Tag Archives: autism

Re-blog: The Problem of Special Needs Siblings

A guest post by Jennifer Janes

Many of you who follow my blog did so as a result of posts on autism. I want you to  know that my support and advocacy for those affected by autism has not diminished. One of the blogs I follow is authored by Jennifer Janes. Jennifer is the parent of a child with autism. Jennifer and I met at The Gathering of Authors in Texarkana, Texas during the first weekend of November. I’ve since learned she is a prolific blogger who recently posted this article on addressing problems between special needs siblings.

Welcome Jennifer!

Jennifer Janes

The following content is from Jennifer Janes’ blog.

My older daughter is a great kid. After she turned three years old and finally began sleeping, she’s been a pretty easy kid to raise, overall. She is loving, kind, understanding, funny, and smart. So what’s the problem?

The problem is that she’s the sibling of a child with special needs. It took me a while to realize it, but that means she has special needs of her own. As I talk to other special needs parents, I’m beginning to realize this is not unusual.

To read the rest of this post, click here The Problem of Special Needs Siblings

 

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Autism Follow-up: Wandering and Other Dangerous Behaviors in Autism

I’m honored by the return of Bobbi Sheahan and Dr. DeOrnellas. In this post they have agreed to share insights into  behavioral risks associated with Autism.

Wandering and Other Dangerous Behaviors in Autism

By Bobbi Sheahan and Kathy DeOrnellas, Ph.D.

Thanks you, Rich, for having us on your blog!  We are back for part 2.  Our first segment was an introduction to autism. In Part 2, we are going to discuss some dangerous behaviors that are often part and parcel of raising a child on the autism spectrum.  Many of these are things I (Bobbi) would never have imagined before having an autistic child, and I have a pretty good imagination.

We’ll start with one of the more alarming behaviors sometimes exhibited by children with autism:  wandering or running.  We expect toddlers to take a run, if you will, at running away from Mom or Dad.  When a child has autism, that phase can go on for year after hair-raising year.

One mom, let’s call her Oona – has an elementary-school-aged son who has given her more than a run for her money:

“He would run out the door, in the street, thru parking lots, down the block, away, away, away. We had to install key-to-key deadbolts & flip-locks on all of our doors. We got handicap parking tags so we could park right next to the door. And sometimes I made him wear a strap from my wrist to his or from the shopping cart or stroller to his wrist. It was horrible & terrifying having to always be worried that someone forgot to lock a lock & he could be two blocks away at any time. On top of the running, he had absolutely no fear/safety boundaries. He would run into traffic or stop & talk to *anyone* telling them within minutes that they were his best friend & he loved them. Very scary stuff.”

I can relate to the Extreme Locks – I have had friends actually laugh at our locks and alarms, and the one on our front door actually once foiled a burglar (!), but Oona risked the scorn of the community – and certain members of her extended family — by taking the Next Step and using a leash.  I asked her how that was received. She said:

“I never got a ton of questions, usually just the sideways looks. Right after diagnosis, I was happy to volunteer answers to the looks – “he has an autism disorder, he runs away”. Later, I just stopped caring what people thought. I don’t have the time or the patience any longer to explain to everyone that I’m not a horrible parent.  I did get comments from my family (who do not understand his diagnosis & what it means for him, or care to educate themselves) like “a leash?!” or the ever popular & interchangeable, “Bring him to my house, I’ll straighten him out” & “you just need to spank him more” (typically said much more crudely by my mother-in-law as “beat his a**” – lovely).

Stories like this make me less likely to judge.  I certainly did judge myself a lot when my own child showed tendencies to flee.  My daughter’s running phase lasted for four years.  Four. Long. Years.  I remember vividly the day that she stood transfixed, staring at an open gate, repeating the cautions I’d been saying to her for years.  I admit it – I cried.  For joy, for relief, and for finally being able to laugh about the time she escaped on a tricycle and took years off the end of my life.

But wandering is no laughing matter.  According to multiple press and online reports, one father in Canada experienced the nightmare of having his nine-year-old daughter wander from their fenced yard, only to be found some hours later in a neighbor’s yard; authorities subsequently took the girl from her father’s custody based on this incident, according to this source http://www.autismkey.com/child-with-autism-taken-by-authorities-ayn-van-dyk/ and scores of others like it online.

