In my previous post I included a chart that showed the ages at onset of deafness. Three-fourths of all people who are deaf lose their hearing after age nineteen. One interesting outcome of deaf mobilization has been the gradual acceptance of sign language as a viable form of communication for those who lose their hearing late in life.
When my hearing loss was first diagnosed, HLAA (founded in 1979) was in its infancy. There was literally no place for someone with late onset hearing loss to get support or help from others. At first HLAA focused on oral deaf people whose accommodation needs were different from the ASL-deaf. At that time the ADA Act was being written. HLAA’s mission was to ensure that oral deaf would not be forgotten. For example, though we cannot hear, ASL interpreters are not as helpful to us as captioning. HLAA’s goal was to advocate for those oral deaf whose first language was English.
However I think they developed tunnel vision in the process of focusing too much on certain accommodations to the detriment of others. They became a bit exclusive and some oral deaf got lost in the shuffle. I recall an oral deaf friend who showed up at an HLAA meeting signing. Signing was her only option since hearing aids didn’t help and cochlear implants had not been invented. She was told she was ‘too deaf’ for HLAA! Those were the early days.
When ALDA came on the scene, their motto for communication was “Whatever works” Late-deafened signers were welcomed from the beginning, and HLAA followed suit. ASL vocabulary even became part of the program for my local HLAA chapter. Just a few words each month would be taught. Club members found it interesting and useful. It is common today to see people using sim-com and ASL at all HLAA and ALDA functions.
One thing I’d like to point out is that both HLAA and ALDA welcome those who were deaf from birth. There is a common misperception among oral deaf that HLAA or ALDA might turn them away because they were born with hearing loss. While it’s true the majority of oral deaf are late-deafened, both organizations are welcoming of ANYONE who wants to join their cause. I suspect this is because their main focus is on advocacy not culture.
But also, many people fit into a gray area. Lots of people grew up with some mild hearing loss, then became profoundly deaf later. Are they born deaf or late deaf? Who cares? Or perhaps you were born deaf, but you’re married to a late-deafened individual, and maybe one of your kids is Deaf while the other is HH. Or maybe you are late-deafened, but ASL was your first langauge because your parents were Deaf.
One positive effect has been that deaf people of all stripes began coming to our events. In turn, we began to recognize that their experiences and perspectives are a great asset to our community. Comfortable in their own deaf skins, they are wonderful models of self-actualization– something the newly deaf struggle with as they come to terms with the internal identity shift from hearing to deaf. The born deaf often exemplify what you CAN do as a deaf person, instead of what you can’t.
Additionally, the born deaf sometimes blossom in our presence as they find themselves in leadership roles amongst former ‘hearing people’ looking for answers. Here, we look up to them as people with information and expertise. It’s natural for them to pass on a few signs.
So what I have personally seen over the past thirty years has been a gradual blending of people who were once polarized within the oral deaf community. We’re recognizing that we ALL need accommodations whether it’s an interpreter, CART, a dog for the deaf, or an FM system. Being deaf is no longer about dividing people according to their accommodation needs. The ADA was passed twenty years ago.
I can’t speak for the Deaf community, but it sounds like the walls are coming down there too. With that comes greater acceptance of ASL in the oral deaf communities.

In this picture, his class is signing to a song, though I can’t remember which song they signed to now. I loved these concerts so much!! Every year all the ASL classes put on a show and invite hh/deaf people in the community to attend. It’s such a fun night. The kids choose the songs, make the stage back drop, bring props and choreograph the performances. It’s so great to see so many young people who know a little ASL. I often run into former students working in restaurants and at Starbucks around town who can sign a little– thanks to this program and others like it. My son is not fluent in sign. His first language is English, as is mine, but he can sign enough to help clarify what he’s saying with his mouth that it helps our communications quite a bit. He is the fifth from the left in the top row– black shirt
I’m so excited. I finally got my Sorenson working again. Last night a Sorenson guy showed up out of nowhere. He needed to give me a new number because of some new FCC regulations. But it was strange the way he showed up so late at night. I told him my Sorenson wasn’t working, then he tested it and said it WAS working, but I kept telling him I didn’t think it worked. Then he assigned my new numbers, and tried to call the CIR (I do not know what that stands for but I think it meant he was calling an interpreter because that’s what he did next.) and then the interpreter told him she wasn’t getting my connection or something. So he had to put in a new router that would piggy back onto my old router. He’s coming back tomorrow and then everything should be all fixed!! And I will be able to call anywhere!!! 



