Healthy Living

Friday, July 25, 2008

Autism: Should there even be a cure for it?

For a long time, I've felt compelled but put off writing about autism. I haven't done this because I in any way disregard the relevance or sensitivity or critical nature of autism in the world we live in right now. I've done it because, frankly, I am scared of it. Autism frightens me.

I'm not afraid of children with autism or learning about autism or discussing autism. As hard as it is to admit, I have been nervous to let autism enter into my writing just as I have been nervous it would invade my home. That's why, when I read this moving and forthright article by Julie Deardorff in the Chicago Tribune, I felt called to finally put autism at the center of my screen.

Deardorff's look at autism isn't about vaccines or supplements or diets, the controversy and conversation we have become used to hearing in the last few years whenever autism is mentioned in the media. Rather, it is about whether or not autism is treatable at all, and whether we should embrace all that autism brings instead of seeking a cure that will halt its symptoms.

The arguments on either side are fascinating and passionate. But then, I don't have a child with autism and I am not a person who lives within the spectrum of its "disorders." This place, where I've stepped back in fear, is where Deardorff pulls me in.

She begins it all eloquently, evocatively, speaking straight to what gripped me and I am sure grips many parents who study their children for smiles and hugs and how they relate to anyone, everything around them in the early years:

One of my greatest fears is that autism will break into my house and steal my son. It may be irrational, but it's there: He'll wake up one morning and vacantly look through me. He'll lose his words, open and close doors for three hours, or begin screaming, as if in pain.

Then, bam! The child I know and desperately love will disappear into a mysterious world where I can't reach him.

She continues on to note that, "[t]o some parents, kidnapping is a near-perfect metaphor to describe the agony of autism," and I imagine you've heard many of these parents lobby and argue and rally passionately on behalf of their children. I imagine you've seen them on Oprah taking a stand against vaccines and promoting gluten-free diets (like Jenny McCarthy, now as well known for her entertainment resume as her autism awareness), you can hear that passion and commitment and sometimes, desperation.

Maybe that's what is scary as well as hopeful -- what can be involved in caring for an autistic child, what some parents have to go through just to get a diagnosis or therapy or the help they need. It is overwhelming.

This is also why it is scary and hopeful to debate whether recovery is necessary at all for people who are autistic. Most of us are probably most familiar with the race toward recovery -- from alternative treatments to day therapy programs to diets -- that we've known families who participate in or raise money for or that we've just seen on a news magazine show. But there is also, as Deardorff points out, growing support for what is referred to as the "neurodiversity movement."

The neurodiversity movement advocates embracing the unique thinking and ways of being associated with autism rather than seeking a cure or referring to it as a disorder. It's no surprise that, while sounding idyllic, it is controversial, particularly among some parents of kids who are unable to live independently, low-functioning or highly removed from human-to-human connection.

Whereas someone high-functioning or on the Asperger's end of the autism spectrum might not want to "cure" the way their brain works differently than other people, Deardorff and others say that this only tells one part of the autism story. Just like diet or other treatments may not lead one kid into "recovery" from the ways his autism manifests, accepting (let alone embracing) neurodiversity and all it means may not work for every family.

What helps my fear -- and I wonder if this is true for any of you -- is that the talk around autism is building and that how and what and why we discuss it is widening. There's clearly much more to be learned, and as a mother, I hope that there are one day many more choices for parents of children with autism and for those kids as they grow into adults.

Until then, I hope we all can keep talking (and writing) honestly when autism is the topic of conversation. It may not alleviate all the fear but it sure can help with the hope part.

What are your thoughts on the neurodiversity movement? Is recovery necessary for everyone with autism?


Read on:

[photo credit: Getty Images]
Syndication:

From the Community…

Comments 1-10 of 26
  • Bbee's Avatar
    Posted by Bbee Wed May 14, 2008 5:20am PDT

    Hi Jessica!

    WOW, what a great post and thank you! Your courage to face your fear is moving.

