Autism Awareness Poetry by Autism Santa


Toys Across America Autism Santa

Toys Across America Autism Santa

As part of our promotion of Autism Awareness Month we would like to share with you two poems by Michael Miller the Autism Santa. At the same time we would like to keep you up to speed regarding his brilliant project Toys Across America. He shares “I run a page on Facebook where my son and I send toys to children on the spectrum all over the USA hence the Autism Santa pen name. As a matter of fact I created an event for this month “Autism Christmas” we are sending out close to 300 toys all to be opened on April 25th. Ok thanks for your time. ” Michael is himself the father of a son who has been diagnosed with ASD. He is also the COO of KultureCity.

You can check out more of Michael’s poetry here.

Meltdowns by Autism Santa

Is it a tantrum or a meltdown.
It’s not an easy thing to know.
Does he really hurt inside.
Or is he putting on a show,

I have dealt with both.
Or maybe they’re the same.
I know not to judge him.
I don’t think this is a game.

Maybe he can’t control it.
This temper I often see.
I wish I could help him.
Or try to set him free.

Rather than adding fuel.
I should step away for now.
But it is not that easy.
I am still learning how.

So for now I’ll tell you this.
It’s not your choice to make.
He is the one who suffers.
I know it is not fake!


Autism Awareness by Autism Santa

I think the world should know.
Autism is here to stay.
In fact it might be growing.
1 in 68 as of today.

So we are asking for a favor.
From you and one and all.
To help us spread the word.
That number will not fall.

So grab a pen and paper.
Or use your Facebook page.
No matter where you live.
No matter what your age.

Perhaps you like to Tweet.
Or sing just like a bird.
Using social media,
The latest craze I have heard.

So go and tell your story.
Or tell it for a friend.
Tell it to the world.
Or who ever will attend.

Tell them about the Spectrum.
Tell it with such clearness.
You can join the cause.
“Autism Awareness”

Michael “Autism Santa” Miller

Personal, Solitary, Parenting Pain: The Emotional Turmoil Surrounding Extremely Aggressive and Behavior in Your Child with ASD – a guest by Amanda Ronan shared by Round Table Companies

Advice for autism parents

Advice for autism parents

Our friends at Round Table Companies have shared with guest blog post , by Amanda Ronan, with us.

Ronan share tips and ideas for helping parents with a child on the spectrum who live through extreme meltdowns and aggressive behaviour. You can read the original article here Personal, Solitary, Parenting Pain: The Emotional Turmoil Surrounding Extremely Aggressive and Behavior in Your Child with ASD.

Ronan writes “Please . . . please don’t wake up, Nora pleaded silently. A dog barking somewhere in the neighborhood had startled her fully awake, though she hadn’t really been sleeping; she’d been in the half-sleep state she’d been surviving on for as long as she could remember.

Yesterday had been the hardest day yet, and that was saying a lot, given what her family had been through over the past 15 years of living with her son who had an autism spectrum disorder (ASD), and extreme behavioral problems. They had been heading into lunchtime after a morning during which Ander had enjoyed all of his normal routines—the same breakfast he’d eaten every day for years, a quick shower, and a few hours of homeschool instruction. Now he was engrossed in his normal weekday TV show as she prepared to make his normal lunch. Routines were important, even crucial, to Ander—and to the peace of the household—so Nora had arranged her life in order to maintain them. Spontaneity, and doing things in the spur of the moment, were four-letter words in their home.

Ander would only eat nachos. There had to be only a small pile of chips, whole triangles with rounded corners, not pointy. The cheese had to be a Mexican blend with both white and yellow-orange shreds visible. The salsa had to be red and mild, pureed with no chunks. This was part of the obsessive-compulsive disorder that the new psychiatrist said her son had, along with ASD and attention-deficit hyperactivity disorder. But as Nora looked in the refrigerator, she cursed under her breath. They’d run out of cheese the day before and she hadn’t had time to visit the store.

