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http://seattlepi.nwsource.com/local/3617...ism05.html

Parents are autism's hidden victims
Baffling disorder hurts more than just those who have it

By PAUL NYHAN
P-I REPORTER

Sharky Munat was 2 years old when the police came.


For 45 minutes the toddler's screams pierced the thin walls of his mother's two-bedroom apartment, until a neighbor finally called the cops.

His mother was used to screaming from her unusual child, who cried for hours if she simply laughed while watching television. But Lillie Addams felt sick when a police officer stopped them to check her son for bruises as they walked to the park.

The officer quickly realized there was no attack -- he was just one of "those kinds of kids" -- but his mother wouldn't know the kind was autistic for two more years.

"Check it out, buddy. If you keep it up, they are going to take you away," the one-time ballet dancer told her son once the officer let them go. Then she sat on a park bench and cried for an hour.

Children have autism, but parents are often invisible casualties. Their child's disorder ricochets through their lives, breaking up marriages, draining bank accounts and robbing them of sleep. University of Washington researchers found these parents, among all with disabled children, suffer the highest levels of depression and anxiety symptoms, and parenting stress.

Since Sharky was diagnosed, his mother has dealt with depression, chest-seizing anxiety attacks, insomnia and incessant guilt that she wasn't doing enough.

"It's this overwhelming sense of powerlessness," Addams said. "I feel blamed by society, by insurance companies. As if it was somehow our fault."

Seattle may be a leading center for autism research and treatment, but its therapists and the medical community can't handle the growing number of families dealing with the disorder. Today, as many as one in 150 children are diagnosed with autism, up from three to four out of 10,000 a decade ago.

More than a year after Sharky's diagnosis, the Addams family felt alone and stressed. Without a map for treatment, they, like other Seattle parents of autistic children, were stuck in a maze of therapies for a disorder with no cure.

There are few insurance plans that cover touted behavioral treatments and not enough therapists or slots at specialized schools. Parents can wait 18 months for services -- after doctors urge them to begin treatment quickly -- and pay tens of thousands of dollars a year out of their own pockets for therapy.

Over the past year and a half, Sharky's three parents -- Lillie, her ex-husband, Ted Munat, and her partner, Stormy Addams -- have visited a dozen doctors, therapists and classrooms, yet they still can't fill big gaps in their son's treatment. "Everywhere we have gone they are pushing you in different directions," Stormy Addams, 43, said. "Or they are pushing against you."

On a cool afternoon in April 2007 while many 4-year-olds play at nearby Miller Park, Sharky comes home from school and stays inside his Capitol Hill apartment, running across the wood floors like any kid his age, and talking about Spider-Man and Big Wheels.

But he runs across the same area again and again, his ponytail and hands flapping around him, uttering words often impossible to understand. By his third birthday, this engaging child had choked a baby and wanted to kill the family cat.

His behavior meant there were no raucous birthday parties, play dates or big dinners out for this family because Sharky could get overstimulated, lash out and throw tantrums that lasted for hours, or simply invite unwanted glares and advice from others parents.

"Our world has become very small," said Lillie Addams, a registered nurse at Group Health Inc.'s cardiac unit.

The Seattle P-I talked to families, therapists and researchers around Seattle dealing with autism who echoed her alienation, anxiety and lack of support.

The daily grind

Like an invasive weed, Sharky's autism permeated most daily routines for his first four years.

At dinnertime in June, Stormy Addams snatches Sharky's broiled salmon from their tiny oven, puts it in the freezer and then onto his Hello Kitty placemat, hoping to avoid a scene.

"Make it colder. Make it cold. Make it cold," Sharky begs again and again because if it's warm, he likely won't eat, he will shriek with the same terror as when his bath is too warm.

Then a bite of salmon falls onto Sharky's Spider-Man T-shirt and he begins swiping at it compulsively. When another morsel drops to the floor, he finally screams, and Lillie Addams ushers him to the first of four timeouts in his bedroom.

After two hours of this, dinner finally ends, and it's off to the bathroom, where one parent holds him down so he won't thrash while the other brushes his teeth. Even after the 4-year-old falls asleep in Stormy and Lillie's queen-size bed that night, he thrashes, eventually bloodying Lillie Addams' nose.

"Everything is all drama," Stormy Addams says.

