Tuesday, December 29, 2009

In a Dark Place You're Likely to find.....

A MUSHROOM!!!! lol K got her mushroom haircut back and couldnt be happier! She forgot her glasses when we left the house so she looks kinda weird, not to mention this is a pic from my cell phone. She's so happy with her haircut and getting to go to the Salon and let Miss Lindsay cut her hair!

So today was a little bit better behavior day... I think the meds are starting to kick in. We havent had any major blow ups today anyway!

Monday, December 28, 2009

Waiting on the Meds

So I'm waiting on the meds to kick back in here with Kaitlyn. Today I had to run an errand to the bank and she had a huge screaming tantrum for about 20 mins because she couldnt draw some triangles right. Here I am sitting with the man at the bank in his cubicle trying to fill out a dispute form and I have a 20 month old sitting quietly playing with his mittens and a 4 1/2 yr old screaming, crying and flailing around in a chair because of her lack of ability to draw the way she wants to... oh the joys of Aspergers. I just apologized to the poor guy sitting there having to listen to that and explained that sometimes she cant get control of her emotions. Hopefully he doesnt think I'm a complete nut or what I'm SURE he was thinking... "Cant this chick control her kids in public?"

Whatever... I'm going to get a T-Shirt to wear EVERYwhere that says Proud Mother of an Asperger Kid. Then when people look at me funny during a tantrum I can just open my coat and smile! :) Let them go home and Google it!!! hahahahaha

Ok just had to get that out...

Sunday, December 27, 2009

Sans Meds

So I decided to take K off the Tenex as I didn't think I was noticing much improvement... well... I admit, I was wrong! There WAS improvement on it... not much but after her being off of it a week she has been a terror. Tantrums (the long ones again), screaming fits, all around nasty behavior and not being able to control her behavior AT ALL. Maybe it has nothing to do with the meds, maybe it does... but we started her back on and will be putting her back on 1/2 pill twice a day. The past few days have me worn to the end and there are times when I want to give up... but I know, for her, I cant. She needs me even if she is treating me terribly. I love her and I will be there for her through good and bad... unconditionally.

She's also having an asthma flare up so we're doing albuterol & pulmicort in the nebulizer for a bit to try to get rid of the cough and then I think we will finish out the winter on the pulmicort once a day. She must have gotten a touch of the cold her brother had and then triggered the asthma. If she keeps coughing I'm going to take her in to have her checked out and let them help me out with the dosing in the Nebulizer... maybe she needs twice a day for a bit to get rid of the cough and yucky breathing.

Anyway... hopefully we will see an improvement in her behavior and I'm also hoping in Jan we can get her started with a private therapist, work on getting her more services through the school district and/or getting her into Crossroads so she can get some intensive treatment.

We'll just have to see how the new year will go.

Saturday, December 26, 2009

Holiday Letter

Though I think this "Letter" should be rewritten for ANY time you're going to see family it really brought tears to my eyes because if Kaitlyn could, this is what she would be saying!!!

Holiday Letter
This article appeared in the holiday 1999 issue of ASAP News! (Volume 3.5) The Autism Support and Advocacy Project, and Potential Unlimited Publishing.
"Dear Family and Friends:" was written for the purpose of it being sent to relatives and hosts of holiday gatherings who might need a crash course in what to expect from their guest with autism.

"Dear Family and Friends: " I understand that we will be visiting each other for the holidays this year! Sometimes these visits can be very hard for me, but here is some information that might help our visit to be more successful. As you probably know, I am challenged by a hidden disability called Autism, or what some people refer to as a Pervasive Developmental Disorder (PDD). Autism/PDD is a neurodevelopmental disorder which makes it hard for me to understand the environment around me. I have barriers in my brain that you can't see, but which make it difficult for me to adapt to my surroundings.

Sometimes I may seem rude and abrupt, but it is only because I have to try so hard to understand people and at the same time, make myself understood. People with autism have different abilities: Some may not speak, some write beautiful poetry. Others are whizzes in math (Albert Einstein was thought to be autistic), or may have difficulty making friends. We are all different and need various degrees of support.

Sometimes when I am touched unexpectedly, it might feel painful and make me want to run away. I get easily frustrated, too. Being with lots of other people is like standing next to a moving freight train and trying to decide how and when to jump aboard. I feel frightened and confused a lot of the time. This is why I need to have things the same as much as possible. Once I learn how things happen, I can get by OK. But if something, anything, changes, then I have to relearn the situation all over again! It is very hard.

When you try to talk to me, I often can't understand what you say because there is a lot of distraction around. I have to concentrate very hard to hear and understand one thing at a time. You might think I am ignoring you--I am not. Rather, I am hearing everything and not knowing what is most important to respond to.

Holidays are exceptionally hard because there are so many different people, places, and things going on that are out of my ordinary realm. This may be fun and adventurous for most people, but for me, it's very hard work and can be extremely stressful. I often have to get away from all the commotion to calm down. It would be great if you had a private place set up to where I could retreat.