“Hey buddy?” she called out. “How about I make us some pizza for lunch today? I know you love pizza and it’s pepperoni – your favorite!” She peeked around the corner into the living room.

Though Ander had headphones on, she could hear the sound. His expression was one of concentration, as though he’d found a moment of peace from his constant struggle to self-regulate, communicate, and actively participate in the world. She waved a hand at him. He didn’t respond.

She knew better than to remove the headphones for him. She’d tried that a few years ago, right after he hit puberty. That was the first time he’d hit her hard, a succession of several slaps to her head until she dropped the headphones and backed away. It was shocking and gut-wrenching. Before that he would lightly hit her—more in a way to get her to leave him alone.

Aggression itself wasn’t new; it had started a few years before kindergarten when he bit both his sister and the family dog, just days apart. Both had howled and become nervous around him after that, having lost trust for a period of time. Nora lost something, too at that time—the hope he’d be ready for school. Despite all the interventions, medical appointments, and therapies, she realized as she tended to her daughter’s wound that Ander might not successfully go off to kindergarten, play with the other kids, and maybe become a teacher’s pet. The journey ahead could be long and difficult; she could no longer deny it.

Not long after the biting, his meltdowns, which once had resembled a whining child’s tantrums, took another unexpected and dangerous turn when he started to throw things in the house and punch the walls. The sound of his knuckles against drywall made her stomach turn. She learned to go into the kitchen for some bandages and ice to apply to his hand when he had calmed down.

Then came the day of the windows. She would never forget the first time she heard the sound of glass shattering. Ander had put his head through the window; incredibly, though, he was unscathed. He turned around to face her, then curled up on the floor and rocked himself until he fell asleep. It took two more broken windows for them to hire contractors to install shatterproof glass windows.

Nora knew that the increased agitation, self-injurious behavior, and aggression stemmed from Ander’s difficulties with communication, social interaction, and self-regulation and that he never truly meant to cause harm and hurt himself or others. But there were times when, for his own safety and the safety of their daughter, Nora and her husband Peter had had to use the physical intervention techniques they’d learned from Crisis Prevention Institute (CPI): carefully wrap their arms around him, remove him from the circumstances, and attempt to defuse the situation. Physical restraint was always a last resort; no parent, Nora was sure, ever wanted to restrain his or her child. As he got bigger, though, she worried about what would happen if this “last resort” was no longer an option due to his size.

She found this out the day there was no cheese in the refrigerator.

When Ander saw that lunch was not what he’d expected, there was a sudden shift in his demeanor and affect. His eyes narrowed, his head shook from side to side, and his feet stomped the ground. A flush also began to creep up his neck.

“It’s okay, buddy,” she said. “The pizza is just for today. We’ll have nachos again tomorrow, just like we always do, ok?”

Ander opened his mouth and screamed at her, flapping his arms so that one palm smacked the glass breakfast table making it jump a bit. Nora jumped herself, backing up slightly. She couldn’t help it: she was actually feeling afraid of her own son. He had hit the table so hard…It wasn’t supposed to be this way…she thought to herself.

And then, in a sudden burst of movement, Ander jumped up, ran towards her, and tackled her. Nora fell backward, her elbow cracked against the tile floor, and the impact knocked the air from her chest. She was gulping like a hooked fish when Ander landed his first punch on her cheekbone. The next one caught her neck and the third her right ear, and her head reverberated with shrill ringing. Finally, with a gasp, she filled her lungs, but she couldn’t push free. Ander was stronger. So she cried helplessly as her baby boy howled and beat her. The once chubby hands that used to grasp at toy cars had become powerful fists that continued striking her until, mercifully, her husband opened the front door. Then it stopped as quickly as it had begun; Peter was still strong enough to pull Ander away from Nora—for now.

After the barking dog woke her, Nora wondered through her familiar exhaustion whether she really knew her own child, knew how to care for him, what he needed, or even knew how to be a good parent. She closed her eyes and willed the barking to stop. When it finally did, she exhaled, not even realizing she’d been holding her breath.

