Let’s Not Make People Afraid To Open Their Mouths

From the New York Jewish Week’s blog, The New Normal: Blogging Disability, April 11, 2013.

Special needs. Developmental delay. Cognitive disabilities. Disabled. Learning disabilities. Retarded. Autistic. Mentally challenged. Slow. Special. Blessed. Pure of soul.

Language is power. From the first words we form as toddlers, making our needs and wants known, to the daily information we share online, from 140 characters on Twitter and beyond, language has meaning and weight. The better we can say it, the stronger our positions, our beliefs and our passions, whatever they are.

Language can also constrict, preventing the honest sharing of our thoughts, especially if we fear putting our collective feet in our mouths. In these politically-correct times, language has become increasingly dangerous, as descriptive terms and labels change at a pace that many find hard to keep up with, let alone understand and accept. Heeding the dictates of the language police is not only recommended, it’s required, or you’ll suffer the ignominy of using the wrong term.

A colleague who’s involved in the development of camp programs for children and teens with disabilities in the United States had an uncomfortable moment recently when she used the wrong term in a discussion about people with disabilities. After being chastised by a fellow advocate, she commented to me, “I want to use the right language, of course, but I don’t want to feel like I can’t speak for fear that I’ll offend.” Even worse, as a parent of children who do not have disabilities, she already felt tentative when talking about it, wondering if she had the right to express her opinion. Now, she’s just uncomfortable, worried that she’ll do it again, use incorrect language.

I know how she feels. Recently, I was summarily informed by a colleague that there had been a language shift in the field of disability. “Didn’t you know, that it’s people with disabilities now, and not people with special needs?” she told me. I adjusted my speech right away, but was put off the more I thought about it. What word is truly right, and who gets to decide what’s in vogue or not?

Ever since my youngest, who has Down syndrome and autism, was born, I’ve felt the need to be blunt about how I talk the talk of disability, especially when it comes to developmental issues. Take the word retarded. According to my Google dictionary, retarded means “less advanced in mental, physical, or social development than is usual for one’s age.” Okay, check. I also like this use of the word retard, when referring to bread baking as in “to slow down…[as in] a long, cool rest for the dough, during which it develops flavor and gluten.” Interesting. Needs time to develop in all sorts of ways. Checkmate.

Point is, “retarded” isn’t an evil term, it’s a descriptive term. When used pejoratively, of course, it isn’t acceptable, any more than “Mongoloid” was when it was used to describe the somewhat Asian features of kids with Down syndrome, or “Spick” for a person of Latino background. And I’m not arguing that language shouldn’t change along with attitudes towards inclusion and people with disabilities in general. What I am arguing is just this: If we’re looking to break down barriers, let’s not raise new ones by fiddling with the language so much that people are afraid to open their mouths.

When I talked about the new terminology with my Shutaf co-founder and colleague, Miriam, she commented that she preferred special needs to disability. Special needs, she argued, is what it’s about, that is, “the unique issues faced by each person,” as opposed to the perhaps harsher term, disability. She added that special needs also refers to the family as well, dealing as they do with the member of the family who has a specific issue. Or, in the words of my husband, “families of children with special needs, have special needs.” They’re not disabled by disability, but they are rendered special by the experience. It’s got a nice ring, I think.

With that in mind, I hereby suggest that we react more sensitively when we hear a term that we consider questionable when it comes to disability. Consider that the person who used the term may actually feel a connection to that word. Or they may not realize that the language has shifted. Or they might not know that the word is no longer in style, or that using it suggests they are insensitive or ill-informed.

Education and engagement will go a long way towards bringing us all together, while challenging all of us as a community of caring individuals to step up and use our words wisely, just like we encourage a toddler to ask and not point. Language is the point of contact. But tone and the desire to learn is more important than what’s the newest flavor in the disability lexicon. That’s how we’ll create a more inclusive and welcoming society in which well-intentioned people feel at home no matter what language they use.


  • Stephen Weiss May 12, 2013 14:31

    I appreciated this article, and I do think it is important not to get caught up in language and to empower those who care to feel comfortable to speak on these issues. I like the term special needs but I want to put in a word for the term disabilities. My daughter and I were at a conference last year at Lynn University called Post High School Transition for Students with Learning Disabilities. It was one of the most helpful conferences I have ever attended. One of the main speakers, Rick LaVoie, haas written many important books on the subject and is widely respected. He himself is ADD and talks about his own experiences. he encouraged students in the room to proudly own the term “disabilities” and pointed out that in college, for better or worse if you don’t use the word disability, you do not get the help you deserve and need because the law that protects those rights is the Americans with Disabilities Act. He encourages those with disabilities to prepare an elevator speech in which they can outline their disability and needs in two minutes and to lerarn to advoctae for themselves. That was very hard for my daughter (and me) to hear, but the truth is it was empowering and enabled her for the first time to take ownership of her special needs, to consciously seek a place that would meet those needs and to insist on them as her right.

    • Beth Steinberg May 13, 2013 10:40

      I appreciate your comment and I think that taking ownership in general, is a huge issue, and it’s one that holds us all back – those with and without disabilities, the children, teens, adults and their families. The word disability is a harder one, perhaps, and that might be the instinctive problem with it but again, we need to look past terms and start accepting and including and providing the needed services so that everyone can succeed.

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