If I can not sit at the meal table, do not think I am misbehaved or that my parents have no control over me. Sitting in one place for even five minutes is often impossible for me. I feel so antsy and overwhelmed by all the smells, sounds, and people--I just have to get up and move about. Please don't hold up your meal for me--go on without me, and my parents will handle the situation the best way they know how.

Eating in general is hard for me. If you understand that autism is a sensory processing disorder, it's no wonder eating is a problem! Think of all the senses involved with eating. Sight, smell, taste, touch, AND all the complicated mechanics that are involved. Chewing and swallowing is something that a lot of people with autism have trouble with. I am not being picky--I literally cannot eat certain foods as my sensory system and/or oral motor coordination are impaired.

Don't be disappointed If Mom hasn't dressed me in starch and bows. It's because she knows how much stiff and frilly clothes can drive me buggy! I have to feel comfortable in my clothes or I will just be miserable. When I go to someone else's house, I may appear bossy and controlling. In a sense, I am being controlling, because that is how I try to fit into the world around me (which is so hard to figure out!) Things have to be done in a way I am familiar with or else I might get confused and frustrated. It doesn't mean you have to change the way you are doing things--just please be patient with me, and understanding of how I have to cope. Mom and Dad have no control over how my autism makes me feel inside. People with autism often have little things that they do to help themselves feel more comfortable. The grown ups call it "self regulation," or "stimming'. I might rock, hum, flick my fingers, or any number of different things. I am not trying to be disruptive or weird. Again, I am doing what I have to do for my brain to adapt to your world. Sometimes I cannot stop myself from talking, singing, or doing an activity I enjoy. The grown-ups call this "perseverating" which is kinda like self regulation or stimming. I do this only because I have found something to occupy myself that makes me feel comfortable. Perseverative behaviors are good to a certain degree because they help me calm down.

Please be respectful to my Mom and Dad if they let me "stim" for awhile as they know me best and what helps to calm me. Remember that my Mom and Dad have to watch me much more closely than the average child. This is for my own safety, and preservation of your possessions. It hurts my parents' feelings to be criticized for being over protective, or condemned for not watching me close enough. They are human and have been given an assignment intended for saints. My parents are good people and need your support. Holidays are filled with sights sounds, and smells. The average household is turned into a busy, frantic, festive place. Remember that this may be fun for you, but it's very hard work for me to conform. If I fall apart or act out in a way that you consider socially inappropriate, please remember that I don't possess the neurological system that is required to follow some social rules. I am a unique person--an interesting person. I will find my place at this Celebration that is comfortable for us all, as long as you'll try to view the world through my eyes!"

I thank, with all of my heart, whomever wrote this.

Bouncing Ball

Really this will be short... Kaitlyn was BOUNCING off the walls the entire day Christmas Eve and yesterday. I have no idea why she was acting out so badly but she was being rude and talking back and not listening. She was getting Time Outs over and over and just overall a complete mess.

Christmas morning was good, she loved all her presents.

Friday, December 18, 2009

Oh the Screaming!!!!!!!!!!!

All night... Screaming.... Screaming... SCREAMING!!! K is not feeling well and her stomach hurts but with her sensory issues (and flashbacks of reflux puking I'm sure) she cant tell if her tummy hurts to puke or poop and so all she does is SCREAM... why is that her only response to things.... SCREAMING!!!!!!!!!! AHHHHHHHH I can't take anymore tonight. I just gave her some Pepto in hopes that if it is one or the other it will take care of it and she will feel a little better and be able to go to bed and not be screaming out all night keeping her brother awake - or me for that matter.

I'm so terribly exhausted from everything these past few days and I'm barely making it to Noon before I crash from exhaustion. I'm heading to bed here in about 5 mins with the kids!

Wish us luck that this is just something she ate and she will be all better in the morning. She has dance and the Christmas Pageant rehersal at Church tomorrow! Ok off to get these guys to bed.

Thursday, December 17, 2009

What a Tightly Capped Bottle!

Well we went to Long Island this past weekend and went into NY City to see the tree. There were tons of people, lights, we rode the train and the subway which were also cramped and crowded. Kaitlyn (though we know she needed to) did so good and held it all in and controlled herself so well! She was SO overstimulated but didnt want to lose control and misbehave. I'm so proud of her!! You could see she was a balloon ready to pop! She also handled having the family over Sunday morning to Grandma's like a champ. She was a little snippy and her brain was so stressed and she was a wreck inside she couldnt even think to write letters or numbers correctly. The poor girl was writing backwards because she couldnt focus! It was crazy to see her doing that. I was told the scientific reasoning behind that and it was interesting that I noticed. It's pretty much that her amygdala was getting all the blood flow and therefor there was only a little going to her hippocapmus. Yes, I've been learning about the brain lately!! lol :) Anyway, by the end of the day Sunday we finally got the tantrums we'd been waiting for. She had one in the bathroom at Grandma's for about 20 mins and then another one for about 20 mins again in the car while strapped in her carseat. She really needed those for a release but she tried so hard NOT to have them. I'm proud of her but then there are times where we can see how bad she needs to release the stress and tension and we WANT her to have a tantrum! It's all crazy!
I am going to be doing some more reading on this whole amygdala/hippocampus thing because it amazes me that I can see things in people and know whats going on and then there are scientific reasons behind what I am seeing and noticing. I really do need to be a therapist... maybe one day when I'm older and the kids are in school I can move into that profession... we'll see!