What Can We Do About Running?  It took our family several years to instill the “do not run away” message, and it will take some folks even longer.  What can parents do in the meantime?  Besides the aforementioned locks and other physical protections, some families employ personal GPS monitors or autism service dogs who are trained to stay with the children and whose leashes are also snugly attached to the child’s wrists.  The question of why our kids wander is a tough one and beyond the scope of this article, but some folks say that the service dogs may also alleviate some of the anxiety that leads to wandering.

Police departments in the U.S. also have free biometric registries where you can provide your child’s fingerprints, pictures, and some basic information.  Many of us also have medical alert bracelets for our kids.  Special Education classrooms often have an aide dedicated to watching the doors, and I spoke with one mom who rejected an otherwise good school solely on the grounds that the front door opened up onto a busy parking lot and an even busier street.

The National Autism Association has a wonderful twelve-point list of action items to address safety concerns.  The list, which can be found in its entirety here, http://www.autismsafety.org/prevention.php?way=12  , includes several of the items mentioned here, plus some others such as designating an Adult In Charge at gatherings so that it’s clear that someone is watching our kids.

Wandering isn’t the only danger that our kids can get into. Jenny Herman, who is the Social Media coordinator for Home Educating Family and blogger extraordinaire at www.manyhatsmommy.com, tells the story of her son’s penchant for underdressing:

“The other day Josh and a friend left the apartment ahead of another mom and I. They went down the hall and out the door. They were waiting next to the friend’s van, but Josh was in shorts and NO SHOES in 30-something degree weather!”

Jenny also had a lot to say about property damage, inflicted with objects that could also be dangerous to life and limb:

“Josh has an obsession with using a tack (push pin, whatever you want to call it) to dig in the wall. He has many dime-sized holes around his room. In this incident, I came in to check on him, and he was digging at the wall next to the night light with a tack to “let more light into your room, Mommy.” At that point, he had only taken off the white paint and you could see the brown covering of the sheet rock (or whatever it is).

This FOOLISH mommy did not cover up the spot. Six weeks later, he came out to tell me he was having a hard time sleeping. Then he told me his body just had to carve something. I went into his room, and there was sheet rock dust all over the wall, the night light, his radio, and the floor. His toy screwdriver was on the floor. He had used his toy screwdriver to dig THROUGH the wall, a Real Live Hole in the Wall, as in you could see the dark space in between the walls. I said, “What did you use to dig that hole?”

“A piece of glass.”

“GLASS! What glass?” trying not to jump out of my skin.

“The glass that was by the ladder.”

“Where is it?”

“I put it in the hole.”

He had no cuts or blood, so I think he found a piece of plastic that looked like glass. I covered the hole w/paper and masking tape and amazingly nothing more has happened there. However, he cannot leave the wall alone! I’ve found other small spots…

Jenny also shared this photo with me – which I hasten to add does not reflect any physical injuries to her son –but I won’t even ruin it by attempting to caption it. It’s already well over a thousand words, I figure:

The lack of caution that we see in some kids definitely extends to safety concerns around water.  Erin McMinn Nieman, in her blog called Noah’s ARC, tells the harrowing story of her son’s close call in “Mothers’ Day Under the Sea,”  http://www.noahs-arc.com/archives/972   Her story of her son’s plunge into a murky lake and her quick rescue of him is harrowing, but what really resonated with me was his response to being saved from drowning:  “Noah walked happily on, holding my hand as if nothing had happened.”

These stories highlight the importance of safeguarding our children.  While these stories may be amusing to someone who did not experience them, our children are in significant danger and have a much higher risk of engaging in dangerous behaviors that result in an injury.  They are more likely to suffer head injuries and to poison themselves accidentally; they are also more likely to end up in hospital emergency rooms.

This is true for several reasons. Many children on the spectrum do not experience pain the way the rest of us do and, rather than learning that the stove is hot on the first trial, they touch the stove again and again.  They also do not understand that certain situations are dangerous.  For example, our children may not understand that running out into traffic can result in injury or death; rather, they are focused on escaping an uncomfortable situation.

