The Ukiah Daily Journal

America, it's time to talk honestly about autism

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SAN DIEGO >> I tell my teenage kids that it's important to know what you don't know, and even more important to never stop learning.

One topic I need to learn more about is autism. I see people talking about it everywhere much more these days, from television shows to profiles of the rich and famous.

Asperger's Syndrome is what some call a form of Autism Spectrum Disorder that can affect social behavior. You may find it in super focused but socially awkward high-achievers. Elon Musk, the richest man in the world — while recently hosting NBC'S “Saturday Night Live” — told the audience that he has Asperger's Syndrome.

Since April is National Autism Awareness Month — or what neurodiver­sity advocates want to rename “National Autism Acceptance Month” — I reached out to an expert with a unique take on the topic.

Kristina Lopez is a professor of social work and psychology at the School of Social Work at Arizona State University. Her specialty is helping Latino children with autism.

Latinos, eh? Clearly, we have a lot to talk about.

According to Lopez, autism in children can be “reliably diagnosed as early as 12 months.” The disorder is centered around “social communicat­ion.” Not limited to the spoken word, it can extend to difficulty in making eye contact, displaying emotion, taking social cues and holding one-to-one conversati­ons.

Lopez says that, for parents, one warning sign is that a child isn't speaking at 3 or 4.

By zeroing in nearly 20 years ago on Latino children with autism, the fifth-generation Mexican American was way ahead of her time.

One reason: her epilepsy. Lopez grew up with what she calls her own “developmen­tal disability.” It wasn't diagnosed until she was a teenager, and it led to lots of bouncing between schools and multiple brain surgeries.

Her struggle gave her a builtin connection to those whose brains are wired differentl­y. It also provided her a window into how the public schools and the medical profession fail Latino students, patients and families.

“There was stigma,” Lopez recalled. “There was resistance from the schools and medical system to let me continue my education and get me the right treatment to manage my seizures.”

When she was still a student, she was put in a special education class because of her epilepsy. Even then, she could see that not everyone in that class was treated fairly or received the same services. Later, while attending college, she worked in a special education classroom.

“I saw the disparity,” Lopez said. “I realized it wasn't just me. This was a systemwide issue. The Latino kids in my classrooms who clearly had autism had another label attached to them. They were the `bad kid' or they had some behavioral diagnosis. Meanwhile, the one White kid in the class had all these people hovering around him, trying to help him.”

Now her mission is to bring about equity for Latino children with autism by making the public schools and medical system more responsive.

It's an undeniable fact — borne out by research — that White children with autism tend to get more services than Latino counterpar­ts. The squeaky wheel gets the grease, and Latinos don't squeak.

Many academics with a PHD in psychology — in Lopez's case, from the University of Michigan — would be satisfied to study

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