Friday, December 11, 2009

Lights, Camera, Action!

Well... since we went to Long Island last we've had a couple of rough weeks with behavior. Tantrums, nightmares and just overall irritability and easily set off. Just yesterday IN Wal-Mart Kaitlyn had the hugest meltdown. She started arguing with her brother over something - she didnt want him touching it - and so I took it away. My goodness did she ever BLOW UP! She was in the basket part of the cart and started crying (of course, thats normal!) and escalated to her kicking, screaming, thrashing around shaking the cart and all kinds of craziness while I simply walked along doing my shopping. I was sure to calmly tell her "her behavior is inappropriate" but other than that, I was unresponsive. It makes me wonder what people must be thinking to see a kid Kaitlyn's age doing that and me just walking along like nothing is going on!!! hahahahaha Anyway, all the crying and screaming got Tyler upset so HE started crying and freaking out... so there I was, walking in Wal-Mart with TWO screaming kids in my cart! hahahaha After the 20 min? or so ordeal little miss Kaitlyn was still upset but had run out of energy I think with all the hard work she was doing to shake around the cart and everything. She then just cried the rest of the time and began the begging me for a hug and kiss to make her feel better and she just kept saying "I'm sorry mommy," "I'm really sorry mommy for doing what I did, I dont like it," and "I dont want to do that, I was sad about the Candy canes, I'm sorry mommy." She was saying all of this VERY quietly while crying in the cart... not sure if it was REALLY to me or just her talking out loud to herself??? I wonder if I could get the Security tapes from yesterday?!?!?!? hahahaha Just to be on the outside seeing that happening would be interesting!

Kaitlyn did have her Dance Studio Holiday Party this past Monday (12/7) and they did the same dance routine as last year and Kaitlyn was so scared (she told me) she stood there with her hands to her face and didnt do any of the dance really... I spoke with the Dr about the drastic change from last year when she did EVERY move. We came to the conclusion that she is more aware of her anxiety - especially when she tells me "it felt like all the people were looking at me." So we'll see how the rest of the dance shows go from here. She did tell me she likes dancing on the stage just not on the roller rink, which is where there little holiday thing was. All we can do is wait.

Anyway, once again we're headed to Long Island this weekend so I'm sure I'll have more than a few days filled with tantrumish behavior once we're back. It's a short trip so hopefully it's a short run after! I hate when there are changes in the routine but we need to get this overwith so we can have a few weeks at home with uninterrupted routine to see how she is really doing. She is on .5mg of the Tenex in the am and now we added the pm. If we still see no change in her by the end of December we're going to pull back and take her off the meds and see how she is then and figure out what to do from there.

I've also been doing a lot of looking around into where we can get money to get her into the program at Crossroads Center to get her some real help. She is going to be starting with the Social Worker the school is providing today! She will be getting that whole 30 mins per week at school but we did ask the girl if she would come here, to a "safe" and "familiar" enviroment to meet Kaitlyn rather than just going to the school. I've also contacted a lawyer to see what kind of options we have as well... I'll update once I know more, right now everything is so "up in the air."

Oh tomorrow is also the annual trip to NYC to see the tree... I just KNOW thats going to be Sensory overload... all the people, the lights?? Yeah... thats going to be an AWESOME tantrum waiting to happen!!!

Tuesday, December 01, 2009

Mysteries of Moon Phases

I am fully convinced that Kaitlyn's moods are connected to the phases of the moon. It's a full moon today/tonight and poor Kaitlyn has been "losing it" all day and been having screaming tantrums about NOTHING. Tonight the biggest "fit" was about WHERE she wanted to eat dinner. She screamed and cried about not wanting to eat at the table. I'm not sure where it came from, either. Then after about an hour of screaming (she's started throwing things now too) she came to me crying and begging for a hug and said she was sorry couldnt stay in control (not exactly her words). The poor kid... had to put her to bed a little early (can only handle so much screaming), dragged her up the stairs screaming, put her in her bed - a few times - where she continued to scream and thrash around... all of that because of her brother touching puzzle pieces which I warned her of before she started playing with it.

We did just get back yesterday from a 4 day trip to Grandma's and I'm sure being all thrown off whatever sort of routine we had was hard for her and coming back to it must be harder. I wish there was a magic button sometimes to just make it all better. Hopefully after a couple days of being back home and back to the routine she will settle back down.