Archive for the ‘autism’ Topic

Why are medical tests so ‘autism-unfriendly’?

Sunday, April 1st, 2012

I would really like to know are why medical tests so autism-unfriendly. For those of us with children on the spectrum, we know the risk of potentially life-threatening, concomitant medical issues is high. Seizures, brain injuries and genetic and metabolic issues are only a few possibilities that we need to test for, and as such our son has had blood tests, urine tests, x-rays and ultra sounds on every organ in his little body.

These test are stressful, and in my opinion, unnecessarily so. Let’s take EEGs. In a world where everything is going wireless, why does it take 37 wires to connect a child’s head to a monitor? In a time where easily-removable stick –ems can hold a 40 pound wall sculpture, why do tiny little sensors need to be attached with an adhesive so strong that it takes acetone to remove? And if the sensors must be removed chemically, why use acetone? It’s cold, and it burns. Why is masking tape needed to cover the electrodes? If the devices are going to fall off anyway, does anyone really think that tape stuck in a child’s hair will keep them in place? (By the way, that tech owes me $20 for a hair stylist to cut said tape out of my son’s hair without looking like he had the mange).

And what about MRIs? Why do they take so long? Why are they so noisy? And, why pray tell, when doctors for years have been prescribing oral tranquilizers like Skittles do they insist upon putting a tranquilizer via an intravenous line BEFORE inserting a sedative?

It doesn’t make sense to me at all. So, to you innovative geniuses who make medical diagnostic equipment, please listen up. All of our tests so far have thankfully been negative. But so have our experiences, which have been traumatic for our son. Fix it. Now. Please.

Ahem…legislators? Some thoughts on Autism Policy

Thursday, November 17th, 2011

For legislators, some thoughts on autism policy:

1. Promote and respect our kids as valued human beings. Until then, all the policies and legislation we’ve worked so hard for will be circumvented by discrimination and the “law of unintended consequences.” For instance, policies against restraint and seclusion are working in some schools, but others simply call the police, who arrive with handcuffs and pepper spray to handle meltdowns and remove troublesome students. State run hab centers are finally being phased out, but ex-residents may have few options when community leaders attempt to limit the number of people with cognitive disabilities living in their neighborhoods. Schools are required to offer the least restrictive environment, but parents still fight for their children to be in a general education classroom versus a segregated one, and often witness their children being loaded onto school buses at the end of the school day up to an hour before their typically-developing peers.

2. Let the money follow the person, not the institution. With thousands of individuals on waiting lists for services, where are the millions of dollars in state and federal funding? If every child enrolled in special education received an average of $14,000 per year from the state, why are children with IEPs not graduating from high school? Why are less than half proficient in math and language arts, even when the US Dept of Education has produced studies proving that children with even severe cognitive disabilities can learn challenging academic content at a level never before imagined? Or that standardized IQ tests can greatly understate the intelligence of children on the autism spectrum? Let the money follow the person to allow parents to seek out the best education possible so that our kids can realize their potential.

3. Support families. How can parents be doctors, lawyers, insurance experts, teachers and parents at the same time? How can we handle our substantial day-to-day challenges? How do we know what’s available to help our kids? Let’s keep those face-to-face supports near us, and cut the overhead and administrative costs from their higher ups. Parents can figure out what their kids need – we are just in the dark about what’s available – and we can desperately use some respite and a caring somebody to keep us sane when the very institutions that are supposed to help us let us down.

Unbind us, legislators. Free our kids from the unwarranted stigma of disabilities, reallocate the cash that’s currently not going where it is most needed and send us a loyal coach to help us navigate the maze.

Advocacy Training – A transformative experience for parents of special needs children

Saturday, June 25th, 2011

Advocacy is good for our kids, but many of didn’t realize that it is good for parents, too. A new study completed by doctoral student Michelle Reynolds for the University of Missouri cites that parents who take advocacy courses become stronger and more confident advocates for their children with disabilities. Among the main benefits of advocacy for parents are:

A decrease in intimidation. Confident advocates felt less likely to be afraid to express their options and disagree when dealing with medical and educational staff.

Hopefulness about the future. Parents learn how to navigate the maze of organizations, manage transitions and learn about success stories of children who have ‘made it’ in the real world.

A sense of community. Parents can also rely on each other, thus lessening the sense of isolation that many of us face.

More respect for our children. Sidelining the focus on ‘fixing’ our kids, we learn how to celebrate their individuality, while identifying and meeting their needs.

The increase in control, hopefulness and community help reduce the oft-mentioned symptoms of combat-fatigue which parents of children with disabilities encounter due to fear, worry, isolation and guilt. Advocacy training marks a transformative experience where parents obtain an increased sense of control and learn to feel better about themselves and about the future for their children. Read the full report here.

Stuff that works - for us

We  don’t assume these products will work for everyone–that’s why we ended the title with the parenthetical (for us). But if you are looking for new things to try, please read the accompanying blogs to view our experiences with these products. 

Mama, Don’t Cry for Me a song written by Mandy Harker and Sharee Wolfley and Sung by Kalii Palmer. Listen when you really, really need the strength to keep believing that everything will be okay.

 Model Me Kids

Model Me Kids® has broken the code on tools to teach social skills to children on the autism spectrum.

Click here for our success story and a full product review.

 

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L. Mae Wilkinson:

National Examiner for Autism and Education

National Public Policy Examiner

St. Louis Examiner for Autism and Parenting

Co-moderator, The Coffee Klatch blog talk radio and tweetchat 

Reporter,  Autism Hangout 

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Twitter, AutismisnotBoss