What I want for my son

Yesterday was IEP day. We had to amend his current IEP for the rest of the school year due to Morgan slipping in reading, though his grades are great, and I went ahead and got the ball rolling for third grade. During the course of the meeting, a lot of questions were asked on all sides concerning Morgan's welfare. This is typical IEP stuff. We hammered out a great new IEP for Morgan which, I hope, will serve him well in the coming months.

There was one question, though, toward the end that will stay with me for years. The Occupational Therapist (OT) asked me, "Where do YOU see Morgan?" Since it was an open question, I answered without hesitation, "I see my son growing up and hopefully going to college. Empowering himself with knowledge. Advocating for himself; maybe one day sitting in front of Congress and advocating for his Autistic peers. That's what I see for him." She looked me and replied, "Great answer... but I was talking about third grade."

That's the thing. Whenever I go into an IEP meeting, of course I'm looking at the current school year and the next one. I'm anticipating how this current IEP will affect him one, three, five, ten years down the road. I assume others do this, too. 

What do I want for my son? I think I know.

I want Morgan to grow up knowing he's loved. I think most all parents want that. But I really want my child to know that his family loves him. 

I want my son to grow up with the knowledge to advocate for himself, not just on the Autism front, but on any front. Self advocacy is an all encompassing area and something that not too many people are good at. I want for Morgan to be diplomatic when needed, but also forceful when he has to be. 

I would love for him to advocate for others. I meant that. Morgan, even at this age, has a clear sense of right and wrong and I would love to see this put to good use. Who better to advocate for Autistics than an Autistic? Morgan will have grown up seeing the wrongs in the system and having his parents explain to him exactly why those things are wrong. I don't see those issues disappearing in ten to fifteen years, so I don't see why my son can't participate in the discussion on how to solve them. 

I want for my son to go to college. That's a given in this household where higher education of any kind is some sort of gold standard. We want him to have that experience because it's an experience we've had. Call us selfish, but we push our son to try his hardest and he does.  

I see Morgan being an engineer one day or a mathematician. Or, as I said in the IEP, "some sort of other geek related career where he's happy as a lark."  I believe firmly in pushing his strong points and interests and I'll continue to do so.

I want, one day in the very far (FAR) future for Morgan to be married. Have kids. Own a house. But God, he'd better wait a long time because I don't know how well I'd handle it. 

I view my son's disabilities as different abilities most of the time, not things which cripple him. Granted, I've let them get me down at some points, but I don't want them to get him down. 

I want so much for my son. I'm determined that if he wants it, too, he'll get it. I'm not raising people who give up. I'm showing them by example that this is never an option.

Year End Stream of...Crap

Today wasn't a great day. For starters, I awoke to find what I thought was chocolate covered cherries by my Christmas tree. I even picked one up. Guess what? It was dog crap. Yep, that's how my super early morning started- with dog crap. Oh well, I thought.

Then, things just went... blah. I couldn't set anything to rights. So, therefore, I decided to hit a mental and physical (I was in pain due to an RA and lupus flare) "reset button." It lasted all of 20 minutes, but you know what my sweet moment was? My sweet, sweet, adorable, oldest child coming in and giving me "night, night" kisses. It was lovely. He thought I needed it. See there, Mr. Baron Cohen? That's called EMPATHY, ya jerk.

While I was laying in bed, thinking of all I needed to do, it occurred to me that I needed and wanted to write. I want to write more in the new year because I enjoy the hell out of it, even if five people read this thing. I ran through my mind all that has happened this year and believe me, a lot has. It would take a novella to describe all that has happened directly to me, but this is about Morgan and my life with him. Actually, I've written a lot about Morgan's major things lately, but I wanted to touch on the milestones again or the ones I've missed. So, here goes...

Morgan, this year, has learned to read! He cracks us up while we drive down the street by reading signs out loud. Sometimes, since we live outside of New Orleans, those signs aren't exactly "kosher," but we still laugh because he's reading. I love that.

