Showing posts with label Nat'l Council on Severe Autism. Show all posts
Showing posts with label Nat'l Council on Severe Autism. Show all posts

Wednesday, April 6, 2022

Severe Autism Awareness: An Interview with Isaac


April is Autism Awareness Month. 

Severe autism takes many forms, but lets be honest, it makes many people uncomfortable. It is not well understood by the general public. Even families that have been living with severe autism for decades and can tell you exactly how it affects their family member, are almost as clueless as everyone else as to its cause and how to treat it effectively. Sometimes there is a reluctance to speak about it because it contradicts the rosy picture that is painted by advocates for people with autism who are not intellectually disabled and have average or above average abilities. It is as if using the autism label for people who are not performing at this level will reflect badly on people who are. 

In this video, Irene Tanzman introduces her son. She projects their affection for each other, but without needing to wear rose-colored glasses to see severe autism clearly.

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An Interview with Isaac, Diagnosed with Severe Autism

Apr 1, 2022

Irene Tanzman

This is my interview with my son, Isaac, an adult diagnosed with severe autism. I filmed this video in April 2022, Autism Awareness Month. Most often, the autism you hear about is not the type of autism that my son and many others have. It seems to me that Autism Awareness for this type of autism seems at its lowest point since my son was diagnosed. The kind of autism that the public is aware of is not the autism that Isaac has. Individuals like Isaac need quality disability specific programming and instruction to lead productive and fulfilling lives. They need therapies such as behavioral, speech, and occupational therapies. This type of help is nearly impossible to obtain. While Isaac is quite loveable and endearing, the idea that he will work in competitive employment is not realistic. He needs the type of services that the National Council on Severe Autism advocates for. Please be aware that this type of autism exists, and that people like this need help and services. Thank you for watching my video.

Visit my website at: https://irenetanzman.com/ . 

Follow me on Twitter: https://twitter.com/itanzman . 

Visit the National Council on Severe Autism: https://www.ncsautism.org/

Friday, October 23, 2020

Death by Severe Autism

"Death by Severe Autism" is an article from the National Council on Severe Autism by Lee Wachtel, MD, a pediatric neuropsychiatrist and the Medical Director of the Neurobehavioral Unit at the Kennedy Krieger Institute in Baltimore, Maryland. The Kennedy Krieger Institute is an inpatient unit serving youth with neurodevelopmental disabilities and severe behavioral and psychiatric disturbance. She is also an Associate Professor of Psychiatry at the Johns Hopkins School of Medicine. 

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Death by Severe Autism  

October 19, 2020

In the wake of senseless tragedy, a psychiatrist reflects 

on severe autism’s painful realities.

By Lee E. Wachtel, MD

With the presidential election only two weeks away, our country stands at a tremendous crossroads during an era of unprecedented health and social challenge. Our lives literally seem at stake. As Republicans and Democrats spar on hotly contested issues ranging from Covid-19 to racial and social equity, climate change and the Supreme Court, disability activists are also jockeying for power and planning their next steps in whatever administration the American people elect.  

I had been quite excited to participate in some of these political advocacy initiatives, until I was upbraided and accused of “ableism” and hurting others’ feelings when I asked what plans might include those with severe autism and intellectual disability. I was informed that “severe” was an unacceptable term, and as discussion of this topic was deeply upsetting to some individuals, I would be dismissed from the committee if I mentioned it again.

Let's be clear. There is obviously, without any doubt, such a thing as severe autism. The tragic death of autism advocate Feda Almaliti and her autistic 15-year-old son Muhammed (often called “Mu” or “Hammoudeh”) in a house fire in the early hours of September 26 underscores this reality, and also just how critical it is to never back down. We must never allow the plight of children and families dealing with severe autism to be suppressed by advocates who actively seek to downplay the serious mental challenges that ended up killing both Mu and his mother.

 

Feda, her sister Maysoon and Maysoon's daughter safely exited the burning home, but Feda ran back inside and upstairs to save Mu. Maysoon described what happened next:

“I ran back to the front door to scream for Feda again- as if that would help her come down faster. I can hear the popping of glass and the faint noises of Hammoudeh crying, “No, No, No" in response to Feda pleading with him. ‘HAMMOUDEH COME ON WE HAVE TO GO, NOW, WE HAVE TO GET OUT NOW!’

“The crying and screaming start to fade, probably not lasting more than thirty seconds. Then it stops and all I can hear is myself screaming for Feda and the words ‘my family.’ The realization of how useless and helpless I became made me sick and I wondered if my heart would give out any second.”

In other words, Feda ran back into the burning two-story structure to coax her 6’2”, 280-pound autistic son out of his room and down the stairs. But he would not budge, and Feda stayed. When the fire officials found the bodies, Feda was embracing Mu.

After a colleague and autism parent commented that “Autism killed Feda and Mu,” I had the chilling recognition that these two incredible people died a horrific death precisely because a severely autistic and intellectually disabled kid was unable to transition from point A to point B. 

I’ve worked with autistic youth for nearly two decades and have seen countless behavioral protocols developed with intricate layers of reinforcement to gain compliance with necessary daily transitions. Yet while I’ve had kids plop down in the road or tantrum naked in busy airport hallways, I’ve never had any autistic child suffocate and burn for failure to move.

Typical teens in this crisis would have immediately run down the stairs. Indeed, most people with autism would have done so as well. The autism and disability advocates who attend college and graduate school, tweet their condemnations of autism parents, and campaign for policy reform and who are largely capable of high levels of independent stewardship, would have not hesitated. And those with physical handicap without severe mental and intellectual disability would have grasped the urgency of the situation and likely followed a planned and practiced exit strategy.

