Showing posts with label late deafened. Show all posts
Showing posts with label late deafened. Show all posts

Wednesday, August 14, 2013

Deaf man mocks a "deaf" beggar

A recent video came to my attention of a Deaf man mocking a beggar at Las Vegas seen here in a Facebook video. This beggar was holding up a sign saying "Deaf. Hungry." Plus another word below which could not be read due to the blurry video.

Ted, the Deaf man signing in the video, made an assumption that the beggar could not possibly be deaf but hearing simply because the beggar did not know sign language.

Now, there are two possibilities.

1) The beggar could be deaf or hard of hearing and does not know sign language.

2) Or the beggar is hearing and does not know sign language.

Ted assumed the beggar is hearing on the basis he did not respond to Ted's signing to him. And thereby concluded the beggar is lying about his medical condition and not deaf at all.  But the beggar could have been born with a hearing loss or is a late deafened person who is homeless.

There are many deaf people in the United States who do not know sign language.
The majority of people who are deaf and hard of hearing do not know sign language. According to a Johns Hopkins study, more than 48 million people in the United States are deaf or hard of hearing, or a fifth of all Americans. Of these, almost 99 percent lost their hearing or were raised orally–not using sign language–and rely on their residual hearing (aided by hearing aids or cochlear implants), speech reading, and the printed word for communication access. This group of people are greatly aided by text forms of access.
Just because you see a deaf person does not mean the person knows sign language. Bad assumption. Best way is to get the facts first. If indeed the beggar is hearing, then shame on him. If indeed the beggar is deaf/hh, then double shame on Ted.  Either way, it's a bit disgusting to watch.



UPDATE: Good friend of mine, Barry Sewell and his wife, Crystal, produced their own captioned video about the disturbing video they saw in Facebook.

Sunday, April 28, 2013

The Walking Effect

The difference between Walk4Hearing and Walk for ASL?

Walk4Hearing involves the community on a much larger scale with thousands of people every year in 22 different cities from June through October. The local media reporting in each city help generate more public awareness about hearing loss. It's a public relation dream machine. Walk for ASL on the other hand involves 15 culturally deaf people who will walk for 30 days from San Francisco to Santa Monica, California with the hope that their actions and message will capture the attention of the media.

Walk4Hearing is again raising money and has a very successful formula since 2006 because approximately 1 out 8 Americans with hearing loss have something that they can relate to each other with a common condition. There are many more hearing parents, friends and families who know someone with a hearing loss.  It could be their grandpa who experienced hearing loss later in his life. Or have a deaf or hard of hearing brother or a sister. A parent with a hearing loss. A hearing person whose best friend wears a hearing aid. A next door neighbor whose teenager experienced hearing loss from Meningitis.  Hearing loss is such a common condition in the United States the majority of the population are familiar with it. And because of the familiarity about hearing loss they become much more approachable about auditory-oral education, hearing aids, cochlear implants, or implantable hearing device that uses the eardrum as a natural microphone. No wonder auditory-oral schools are succeeding in their public relation efforts with their communities.

In its first year in 2006 the Walk4Hearing raised over $300,000. Since 2006 they have raised several million dollars. In 2011 Walk4Hearing successfully raised $1.1 million dollars in a matter of months. In 2012 they surpassed the $1.2 million dollar mark. This year their goal is to raise $1.4 million dollars and so far they are 24% of their goal with $336,000 raised already and they are on track to surpass the $1.4 million dollar mark before the first walk to start in June of this year.

Money raised is shared between national and local programs and services including support of children with hearing loss at www.kidsandhearingloss.org.