We moved this year and Morgan, while he misses TN, loves his new home. It dawned on me not even two hours ago, that in the six months we've lived here, we've had more kids come over to play and vice versa with Morgan than we've EVER had in his whole little life. That's sad, but I'm wanting to celebrate it more. It means that the wonderful people we're surrounding ourselves with (if you're reading this, Mrs. S and Ms. A, especially!!!) are truly great people and that they don't judge our child for carrying the "A-card" like a disease or for being different. It helps that these two particular women I've mentioned are both funny as hell and love Morgan.

Morgan loves his new school. I mean, really loves it. He loves his teacher, has made friends, loves his paras (aides), and has buddied up to a male figure that "puts him to work" to make him feel special. His school is a great place and though we're still working out kinks, he's doing really well.

He's cutting his own food!

He put together his own Lego truck!!! I know, I know, I did that whole post about "what not to buy my autistic child," but my hubby and I caved and bought the kiddos the 405 piece tub of catch in the feet in the middle of the night Legos for Christmas. They begged, okay? Then, the day after Christmas, Morgan startled me with this:


Morgan showing off his "lorry."



I am not saying that this year has been all roses, because it has not. My son has watched me be sick more than healthy at times. I have a disorder that made him think on a few occasions that I was DEAD- that sucks. He still tantrums, but not much.

What I'm choosing to highlight in this current climate of "panic about autism leading to psychotic behavior" (thanks, media!!), are our great moments. We're in a good place. We're happy. We're healthy. Morgan's in a safe and welcoming environment. And man, I'm damned proud of my child.



An Autism Wishlist

Dear Santa and the general public,

For Christmas, there are some things I would like for my son and the estimated 1 in 88 other people like him.

Understanding. I want for people to understand that autism doesn't mean that my son and other people like him are less. They are not unable to feel, they are not unable to function, they are not unable to think. They just do it differently than neurotypicals do. You know what? That's okay with me and it should be okay with other people, too.

Acceptance.  I want for my son to be accepted by his peers, not just his autistic peers (they parallel play just fine, thanks), but by the little boys and girls that you other neurotypicals are raising. I want for Morgan to be able to go to school and not get teased for his monotone voice, his vocal stims, other stims, or love of the demonic blue engine. I want for other autistic people to be able to gain acceptance in society by people looking at them as PEOPLE, not science experiments. Let me know if I'm wishing for the moon here.

Services. We're wasting precious time and money, I think, pushing for cures and looking for causes when we could be looking at the big picture- services. Teaching people (note that I keep putting this in italics?) on the spectrum life skills is important. Funding ABA (Applied Behavioral Analysis) is damned important, something that insurance companies all too often don't do and it's costing a lot of us somethings that we don't have- time and money.

If we're parents, we're freaking out wondering how our children are going to manage as adults in a very cruel world that will not accept our children. Because that world is not likely to change, as evidenced by some of the behaviors shown at the recent Congressional hearing on autism. Congressman Issa was good enough to call this hearing- the first in a decade, but some of his peers, some of the people who spoke, referred to autistic people as "burdens." My son is not a burden. However, paying through the nose for services and going deeply into debt for those services can be, yes.

Congressman Issa, thank you for showing that you care about us and about our people by heading that hearing and implying that there would be more in the future. There has to be. Services need to rendered. Our 1 in 88 can't wait any longer.

Just, please... Let's please, for once, get our crap together in the autism community and have a community! Please?

Warning, going into a rant now...

Why won't some of us <parents and lawmakers> listen to autistic people?! Some of us NTs listen to and applaud autistic self advocates such as Temple Grandin, Landon Bryce, Karla Fisher, etc., for what they have achieved not in spite of their autism, but because of it. When will people get that autism isn't this "burden" (borrowing a phrase here)at all times. I understand that the people I named are so called "high functioning" individuals, but what about other people that aren't? Don't their lives have value? Is there a run on life tickets if autism is caused by something in utero or by something in the environment? Does it really freaking matter?