Nora strained to listen for any slight noises, any movements that might indicate that Ander’s sleep had been disturbed. Not hearing anything, she let her neck muscles relax and her head sink back into the foam pillow. The bedside clock saturated the otherwise dark room with the same deep red hue as the bruises on her body. In two hours, a new day would start. And she had no idea what it might bring.

As a parent of a child with ASD and extremely aggressive behavior, perhaps you can envision yourself in this story, which reflects actual parent interviews and other informed sources. Maybe you, like Nora, are feeling alone, lost, hopeless, and more disconnected than ever before.

If you are living constantly on the edge of your seat, “walking on eggshells”, trying to avoid another meltdown or manage the aggression, the self-injurious behavior, and the violent outbursts, you aren’t alone. With the U.S. Centers for Disease Control and Prevention reporting that one out of every 68 children is being identified with ASD—a huge increase from 2000 to 2010 alone—the emotional and physical turmoil associated with ASD and extremely aggressive behavior is becoming is becoming a more common scenario.

When you begin to fear your own child, it’s time to ask for help. Here’s what some parents and experts recommend:

* Build your team. Seek the assistance of a therapist with expertise in autism spectrum disorder and behavioral approaches. This person can help you assess your environment, identify triggers for behavioral problems, help with structure and routine, and provide strategies at home to prevent meltdowns and aggressive behavior. Speech therapists, occupational therapists, special education teachers, and autism in-home providers can also provide you with strategies to teach communication, social, and self-regulation skills. Respite providers and support groups can also offer provide a great deal of support for you and your family.

* If what you’re doing isn’t working, then try something different. Maybe it’s time to consider medication. Psychotropic medication does not “cure” ASD but it is often helpful for extreme emotion and behavior problems. While many parents feel fear or hesitation about using medication with their child, the right form of psychopharmacological intervention may be helpful for symptom relief and also allows therapeutic approaches to be more successful, ultimately, so that medication is not necessary in the future. Also, if your child’s therapist is not providing you with ideas and strategies to try at home to minimize the behavioral outbursts – and it seems like they are just doing a lot of “talk therapy” with your child – then it might be time to seek a second opinion. Most insurance companies will cover this type of service. If your child is in special education, and you believe that there is not a “good fit” between his needs and the services provided through the IEP – remember: you have the right as a parent to meet with the IEP team to discuss your concerns and potential changes to the plan.

* If it’s an emergency at home – then act like it – call the police or a crisis response team. Contact the Department of Human Services (DHS) in your county or jurisdiction and inquire about emergency crisis services. This is a good proactive step. The police should always be contacted if necessary but remember their primary responsibility is to ensure safety – and they are not usually very familiar or trained in how to effectively work with children with special needs. Always take necessary action to keep yourself and your family safe.

* If you’ve truly exhausted your emotional resources–then consider out-of-home care. Community-based homes and therapeutic residential treatment programs are available through county and school district funding and provide access to therapeutic care that is consistent with the individual needs of your child. They can be short-term or more long term options. Contact your local DHS or do a websearch on programs in your area – and then start making phone calls to learn more.

Parents: Remember, you don’t have to feel afraid and isolated in your own home. If you are in a very difficult situation with your child with ASD and extreme aggression, remember that you have not failed. You’ve done your best with what you’ve been given – and it’s time for more help. You are a loving, concerned parent who is trying to manage a situation that has become unmanageable. Having an awareness that you need help – and it’s okay – is one of the first steps necessary in doing what’s best for you, your family, and your child.”

Amanda Ronan is a writer, an editor, an educator and a dreamer. She has her Master’s in Education and was a teacher of elementary and middle-school aged children for nearly ten years. While engaged with her work in the classroom, Amanda rediscovered her first love — writing.