    It is too late to save my little boy from autism. And I can tell you first hand that I was crushed when we found out Mitchell had it. We were in denial, then agony and then a deep depression with all the ugly things that go with it. I am no longer married to Mitchell's father. I grieved as if I had lost a child due to an untimely death.

    As Mitchell grew from a baby to a tot I knew cryin' in my pillow night after night was not helping him in any way.

    So, I brushed myself off and with very little support from the public school system or my dr.'s I did the only thing I could think of to help him. I literally got down on the floor and eye level with this sweetie of mine and almost forced him to look in my eyes and connect with me. I did this for five long years day after day hour after hour. To my surprise he started looking at me first and wanting to play trucks and dolls and what not.

    I also invested in the PECS system for those of you that do not know what that is it is the Picture Exchange Communication System invented by Andy Bondy. And to clarify what PECS are they are little hand size pictures of everyday items like a ball or a puppy. These little pictures helped Mitchell identify all the things around him. IT WORKED ... and I mean to tell you it opened the door to Mitchell's communication skills in a HUGE way.

    Mitchell is nine years old now and he won't stop talking! YEP, you got it *non stop chatter! How wonderful is that?!

    We go through some very *difficult times and our fight will never be over ... tears are streaming down my face as I write this because of how proud I am of Mitchell and how I admire his ability to laugh and smile day after day.

    I could go on and on and on about our *daily struggles and worries and my fear for his *future after I am gone.

    If there is a cure then I think we need to do everything we can to save the next little boy from this awful thing called autism.

    And again, I am so proud of you ... you faced your fear and have now become an educated voice sounding off about autism.

    GREAT POST!

    *I have so many funny stories, heart breaking stories and much more to share about autism and my Mitchell ... I really could go on for days!

    Report Abuse
  • celticangel1969's Avatar
    Posted by celticangel1969 Wed May 14, 2008 8:14am PDT

    As a mother of three wonderful kids, I felt more than compelled to write. My 17 yr old daughter was diagnosed with Asperger's syndrome at the age of four. I had had a difiicult pregnancy and tried for years to find out what I did wrong to inflict this disease on my child. My doctor finally pulled me aside and told me that I could spend all my life blaming myself or take the best care of my daughter that I could and accept the fact that she is "different". I have stopped blaming myself and take care of her the best that I can. We are lucky in the fact that she goes to a wonderful public school that has actually found a college for her to attend when she graduates. She has grown into a beautiful young lady with an amazing artistic talent. As to the finding of a cure, I'm all for it! But, shouldnt we all focus more on prevention?

    Report Abuse
  • Jenae's Avatar
    Posted by Jenae Wed May 14, 2008 8:38am PDT

    What are your thoughts on the neurodiversity movement? Is recovery necessary for everyone with autism?

    I think it is great that people are accepting people with autism and talking about it more. For people with Asperger's I can understand the neurodiversity movement because most of them are so much high functioning than kids with just regular autism. My cousin is Autistic, he can't talk, he can't take care of himself, he's almost 5 and they can't get him potty trained. Something NEEDS to be done about this. For him it is not about being diverse and about thinking differently. For his parents it is like he is 'kidnapped' they need help. It is not about thinking differently for him it is about being about to live and function enough to speak and take care of himself. What about those kids? I think they deserve prevention or a cure. Jakob deserves better and as much help as he can get and so do so many kids out there.

    Report Abuse
  • Jessica Ashley, Shine staff's Avatar
    Posted by Jessica Ashley, Shine staff Wed May 14, 2008 8:40am PDT

    Bbee and Celticangel, thank you so much for sharing your stories and a bit about what has worked for your families and kids. Celticangel, I think you raise a really important point that we should turn our eyes to prevention as well as recovery and that makes me wonder where we are scientifically with that. Anyone know?

    Jessica.