I think what matters the most, if we are the parents of an autistic child or children, is finding the best way to help said autistic child or children through life and into adulthood. We have to love them. Not treat them like they are our cross to bear in life or society. Not treat autistic people as anything but human beings. Am I the only person getting that we are doing more to help with foreign aid than autism? Am I the only one that sees that helping Egypt's military since 1979 as compared to helping autistic people with healthcare might be wrong? Or am I the one that's wrong? 

**Also, it is incredibly offensive to call an autistic person a burden. I cannot repeat that enough. The burden lies in the way NT people think about autism.


So please, Santa, the general public, the five people reading this... please take some of this to heart. We have "stuff" we need to work on in our community.

Thank you,

Jessi

Mostly smiles, some tears, no jeers

The title pretty much sums up what yesterday, the Louisiana Autism Speaks inaugural Walk was for us, as a family. Morgan had the greatest time! We had explained to him what the walk was about, leaving out Autism Speaks' mission about finding a "cure" for autism. If we had done that, he would have balked outright. He kept looking around and asking me "are ALL of these people autistic?" It kind of cracked me up. But after a while, he just, well, let go.

Pre-walk

He became MORGAN. The Morgan that very few people really get to see. The one that toots like a train, grumbles and grunts low in his throat, tells Thomas stories non stop, and had a blast. He played with so many auties, it was just wonderful. All of those people, being themselves, in an environment where they could be themselves.

Walking and SINGING!

I met a lot of lovely people yesterday and witnessed wonderful, sometimes heartbreaking, tender moments. I thought I might spend my day crying. For one, that a Walk like this is even needed breaks my heart a bit. But it breaks my heart no more than childhood cancer, adult cancer, AIDS, etc., walks do. It's here, we have to deal with it, don't go all Chicken Little with it, and COPE.

 
You could see "it" in a lot of our faces. I say "our" because my husband and I captured it for both of us, completely candid- the LOVE. During the singing of the National Anthem, there was a mother and her daughter standing in front of us. The daughter, who must have been nearly my age (almost 30), was flapping her left hand and starting to make a keening sound. I believe she was starting to have sensory overload. She was profoundly autistic and had her left hand's fingers arched back at such an angle I honestly wondered how they didn't break. Then, her mom did "the beautiful thing." She took her daughter's hand (the left one) and converted the flapping and arching fingers into a waving motion. The autistic woman went from looking like she was going to have a meltdown to looking as if she were directing a beautiful concert; a smile came upon her face. I cried.

I walked up to the mother after the Anthem was over to tell her "what you just did for your daughter was beautiful. The world needs more parents like you." She, too, had tears in her eyes and said, "We can't help but love them, can we? They're only our children once." That statement alone made me tear up even more.

"They're only our children once." How true. Morgan and his daddy.

I love my son, no matter what, as do (I hope) all of those parents there yesterday. But you could see another "it" in a lot of their faces: the agony, the stress, the pure anger, almost malice, and the "I'm not coping, I'm going through the motions of having an autistic person amongst me" in their faces. Thing is, a lot of those parents had kids that seemed a lot like my child. These weren't the parents who had kids in strollers at the age of 10, who had non verbal children- they had high spirited, highly intelligent children that wouldn't, for the lack of a better term "shut up," lol.

That's what killed me. The ones who seemed, to an outsider, to have it "the worst" smiled the most.

My family and I walked for a little boy who loves trains. He was singing his Thomas the Tank Engine songs, telling the stories, talking about anything and everything, petting the dogs people brought, trick-or-treating along the path (great idea, Autism Speaks!!), tooting  and beeping, and NO ONE CARED! I loved it.

With the boy I walk for, walking with me

The nice man who took this chopped off Bay's head- whoops.

I had to laugh at one woman who crawled her kid's butt for slapping one of the AS signs. He was clearly stimming his happy little behind off and I had already shooed him away from the sign, as I was taking pics of all of the signs. She apologized for her son's "behavior" and I outright laughed saying, "lady, if there is a place and time for our kids to stim and be themselves, it's today and NOW!" She smiled uncertainly and walked away.

