Monday, April 26, 2010

Autism Awareness Day: Guest Post By Catherine Parry


Did you know that April is Autism Awareness Month?
Did you also know that 1 in every 166 children in the U.S. has Autism Spectrum Disorder? Today on all three of my blogs we are talking about Autism. This is a guest post written by my neighbor Catherine Parry and her son Will:



Catherine and her son, the imaginative Will Parry

I write this as I sit beside my son in his tenth grade Human Biology class. He’s taking an open-book, multiple choice and true/false test over the evolution chapters he studied the past week. Based on his frantic page-flipping and worksheet rattling, I can see that I’m using the term “studied” loosely. Apparently this is one of those weeks when little information made it past his tympanic membrane (a term I picked up this year in Human Biology) and into his brain. I’m never really sure whether he’s paying attention to his teachers or not, because in classes he always looks as though he’s mentally escaped to Uranus. “Will,” I often say in an attempt to bring him back, “you’re on Uranus again.” “Mom, that’s obscene!” Only sort of, and it’s so fun to shock him.

For eight grades now (we packed it in for fifth and sixth grades and homeschooled), I’ve acted as Will’s aide in the classroom. The reasons for this unusual arrangement are various: suffice it to say that over time we’ve learned that it works best for Will. He was four years old and enrolled in BYU’s preschool when we received a call from the head teacher requesting that we have him tested for developmental delay. We were a little puzzled why she would think that our exceptionally bright son would need such a test, but he had been born ten weeks early (three and a half pounds), so we reasoned that perhaps her teaching expertise let her see delays that we thought he had outgrown. You can imagine our surprise, then, when the testers told us that he scored extremely low on all the tests. His best was math, on which he earned a 25%. As we left, one of the testers handed us a paper with three names, addresses, and phone numbers--the middle one circled—and said, “I strongly urge you to have him tested for autism.”

Autism? That was what the oldest child of my mother’s visiting teacher had had. He didn’t talk, spent most of his time sitting in a corner banging his head against a wall, and they put him in an institution when he climbed on top of the refrigerator and jumped down on somebody. That didn’t sound like Will. I’d learned in a college class in the 1970s that autism was caused by “refrigerator mothers,” who denied their children their nurturing warmth and affection, causing them to turn inward and shun human sociality. That didn’t sound like me, who was so excited finally to have a baby at age 39, that after his birth no other responsibility got its due time and attention. Nevertheless, as we walked from the building to the parking lot, carrying our short list of autism specialists, my husband and I knew that the tester’s informal “diagnosis” was correct. We learned later that she recognized the characteristics because she, too, had a son with high-functioning autism.

While we waited to see the specialist, we read about the disorder and began learning how to help our son. I won’t pretend that the bottom didn’t fall out of our little world. The exceptionally beautiful colors of that fall contrasted with our bleak inner landscapes as we read that a child with “mild” autism and no mental retardation would function in life as if he or she were mildly mentally retarded; that autistic people rarely marry or have children, and when they do, those marriages more often than not fail. We read about a young man with exceptional talent for enjoying and understanding beautiful music, who ended up sweeping the floors in a music library because his autism impeded his ability to finish school and cope with the pressures of a career. We grieved for the death of our son’s future as we had assumed it would be--scholastic achievement, a church mission, marriage, children, a career, church service--knowing now that such events would either not happen or would happen differently for him and us. There’s no use pretending, either, that our joy at the achievements of our friends’ universally brilliant children hasn’t been tinged with thoughts of what might have been for our own son. We began, though, to wonder fairly early whether we truly grieved for Will, or whether our parental egos grieved our inability to live and achieve through our child. The longer we have been parents, the more we have learned to distrust our motives for responding sharply if Will melted down in public, or for demanding obedience just because we said so. Will’s most challenging task may be training us to act in his best interest, without worrying about how our decisions affect our parental image.

None of these musings, though, give you a sense of Will’s eccentric charm and how interesting life with him can be. His often quirky interests have taken us through studies of bats, cacti, lemurs, volcanoes, and cephalopods (the family octopi belong to). At one time, thanks to Will, we knew more than any of our acquaintances about the mating habits of cuttle fish. When he was four, he was a firefighter. Assuming that was what he would be for Halloween, I asked about some costume detail, to which he replied that he wasn’t going to be a firefighter. Astonished, I asked why. “Because,” he replied, “for Halloween you dress up as something you’re not, and I am a firefighter.” One day during his pirate phase we became quite angry with each other, and he shouted at me, “You blackguard! You scurvy knave!” Often I learn unpleasant things about myself, like the time we visited the Louvre during a BYU Study Abroad. I unwisely decided he and I could manage lunch in their tearoom, but before I could catch him, Will darted away from me and ran smack into a French waiter carrying a large tray laden with dirty dishes which crashed to the floor. As he began swearing at us in French, I grabbed Will and fled in embarrassed panic from the restaurant, not stopping until we reached the anonymity of the gift shop several floors below. Not even the wrath of a wronged French waiter could keep Will and me out of a museum gift shop: for several years they were his favorite places.