While all children are impulsive at times, children on the spectrum are especially so and do not think through the consequences of their behaviors. As a result, they can end up in some precarious situations. Although keeping our children safe can be very difficult, it is critical. I suggest that in any situation you have a “designated watcher” for your child – someone who is responsible for seeing that he or she remains safe. This is especially important in crowds, unfamiliar settings, or anywhere your child feels uncomfortable.

Bobbi Sheahan and Kathy DeOrnellas, Ph.D. are the authors of What I Wish I’d Known About Raising a Child With Autism; A Mom and a Therapist Offer Heartfelt Guidance for the First Five Years (Future Horizons, 2011).   Portions of this article are excerpted and adapted from the book, which is available at www.fhautism.com and wherever books are sold.   Readers of this blog can use the promotional code BOBBI for 15% off of What I Wish I’d Known About Raising a Child With Autism  and any other Future Horizons product or conference, plus free shipping.  Bobbi’s website is www.bobbisheahan.com, and she would love to hear from you at me@bobbisheahan.com.  You can also connect with her on Twitter at  @BobbiSheahan or on Facebook.

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Book Review – The World According to August by Sandy Westendorf

The World According to August – One Good Friend” opens with an effective statement of purpose; what it is and what it is not.

The book touched me deeply. It gives readers a deeply personal, yet insightful picture of a child with autism; how he and they are similar in many ways and yet different, as well.

It is the intent of the author to dispel common misconceptions about autistic children. The author uses a true story to illustrate the common, shared emotions that we all experience. We learn of concerns and needs they experience. This is a moving, touching and emotional read.

Quotation from the book.

Author

“Every child is unique; the extent to which they are affected is also individual. If you are not living with autism, it is easy to miss the child and only see the diagnosis. The book was written in an attempt to demonstrate, although outwardly, these children may appear different; but inside—where it counts—they are the same as you or me. Children with autism love, have an ego, feelings which can be hurt, a sense of humour, and even a mischievous side.

The book was written in an attempt to demonstrate, although outwardly,
these children may appear different; but inside—where it counts—they
are the same as you or me.Children with autism love, have an ego,
feelings which can be hurt, a sense of humour, and even a mischievous side.”

§

Comments and order information:

Print quality is good. Illustrations are effective and well done. I highly recommend it to everyone.

If you’re interested in purchasing, Click here “The World According to August.”

Use this link for the Kindle version of “The World According to August.”

I want to follow this review with a poem thatwas inspired by the book:

Poem for an Autistic Child

A Tribute to August

from “The World According to August —

To soar on wings of eagles

to glide along the glade

to bounce and jump and whirl and twirl

to dream and search and sway.

He has so much in common

with you and me you see —

a bright and charming sweet young boy

who senses all with clarity.

To hear, to see and touch and smell,

he takes all in so well,

his self expression is unique

his feelings hard to sell.

We might whisper, he might yell

but one can never tell.

He likes himself and folks like him

and that works out quite well.

August has needs and we have ours,

life comes with give and take ―

love and comfort, peace and joy

needs all share, so we partake.

A smile, a doubt, a look askance

a wave, a nod, a sigh —

He needs hugs and love at times,

same as you and I.

He gazes on the sights nearby,

is stirred by beauty there.

A swan takes flight, a songbird sings,

if only he could fly.

Unspoken words may bite his tongue,

but thoughts within belie.

A word from Mom, a smile from Sis

unspoken things give him answers to why.

Show him love and friendship now

his joy you’ll never miss.

  Don’t ever leave just stay nearby,
he just might make you cry.

August is a special child

and August needs a friend.

August is a special child

And August is my friend.

a poem by Rich Weatherly, October 7, 2011

For more information about autism and “The World According to August – One Good Friend” by Sandy Westendorf  refer to http://purplebirch.com/books.html .

Sandy managed a team of behavioral specialists and is the mother of an autistic child. According to Sandy:

The book was written in an attempt to demonstrate, although outwardly,
these children may appear different; but inside—where it counts—they
are the same as you or me.Children with autism love, have an ego,
feelings which can be hurt, a sense of humour, and even a mischievous side.