My big embarrassment (for me, as a parent, not a member of the autism community) was that Bay was acting like such a jerk,  no less than 13 people asked me how did I deal with have two auties. Do I medicate him, and my personal fave "how long has he been diagnosed?" I had to explain to those good people that as far as I can see, Bay is a NT, but very jealous of his brother's ASD. We're going through a rough patch right now and he was really showing his behind yesterday.

Pre-walk, bay getting a lecture on how to behave. Already had five people ask about his "autism." I actually told someone he just had "gingeritis."

All in all though, yesterday was beautiful. Cold, but beautiful. I think I saw more of humanity than I ever dreamed existed in the world. The best part? Morgan was "with his people." Love that boy.

Sticks or stones?

The old saying, "sticks and stones may break my bones, but words will never harm me" was obviously thought up by an asshat parent trying to comfort their child.

Sticks and stones, while they leave there visible marks, have a way of traumatizing yet making someone angry in the NT and Autie world. But those marks fade, they always do, even if scarring occurs. I'm not saying that assault in any form is acceptable, but let's face it- most of us would probably rather take a literal slap than a verbal one. I would.

Morgan seemed "fuzzy" this afternoon. He was hyper- for him. He couldn't focus at all and was over emotional, even by autistic standards.

I had to run over to a neighbor's apartment to print something off for his homework and her son came running in to inform me that Morgan was crying, a LOT, because the kids wouldn't play a game of tag. The neighbor and I, being adults, just said, "play the dang game and be a big kid- set the good example!"

When I came out to the stairwell, the kids were all in a huddle around Morgan, chattering like magpies. I knew that would set him to crying. Well, he already was- a LOT. My "mommydar" went off. I knew something wasn't right.

B, a girl that has become Morgan's bestie lately, piped up that Morgan had been bullied by two boys at school today. God, I felt my heart just... squeeze. With all of the kids around us, I coaxed out what had been bugging him (three cheers for him even telling, I think he felt encouraged due to the other kids being there). Apparently, some little jerks named Z and let's call him B told Morgan that he's fat. "Lard ass" is the word Morgan later used. That is NOT a term I allow in my house. Derogatory terms referring to weight rank right  up their with gay slurs and racist terms.

After Morgan confided in the crowd, I pointed out that those morons aren't his friends and that he needs to stay away from them. Also, that everyone standing there IS his friend. The kids were very quick to chime in (they're super sweet, honest to goodness great kids!). Then, J, the comic in the group, raised his shirt, grabbed his tummy and shook it yelling "Morgan, THIS is fat!!" J does have a bit of chub. Funnily enough, he's the exact same size as Morgan, but six years older!

I think this has been going on for a while. Morgan has been making comments since last month about being fat. The child stands 5'1 and weighs 110lbs. He's a big kid! Overweight some, yes. But geez. HE TURNED DOWN CANDY TONIGHT, PEOPLE!

My point in all of this is this: I've been on a tirade lately against the word "retard." Begging, ordering, asking, etc., people on Facebook, Twitter, in my everyday life to just eliminate it for fear that (a) it'll reach Morgan's ears, (b) they need to get a flippin' thesaurus and another word, anyway and (c) why use it?

Don't people understand that words hurt? I know that I still sting every time I think of my former stepfather telling my mom that I was "fat as mud," "could be pretty if I laid off the food," and a zillion other things. I know that my sister still hurts from the godawful crap I said to her about her speech and gums (Sorry, Riah- I really do love you and you are a beautiful person... hate that I gave you that phobia about closed hands and spiders).

I lay awake some nights, like most parents and mentally replay my day. More than 80% of the time I can come up with something that I've said that will likely scar one of my kids. I'm ashamed as hell and yet, it's probably small beans compared to what other parents do to there kids. This is in no way excusing my own behavior. I've gone on tirades that would make Marilyn Manson blush.

I just want my 10 readers to ask themselves... would you prefer your child to be bullied for something they cannot help (like autism), be made fun of for their weight, or be physically hurt? Of those things, which do you think would hurt worse? If it has happened to you, what are your thoughts? 