Autism and Challenging Behaviour Part Five- Getting a Haircut

Autism and haircuts

Autism and haircuts

Now when I was my son’s age I have to admit that I hated getting my hair cut.  I think it was the boredom of waiting so long for the barber to get round to me that did it.

But with our son John this is not the case at all.  He hates having a haircut and when I mean hate I really do mean hate.  So much so on one of his first outing to my mother’s hairdresser the people from the shop next door came over to see if there was a problem.  So meltdowns were the order of the day.  You can find some great tips for dealing with meltdowns in the comments section of one of our older blog posts here https://patienttalk.org/?p=2349.  Why?  Well in John’s case he has sensory processing disorder which means the feeling of having his hair cut is, to him, one of massive overload of the senses.

Over the years we tried various strategies.  These included cutting his hair at home by a professional hairdresser who is also a friend.  The poor woman ended up cutting her hand with her rather sharp scissors during the haircut as John attempted to do a runner!  We also went to a specialist autism hairdresser.  The problem was that she was only available during the hours that my wife and I were at work.  Even if we could have made it would have taken around an hour’s journey to get to the venue.

So how did we solve the problem?  Well actually luck rather than judgement.  He rather desperately

Autism and haircuts

Autism and haircuts

needed his hair cut and our then nanny Willow offered to take him.   It turned out that she had spotted a local barbers shop which she thought could help.

I had a haircut there yesterday so I thought I would take the opportunity to show what the big draw for Willow was in two pictures illustrating the blog.  As you can see they have a car.  One John could sit in.  And you can see the TV as well – offering a section of the finest space-related cartoons that humans can make.  Not just that – in his hand was Willow’s iPhone with an exciting game of “Angry Birds” on the go.  Did it work?
Well more or less.  His hair got cut and no one went to hospital.  But most importantly he started to calm down when his hair was being cut.  So yes it is a rather incremental thing but it worked for us.

In fact these days he is happy to grasp an iPad and  have his head clippered as long as it takes less than five minutes.

That’s how we did it.  How about you?  One of the objectives of blog posts like this is to get other members of the autism community to share their experiences with others.  It would be great if you could share your story about getting haircuts either for yourself or your loved one.  Please feel free to use the comments box below to share.

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You might like to think in terms of the following questions:-

a)                        Did you have particular problems with haircuts?

b)                       What was the root cause of the problems?

c)What techniques did you use to overcome the problem and end it with a cut which worked?

d)                       What advice would you give to a parent about to embark on the hair cutting  autism journey?

And finally there is another option.  Don’t bother.  One of the boys in John’s class (they all have ASD) just has long hair.  It’s clean and looks great.  Albeit a bit heavy mental fan circa 1980.  So that may prove the best way out.

 

Kylesmum My 5 year old will have a meltdown with every haircut but the funny thing is that he will keep still … it’s so hard for me to watch cause what we do is that my husband will cut his hair with the clippers whist my son is sitting in the bath (empty of course) and he puts up with with about 10-15 mind of very emotional crying, trembling and sweating but once he is done he hits the off button on the machine and my son will start so sing and laughing with relief.
We have tried to put him in the empty bath with lots of thing to try to distract him but nothing seems to work e.g. iPad, favourite toys, turned the bath into a ball park nothing seems to calm him but as I said the only good thing is that he wount fight it and he can get his hair done quickly
Kylesmum My 5 year old will have a meltdown with every haircut but the funny thing is that he will keep still … it’s so hard for me to watch cause what we do is that my husband will cut his hair with the clippers whist my son is sitting in the bath (empty of course) and he puts up with with about 10-15 mind of very emotional crying, trembling and sweating but once he is done he hits the off button on the machine and my son will start so sing and laughing with relief.
We have tried to put him in the empty bath with lots of thing to try to distract him but nothing seems to work e.g. iPad, favourite toys, turned the bath into a ball park nothing seems to calm him but as I said the only good thing is that he wount fight it and he can get his hair done quickly .
MylaBides my husband and i used to wait until my daughter was asleep before we cut her hair. that was until she was 8-9.

then we bought clippers which we first used on my younger son while she watched. when it was her turn, she didn’t protest. maybe because she saw my son was alright. or maybe because she was playing around the playground, walking around while my husband followed her around.

of course he had to use rechargeable clippers. the wire simply will not cut it–pardon the pun!