I heartily encourage you to support research into autism by purchasing this book.  A percentage of the proceeds will be donated equally to support Canadian-American Research Consortium (Autism Research) and the International Society for Autism Research.

For more information about Sandra Westendorf, check her Purple Birch Publishing Website. For that you can click right here. 

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Filed under Book Review, Poetry

Guest Host – Autism Discussion Re-Visited

I am honored that Sandy Westendorf has agreed to continue her discussion on autism.

Author of The World According to August

She is the author of, The World According to August – One Good Friend.

Sandy’s book inspired me to write Poem for an Autistic child and has agreed to answer questions related to comments from the introduction of her book.

Interview questions

Your book, “The World According to August” touched me deeply. You give us a deeply personal, yet insightful picture of a child with autism; how he and they are similar in many ways and yet different, as well.

During our previous interview we discussed the reasons you authored The World According to August – One Good Friend.

In that interview you addressed challenges and rewards parents and children themselves faced and stressed the importance of recognizing uniqueness. We ended with you calling on others to learn more about those with disabilities.

Since then our conversations have touched on a couple of topics you feel strongly about. From this point forward, feel free to consider yourself the guest-host.

You and your family have been encouraged by a therapy that you now heartily endorse. Please don’t hesitate to step up on your soapbox. What do you have to say on this?

Correct, the therapy our son made the most significant gains on was the Lovaas Applied Behavioural Analysis therapy, commonly referred to as ABA.  This therapy was developed over forty years ago by Dr. Ivar Lovaas, a world renowned autism expert. Dr. Lovaas’s program was, at the time, the only peer reviewed, scientifically validated therapy. It uses Discreet Trial Training, where new skills are built upon in sequence and each mastered, much like constructing a brick building. The therapy includes Intensive Behavioural Intervention, which helps the child learn to manage their behaviors so they are able to focus and learn. There are many who still believe ABA is based on the use of negative reinforcements and/or the use of aversives, which is not the case. I know dozens of families who use ABA with great success, and not one has ever used aversives. They are not used in a correctly managed, modern program.

In conjunction with ABA we incorporated a play therapy called “Floortime”, which was developed by Dr. Stanley Greenspan. We saw the most gains utilizing these two programs in concert with each other. We explored several options in an effort to find the right fit, trying other diets, supplements and therapies – with little or no results. The one program which worked best for our child was the one we stuck with. It is what works best for your individual child which is the best treatment for them! Every child is unique, therefore, their responses to a treatment will be unique as well.

Parents should investigate their options, research, ask questions, and use common sense. Now we have many therapies, and diets available to families, some better than others. Sometimes it is the combination of programs or diets which  reveals the best outcome.

We discussed a controversial issue related to evidence linking vaccinations to the onset of autism. It might help others if you share what you’ve learned on the subject. Back to you…

This is a hot button issue, with many parents, not just myself.  For years the Pharmaceutical companies have been saying there is no link between vaccines and autism. I beg to differ, as do thousands of other parents, judging by the overwhelming anecdotal evidence many doctors still choose to ignore. I have heard my son’s story repeated too many times to count, by other parents of children with autism. The scenario is all too familiar, healthy, neuro-typical toddler goes to doctor to receive vaccinations (usually it is the MMR), within minutes to hours, toddler appears unresponsive (doctor’s will refer to this as an ‘infant faint’) they cannot explain why the same toddler now no longer speaks, makes eye contact, cries incessantly or in our son’s case has stopped walking.  Beginning in the early 90s the number of recommended childhood vaccines doubled! Thimerosal the preservative used (still in flu vaccines) contains over 49% mercury by weight.  Because of the known side effects of mercury poisoning, which mimic the symptoms of autism, there is now at least one version of the Thimerosal-free vaccines available.  With the huge public outcry against the Pharmaceutical companies, there were studies conducted to determine whether or not vaccines contributed to autism. The findings concluded there was no evidence to support the claims linking autism to vaccines.  Out of the 23 studies conducted, 18 of them were funded by major Pharmaceutical companies.  This appears to be a gross conflict of interest. If the studies were to find a link between autism and vaccines – what do you think the size of the class-action law suit against Pharmaceutical companies would be?  There appears to be no accountability and our children are being hurt.