Our Autism These Days

Since my last post, we've packed up the family and moved from Deliverance, TN, to the greater New Orleans area, LA. We. Love. It. Here. 

Morgan is not as ostracized here for his differences as he was in TN. Maybe it's because in the land of odd, he's not so damned odd. Or maybe it's because we're living in an apartment complex where a whole bunch of kids (some his age, some younger and some older) have embraced Morgan and protected him from the very few bullies that roam the complex.

In his class, he actually has four other auties around him! You know what that means? A para (paraprofessional) is in his classroom at all times giving the teacher - and the auties - much needed support. Morgan even gets his speech in class, thus not being singled out.

Morgan is HAPPY!

Best part about living in Louisiana? With six months of residency under our belts, Morgan will qualify for something that is nonexistent currently in TN- autism insurance! I commend my friends fighting for it still, but state senators there told my husband point blank that it would not happen, period. I hope that this will soon change, as many people would benefit from autism insurance reform.

This has been a great change for our family. My own outlook on autism has changed.. While I never really have, I don't want to cure my son. Or fix him. I want to help him succeed.

Some might ask why I don't support a cure... well, if I were to cure Morgan's autism, I would being "curing" my son of everything that I hold dear.  The things that I would do with away- such as his lack of friends, are what make him Morgan. And... He's the friendliest kid I've ever met, but society deems him "weird." So he takes things literally, talks too damned loud, and stims like crazy over things that I cannot possibly understand. So WHAT if he likes Thomas the flippin' Tank Engine (still) at the age of almost eight? WHO CARES? 

Why would I want to cure my sweet, caring (squash that not having empathy thing, people- my kid has it in spades!), quirky kid. We got lucky in a lot of way on this spectrum of ours. Morgan is verbal, in a Yoda sort of way. He's a whiz at math. He has an ear for music. He's just... different from how society wants him to be.

You know what? My view on autism has changed a helluva lot in the year. When I began this blog, I was mad as hell that someone had finally labeled my kid with something that I viewed as nearly a death sentence. I was so very ignorant and wrong. 

Autism, in so many ways, is a beautiful thing. I wish more people would see it as I do. Sure, sometimes I flip out and stay awake worrying, like a lot of autism parents, but not as much as I used to. There is no light at the end of the tunnel- yet. However, there are a lot of colors in my kaleidoscope. 

The Junior Advocate

As I've mentioned before, I worry- a lot. I worry about Morgan 24 hours a day, seven days a week. If I were to be given an extra hour in a day, I'd use it to worry even more. However, I'm proactive in my worrying sometimes. Some people call this crazy, I call this being an advocate.

I get the whole family in on this act, down to our toddler, Bailey, or Bay, for short. Bay is a real spark plug. He knows the basics of autism and Asperger's. People, who shall remain nameless (you know who are you are), think that I am over burdening a child that already has and is going to have the "heavy burden" of an older brother that is "different" to help guide through life. They think that I give my children too much information about autism and life in general. I call bullshit. That's right, I said bullshit. Allow me to enlighten.

Bay is an exceptionally bright four year old. He already can spot differences in how he operates from how his brother does (interactive play, imaginative play, dressing up, making up names for himself, appropriate answers to small talk, no stims). It saddens and frustrates him that his brother doesn't play with him like he wants Morgan to. It does the same for me and my husband. Tonight when it was brought up to me by Bay (for the millionth time, I might add), I decided to break it down and be deadly honest with my son.

You see, Bay is about to enter preK. He's nervous about the other kids being mean to him like some kids have already bullied his big brother (thank, bullies!). I told him, as bluntly as I could, that bullies, while they are everywhere, aren't as likely to bother him as they are Morgan. Bay doesn't do things "differently." He's neuro typical. The most he might get teased for is his slight speech impediment and ginger hair. Oh, and the kid loves pink and purple. But other than that, Bay's 100% neuro typical, all around American, boy.

