Showing posts with label aspergers syndrome. Show all posts
Showing posts with label aspergers syndrome. Show all posts

Autism and the God Connection Review

Autism and the God Connection
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Several years ago, I penned an article for "Angels on Earth" Magazine (Loving David), regarding my young daughter's belief that an angel often visited, and watched over her brother, David, who has autism. I had no idea when I wrote that story of reverence for my nonverbal son, that the severity of his autism would lead us full circle back to our core beliefs about his diagnosis.
Now, years later, while reading this luminous work by William Stillman, I felt validation of a truth we had always suspected, but came dangerously close to losing touch with: our autistic children are creations of God and a manifestation of His Divine Plan. It feels so good to come out of my closet again! :)
William Stillman has woven moving, haunting accounts either by people with autism, and/or those who love them to explore spiritual realms where clinicians often arrogantly refuse to acknowledge as anything beyond "hogwash". Buried in this sensitively treated text, Mr. Stillman reminds us, above all things, to show the same sensitivity and respect in our daily dealings with people who have autism as we would our "neurotypical" acquaintances. More importantly, he builds a compelling case as to why we should always assume the intellect and competence of persons with autism.
The arrogant presumptions by those who label themselves "behaviorists", "educators", and "clinicians" drive home a painful, common message: autists, especially nonverbal ones, are hopelessly retarded, largely ineducable, and spiritually "empty" souls. As a parent of two with autism, I am often left with the the feeling that these "professionals" have spent little, if any time at all, truly getting to know, and understand, a person with autism.
While our youngest son who has autism was always verbal enough to make his intelligence apparent to would be skeptics (J. was born knowing how to read--nobody taught him), our older, nonverbal son struggled greatly to "prove" his intellect. His extreme sensory dysfunctions complicated things further. A brief spell of beautiful, peaceful years when David used pictures to communicate brought him some welcome respite, and access to more "intelligence assuming" curriculums. Then as he aged out of early intervention, his pictures began to fail him as a trustworhty form of communications. Our beautiful boy had more to tell us than what he wanted to eat, drink, or wear, and his pictures could not account for his maturing communications needs. Predictably, as his world narrowed, his behavior began to grow severe. In response, his "teachers" and "behaviorists" began to narrow his world further in response to his anger and frustration. Mental Retardation was slapped onto his list of labels, further narrowing his options. The light in my son's blue eyes grew painfully dim. We were losing David.
No amount of arguing could budge his school district into moving him towards intensive augmented communications training. They felt they'd done their job. Our child could communicate basic wants and needs. While we struggled to find resources to advance our little boy's communications further, we lost our child. His marathon episodes of aggressions and self abuses became so frequent and severe that his school district placed in a behaviorally focused group home in a program designed to force him into "compliance" with a rigid set of behavioral tasks. We were told by experts, that this was his only hope for a life outside of an institution. He grew worse, and worse. In the name of "treatment" our son faced injuries, human bites, pinching, hitting, food deprivation, falls through windows, and finally, witnessed and documented sexual molestation. Against all "expert" advice, we bought our little boy home, where at least we knew he'd be safe. Nobody could argue that he never got wounded or molested on our watch.
It wasn't until we set aside "expert" notions about autism, and began to operate on our original assumption that our nonverbal son was an intelligent and competent human being that we finally began to get over the hump of his seemingly insurmountable "behaviors". Seeing some changes from the first day of our "new attitude", we committed ourselves to previously "Unthinkable" approaches--the only ones we hadn't tried.
Here, during my son's eleventh year, we abandoned everything we were taught to believe about "how" to teach a person with autism. Daily, we are rewarded with increasing amounts of time where our son feels able to reveal the bright, luminous, funny--and wounded, traumatized individual that he is.
Today, our eleven-year old is an amazing young man by anyone's standards. He communicates with a letter board, he has pen pals, he writes poetry, he craves material about astronomy and ancient cultures, and no, we don't facilitate. He accesses grade level curriculum using the Rapid Prompting Method, and we are in the process of trying to convince his school district that behavioral approaches do not work for every child.
In trying the one thing clinicians warned us to never do---assume our child a capable, intelligent human being---his lost childhod was unearthed and reborn--hopefully before the wounds ran too deep to salvage his boundless spirit. While I can't change the painful mistakes we made in trying to help him live with autism, our son understands that we did the best we could with the tools we had available at the time.
In truly accepting autism, and embracing it as an integral part of the children I have, all of our lives are once again filled with reverence, joy, and miracles. I often find myself describing myself as a woman redeemed by her children's struggles. The best there is to say about me....or anyone in my family....revolves around having known, loved, advocated for, and accepted as the miracles God intended---two amazing children with autism.
Does that mean that in accepting our son's autism as a gift, we don't seek improvements which will ease their paths and broaden their worlds? Absolutely not! We simply operate on the same set of assumptions for our children with autism that we would for any child---we want them to become happy, healthy,contributing human beings.
In closing, my son David, has a message hew wants to share with Mr. Stillman, which he wrote in response to reading some of Mr. Stillman's work on the fundamental rights of autists to communicate:
When you look into the sky
The stars are all you'll ever see.
I have chosen instead to see
The possiblities lying in between.
"Autism And the God Connection" is a book about just that...choosing to see the possibilities beneath the label. Thank God we revisited that choice before our son's radiant spirit was dimmed forever.