Fast-forward 10 months, and Sharky has taken impressive strides. His sweet social nature now far outweighs more typical outbursts of 30 minutes or less.

But his speech and comprehension remain noticeably delayed, and his mother's worry is just as intense, though now focused on finding and paying for therapy and the right school.

That means Lillie Addams often sleeps in bursts of two to four hours. She tried Ambian, Lunesta and Trazodone, but those sleeping pills worked only for a few months.

"What I am not doing?" Lillie Addams, 39, asked.

Last fall the worry got so bad, she thought she was having a heart attack when her chest began tightening. It turned out to be anxiety attacks.


Since autism remains such a mystery, parents battle this anxiety for years and constantly manage their expectations. When Sharky turned 4, Lillie Addams thought he would never go to college. Now she is not sure.

"Now I just hope he can lead an independent life, and have a girlfriend, or someone to love."

Her maternal hopes fluctuate because her son's autism is impossible to pigeonhole. With an infectious smile, he plays peacefully with his 5-year-old neighbor in the apartment courtyard one day and tells his father he loves him 20 times the next.

"Lots of friends of mine, their first comment is: 'What a happy child he seems to be,' " Munat said.

But Sharky always struggled to speak and understand. In the fall of 2006, a group of therapists, psychologists and nurses told them why, diagnosing him with autism, but not much else.

"It was kind of like this is what you got. See ya bye. We'll send you some paperwork," Lillie Addams said.

Since then, Addams has struggled to understand a disorder that's so hard to define that children are diagnosed on a spectrum. She still doesn't know where her son falls on that scale.

Meanwhile, treatment costs easily overwhelmed this family, which earns a combined $70,000 a year. They would love to get Sharky intensive behavioral therapy, for example, but they can't afford it.

"It's like having a carrot dangled in front of you," Addams said. "I make $30,000 a year, and often the cost of ABA (behavioral therapy) is $30,000."

Health insurance is little help. Few company plans cover behavioral therapies. After Sharky's two working parents cover co-payments for speech and occupational therapy there is little left for such promising therapies.

With little extra money, the three parents patched together Sharky's treatment plan over the last year, and worried his window to progress was closing because of what he missed. Sharky was diagnosed at age 4, later than many children with autism

The expense is one more layer of worry on an already complicated family. Lillie Addams and Munat divorced in 2002, and now split custody.

Yet this three-parent arrangement works, and Stormy Addams' role as stay-at-home mom and ad hoc therapist is clearest, etched in a tattoo of her cradling Sharky that runs down Lillie Addams' entire thigh.

Plans for the future

Autism is everywhere these days -- in People magazine, on Oprah, the presidential campaign trail and YouTube -- but none of this attention, or fresh state and federal money, has reached this family.

Instead, Lillie and Stormy Addams are so desperate that they may move to Colorado, California or Canada, anywhere that promises better support when Sharky's state benefits run out at age 7.

Amid their worry, Sharky makes progress. Over the last year, he learned to use the toilet, ride his Big Wheel, sleep in his own bed and brush his teeth.

To reduce their stress, the family now does yoga together every morning, and his mothers just resumed their only other stress reliever: going to the gym.

His meals and baths, though, are still served cold, and his mother still worries.

That's because Sharky will finish kindergarten this June at the UW's Experimental Education Unit. His parents wanted him to spend another year at the school because he lacks basic skills, such as writing his name, but he has to move on. They haven't been told where.

But Sharky has improved outside special schools and therapy sessions. A year ago, he slipped on his first pair of black ballet slippers.

Now every Thursday inside a North Seattle studio, Sharky glissades alongside his teacher and assumes a classic port de bras, his intense focus intermittently broken by a toothy grin.

"The more time I spend, the more hope I see," Lillie Addams said.


FAMILY BLOG

Ted Munat, Sharky's dad, has begun chronicling the family's story at the blog Still Life With Shark, stilllifewithshark.blogspot.com.

P-I reporter Paul Nyhan can be reached at 206-448-8145 or paulnyhan@seattlepi.com. Read the Seattle P-I's parenting blog, Working Dad, at blog.seattlepi.com/family.
parents again...never mind us, we're just kids of the devil come here to make our parents life a total mess with no thoughts expect to destroy (end sarcasm).  sounds too much like the "autism every day" garbage.

we already have coverage on parents and not enough coverage on the people most affected with autism, autistics, especially of the adult variety.

bravesj858 Wrote:
parents again...never mind us, we're just kids of the devil come here to make our parents life a total mess with no thoughts expect to destroy (end sarcasm).  sounds too much like the "autism every day" garbage.

we already have coverage on parents and not enough coverage on the people most affected with autism, autistics, especially of the adult variety.