I explained to Bailey that God makes all children special. I mean, really, really, really special. However, he made Morgan with an extra dash of special with his autism. Autism wired his brain differently and makes him see the world in a different way, takes away his ability to filter sounds, find patterns in things, notice things that other do not see, and most importantly, in a social way, it hinders Morgan's ability to act like other kids (in my case, I silently scream thank God when I go to the grocery store and observe other people's offspring). I told Bailey that one of Morgan's special talents include echolalia, which is how Morgan can spit out phrases of a movie or the actual whole movie when they're playing. However, I asked Bay if he's ever noticed that when someone asks Morgan a question, Morgan might answer with a movie phrase that makes no sense. Bay answered in the affirmative. That, I told Bay, is echolalia. That, I told him, is an ugly side of autism, according to the looks we get.

Another one of his brother's talents is building. Morgan loves to build- train sets only. This irritates Bay to no end since he wants to builds lots of things. I told Bay not to take that away from his brother by making Morgan feel wrong for that. Morgan already got teased, you see, for his love of Thomas the Train and all things train related at school and only at home and in his homeroom does he really get to express that love. Realization dawned on Bay. He'd been really mean a lot to his brother, without really realizing it. I've always told him "no teasing or hurting your brother."

As I explained to Bay that, because of things related to autism, Morgan has to be taken out of his regular classes for therapies and resource, something that Bay will never have to do, Bay looked sad. He asked, "but why? Why does Morgan have to do those things? Can't you tell them to let Morgan stay in classes?" I told him, "Baby, I signed papers saying that Morgan has to be there; those extras help your brother learn better. The classrooms are too loud and the other places are giving him skills so that he can be more independent one day." "But I won't have to do that?" "No Bay, you'll be a regular student, learning reading, writing, math, geography, and going to recess- when you're good and do your work."

Then the hardest part... Bay asked why his brother didn't want to play with him a lot. Morgan can usually manage maybe 15 minutes, tops. After that, he needs what I now recognize as a sensory break (soccer practice and games take some slick maneuvering). I've tried explaining it to Bay before, but he's either been too young or ignored me. I explained tonight in the school terms that although he wants to, Morgan can't take the overstimulation and the noise. It sends his brain into a tizzy and causes it to crash, like a computer. Bay got it. He asked what he could do to help his brother.... and that's when I explained about God making HIM with an extra dash of special, too.

As best as I could explain to a four year old, I laid out what I expected from my younger son. I told him that some day, he might feel like the older brother. He might feel like he is guiding his brother through life and that's okay. It might not feel fair, but that's why God gave him that extra dash of special. That dash is made up of compassion, love, and all good things. It is going to help him and Morgan. That when he sees his brother getting teased and Morgan's not understanding it, Bay is to stop it ("yeah, I'll stop those bad guys!"). That when we're in public places and he sees Morgan wandering, to hold his hand or to call out to him. When Morgan's needing space, give him space. That when someone asks, tell them, "My brother has autism, and you're issue is?" That might be wrong of me, but Bay already sees me doing all of this and is my own personal mynah bird, you think he's not going to copy me?

I pointed out to my younger son that Morgan wants lots of friends, and even has a few. He asked me, then, why didn't I have a lot of friends. Hmmm, I thought.... Well... I told him point blank that I'm very protective over him and his brother. That I can't take people being thoughtless of either of them and treating them like crap. Case in point, the "friend" that stupidly told me that she imagined shopping with Morgan must be like shopping with a two year old. She smiled as she said it. It was like being stabbed. He's one of the best behaved children I've ever met and sweet, to boot. I told Bay about that and he nodded and agreed that the former friend was, indeed, mean to him, too.

My point in all of this is that if your child on the spectrum has a sibling, it's never to early to turn that child into an advocate for their sib with autism- and the thousands of kids similar to them out there. Your NT child will one day grow up as all children do. Your child will hopefully be compassionate towards everyone they meet, but especially those in the special needs community. I hope that my own ginger haired younger child will see one of his classmates in gym, one that acts an awful lot like his brother and is getting teased, walk right up to that kid and announce, "Hey, you overstimulated? You want a friend? I'm your guy!"

I'm raising an advocate, not a jerk.