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‏إظهار الرسائل ذات التسميات Suzanne Wright. إظهار كافة الرسائل
‏إظهار الرسائل ذات التسميات Suzanne Wright. إظهار كافة الرسائل

Neurodiversity Cultists Take Note: My Son Is A Joy; His Autism Is A DISORDER


Conor walking the North Riverfront Trail along the St John River, Fredericton

Many in the Neurodiversity cult, which irrationally embraces and worships the autism segment of the autism disorder diagnosis they sought for themselves, or their children, while discarding the DISORDER component of that label have, once again, attacked parents and other family members who dare to counter their perverse, ill informed ideology with honest depictions of their own kids autism disorders. Suzanne Wright's recent, honest, accurate, depiction of the challenges faced by so many with autism disorders and their families, has sent the autism cultists into what Autism Jabberwocky has called a collective conniption. Among the usual hate filled, knee jerk reactions is the allegation that family members, including parents, who talk honestly about the autism disorders they experience are describing the ND cultists' kids as monsters.  In truth it is only the ND cultists, those who praise autism as an Einstein like gift, who use the term monster in describing their autistic children.  

On this comment I am posting two sets of pictures (1) showing the joy we call Conor and (2) showing some of the harm inflicted by his autism DISORDER .  I have posted most of these pictures before and I don't expect the ND cult mongers who praise and misrepresent autism as a gift to actually pay attention to such evidence. They presume to know more about my son than I do.  For those, however, whose minds have not been frozen and locked forever in the Neurodiversity cult that worships here are these two sets of pictures which showns the realities of life with out son, the joy of Conor and the harm he suffers from his autism DISORDER. I believe the joy pictures speak for themselves.  The harm pictures will include a brief explanatory description.

(1) The Joy  of  Conor 














(2) The Harm of Conor's Autism Disorder

Conor engages in Self Injurious Behavior,
 including biting his hands and wrists. 


Conor has put his hands through glass windows and has to be 
watched closely when he is upset to ensure he does not do so again.


Conor's Self Injurious Behaviors include hitting himself in the head when frustrated/having a meltdown.  The picture above resulted from an incident at 3 am when Conor was hitting himself in the head with considerable force. I tried diversion strategies unsuccessfully and tried to grab his arms to prevent him from injuring himself.  He is much quicker than his old Dad and lunged forward and bit me on the bicep, biting through the skin and into the muscle resulting in the bruise above and calcium buildup. NO he was not trying to injure me, it was an example of what Dr. Sanjay Gupta called Reactive Aggression. 


Conor is very sensitive to noises usually the type of noise rather than the volume.  Some telephones ringing and some cars and motorcycle noises will set him off.  We use mobile phones in our home almost exclusively now because Conor has ripped the cords of our land lines out of the walls so many times. 


Conor, like a substantial number of the 50% of the autism spectrum who also have an intellectual disability also suffers from epileptic seizures. He suffered two grand mal seizures requiring attendance by ambulance at the Emergency room.  He ALSO suffered an adverse reaction to his medication which almost took his life and resulted in 2 weeks in hospital including 6 days in the ICU.  (Thanks again to the wonderful ICU Team at the Chalmers Hospital!)


10 years ago when we lived on Hillcourt Dr. above, just behind the parking lot of the Red Lantern pub marked above on the Google earth map, Conor wandered out of the house unnoticed.  Heather was in Nova Scotia and I answered the phone on a business call.  When the call ended Conor was nowhere to be seen.  After a frantic 911 call I recovered him from the Ultrasound gas station/convenience store on the corner of Main and Fulton above. Conor had crossed the busy parking lot of the Red Lantern Pub and also crossed a busy Saturday afternoon Main St.  Traffic was stopping to avoid hitting him and a good Frederictonian stopped his truck to take him to the Ultramar and alert 911.

I love my son dearly and I owe it to him to speak honestly about the autism disorder which limits his ability to function in this world and limits his life prospects. I will not misrepresent the nature of his autism disorder to make myself feel good.  I will fight all those who do misrepresent autism disorders as gifts. That is a promise I make to all including those at ASAN, TPGA and others who misrepresent autism to the world.  

An Excellent Week For Autism Advocacy! Suzanne Wright Speaks Out and John Elder Robison Resigns



Thank You Suzanne Wright!

It was a good week for reality based autism advocacy for two reasons. First, I was very encouraged by Suzanne Wright's very honest description of the many challenges facing persons with autism disorders and their families in Autism Speaks to Washington - A Call for Action. Second I was very pleased to see John Elder Robison, an extremely high functioning and very successful, free ranging Aspie, who refuses to acknowledge that autism is a disorder that should be cured, resign all his positions with Autism Speaks.  It appears that Autism Speaks may be abandoning its attempts to mollify the Neurodiversity ideologues that have caused so much harm to those with severe autism disorders. Hopefully its fund raising expertise can now be used to encourage the research necessary to help all persons with autism disorders and to develop national autism strategies to implement evidence based autism interventions in the US ... and in Canada.

I encourage everyone who actually cares about helping persons with autism disorders to read Suzanne Wrights powerful article in full.  I am very impressed with her courage in speaking so openly and honestly about the realities faced by many with autism disorders, their families and caregivers:

"Each day across this country, those three million moms, dads and other care-takers I mentioned wake to the sounds of their son or daughter bounding through the house. That is - if they aren’t already awake. Truth be told, many of them barely sleep—or when they do – they somehow sleep with one ear towards their child’s room—always waiting. Wondering what they will get into next. Will they try to escape? Hurt themselves? Strip off their clothes? Climb the furniture? Raid the refrigerator? Sometimes – the silence is worse. 

These families are not living. 

