Why I’m not feeling blue on Autism Day

By Fiona O'Leary

 

The message being used by one organisation is instilling fear and hatred about the condition, says Fiona O’Leary, who has Asperger’s.

TODAY is World Autism Awareness Day, and the sound of alarm bells ringing is eerily unsettling to me, and to many other people who are on the autism spectrum.

I did not use the term ‘disorder’, as I do not feel disordered and I object to this negative language. But who will speak for me, and for the autistic community?

We have a voice, we are connecting and supporting each other, yet we are not being heard above the mainstream portrayal of autism as a ‘devastating disorder’. We are being left out of most discussions regarding our future, because the stereotype of us is so debilitating.

Nineteen years ago, my son was diagnosed with autism.

It was not easy then, but as challenging as it was, I feel the parents whose child is diagnosed today receive a barrage of negative information from powerful ‘awareness’ groups.

One such organisation is Autism Speaks, which is the driving force behind the ‘Light It Up Blue’ campaign that has been adopted by many of the prominent Irish autism charities and awareness groups.

I, for one, and many other individuals on the spectrum, along with the majority of self-advocacy groups, will not be lighting anything blue, and for indisputably good reasons.

Firstly, Autism Speaks’s senior leadership does not include a single autistic person, and excludes autistic adults from its board of directors, leadership team, and other positions of seniority.

In November, 2013, John Elder Robison, the only Autism Speaks advisory board member who is on the autistic spectrum, resigned his post.

Elder Robison was protesting the organisation’s portrayal of ‘the problem’, which described the families of autistic children as not living, but merely existing.

Elder Robison stated in his resignation letter that after four years of attempting to reform the organisation from the inside, he had been unsuccessful, and he could no longer be a part of the “only major medical or mental health, nonprofit organisation whose legitimacy is constantly challenged by a large percentage of the people affected by the condition they target”.

In one of Autism Speaks’s most prominent fundraising and awareness videos, one of its executives says how she had considered driving off the Washington Bridge with her autistic child.

She didn’t, because she had a ‘normal child’ also. Her words were spoken while her autistic child was playing, within earshot, in the background. Another video, the now infamous ‘I Am Autism’ ad campaign, tells the listener that ‘autism’ knows where you live, that it is an epidemic worse than cancer, AIDS, and diabetes combined, that it will destroy your marriage and make you bankrupt, that you will never go to a church, a park, a birthday party again, without a struggle, without embarrassment. Is it any wonder that lady felt like driving off a bridge: how long can one breathe in this demonisation and horror?

There is much more to highlight about this organisation, but if the reasons here are not alarming, then we need to wake up from the utopia of ignorance in which we doze.

Because Autism Speaks does not speak for me and I have Asperger’s.

It does not speak for my two wonderful and gifted boys, my reasons to live, who are on the autistic spectrum.

Yet Autism Speaks is ‘sounding the alarm’ with their latest awareness campaign, around the world and, most worryingly, right here in Ireland.

I participated on the panel of the final public consultation meeting of the IARB (Irish Autism/Neurodevelopmental Registry and Biobank) held at University College Cork last month.

The proposed Registry and Biobank is a partnership between Trinity College Dublin, NUI Galway and Autism Speaks. When I saw Autism Speaks’s logo — of a blue jigsaw piece — occupying equal space on the literature and advertising of a proposed biobank, I was more than a little unhappy. I was stunned at the logic of including an organisation that is controversial within the autistic community in a venture that needs that community’s cooperation if it is to be successful.

I expressed my concerns and I was invited to participate.

Myself and a small group of advocates went to object to the involvement of Autism Speaks, making the logical point that by including Autism Speaks they would be excluding a huge number of autistic people and their families, who rightly boycott that organisation.

Our premise, ‘nothing about us without us, is a good place to start.

Any research that will bring positive benefits to people on the autistic spectrum is welcome. However, the propaganda used by Autism Speaks is instilling fear and hatred about a condition that is struggling to find acceptance in society.

Autism?