Feda Almaliti was an autism trailblazer beyond compare, and her autistic son Mu was cherished for his infectious joy. But by any reasonable measure, his autism was completely unlike that of the autism self-advocates. It was severe – Feda herself described him as “Autistic as F&@#” — and was compounded by severe intellectual disability. Most importantly, in a dire situation his severe impairments rendered him incapable of taking a simple action to save his own life. If Mu had mild autism, and lesser intellectual disability, I have no doubt he would have heeded his mother's words and fled the fire. Mild and severe. More and fewer IQ points. It all matters. It matters so much that in this case it meant the difference between life and death.

My one hope is that this tragedy may actually serve as a lesson to disability activists who dismiss the reality and plight of the severely disabled while narrow-mindedly pursuing their own agendas. There are so many Mus and Fedas out there facing horrendous hardships. Dismissing their realities — as I was essentially asked to do by current disability leaders — would not only have been a grave violation of the medical ethics to which I adhere, it would carry potentially devastating consequences for national disability programs and policy.

Whichever administration is in power after the election, they need to hear about severe autism. They need to hear about it loud and clear. Lives are on the line.

Tuesday, September 29, 2020

A founder of the National Council on Severe Autism perishes in an accidental house fire

I have been a follower and admirer of the people who founded  the National Council on Severe Autism  in May 2018. One of their founders, Feda Almaliti, died Saturday in a house fire with her beloved son Mu. This is a tribute to her and her son from her NCSA family.

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On the Passing of Feda Almaliti, 1977-2020

September 27, 2020

Yesterday was a day that rocked the autism community. Feda Almaliti, one of the founders of the National Council on Severe Autism and who was recognized nationally for her outspoken and often brash and hilarious advocacy for individuals and families impacted by autism, perished in an accidental house fire with her beloved son Muhammed. Feda was able to run out of the house along with her sister and niece but then went back in to bring out Mu. She could not carry him but kept fighting till she lost her breath due to heavy smoke. When the fire officials found the bodies, Feda was holding Muhammed.

Our hearts are broken....

...When we heard she had died trying to save Mu, a friend remarked, “Of course she did, she would not have been able to live with herself otherwise.”

Read the full post here.

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See also, Ways to Honor the Late Feda Almaliti and Her Son Muhammed

The NCSA Blog is full of posts that describe the hope and despair of severe autism and give voice to people who have been underrepresented and misrepresented by people presuming to speak for them.

Wednesday, January 16, 2019

New Organization on Severe Autism

Autism is not one of the disabilities that my two adult sons have had to deal with. My awareness of autism goes back to the late 1970’s and the struggle to get schools to fulfill their obligation to make available a “Free and Appropriate Public Education” (FAPE) to every disabled child. Autism was not an official category defined by federal regulations at the time, but most children with autism fit under one or another of the categories listed and because of their disabilities needed special education. 

I knew families whose children had been diagnosed with autism and other related disabilities that would fit the definition of autism as it is now understood. The difference is that forty years ago, I never heard anyone talk about “high-functioning” autism or any of its milder forms. The manifestation of the disability was almost always severe and was often combined with intellectual disability, severe language impairment, and behaviors that interfered with education in regular classrooms and sometimes caused self-injuries or injury to other family members.

As a non-expert, I do not pretend to know enough to explain the explosion in autism diagnosis, but cases of severe autism have not abated. The needs of this population are growing, especially with the aging of family caregivers and the tendency for some advocacy groups to turn their backs on people with the most severe disabilities in favor of presenting an optimistic and more palatable image to the public and policy makers. If I had to rely on presenting a “positive” image of my children now and in the future to justify spending on services for them, I would be sabotaging the prospect of them receiving services that are both appropriate to their needs and effective in preventing harm.

A new organization called the National Council on Severe Autism (NCSA) has been launched “Pursuing recognition, policy and solutions for the surging population of individuals, families and caregivers affected by severe forms of autism and related disorders.” 


This from a press release on 1/10/19:

“…The new organization is created to address pragmatically the many serious challenges in services, housing, and policy facing families, caregivers and individuals affected by severe forms of autism and related disorders.

“‘Autism is often romanticized and sugar-coated in the media and social media,’ said Jill Escher, NCSA President. ‘In contrast, our efforts will be guided by pragmatic realities. For countless families devoted to the well being of their disabled loved ones, the daily challenges can be overwhelming, and the prospects for the future extremely bleak. We will work to increase capacity and a range of new options for this population.’….”

The organization has gotten off to a good start with a Website that presents their reason for being, policy statements, and an active blog .

From the NCSA blog:

If you wish to Share your story, the NCSA wants to hear from you:

Please share with us your story and concerns, and also your ideas about how to improve the lives and prospects for all those affected by severe forms of autism and related disorders. Topics may include, for example:

• Housing and long-term supports
• Education and training
• Day programs and employment
• Medical care and therapeutics
• Behavioral crisis and crisis care
• Financial issues
• Autism research
• Individual, parent and family well-being

Your information will help inform NCSA’s efforts, and will be kept confidential. If follow-up information is needed, we will contact you. Thank you for your generous assistance and time...


Amy Lutz, a parent of an adult with severe autism, writes about the organization on the Inspectrum blog from Psychology Today: "National Council on Severe Autism (NCSA) Launches; New organization will advocate 'for those who cannot speak for themselves.'", 1/14/19.

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For more information: 

Website: ncsautism.org
Email: info@ncsautism.org
Facebook: https://www.facebook.com/ncsautism/
Twitter: @ncsautismorg

Mail:

National Council on Severe Autism
PO Box 26853
San Jose, CA 95159-6853