They are existing. Breathing – yes. Eating – yes. Sleeping- maybe. Working- most definitely - 24/7. 

This is autism. 

 Life is lived moment-to-moment. 

In anticipation of the child’s next move. In despair. In fear of the future. 

This is autism. 


On the good days my daughter Katie and all the other moms out there – 70-million around the world – see the sun shine. They notice the brilliant colors of the autumn leaves. On bad days, they are depleted. Mentally. Physically. And especially emotionally. 

Maybe they have been up all night caring for their teenage child who’s having a seizure. 

Maybe they are up yet again changing the sheets because there’s been another bed wetting accident. 

Maybe their child has been trying to bite them or themselves. 

Maybe they can’t afford the trip to a doctor specializing in autism. 

Maybe there is a waiting-list for ABA, speech and OT. 

Maybe their insurance won’t pay. 

Maybe they don’t have the money to pay a special lawyer to fight for school services. 

This is autism.

If any of this sounds familiar, you know autism. And if you know autism, you know we are looking at a monumental health crisis. And, we have no national plan."


I have a 17 year old son who suffers from severe autism disorder who has hit himself in the head repeatedly, bitten his hands repeatedly day in and day out until he was removed from the mainstream classroom and received his ABA based instruction (for which I and other parents had to fight) in a separate learning environment.  He has put his hand through glass windows.  He suffers from seizures and almost died in an adverse reaction to his previous seizure medication (as determined by the ICU team that saved his life at our local hospital).  He has suffered serious meltdowns as a result of obsessive behaviors. Disruptions of routines can also be extremely difficult.  He once left our home unnoticed and wandered across a very busy street oblivious to car traffic dangers until a good citizen of Fredericton stopped and took him to a nearby Ultramar service station/convenience store, called 911 and waited until I arrived to bring my son home.  The consequences could have been much different and I have never lost sight of what might have been.  24/7 care is absolutely the rule in our house. 

I am all too familiar with Suzanne Wright's list. I know autism.  I believe fervently that researchers should be focusing on finding cures and treatments for all autism disorders not the meaningless "remediation" advocated by the very high functioning J E Robison who opposes the very concept of curing autism.  I am very happy to see that Mr. Robison has abandoned his attempt to persuade Autism Speaks to stop seeking  real understanding of autism, to stop seeking treatments and cures for autism.  Above all Mr Robison's departure may help Autism Speaks find its way to once again speaking honestly about the challenges facing all persons with autism disorders including the 50% on the autism spectrum identified by the World Health Organization as also suffering from an intellectual disability.

Thank You Suzanne Wright!

Autism Speaks Tackles Autism Crisis in South Florida Mar 24 - 28


Donald Trump, Bob Wright, Suzanne Wright, Melania Trump
Photo: TOWN-CRIER Online

Autism Speaks is continuing to show outstanding leadership in tackling the Autism Crisis in the US and around the world. Co-founders Bob and Suzanne Wright have joined with Donald and Melania Trump, local parents and autism advocates in organizing a South Florida autism awareness and fundraising initiative to take place during the last week in March. Autism Speaks Week, March 24-30, will include a number of activities including a Television News Series on the autism crisis of escalating rates of autism diagnoses, March 24 to 28 on NBC stations in the area, an on-line auction, ING Direct Ride Now South Florida motorcycle ride, Saturday, March 29, a telethon and broadcast of 'Autism Every Day', and a concert for Autism Speaks, headlined by Lionel Ritchie, Sunday March 20.

As stated by Bob and Suzanne Wright in TOWN-CRIER Online:

“Autism is a national health crisis that is affecting families in every corner of this country, from Florida to Alaska,” Bob Wright said. “Autism Speaks Week will shine a spotlight on the struggles of South Florida families and inform people about what they can do to improve the lives of individuals with autism in their community.” “Our hope is that this series of events will increase the level of understanding and acceptance,” Suzanne Wright added. “The money we raise will help Autism Speaks fund autism research and support community organizations here in South Florida and across the United States that provide critical services to children and adults with autism.”

The ability of Autism Speaks to generate public awareness of autism, raise funds for autism research is amazing. And now Autism Speaks is turning its considerable abilities to assisting local autism support organizations. Not content to engage in endless peurile debates over the appropriate metaphors to use in describing autism or whether to say "autistic person" or "person with autism" Autism Speaks is actually doing something constructive, in a big way, in addressing the Autism Crisis.

Autism Every Day At The Nantucket Film Festival

'Autism Every Day' was scheduled to play this past week at the Nantucket Film Festival. The film has been a key element in the efforts by Autism Speaks and Bob and Suzanne Wright to raise autism awareness, real autism awareness, around the globe. The film generated much hostility from those who wish to portray autism as simply a natural variation, a subgroup of people with different ways, perhaps even superior ways of thinking. For daring to portray the real challenges of their autistic children's neurological disorders the parents of Autism Every day were vilified by the Neurodiversity movement on the internet.

Autism Every Day, and the courageous parents who participated in the filming, helped shatter the propaganda of the 'Autism is Beautiful' movement, the nonsense perpetrated by the Neurodiversity ideologists, those who make a career of pretending to be the voices of autistic people and those who like to hold 'acceptance projects'. For the Neurodiversity movement 'Autism Every Day' could not stand without challenge. And so they lashed out at the loving parents who appeared in the video.

Autism Every Day presented autism as it really is - a neuro-biological developmental disorder characterized by impaired communication, deficits in social interaction, and in some cases dangerous behavior. As the father of a profoundly autistic boy; a father who loves his son dearly and takes joy in each moment with him, while dealing with the hard realities of his autism, I thank the Autism Every Day parents for their courage and candor.

I hope they and their children are doing well.

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