As I finish this little essay, it is the late evening of an exceptionally full Sunday. Today, my fifteen-year-old son, who deals with the challenges of autism, bi-polar disorder, and obsessive-compulsive disorder, admirably fulfilled his duties as president of the teacher’s quorum in our ward. He arrived at church in time to help prepare the sacrament, attended a meeting in which they discussed how to help other kids in need, went with his dad to visit an elderly couple, and attended a fireside in the evening. Sure, he needed help shaving, putting on his tie, buttoning his cuffs, and as usual, he refused to comb his hair. In an attempt to be funny, he doubtless made inappropriate comments during his classes and the meeting, and he compulsively ate cookies after the fireside. So did I. None of Will’s mental challenges will ever go away, some aspects of them will even worsen with age, but in facing those challenges he has shown intelligence, courage, and determination. He is good natured, fun, and funny. He takes seriously his religious principles and duty to God, and is learning his duties to society, though those lessons come more slowly. I love him, and can ask no more.

Catherine Parry is a wife, mother and professor of the English arts. She also happens to be the woman I want to be when I grow up. Or the woman I want to be right now. She's intelligent, unique and completely enjoyable. She's also my Relief Society President. You can read more about Will and his upcoming novel Chronicles of the Scarred by going here.



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Awesome:






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On my other blogs today:

c jane's Guide to Provo
The Provo City Half Marathon & 5k benefits children with Autism find out how



dear c jane
don't miss this Jammin' Jen video--music therapy for children with Autism
click here
(hint: you might cry like I did).


I am c jane and this is Autism Awareness Day.
contact me:
cjanemail@gmail.com



57 Pieces of Opinion:

Tanya and Colin said...

Will sounds like a great guy with a wonderful family. It also sound like he has his priorities in order! Good luck Will!

Molly said...

Thank you for this - thank you so, so much.

Brenda said...

Does the author have a blog? Please do let me know. Thank you so much, Brenda

The Boob Nazi said...

Thank you for this story. I've worked with children with autism, and they are wonderful children who have to deal with such an awful disease. My nephew has PDD-NOS, and he can now communicate well at 5 years old.
Sigh, also, thank you for not talking about a "cure." Sigh. I'll save that rant for another time and place.

Christine said...

I too have a son who is on the autism spectrum, He is a high functioning Asperger's syndrome guy who was absolutely devastated when he was turned down to serve a mission.
Like you, we knew so many in depth subjects, his favorite being dinosaurs, sci-fi and Legos.
He may bring many challenges, but with those challenges comes learning and blessings!

kirsten said...

As a mom with a spectrum kiddo - thanks for this! The more my neighbors/friends/his teachers, etc. understand Autism, the better our lives are!

I have to point you to this post:
http://momnos.blogspot.com/2010/03/on-being-hair-dryer-kid-in-toaster.html
The best 'What is Autism' post I've ever read.

Anonymous said...

awesome-thank you.

Marie said...

BEAUTIFULLY written!
As a Mom to a son with Autism...Your words at the end brought a tear to my eye..
"I love him..and that's all I can ask for"

Extraordinary Housewife said...

I don't know if you watched Celebrity Apprentice last night (I'm totally addicted, kind of like watching a train wreck.) but they raised $347 thousand for the Hollyrod foundation. Absolutely wonderful.

Brandy Wheeler said...

Oh, thank you so much for mentioning Autism Awareness month! We are a family who deals with this daily. I appreciate your featuring a family. The one point I would love the world to understand is that not all Autism looks or acts the same. Most often when I tell people that my son has Autism, they ask what his special talent is? I can appreciate where they came to even know about Autism (thank you rainman) but, that's just one very rare type. So, if I may ask your commenters and fans to take a moment and Google Autism Spectrum, they will get a litte clearer picture of what Autism looks like!

Brandy

Ruthanne said...

Thanks for sharing this, it was really an eye opener for me, and made me love you and your son even though I don't know you. I also want to be like Catherine when I grow up, what an inspiration!

Anonymous said...

Hugs to that extraordinary woman!

Salmon Tolman Family said...

