Friday, January 25, 2008

Autism Sucks

So, I am sad and angry today.
I have been all week.

It's here again. The depression stage that I had successfully kicked to the curve last fall.

For the last couple of weeks he has hit a plateau. In fact, now the stimming has increased. When stimming increases you are reminded more than ever about the A word: Autism. I find it is possible to forget about it a bit when the stimming is not there.

He has increased the nose snort thing he does along with the throat one he does. In addition, he has started to shove and throw things high into the air. Things like toys, shoes, balls, etc.....

Exactly one week ago we set out for Disney. Me, the big Disney fan, was actually stupidly hopeful it would be heavenly. While some good did come out of it, it was mainly miserable. The good was ok but the bad was baaaaaaaaaaaaad. While watching the "Dreams Can Come True" show in front of the castle I almost left in full tears and with a nervous breakdown. My son wanted nothing to do with it and it was almost the end of the trip already. He insisted in shutting his eyes and not look up as he covered his ears and hummed. My mom bickered with my husband and while all of this was happening the cast was making the audience chant "Dreams can come true, dreams can come true" over and over. I could not help but look up at the stage and wish they would all shut up and go away. As I watched the audience under the "magic of Disney" spell I felt so stupid standing there while everyone chants and here I am looking at my son who wants nothing to do with the show and is stimming like crazy. What dream? certainly not mine! My dream is far from coming true. This was more like a bad dream. I fixed my eyes on the top of the castle and tried to tune it all out and waited for the happy ending of the darn show.I could not walk out because we were in the middle front section and impossible to leave out of it. I fought back the tears hard. But, enough about Disney, that's a whole other post. Just sharing why today I am feeling sad.

This post is about the rest of the week when we got back from Orlando.

On Monday we went to see our DAN doc. We were escorted into the tiny room and the doctor came in a half hour later. While the doc reviewed where we last left off last August my son stormed through the closet sized room which already contained 3 adults , a tv and some toys. Things were flying, stimming was high, he was climbing the sofa and just creating a lot of chaos. I was glad so that the doc saw how he can be but I was mortified that he was being this hyper. He really isn't really like this usually. Or is he? I started to realize that we might not notice it because at home he roams all over the place and it is spacious. He does run and climb things at home too. Hmmm

After the 40 minute consult was over I felt like I had run a marathon. I was completely beat. $200.00 for the consult and about $ 300.00 in blood tests (to be done soon), urine toxic metals (to be done soon) and a different chelation challenge (you guessed it- to be done later) I wanted to run out! All that money and he was still so far from recovered.

I went home feeling very down.

That same night, well really the next morning at about 1:50am our son woke up crying hysterically. He can't explain what he was feeling but in a sleepy, whiny, crying voice he would say "ear!" and "mouth!". I thought that perhaps he was losing a tooth and it hurt. I also thought he might have an ear infection though it has been years since the last one. This went on for what felt like forever but it was really about an hour. I called the peds office completely anticipating it would not help. My husband in the mean time wanted me to give him Tylenol. I refused because of the reports on decreased glutathione linked with Tylenol. He then used this time to mock our "natural" approach to our son and said "well, what do we give him then". The answer was "I don't know".

The nurse on call, called back. She interrogated me forever and then said Motrin and cold compresses to the ear. My husband left to buy Motrin and I attempted the cold compress but no luck. He fought me off. Sigh. Finally, my husband brought the Motrin back and with that, he went back to sleep in about 10 minutes.

I left him home from school the next day worried and to take him to the doctors office to get checked out. He barely complained . Just said "ear" a couple of times but was in a good mood luckily. Here is the story from the pediatrician's office.

I had a 10:30am appointment. I made sure and walked in at 10:30am to avoid the prolonged waiting. In the waiting lobby there was a little girl who was about 4 and her litttle 2 year old brother. They took an instant liking to my son unfortunetaly. They kept asking him questions to which he would of course ignore and stay silent doing his own thing. The little girl came up and asked "What is his name?" and " Does he talk?". I told her his name and said he spoke a little bit. The little boy started getting upset that he would not answer back. Finally, out of frustration he said " Hey! what's wrong with you punk head?" I swear he said this. A 2 year old. He then procedeeded to follow my son around screaming "What's wrong with you?". Emotionally, I did not want to bring the autism card our to the kids mother and get into it. I just did not want to talk about it. I rather think whatever she wanted and leave it at that. I redirected my son as the little 2 year old boy kept harrasing my 5 year old. The office is usually good about appointments. At 11:00am I finally walked inside uninvited and asked how much longer they would be. My son was starting to get really hyper, jumping off of things and in addition there was this situation with the little boy. They said that because I was a same day appointment it could be another 45 minutes. As usual, I failed to keep my cool and burst into tears. I hate when I do that. I told them to cancel my appointment , that I could not wait outside with my son. I stormed out. I then thought about it and walked back in. I told them that I was not being ungrateful or impatient but that my son has autism and he could not stand to wait yet another 45 minutes. Luckily my son had to go potty and while I took him, my mom pleaded our case with them. By the time I came out they called us in, put us ahead of everyone and the ped. saw our son. No ear infection, nothing wrong with him. He gave the ped a hard time while he examined him but we were out in about 15 minutes.

I walked up to the reception desk and I thanked the girls. I told them that this meant a lot and that they have no idea how much it helped. Before I could continue to thank them, I turned and caught my son right when he shoved a little toddler down to the floor. I rushed over there, picked up the toddler and apologized to him and apologized to the mom. The mom gave me the death look and I made my son say "i'm sorry" to the toddler. BUt you know, it was more echolalia than anything. He had no idea that what he did was wrong. So, I took my son by the hand, said another thank you as I walked out with the toddler still screaming in the background.