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Thorn in My Pocket: Temple Grandin's Mother Tells the Family Story Review

Thorn in My Pocket: Temple Grandin's Mother Tells the Family Story
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Eustacia Cutler's book about raising Temple Grandin answers the two questions I've always had whenever I've heard or read about Temple Grandin. How did Temple survive in a time when everyone was warehousing their kids with autism in mental institutions and how did she succeed so well as an adult?

This is not a "how-to" book on educational procedures or anything like that. By reading this autobiography, you will understand the character of Temple's mother, who quite literally saved Temple's life. Fifty-some years ago, Eustacia was the product of her time in most ways--the stay-at-home wife to a wealthy man who was bent upon institutionalizing Temple, particularly when he got the support from psychiatrists who believed at the time that the reason for Temple's autism was Eustacia herself.

There's a real lesson to learn here. Instead of surrendering her child, the originally compliant Eustacia (women were supposed to be that in the 40s and 50s) changed. She intuitively knew that if she gave up whom she could be, her child would be given up as well. She fought ferociously and even walked away from her marriage and her economic well being to save her child. And at that time, when she faced a family who didn't support the divorce financially and a society that looked down on single mothers, she had four children!

If there's one thing that stands out in this book, it's that you have to be who you are and all you can be in order to give that same gift to your child. Temple Grandin comes by her strength, intelligence, and creativity because she had a mother who studied every angle of whatever or whoever she could find to help her child and wasn't afraid to try anything, from allowing her child to negotiate with a local merchant to fighting for her child's right to the education Eustacia believed would save her.

The reader gets a clear picture of the evolution of the science of autism over the decades with some pretty deep conclusions on Temple's mother's part. It's personal. It's incredibly written. This is NOT a how-to-raise-your-child book. It's a story about the meaning of life and society itself. I'd recommend to anyone who wants to know how character is formed-it's not just parents of children with autism. It's one of the best books I've read in a long, long time and I'm eighty years old with a library of books I've read over a lifetime!


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A Thorn in My Pocket is Eustacia Cutler's story of raising her daughter, Temple Grandin, in the conservative Leave-it-to-Beaver world of the fifties, a time when children with autism were routinely diagnosed as "infant schizophrenics" and banished to institutions. She tells of her fight to keep Temple in the mainstream of family, community, and school life, how Temple responded and went on to succeed, as Ms. Cutler puts it, "beyond my wildest dreams." Ms. Cutler also explores the nature of the autism disorder as doctors understand it today, and how its predominant characteristics reflect our own traits in an exaggerated form.

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