I love this woman and her writing. Thank you so much for sharing your story!
My son is 3 years old, and he's banged his head since he was 9 months old and awakes at all hours of the night. He has difficulties in public situations and severe behavior problems. We've seen countless doctors and specialists. He's been diagnosed with an autistic spectrum disorder. He is a wonderful child, but with only two moods: funny and charming or angry and upset. And we love him so much!!! Thank you CJane for this guest post!

Julie said...

Thank you for bringing a greater undertstading to being human and the challenges it can bring us...Your son seems delightful and happy. I thoroughly enjoyed every word of this post!

Anonymous said...

Love this! Thank you for sharing!

And,(said in tatle-tale voice)...Ohhh, Stephanie used the Chief's name in her blooooggg... You going to put up with that? :)

Jocelyn said...

I LOVE this entry. I knew I would love it from the beginning and then when I read, “you’re on Uranus again.” I knew I was head over heels in love with her and her son.

She is a warrior whom I admire. My son has Sensory Integration Disorder, about as close to the spectrum as one can get without being on the spectrum. I laughed and cried as I read this. Laughed because I go thru similar issues with my 8 year old. Cried because I am grateful I am not alone. Laughed because I can tell she is a mom who loves her son unconditionally, cried because I am not the only mom who feels so proud of achievements in their child with a "disorder" He is phenomenal, and we can tell why, look at his mom and dad, who we can tell support their child. How many moms sit thru school with their child and not just one year either.

I thank-you for sharing your wonderful son with us. He is amazing and you SHOULD be proud of him. These children CAN be worked with and yes, we rejoice in EVERY little improvement. Someone asked me why I rejoiced in such small improvements. I think it's because when my "world crumbled" I didn't think I would have those improvements.

Love to your family.

Carolyn said...

Thank you so much for this post. I too am a mother with a son who has autism and wrote his story this month in honor of autism awareness. Of course it wasn't as nicely written as this poster. :) Thanks again for getting the awareness out there.

lisa said...

I know both of these amazing, funny, wonderful human beings and they are every bit as wonderful in real life!

I want to be Catherine when I grow up too!

springrose said...

Thank you for sharing! I think once you have a child diagnosed with something on the spectrum others seem to come out of the woodwork! That is the way it has been for our family! My daughter has Aspergers with sensory disorder. My nephew has Aspergers with defiant disorder and ADHD, and another nephew has Aspergers with ADHD and some sensory. It is such a hard thing to deal with, but knowing people are becoming educated and are compasionate as you are it helps. Just to get close to one of these fabulous kids is a miracle, but to hear them laugh with an addicting laugh it is marvelous. And thanks for the video on your other blog! How wonderful people are!!

TX Girl said...

I had to read this little snippet over and over. It was just too beautiful.

"We began, though, to wonder fairly early whether we truly grieved for Will,...may be training us to act in his best interest, without worrying about how our decisions affect our parental image."

My parenting challenges are nothing compared to yours, but I for one still need to remember how simple and basic a principle this is.

Elise said...

I took Dr. Parry's Reformation Humanities class this last semester and he spoke about Will a number of times. I loved that class and came to know Dr. Parry to be an amazing man--now I know it's with the help of such a wonderful family. What a lovely, tender post.

Sunny Girl said...

Thanks Cjane! I have two sons who had Autism Spectrum disorders. One is completely well now, on his way to serve a mission and we are still working to resolve our other son's issues. Our sons' conditions were results of their immunizations. The thimerosal--mercury--in the vaccines is toxic to the body and particularly for the brain. This is why autism rates have exploded--10 times what they were in 1970. As we have sought alternative methods of healing, we have been able to have our son back through getting the mercury out of his system and other modalities. Glyco-sugars are very helpful for this disorder and we are confident in time, we will have our second son completely free of this disorder as well. There are solutions out there!

karen gerstenberger said...

Thank you for posting this.
Thank you to Mrs. Parry for writing and sharing about Will. There is a blog (for which I write a monthly column) called Hopeful Parents (www.hopefulparents.org). I wonder if she would ever want to be a guest writer? She has an awesome, inspiring voice!

Elizabeth said...

It's wonderful that you're doing this on your blog, given that you reach so many people! I want to point out that recent statistics state that autism affects, now, 1 in 150 children.

Beautiful post about Will.

Miller Family said...

Thanks for the post. As others who have commented, I too am a mother of a child with autism. C Jane is wonderful for keeping something like this in mind!! BTW, the new stat of American children with autism - 1 in 91.

bethany said...