Yes, but the parents are the ones who have to pay the bills and keep the house running and make sure everyone's needs are met. What's wrong with highlighting those difficulties?
There needs to be MORE stories from the viewpoint of the autistic, NOT LESS stories about parents, does that make any sense...

These situations are the kind Autism Speaks should help in, rather than funding wasted research for a cure.
I don't understand why this child can behave enough to take ballet lessons and screams all the time at home?  If he learned how to brush his teeth why do his parents have to hold him down to do it?  

Maybe time out just don't work for him.  

Sensory issues like cold/hot/warm.  I don't think there is a problem with serving cold food or having cold bath if that is what he wants.  Just cook the food ahead of time.  

I don't think that sleeping pills are supposed to be used regularly anyway.
sorry about my first reply, i was really fired up about all the negative language in the article and reference to victims and felt like a repeat of so much we hear from the cure orgs.  but it's a bit of a shame that parents are being misled to think aba will fix all of their problems.  but this is just a case of failure on autism speaks' part of not providing services that help autistics instead of fixing them to be normal, an agenda that autism speaks is currently pushing.
My parents say I was much calmer than most kids.
I think that four time-outs to his bedroom during a two hour dinner session is excessive for a 4 or 5 year old.  

Sorry, don't have kids.  So maybe I don't know.  If the kid can not control himself then the time-outs are discipline for what?
Hehehe mine too Smile

People say my last g/f, before the girl I'm with now, looked like mortisha Tongue

I was going to post something else, but for the life of me, I don't know what it was anymore, I *** hate that Tongue

Callista Wrote:
Okay. This article has all the usual hyperbole and sensationalism--that's obvious. But there is an issue here that's real, and that is the fact that parents suffer when their autistic kids are rejected, stereotyped, etc.; and they suffer when there is too much to do to raise the child and nobody helps them. Autism almost always means "difficult child" as well as "isolated parent". And that's a state of affairs that shouldn't continue.

When you have an autistic child and you go to the grocery store and that child has a meltdown, most other people have no idea they are looking at a scared, overwhelmed child. They think they are looking at a spoiled brat. You may be left out of the "parents' groups" that form around children's activities because your child doesn't have the skills or stress-tolerance to participate; and even when he can, you will always feel different because your child is different. For a neurotypical parent, the shunning for being "a bad parent" can be truly painful. They feel shut out of other parents' lives, isolated, because there's a stigma attached to disability that makes it hard to talk about life as an autism parent, hard to be open, hard to brag about your child's accomplishments or talk about their day. Most moms with typical kids will just look at them with pity or deluge them with the latest fad autism cures.

For high-functioning kids, the moms will get things like, "You just need to discipline him better." Being told you are a bad mother is very painful when you are trying as hard as, or harder than, everyone else. And remember, these are neurotypical moms. They NEED that social contact the way we need food and water. The reputation of autism shuts them out of a lot of social groups.

On top of that, raising an autistic child can be hard work. I've heard it described as "parenting squared". Maybe your child is an insomniac--sleeps four hours a night on a good day. Maybe your child doesn't have a good sense of danger, and you're forever having to pick him out of trees and make sure he doesn't run onto the highway. Maybe he has frequent meltdowns, and you're getting headaches from the screams and beating yourself up because you don't know what's wrong and you so desperately want to make it better. You need a break, but you can't figure out where to get one, and when your stress level rises, your child's stress increases too and things get worse. You have to deal with the school system, which probably wants to do the bare minimum. You have to deal with relatives who think anything from "He needs discipline" to "Find a good residential placement; he's ruining your life."