Timingreenville At that age he would sit in my, his dad’s, lap.
Timingreenville We were very concerned with taking our 16 year old. I spoke to Christian at Great Clips as she cut my hair. She said to bring him in and they would work with in. A big issue with us is getting him in and out of the car. Transitions can be very hard for him. This time he sat through and shocked my wife and I. Then he got up and had to turn off the lights. I tried to prevent but he had to do it. Then he walked right out like no big deal.
Now with summer we will buzz him outside on the deck. He has gotten better about getting around his ears. It tickles.
SarahMKInnes My (almost) 7yr old (ASD and ADHD) just had his hair cut today. He will only have it cut at Sharkey’s (kids haircutting place) and will only allow the hairdresser use scissors – NO clippers whatsoever. Today there was a minor meltdown when he found out that their Super Mario game had worn out and they threw it out (he is obsessed with Super Mario) but once we got over that he was a bit squirmy but made out ok. I find what helps is if the hairdresser warns him beforehand (eg. “I’m going to spray some more water now”). We also try to make sure it is the same person every time that cuts his hair.
SneakyMumInOmaha Read SneakyMumInOmaha
SneakyMumInOmaha My 5yr old screams bloody murder everytime we try to cut his hair…except for that time when he woke up with a buzz cut. Oh yes I did. The trick is to turn the clippers on from a distance and then walk toward him. They’re pretty loud when you fire them up. And make sure your clippers are well oiled so they don’t pull his hair. You don’t want him waking up with a partial buzz-cut. And you’ll want to lay a towel down for easy cleanup and an itchless night. Good luck 🙂

 
sneedley13 Similar to PeterKijek below , our biggest problem was getting Connor to sit still in the chair. He also like to look around and see what everyone is doing. He now plays with the iPad/iPhone when he’s in the chair. We have found that he is much better when his Dad takes him rather than me, usually because he will get his hair cut at the same time (first) so Connor can see it, although we still have problems around the ears, either with the clippers or the scissors!
marionburns TiffanyIvison  https://www.facebook.com/profile.php?id=106711162797745&ref=ts&fref=ts

get in touch and i will talk you through some tips .

TiffanyIvison I have not found a way to make it work yet and am open to suggestions! My son is almost 2 and was just diagnosed with Autism, we already knew he had SPD. He was born with a lot of hair so we have had to visit the hair dressers many times and it gets worse with each visit. We are due for another cut soon and I have anxiety just thinking about it.
EricaPurtell I’ve found that if my Partner (his father) gets his hair cut first with my son watching we’re all good until we get to trimming around the ears- that’s the only thing we have a problem with….
lifeisarainbowmummy My son is actually sensory seeking at times and he loved my hairdresser who offered head massages even as a baby so he looked forward to getting his hair cut. We had major issues when my hairdresser went on maternity leave but we managed to convince him to let my new hairdresser cut his hair. One interesting thing we have found is that our son dislikes parting with any part of himself, after every haircut he has had, he has got down on the floor and picked up every last hair… thankfully he has the angelic looks to get away with it and hairdressers happily provide him with a bag – and we have a money bag full of hair for every single haircut he has had in the last 6 years! We even have a little tub of nail clippings (bag over head) as he would not let me clip his nails which he despises unless he could keep them. He was also terrified of losing his first tooth and sobbed for an hour when he realised his tooth was wobbling as he was terrified the tooth fairy would take it from him. We had to promise he could keep it in his sterling silver my first tooth box and wrote to the tooth fairy to ask if he could keep it. He still got a pound and a very reassuring letter from the tooth fairy!
marybethpalo I too had the same problems – what I had discovered was that my son not only learned from video but also we could film future events like a hair cut and the anxiety basically disappeared.  So – I used video modeling for years to teach and to familiarize my son with situations.  Seeing a man getting his hair cut up close and being able to watch it over and over seemed to do the trick.  We had been cutting his hair at home, in the bath tub, on the swing – you name it we had tried it!
PeteKijek Actually, I have had a similar experience with my autistic son. His main problem was not sitting still in the barbers chair, and he constantly looks round to see what the barber is doing! As you’ve mentioned, the TV nearby is a great distraction for him, (he’s a bit too big and too old for a car chair now 😉 ) but he also enjoys looking in the mirror at what the person is doing. I think he never quite understood how what was happening in the mirror was what was happening to the back of his head!