Autism is a neurological variation that occurs in about one percent of the population and is classified as a developmental disability. Although it may be more common than previously thought, it is not a new condition and exists in all parts of the world, in both children and adults of all ages. The terms “Autistic” and “autism spectrum” often are used to refer inclusively to people who have an official diagnosis on the autism spectrum or who self-identify with the Autistic community. While all Autistics are as unique as any other human beings, they share some characteristics typical of autism in common.

1. Different sensory experiences. For example, heightened sensitivity to light, difficulty interpreting internal physical sensations, hearing loud sounds as soft and soft sounds as loud, or synesthesia.

2. Non-standard ways of learning and approaching problem solving. For example, learning “difficult” tasks (e.g. calculus) before “simple” tasks (e.g. addition), difficulty with “executive functions,” or being simultaneously gifted at tasks requiring fluid intelligence and intellectually disabled at tasks requiring verbal skills.

Following on from the RTE Prime Time expose of the truth behind the CD Protocol and the use of MMS as a cure for Autism, 'ART Autistic Rights Together' would like to reiterate the need for legislation and Regulation of all Autism treatments, now and into the future.

The abuse will not stop until it is actually illegal to use and experiment on Children simply because they happen to be on the autistic spectrum!

 

 

 

Follow up Prime Time programme exposing the use of MMS/CD Protocol by a Medical doctor in Ireland, further strenghtening the urgent need for legislation and regulation to protect Autistic children from experimentation at the hands of the Biomedical and Quack industry!

 

 

 

 

 

 

 

 

 

 

Aims of Autistic Rights Together


The main objective for which 'ART' (Autistic Rights Together) has been established is to promote the principles of equal rights for Autistic people.


'ART' (Autistic Rights Together) is a Non-Profit Organisation, founded and managed by Autistic people and fellow NT's (Neurotypicals) who share in our ideal to achieve equal rights for the Autistic Community.


Our passion is to empower Autistic people.


To do this we will strive to provide a safe environment where Autistic people of all ages can come to seek advice and support in the knowledge that they will be understood and valued.


The founders of Autistic Rights Together have been working on an individual, purely voluntary level for some time now on many pressing issues effecting the Autistic community. We needed to create an Organisation with the power to more effectively tackle the serious ongoing concerns of the ASC (Autistic Spectrum Condition) Community.


Issues such as:

The lack of inclusion of Autistic people on boards and management of the main Autism organisations.


The continued use of demonizing and damaging rhetoric by Autism Organisations in awareness and media campaigns throughout the world, thereby creating a sickening level of fear under which Autistic people are forced to exist.


The lack of training in the understanding of the Autistic Spectrum by public health sector workers such as Doctors, Nurses, Social Workers, Welfare Officers, Gardai and the Civil Service. Many Autistic People find it daunting and incredibly stressful when confronted with a system which has little or no regard for their needs, be it communicative and/or sensory and the simple supports that would make such a huge difference to the lives of Autistic People.


The growing use and marketing of numerous Dangerous, scientifically unproven, unsafe and potentially damaging so called cures and treatments all throughout the world. The experimentation on Autistic Children and Adults must stop!


The continued use of harmful, damaging and degrading interventions such as the use of 'Isolation Rooms' also known as Seclusion, Withdrawal, or Quiet rooms. Often these rooms are little more than Cells in which Autistic children are locked.
The use of (GED) Graduated Electronic Decelerator, a torture device strapped to Autistic people at the Judge Rotenberg Center in Canton, Massachusets which administers painful, powerful electric shocks to the body at the discretion of staff.


The level of abuse and bullying of Autistic people at the hands of Schools, Care Homes, Service Providers, fellow employees and employers must be addressed and stamped out.

We need to change the public perception of Autism from one informed by fear and negative stigma to one of Acceptance and Understanding, embracing of the concept that Difference is more and not less, Difference is not to be feared and stamped out but cherished, enabled and encouraged!


These are the Ideals which we in ART Autistic Rights Together stand for and will work towards achieving!

 

 

 

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