And everybody seems to want to pity you and tell you your child is either an angel or a demon, either has to "overcome" his autism or else will never amount to anything. You have to deal with the knowledge that your child is being bullied at school. You have to wrestle with special ed teachers who would rather just warehouse the child than teach him anything. And most likely you have to do all that alone, because autism's reputation doesn't leave much room for a reaction other than pity and subtle but ever-present shunning. And when you need a break, how do you get one? Getting someone to take care of a special needs kid is more than just calling up the neighborhood babysitter. Respite care is expensive or unavailable in many places; or else it's allotted in such tiny increments that it might as well not be there--two hours a month was one figure I heard. And then you have to wonder: If my child is not independent in adulthood, can I expect that he will be treated with respect by anyone who assists him? What happens if I die? How do I know if he's being abused or belittled or ignored?

Autistic people do suffer from the prejudice we get. But so do our parents. There's not enough support; they're not included in the community; and in general there's much more trouble coming from prejudice and isolation than there ever was from autism itself.

Great post!

Kinda harsh calling people bad parents, everyone can learn to do better though - often with abit of help.
So are parents being offered this type of help, specifically for their autistic children?  Some people want to say you can't blame the parents if they don't know what to do in certain situations.  I can blame the organizations that support only ABA and genetic research and offer nothing else to these parents.  

I know quite a few teachers who tell me that there are an excessive amount of bad and inadequate parenting skills around.

M Wrote:
I don't understand why this child can behave enough to take ballet lessons and screams all the time at home?


That's really common -- for autistic children to behave in one context and not in another.  Like at home, but not at school, or at school, but not at home.

Quote:
If he learned how to brush his teeth why do his parents have to hold him down to do it?


Knowing how to do something isn't the same thing as being able to do it, and/or being able to do it as often as necessary.

alectrum

atypical Wrote:

Callista Wrote:
Or being able to tolerate it, even if you can do it. Learned to take showers at eight... didn't learn to tolerate them (or take less than two hours) 'til eighteen.



Our son barely tolerates getting his hair washed - it's so hard for him.  Last month he suggested he wear swim goggles - I can't see how it helps, but he submits himself better.  He likes baths but not washing his hair in the bath.... My husband and I have been mentioning this idea to our 11 year old , like once a week suggesting... um, well how about a shower, it's getting warm out you're getting older... He's not interested - he says, well our pool will be open soon... (no shmapoo in the ppol though so it doesn't count ya know?) I figure just like everything else, when he can, he can. He does care baout what he looks like, he likes to keep his face and skin and hands very clean - and will not tolerate body odor - but his hair-- it's been getting pily fast... I'm sure I'll miss washing his hair someday.


I've just had a bit of a mad idea involving cutting the top of a cap and leaving the peak so that the soapy water doesn't run on his face and he can still get his hair washed.

alectrum

atypical Wrote:

alectrum Wrote:

atypical Wrote:

Callista Wrote:
Or being able to tolerate it, even if you can do it. Learned to take showers at eight... didn't learn to tolerate them (or take less than two hours) 'til eighteen.



Our son barely tolerates getting his hair washed - it's so hard for him.  Last month he suggested he wear swim goggles - I can't see how it helps, but he submits himself better.  He likes baths but not washing his hair in the bath.... My husband and I have been mentioning this idea to our 11 year old , like once a week suggesting... um, well how about a shower, it's getting warm out you're getting older... He's not interested - he says, well our pool will be open soon... (no shmapoo in the pool though so it doesn't count ya know?) I figure just like everything else, when he can, he can. He does care baout what he looks like, he likes to keep his face and skin and hands very clean - and will not tolerate body odor - but his hair-- it's been getting oily fast... I'm sure I'll miss washing his hair someday.


I've just had a bit of a mad idea involving cutting the top of a cap and leaving the peak so that the soapy water doesn't run on his face and he can still get his hair washed.


even whenhe is at the hair salon they wash his hair and he dosn't get wet at all.. It's about his perception/worry that he might get wet (I think).  We actually put in a pool, it helped him get over alot of water concerns - he swims under water and gets all wet - he just doesn;t seem to like having only one part wet... fine with me.

Do you mean a swim cap? He is a big inventor, I may give one to him and see what he comes up with.. he is motivated tomake the prcess better.  I am hoping he will just shower (alone) eventually wouldn't he then have control of the water?


The thing I was thinking of was like a cross between a swimming cap because there is a tight band on them that makes them waterproof, and an ordinary cap that has the peak for water to run off.  

Sure he will shower for himself one of these days.  He'll work himself up to tackling it, don't worry.  Smile  Probably when you least expect it and have other concerns he'll surprise you.

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