National Programs and Services    
  • Provide timely and reliable information about hearing loss through HLAA’s website, Hearing Loss Magazine, HLAA e-News, the Hearing Loss Support Specialist Training, message boards/chat forums and annual conventions
  • Advocacy at the national level to affect legislation that impacts people with hearing loss, whether it’s funding for hearing aids, cochlear implants, communication access in public places or other important issues
  • A nationwide network of chapters and state organizations providing peer support
  • Support for parents of children with hearing loss at www.kidsandhearingloss.org
  • Outreach to veterans returning with hearing loss
  • Social networking site for young adults with hearing loss at www.hearinglossnation.org
Local Programs and Services    
  • Captioning and hearing assistive technology at HLAA chapter meetings to make them accessible
  • Scholarships toward college tuition for students with hearing loss
  • Funding for hearing aids and assistive listening devices for people who cannot afford them
  • Installation of hearing assistive technology in public places, such as community rooms and public libraries
  • Captioning of live theater productions
  • Seminars on coping with hearing loss
The www.kidsandhearingloss.org website is to help
empower parents of hard of hearing and/or deaf children by providing the resources necessary for them to make informed decisions about their children’s hearing loss.
Below is a Walk4Hearing video promotion with subtitles.




Walk for ASL is a new venture idea to help raise awareness and seek funding for their own agenda and cause. It only actively involve 15 deaf people who will walk in California the 600 miles from San Francisco to Santa Monica in 30 days along the Pacific Coast Highway. Their goal is to get the attention of the media.

The difference here is that ASL and deaf culture are essentially a hidden language and community. They are more apparent in large cities such as Washington D.C.; Rochester, NY; Seattle, WA; and Austin, TX. Even in large cities the bulk of hearing people go about their daily lives and never get to meet or see a signing deaf person in their life. And for a good reason because the culturally deaf community make up about 0.2% (0.002) of the total population in the United States. The chance to meet a signing deaf person or a deaf group would be quite small. It becomes harder for hearing people to even sympathize with such a small deaf community when they try and raise awareness on ASL, a language and culture that are totally foreign to most of the hearing society. They might hear about signing deaf people in the news on rare occasions or by chance see a deaf character in a television show. But to the hearing society the language and culture of deaf people are still completely foreign to them.

Below is a Walk for ASL video promotion but no subtitles or transcript available.





Monday, April 22, 2013

A win-win-win situation


For any organization that serve the deaf and hard of hearing population as well as for parents of deaf and hard of hearing children should take every effort to accommodate the potentially wide ranging communication access needs for an audience with deaf, hard of hearing, culturally deaf and hearing people when doing live presentations.

The concept and idea are quite simple. Three things are needed at the same time.

1) Real time captioner where the spoken words can be displayed visually for the audience.
2) Sign language interpreter.
3) Voice interpreter.

Using that prescription it wouldn't matter if the people in the audience or the speakers are deaf, hard of hearing, culturally deaf or hearing, communication access wouldn't be missed by anyone. This is how you "walk the walk" instead of talking out of the sides of your mouth.

Using the three communication access points satisfy 6 different possible outcomes for people who are:

1) Culturally deaf people who rely exclusively on sign language can take advantage of sign language interpreters.
2) Hard of hearing and deaf people who are not native signers can get assistance from captioning to help supplement their weak signing skill.
3) Hard of hearing and deaf people who can hear well with their hearing aids or cochlear implants and sign well can take advantage of either voice interpreter, captioning and/or sign language interpreter to help fill all of their communication gaps.
4) Hard of hearing people who can hear well and understand the spoken words well but do not know sign language can take advantage of voice interpreters and captioning.
5) Deaf people who do not know sign language or cannot hear well to understand the spoken words can take advantage of captioning.
6) Hearing people who do not know sign language can take advantage of voice interpreters and, if they need to, captioning.


If you're a 501(c)(3) non-profit organization that caters to deaf and hearing people, and even hearing people such as parents of deaf and hard of hearing children would be wise to use take advantage of all three communication access points if you plan to do presentations at a workshop, training session, or at a convention where the public is invited. It just make smart sense to do this because no one would be left out of the communication loop. No one would feel discriminated or left out. Everybody can participate and be a part of the larger discussion. Catering to only a specific group of people with hearing loss or cultural identity helps no one when the bigger picture is to help everybody understand deafness-related issues and concerns. 