Thank you for this post. As a mother dealing with the reality of my son being evaluated and diagnosed with autism (next week) it was nice to read that someone else has felt the very same feelings that I have. Thank you for being so honest.

Stasia said...

Beautiful post. I don't have a son with Autism but I do have a son who is dealing with severe mental health issues (maybe bipolar?). I need to read posts like these to know my feelings are not just mine but every mother's. Thank you.

Simy said...

Catherine,
You and Will are truly an inspiration to us. We love your family.

Rick and Anne said...

I knew your blog would bring me something special today! My two eldest boys are also autistic. It was so comforting to hear of another young man with the same struggles who blesses the lives of others. My husband and I learn something new every day from our boys and there is always a laugh to be had! I needed to hear this today.

Anonymous said...

Thanks for bringing attention to this issue.

Also, it is National Infertility Awareness Week www.resolve.org

Mrs.Dr.Shot said...

Thanks so much. I'm blessed to have a very loving autistic child, but have the same fears as the mom writing. It's really helpful to hear from others.

Martha said...

that was so beautiful. thanks for sharing.

Jessica said...

My little boy, who is about to turn three next week, was diagnosed with an autism spectrum disorder last year. I had a young friend ask me if I thought he might be a musical genius or have some other amazing talent. I told him that right now my greatest hope for him is that one day he can tell me what he wants and that I will hear him say, "I love you."

As difficult as his disorder can be at times and as much as I have grieved for the life I wanted him to have, Charlie is a light in our home. His spirit shines despite his difficulties in connecting with others and communicating. I love this sweet angel boy and feel priveleged to be his mom.

Thanks to Catherine for sharing her story. Her son's abilities and challenges are different than my Charlie's, but I could relate to so much of what she said.

Christy said...

My little brother is special needs, though not autistic and this was a beautifully written and very honest post. Thank you!
I also have to mention, though I don't know much about it....apparently the EPA is coming out with a study linking autism to some childhood vaccines as a number of them are made from cell lines of aborted babies. Which is rather frightening if you think about it.

Julianne said...

This is one of the best posts I've ever read. We're just learning some things about our son that puts him on this Autism Spectrum. The part you talked about how it affects the parental image -- oh dear me. I'm so worried about how I am perceived, and when you have a kid with these problems, people perceive you a WHOLE lot differently. It's a really hard pill to swallow.

Much less, the pill of "my kid has something different about him, something that will affect him forever" is also a really, really hard pill to swallow. In fact, I'm still swallowing it.

Anyway. Thank you for this lovely wonderful post. Thank you, cjane, too. Your birth story last week was incredible.

Jennifer said...

As a mother of an autistic daughter, I wanted to thank you Cjane for shining a spotlight on this. Also, the CDC released new stats a couple of months ago. Autism now affects 1 in 110 children and 1 in 70 boys.

Rachel C said...

I'm sure this post helped many people today! Thank you.

Jodi said...

I have two boys on the spectrum. I just received an email from my 8 year olds teacher this afternoon informing me he had taken to throwing pencils in the classroom today. I ran into Catherine's post shortly after and it left me smiling.

Thank you for keeping the sunshine in my Monday Catherine.

julia said...

Christy:
If you don't know very much about something, perhaps you should get the info, before you start telling people about it. Vaccines are not made from aborted babies. This is an urban legend that has been propagated for years. I know this, because I am a physician, who knows what she gives to her patients. I have done the research. Vaccines are made from either live or killed virus...I won't get into the science here. Also, the EPA does not have any research studies involving autism, or aborted fetuses. They handle environmental issues, such as mercury toxicity, which may be what you heard.
Juliaj

Debbie said...

Very inspiring. I have an 11-year-old son w/ high-functioning autism and he has also written a story (with my help but mostly out of his imagination) about a super-hero and we're now trying to find someone to publish it. Loved reading about Will.

Katie Price said...

My nephew is autistic and I actually just came back from lunch with him. He's six years old, and possibly one of the most special children I know. There is something so different about him, you can see it in his eyes. It's like he understands what is important more than we do, and doesn't bother with the rest. I salute anyone who deals with autism on a daily basis - you are all my hero.

Keri said...

I wrote last week that it took 11 years for my husband and I to have a son. We are now discovering that our 5 year old has Asperger's. The bliss of finally having a child wore off as the violence, head banging, and other excitements became incredibly bad. Does anyone know of available resources for us to learn how to best help our son? We have been unemployed for 19 months now and the services offered by Medicaid and the school district have thus been greatly lacking. I would be grateful for any information.

Chez Zizi said...

