoyed to have Mommy & Daddy to himself. In fact, he was pretty much in Tripp heaven. Mommy, Daddy, Elmo, Blanket, and the Video Now Jr - does it get any better? The trip was uneventful itself. Our Monkey did NOT take a nap in the car. We picked up fast-food dinner and checked into our motel. We went cheap (like we had a choice!) since it was just one night. The Econolodge was, well, an Econolodge. It was clean.
Tripp thought it was the coolest place ever. He was pinging off the walls. There was more tippy-toe monkey dancin' than I've seen in quite some time. He even kept running into the closet and back out like he'd found a secret hiding place or something. My genius husband had packed his laptop and Tripp's favorite movies so that helped us calm him down enough to eat his dinner and then go to bed. He wasn't too happy that Mommy & Daddy were sleeping in the big bed and he was sleeping in his Winnie the Pooh bed, but he got over it and went to sleep by 9:00.
I turned the TV off at 10:00. I know I was still awake at 10:45. I slept for a while, but from about 3:00 on it was in 20 minutes spurts. There was no alarm clock in the room so we were relying on my watch and Easy's phone to wake us. I was terrified we'd over sleep. We didn't - everyone was up and ready to hit the road at 7:30 which gave us plenty of time to get there....so we thought.
We drove over to the address we had been given. Turns out the the ENTIRE Scott & White medical facility has one address. It also turns out that the valet at the hopsital gives incorrect directions to the pediatric clinic. As does the receptionist at the main clinic information desk. We got to our appointment after WAY too much walking in the cold about 15 minutes late. Fortunately no one complained about our tardiness - I may have blown a gasket if they had.
So, we check in, wait all of three minutes and meet Dr. Montogmery, the psychologist that is the first point of contact on the Autism Team. Our time with her was, well, anticlimatic. (not sure I spelled that right, but I assume you know what I mean) She did a lengthy background interview. There was no paperwork to fill out. The interview felt as much like a conversation as anything else. She choose to not do any testing since he has his appointment for testing through the school district on Wednesday.
So, here's the bottom line based on our interview...........he WILL clinically be on "the spectrum." As for exactly which box on the spectrum we don't know yet. Her inclination is that he will eventually be given the diagnosis of Asperger's. At the moment, however, he is a bit young to be given that label so as we continue throught this process we may be given "high-functioning autism" as our label. So, there you go. And there I sat, hearing the words I expected to hear, and still I found tears streaming down my face. I was surprised by them. It's not like I didn't know it was coming. I don't know if it was that last little part of me that had been hoping this was all a dream finally letting go, or maybe it was simply relief that I am not crazy and the things I've been concerned about are real. Regardless of where the tears came from, they were needed in that moment, and then they passed as we started making a plan.
Here's the really good news........Dr. Montgomery will be coming to College Station once a month starting in January!!! She is referring us to see Dr. Hall, the developmental pediatrician. She said we don't really NEED him at this point, but we will eventually so it's better to see him now and stay in touch as Tripp gets older so he will be "on board" from the beginning. I am supposed to email her after his assessments on Wednesday and let her know exactly what tests they did. If she feels the need to do any additional tests she will work us in on her January visit to CS. We have appointments already booked with her for February and March. She had VERY positive things to say about our school district. There are a lot of more technical things I could tell you about treatment approaches and recommendations and upcoming changes, but I'll save all that for another post.
At this moment I feel pretty good. I am releived that I'm not nuts. As I typed this I fought back tears more than once, and I'm sure that will continue throughout this process. That's just part of being mom. I'm tired, I'm hoping to go to bed early, maybe I'll even go to sleep. Keep those prayers going, we've got a long week and absolutely NONE of it is part of Tripp's normal routine. Pray for my patience, endurance, and please pray for peace in my precious son's mind as his world each day will simply not be what he is expecting.
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