Talking about Autism! Telling your friends and family about autism. Updated

Autism Awareness Month 2015

Autism Awareness Month 2015

Getting a diagnosis of Autistic either for you or a loved one can be a traumatic experience.  Check out our previous blog on the subject (https://patienttalk.org/?p=284) which in fact was one of the first posts we ran on the blog.

In this blog we are interested in kick starting a discussion on how to discuss autism with family, friends and even the wider community.  While we are  not aware that autism is perceived in a negative fashion (see https://patienttalk.org/?p=1668) we are interested in the best ways of getting a positive reaction to an autism diagnosis.   The aim is to make the comments box below a great resource for anyone who has themselves just been diagnosed with autism or has a family member or friend who has just received a diagnosis.

As I mentioned before I found my son’s initial diagnosis very hard and, at the time, did not want to discuss it with anyone in any depth.  I now feel that this was a mistake as along the way we did lose contact with people due, in part, to us not explaining the changes in our lives caused by our son’s autism.  (To be honest most people assume that a five year old who can’t use a potty must be on the receiving end of bad parenting.)

One thing I have noticed is that a lot of people assume that people on the spectrum are savants rather like the Dustin Hoffman’s character in Rain Man.  Not easy to disabuse people of this one I’m sorry to say.

But the real headache, for me, is the meltdowns.  As the years go on they become fewer and fewer, for us at least, but when they do appear they are still an emotional tsunami.   For the onlooker it seems these are just “tantrums” over nothing rather than an upturned world which our son cannot control or rectify.  But the whole experience is made much worse by the looks of contempt and disgust on the faces of passers-by when it happens in public.

So how do you talk to people about it and try to get them to understand?

I know some people walk away from massive social lives finding it easier to just focus on their loved ones.  Others turn to autism advocacy often with great success.

So over to you.  How do you communicate autism awareness and the specific issues which affect your life to those around you and in the wider neurotypical community?  It would be great if you could use the comments boxes below to share your thoughts on these matters.

You might wish to consider the following questions when framing your answers:-

a)      What are the major issues with regard to autism which you feel you need to explain to others?

b)      How has the autism diagnosis affected your relations with friends and family?

c)       How do you explain autism to others?

d)      Are they any resources you think may be of use to others in helping them raising autism awareness?  This might include your own autism awareness resource.

e)      How do you explain meltdowns to those around you?

Please note that these are only a few of the questions the subject raises.  Please do add anything you think may be of interest.

Many thanks in advance.

 