Thank you for sharing. I am a teacher of children with Autism and it is wonderful when you have a family like yours to be so supportive of their child.
Zizette

Steph said...

Thank you for such a beautiful account of life with a child on the spectrum. Catherine, you are amazing!

@ Keri who commented above. I would be happy to talk to you and help you if I am able. I have 3 boys on the spectrum. Please email me at stephanie.blackard@gmail.com

I love this blog and I love it even more for recognizing Autism Awareness month. Thanks, CJane!!

MD said...

I really enjoyed this post. Thank you for sharing. Will sounds like an awesome guy. It also sounds like he has an amazing advocate and mother!

regina said...

i have three children from high functioning to non-verbal still bathing her. we just started the bi-polar phase of this fantastic journey with one of them and you know what? i don't want to change it. the make me laugh far more than they could ever make me cry.

ps. i am all for inappropriate comments in church will, more people would come it we all said what we really thought.

stodmor.wordpress.com

Suzanne said...

I think it is absolutely wonderful that you are so dedicated to supporting your son and his education!
I also think it's great that you nurture his writing and artistic talents. As a family, I'm sure you an an inspiration to many who deal with daily challenges.

Laurie said...

Thank you for sharing. I sure admire this mom and her son.

Pol said...

Thanks for this. I have an 8 year old high functioning autistic son. He cannot keep quite during church, he takes every comment as addressed to him personally, and calls out responses. I used to find it hard, now I know that the congregation love him as he is, and that they are blessed by his enthusiasm for the Lord.

Not just a scientist... said...

Thanks for posting this lovely and thoughtful essay. I hope you won't mind me submitting a counter to one of the comments above, just so an alternate viewpoint is available to your readers. The notion that autism is related to thimerosal in vaccinations has been (thoroughly) debunked, - there is no evidence that this is true, and in fact the original scientific publication making that claim was recently retracted by the journal because the results published therein were faked. Yes, faked. In fact, thimerosal has not been an additive in early childhood vaccines for over a decade, yet incidences of autism have not decreased. More likely it is simply a coincidence that the symptoms become noticeable at about the same time that early childhood vaccinations are given, combined with the fact that autism itself was not included in the DSM until 1980, and other spectrum disorders were not added until the DSM-IV in 1994. Even if your readers don't agree with the above statements, I hope they will spend a little time learning more about some of this issues. Avoiding childhood vaccinations altogether (as the anti-vax crowd sometimes suggests) could lead to the return of absolutely devastating childhood diseases - we are lucky today to have very little societal memory of what was once a very common occurrence - regularly losing our youngest family members to diphtheria, measles, polio, etc. I'm sorry to draw attention away from the larger story, because understanding autism spectrum disorders is important, but even more importantly understanding the *people* who experience them (both those with the disorder, and their families & friends) hopefully will help us understand that constantly focusing, with regret and blame, on the causes of the spectrum disorders leads us to miss the larger lessons and relationships we could be experiencing from these unique people.

Anonymous said...

I have a close friend that ended up having two children with Autism (she has 3 girls). Upon finding out that the baby had Autism, through prayer, she found this site;

http://pecanbread.com/

This diet did offer her youngest daughter a 2nd chance at a normal life. In fact after going on this diet she no longer shows any signs of Autism. And I am sure it was because it was caught and treated at such a young age. The oldest daughter with Autism still does have Autism but her mother has shared that she is impoved tremedously. If you want to read her blog here's the link;

http://ckcclan.blogspot.com/

You have to go back a bit to read about her discovery of the diet and how it has helped the girls.

I just thought I would share. You shouldn't hide good information that has helped one parent - I believe in the power of sharing knowledge. :)

cat~

danette said...

My son does not have autism, he does however have a generalized learning disablity. He has the most tender spirit.
My feeling while reading this, and these are just feelings is that maybe there are more cases of autism because Heavenly Father needs away to protect these special special spirits. These children up in Heaven where Heavenly Fathers chosen kids and they need extra protection down here from Satan. I don't know just a thought. Makes since to me.

Emily said...

I LOVE CATHERINE PARRY!!!

Anonymous said...

Loved this blog post!
Thanks for sharing!!
~ Jess

Christine said...

That was enlightening and inspiring to read. Thank you!

Lilly said...

I agree, please start a blog. It was a truly wonderful post.

Ashlee @ I'm Topsy Turvy said...

Thank you. As a mom to 4 Aspies as well as being married to one, it's so nice to have someone else "get it". My own parents don't like my children or support me because they think the aspergers behavior is because of my "bad" parenting. It's nice to know I'm not alone. Thank you.