    Report Abuse
  • missy's Avatar
    Posted by missy Wed May 14, 2008 10:28am PDT

    As the mother of a 26 year old son who is austic and nonverbal yet mentaly 4 years old.I thank you for the question.I as a mother would love to said yes.But as a mother and a Christian I would anwser no.I love my son and am happy for the love he is able to give and hie wonderful smile,and his caring heart.And for the peopel who do every day what I as a mother could not do.My son lives in a group with his peers and he is happy.I am grateful there is help for people when my son and I need help there wasn't to much postive help.But like me he is warrior.

    Report Abuse
  • lee and ethan's Avatar
    Posted by lee and ethan Wed May 14, 2008 11:38am PDT

    My name is Cristal, and my three year old son, Ethan, is believed to be autistic. I am a single mom, and have gone to every specialist Medicaid can cover. One says "autism", one says "pediatric developmental delay", another says "bipolar with obsessive compulsive disorder". I am so confused!The biggest problem is now when any child falls behind, they group it into autism. I can get no answers from the public school, keep getting referred to another specialist, and some just want to write my baby off as "another case of autism". If I was less stubborn or had less information like so many parents, I would just give up and let them label my son. I have been working with him for over a year now, and he is trying SOOO hard! He wants to learn, communicate, and to "be good"-he just doesn't understand how to get there. I have decided not to label my son and not give up and push a little more every day and endure the heartbreaking confusion on my little man's face and you know what?--I think it's working! Thank you for speaking on this topic-everyone needs to be aware so we can find a solution...never give up!!

    Report Abuse
  • Bbee's Avatar
    Posted by Bbee Wed May 14, 2008 12:18pm PDT

    Lee,

    You said it best ... NEVER GIVE UP!

    I am happy to give you all my PECS and my PECS manual. I will send them to you if you want me to.

    Here is my email address ... we can talk for little if you want to ... kFeinNicholson@yahoo.com.

    NEVER GIVE UP!

    Report Abuse
  • EddieO's Avatar
    Posted by EddieO Wed May 14, 2008 2:14pm PDT

    I have a nephew we believe to be autistic, this article was

    very informative and has shed a light on what I thought was always

    going to remain in the dark. I certainly want to help in every way

    I possibly can.

    Report Abuse
  • Josie's Avatar
    Posted by Josie Wed May 14, 2008 3:55pm PDT

    As the mother of a wonderfully loving, bright eyed, highly intelligent autistic son, i have to say the hardest part has been the waiting for the connection from the action to the verbal expression of the action. For nearly 5 years i waited to hear him say mommy. He knows who i am but the connection between the word most infants knows to me was a long and difficult road. Getting therapy for him is quite expensive since there is a cap on what the insurance will allow. And while the insurance pays a much lower amount after the benefit is used I pay approximately 5 times that amount so after we exceed our benefit he loses the therapy he desparately needs. But aside from all of that, I would not change him for the world.

    Report Abuse
  • jandcholden's Avatar
    Posted by jandcholden Wed May 14, 2008 3:58pm PDT

    Lily is a beautiful, 3 year old girl. 1 1/2 years ago, I started to notice that my daughter wasn't looking at me any more. She didn't say Dadda or mamma or smile at the camera. She didn't respond to her name. She stopped eating food with color. She started walking on her toes and throwing unbeleaveable temper tantrums. Something was different. Her doctor wanted to "wait and see" what would happen. The state recognized that there was something wrong with her but didn't do anything about it (they said that they didn't have a speech theropist in our area) It wasn't until we took her to a neurologist that he diagnosed her as a high functioning child on the spectrum.

    Immediately the state found a Speech theropist and an OT to help her and us. Because of the theropy she has a few words. She now attends special school 3 days a week to work on her social/emotional, speech and fine motor issuses.

    I personally don't believe that immunizations were the cause. We have hope that someday there will be a cure so that she may function in society as a "normal" individual.

    Report Abuse
Comments 1-10 of 26

leave your comment

You must sign in to post a comment

Sign In for personalized information

New User? Sign Up

Updates Chatter on Shine...

Health Byte

Kim Cattrall might not quite be my own personal girl crush just yet, but she is definitely my body image hero.