Do I believe it was the vaccine which introduced autism into the life of my beautiful boy – yes! Do I believe vaccines cause all cases of autism – I don’t know, I only know what happened to my child. I have spoken to a few parents who recognized something different in their child from the moment they were born, but the majority I have had contact with have stories like ours.  Having said this, would I vaccinate my child, knowing what I know? Yes.  I would insist on single dose, no multivaliant vaccines, which are Thimerosal-free, and I would request they be spaced farther apart.  Vaccines save lives – this cannot be disputed. We just have to ask ourselves – how much is too much?

Are there any closing words you want to share at this time?

There is a glut of information out there; it is hard to know what is right for your child. For a parent who has just received the diagnosis of autism, take heart. It is not the end of the world, or the end of your child’s life – it is the beginning of a journey down a different path towards an unknown destination.  It will be rocky, and at times overwhelming, it will also be joyous and beautiful, and you will find your rhythm. Seek out organizations like FEAT (Families for Early Autism Treatment), autism support sites, etc… Don’t be afraid to advocate, strongly if the need be, for your child. You are their voice, their safe haven, and their best shot at a bright future.

.

Additional comments?

I want to thank you for giving me the opportunity to stand on my soap-box and spread the message about people with disabilities. Many do not have a voice of their own. It is up to those of us, who love and care for them, to give them that voice. Parents should know it is okay to advocate for your child, special needs or mainstream. Encourage connections with people with different abilities – it will make all the difference – to you and to them. Eight months after I had finished writing the story and it was in the hands of my book designer, I came across the following link: http://www.wretchesandjabberers.org/screening2.php I was delighted to see other like-minded people. The short clips on the link show two men with autism trying to dispel many of the misconceptions of developmental disabilities. Their message was exactly what mine is – inside we are all the same.

For more information about Sandra Westendorf, check her Purple Birch Publishing Website. For that you can click right here. 

Caveat: Always check with your personal physician or pediatrician for advice regarding vaccinations. Information provided is the opinion of the interviewee and should not be taken as medical advice.

Link to The World According to August – One Good Friend, Trailer.

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Poem for an Autistic Child

A Tribute to August

from “The World According to August —

One Good Friend”
by Sandy Westendorf

To soar on wings of eagles

to glide along the glade

to bounce and jump and whirl and twirl

to dream and search and sway.

He has so much in common

with you and me you see —

a bright and charming sweet young boy

who senses all with clarity.

To hear, to see and touch and smell,

he takes all in so well,

his self expression is unique

his feelings hard to sell.

We might whisper, he might yell

but one can never tell.

He likes himself and folks like him

and that works out quite well.

August has needs and we have ours,

life comes with give and take ―

love and comfort, peace and joy

needs all share, so we partake.

A smile, a doubt, a look askance

a wave, a nod, a sigh —

He needs hugs and love at times,

same as you and I.

He gazes on the sights nearby,

is stirred by beauty there.

A swan takes flight, a songbird sings,

if only he could fly.

Unspoken words may bite his tongue,

but thoughts within belie.

A word from Mom, a smile from Sis

unspoken things give him answers to why.

Show him love and friendship now

his joy you’ll never miss.

  Don’t ever leave just stay nearby,
he just might make you cry.

August is a special child

and August needs a friend.

August is a special child

And August is my friend.

a poem by Rich Weatherly, October 7, 2011

For more information about autism and “The World According to August – One Good Friend” by Sandy Westendorf  refer to http://purplebirch.com/books.html .

Sandy managed a team of behavioral specialists and is the mother of an autistic child. According to Sandy:

Every child is unique; the extent to which they are affected is also individual. If you are not living with autism, it is easy to miss the child and only see the diagnosis.The aim of this book is not to speak to autism as a disorder or to define it; there are many excellent references which address those specific topics…

The book was written in an attempt to demonstrate, although outwardly,
these children may appear different; but inside—where it counts—they
are the same as you or me.Children with autism love, have an ego,
feelings which can be hurt, a sense of humour, and even a mischievous side.

I heartily encourage you to support research into autism by purchasing this book.  A percentage of the proceeds will be donated equally to support Canadian-American Research Consortium (Autism Research) and the International Society for Autism Research.

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