I wanted to dissappear.

I cried on my way home. It had been 6 continous days of this, of autism all the time, day and night! It's never going to stop is it? I mean, I am pretty resilient. Yes, I am a crier but I get over things pretty quickly and move on. They are usually bad at the moment and then I can focus again. But this? this has been wearing me out completely. I might do another posting soon all happy and chipper but not today. Today I am mad. I am angry.

The frosting to the story comes from the reports from school yesterday and today of the increased stimming, shoe throwing and whining. Nice.

If I lived in a bubble everything would be just fine. We have our routine, our son is usually happy and we live. But when put in the very real day to day situations and with other kids, things suck. I am tired of explaining my child's behavior and of pulling out the autism card. I am tired of "friends" assuming that because we have a house with a yard, semi nice cars and are not sweating the gas bill we are not entitled to be angry about our lives! There is no price on the health of your child. There just isn't. I am living with an incredibly cute and happy child who is in his own world. I mean, even a blind or deaf child can have a conversation with you and tell you how they feel. That they are hungy or that , hey, I really like it when I wear that red shirt. It is sad when you are put into that situation of analyzing how much worse it could be or how someone else's misfortune might be better than yours but it's reality.

I am pissed off at the world today. I don't understand this world. I don't understand kids suffering. Why? what good does it do? Is God trying to teach me some sort of lesson because really I am not getting it and if anything it's making me into an ugly version of myself. I don't feel like looking at " on the bright side" today.

I want to scream at the Disney show creators for making the audience chant "dreams can come true". B.S. well, I take that back, I guess they can for some people, just not for me. Why does my little boy have to go through this? Why do any kids have to go through anything remotely cruel?

This is me venting. Take it as it is: one really sad and angry mom

9 comments:

GFCF Mommy said...

Well, I've had a similar week. I don't know if you had a chance to read "Nothing's Going to change my world" on my blog. But I don't want to make you cry more, just that I hear you. I understand.

We need to talk. Forget Starbucks. How about some shots of tequila? (Just kidding, I'm more a Chardonnay kind of girl, but you get the idea!)

Maybe we won't go to Disney after all.

XXXOOO for you and for your hubby, your sweet boy, and even your mom.

Katherine

Queenbee said...

Oh K, I am so sorry!!!
Hey, I am more of a Chardonnay girl too! Actually, lately I am into Malbecs!

I don't want to discourage you from Disney!!! It was my fault with going with high expectations. Last summer we went with none. Zero. We said that no matter what we would let him do what he wanted. It worked.

This time, I had the model of last summer so I had some.

Last night I was talking to another couple. They have 3 typical kids. They ASSURED me that even their kids are obsessed with something one time at Disney and the next time they go it always changes. That made me feel better.

The situation at Disney for me was also aggravated by my mom who gave way too many opinions and got in the way of our parenting iykwim. Had it been just hubby and I, I think things would have been smoother!!!

Ok, off to read your post.

I will email you for us to meet for spiked coffee...;)

bmountjpy said...

We did Disney a couple of years ago. Little Miss was still dealing with sensory issues, and so we had some sticky moments. She spent the whole car crash show at MGM Studios on the floor with a blanket. But we brought the letter from the doctors indicating they had autism, and we got special passes at Guest Services so we got into the Fastpass Lines for nearly every ride. Splash Mountain in 15 minutes instead of two hours! Disney folk were very helpful and accommodating when we asked, even if our child's "disability" wasn't readily apparent. And after we got home, we saw quite a few developments that showed it was a good experience for the kids--it just took awhile to process. I'm sorry Disney didn't go well for you this time, but I wouldn't give up!!
babs

scott said...

Providence pointed me to your blog and boy am I glad it did. Don't take this the wrong way but this post CRACKED ME UP! All I can say that we have been down that road and felt those same things and still do and your post reminded us of all of that in an odd heartwarming good riddance sort of way. Our ASD kids are 15 and 13 so your pain is our pain. Keep up the good work. I feel like you are speaking to me.

visit us at http://mylifeinhisworld.blogspot.com/

Queenbee said...

Thank you all for your support in my crazy post! Isn't it even crazier that you can all relate?

Scott- but I WAS speaking to you! lol

Da Geniius said...

Hi Queen Bee...
I've been reading your blogs for about a month now and I'm really starting to fall in love with you and your son. I realize that it is not very easy to raise a little person that is much different in so many ways. My name is Morrell and I am a high school senior in Memphis Tennessee and we have a senior research project and I choose Autism. My question is Who does it a effect and can it be prevented? & Is there a "cure"??
So, if you could help me with anything or any information I would really appreciate it.
oxox ~The Researcher~

Da Geniius said...

Sorry for this EXTREMELY late message, but yes..
Your answer was very helpful. I thank you for taking time out to response to me and if it is otay, may I have permission to use our blogging conversations (the 's' was added bcuz I'll be back. lol) in my research paper?!? Please and thank...

.:The Researcher:.

whizkidforte said...

I regret your down feelings, especially when you have to deal with a cruddy day at the Magic Kingdom during Dream Along with Mickey (I think it's still showing now), with the "Dreams come true" chant to ward off Malificent! I have a very good suggestion to compensate the grief you've experienced at the resort - maybe AllEars.net would help you!

Queenbee said...

thanks..what can allears.net do? When we recently visited in January there was no centerstage show. It said they were redoing them. Now that he loves everything, not sure how he wou ld react to the show since he is older. Should be interesting. It has been a year since this post. Glad to say some things HAVE gotten much better, others have remained the same.