LynetteConstable JolandaKruithof Looks like it has some great information. Can you translate it to English? I can’t read Dutch. I’m sorry. But I need help explaining my son’s behaviour to his grandfather – who just thinks he is a “miserable sod”
DarvinMcCloud Do we have any data concerning autism and hydrobaric treatment? Shouldn’t we give it a good test, if not why?
JolandaKruithof I am a dutch mom of a 9 year old Aspie. He’s got diagnosed december ’13. Because I want my friends, family and everyone else to know what it does to us and the impact it has on our lives, I decided to go blog about it.
You can find my blog at: http://aylablogt.blogspot.nl/.
Hope you enjoy!
misser31 My 8 year old daughter Dakotah was diagnosed with autism @ 18 months, she has been in early intervention since then. On some things she has improved on and others she needs more help, she is a strong independent little girl who is teaching us that being different is not as common as we think anymore and they are 10x smarter then us. This year has had struggles and triumphs, she now knows how to spell her whole name and is reading a lot more. We love her more than anything and am so glad she is in our family. Love you Dakotah bear!
JulieCamacho Although my son is not recently diagnosed he has started to have meltdowns at his Pathfinder events (club for kids 10-15 yrs of age). He had one almost 3 weeks ago and had a hard time 2 weeks ago at a large event.  Then hospitalized last week from school due to a large meltdown. These events have been hard on his friends in the club and Saturday he missed the club meeting. The kids had lots of questions for the directors who decided to ask me to speak to them about what was going on with my son.

I told them to look up Autism online that there are different areas people are affected in. Juans biggest area of difficulty is his social skills. I told them to also look up famous people with Autism so that they can see how people can be successful with this diagnosis. One child asked if this was a disability, my response was that this gave Juan different Abilities. They liked that comment and then we went over the positive things  Juan has to offer and some of the things like teasing that he struggles with and how they can help him if they notice little signs of fustration for him. They were all intent on listening and very involved with question. I am hoping that this will help understand him a little better and make a difference in him keeping more friends.

knutegems I would suggest you keep things simple. Any parent of an autistic child is under enough stress. Simply state that due to your child’s autism you are dealing with certain behavior issues. Most of these behaviors will change or lesson with age. There are many sources of information for people who are interested. I always felt it more important to educate the children my son was going to be with and help them to understand. They only know what they are told. If they are informed correctly they will have great understanding and be very accepting.
Amanda Rich A) The melt downs…I want one of those bubbles floating above her head to say “I am not a spoiled brat, I am over sensitive and something just pushed me over the edge of my thresholds….please don’t roll your eyes at my Momma” (B) and (C)…our friend base has changed, if they are willing to hear us out and learn they are still our friends…some decided that their kids would “learn bad habits” (ugh) from her. Mostly I miss being able to relax, I am never not aware of her voice, her body language (that warns us that she is about DONE).
I try to read everything I can, always looking for support. My biggest struggle….she looks like any typical child, she isn’t typical- she is 9 and will throw herself on the ground, ears covered, tears flowing and screaming. It is so hard when nothing looks “off” outwardly….I so thankful she is as high on the spectrum as she is, but it makes a barrier to the uneducated….I see the looks, I see the eye rolls, she is obvlious to the social cues, the social intuition is not there, she has speech deficits, and her heart is as big if not bigger than the universe. She is my Angel and I just hope that education for the public continues, if the judgemental could just walk in my shoes for a day!
Thanks
JoannaPapadopoulou I am a mother of a 3 yr and 8 month old big diagnosed with autism at the age of 2 1/2. I will try to address each one of your questions in order to assist your cause. a) I usually need to explain that my son refuses to eat any type of food besides sweets, unless it is served blended in a bottle. Also I need to explained that he has not mastered using the potty just yet and also that he will not reply verbally or look at you often when you are talking to him. b) we usually avoid gatherings when they take place at restaurants or coffee shops. We prefer house gatherings and some play grounds. Also for a long time we did not feel like inviting ppl over our house like we used to. Now we are better with that. c) I try to give basic characteristics that mostly involve my son. I usually describe it as a different way of seeing things, difficulty in communication, lack of sicialzation skills, difficulty dealing with changes and so on. d) I riled mostly on th Internet and on books about autism, Various treatment approaches like ABA, also I find others parents advice and experiences helpful and more practical. e) I usually explain to ppl what triggered the meltdown, for ex that he wanted the chocolate and I didn’t give it to him, or that he is tired and he overreacts to situations.
Thank for reading this. I will be happy to discuss the issue more with you.