Friday, April 22, 2011

Keeping it simple

I like to keep things simple in life and try to look for the more positive things. For me, I refuse to use my disability or my hearing loss as a crutch or an excuse in life. There are ways to educate people that's simple when it comes to communication access. People continue to learn new things when it comes to those with hearing loss. Many people I work or associate with have mild hearing loss and some do wear hearing aids. Few I know have moderate hearing loss. Sometimes in one ear or both. One is a young adult who has a hearing loss but only in the high frequency range but hears just fine but no hearing aids. And of course those who have much severe hearing loss and know signs.

Nothing is worse than to have people look down on you with pity especially if the person plays the game using deafness as his/her crutch. I refuse to see myself as a victim or behave like a victim all the time. Playing the victim card at every waking moment isn't a healthy life while accusing and blaming people all the time.

Accentuate on the positive. Keep it simple by keeping the path clear.

Sunday, June 08, 2008

Deaf America Syndrome

Image Hosted by ImageShack.usAt first glance my blog title may sound like something of a disease or a condition I'm trying to infer. A disease or condition that afflicts Deaf America and that being Deaf or a person who is culturally deaf is an affliction. An anomaly. A contagion. Something that needs to be cured or fixed. We also hear the word “syndrome” almost daily. We hear about people with Down’s Syndrome, Carpal Tunnel Syndrome, Chronic Fatigue Syndrome, Shaken Baby Syndrome, Munchausen Syndrome by Proxy, Rubella Syndrome, and so on and so forth. All of them deal with the negative connotation as being a disease or condition of some sort in association with the word “syndrome.”

You as a reader might be hastened into thinking that this blog entry is nothing but negative things about Deaf people, Deaf culture, and the Deaf community in America. Not so. It is not my intention to present wholly negative viewpoints just for the sake of it but more accurately an attempt to provide a more equitabe and balanced look. Questions need to be answered and how our perspectives view things differently from many different angles.

Now, if we look at the definitions of the word “syndrome” we can see that it has primarily two meanings. From the medical definition it is defined as “a group of symptoms or signs that appear together and that tend to indicate, with some consistency, the presence of a certain disease or other condition.” From a non-medical point’s of view the definition of “syndrome” is defined as “a complex of concurrent things.” This blog entry, “Deaf America Syndrome,” is about the complexities of concurrent things that meshes together with the pitting of ideas, concepts, and long held mythical beliefs between hearing, deaf, Deaf, and hard of hearing people in America. Nothing about illness but the complexities that we see and experience today.

The issues Deaf people in America have to deal with involve all of their own complexities and idiosyncrasies, including how they feel about hearing people, deaf people with cochlear implants, late deafened, or people who are hard of hearing and wear hearing aids. Many people do not always see things as other people do. Of course, this is how people behave. Our perspectives are different about life and of each other. Some perspectives are negative while others are positive. Some people refuse to acknowledge certain things in life thinking it's all a conspiracy, while others simply accept it as a given and seek better ways of doing things. Some steadfastly stick to their words until one day something dawns upon him/her and do an abrupt but humbled 180 degrees turn on their opinions or beliefs. Deaf America has its own true richness in life combined with the unique cultural upbringing that cherishes Deaf family support and friends. People try and lead a good example for others to follow but everybody stumbles along the way. We have the good, the bad, and the ugly in America when it comes to diversity and perception issues. People cannot simply ignore these things and we must face these things head on instead.

Diversity Issues.

When diversity is lacking you would know it right away. So, in the case of the blog aggregator business the best way to assure diversity is to first make sure that you have an example of that diversity in place. For a start, you have a group of people who contribute and maintain an aggregator site that exhibit that very same diversity make-up with those on the outside. Otherwise it’d just be a political tool in the attempt to claim the “diversity” label when it’s really not the case. Such an example of this may be in the form of a group that promote Deaf-centric values but do not reflect the same diversity mixture to those on the outside. Ideally, for a group of people to reflect that diversity mix would be a “cuer,” a person who is Deaf, a person who is deaf or hard of hearing, a person who is hearing and have a relationship of some kind to somebody who is deaf (e.g. hearing parents of a deaf/hh kid), CODA, late deafened, a deaf person who wears a cochlear implant and so on. Though philosophies may differ in the area of language or communication but you have a diverse group of people who share a common ideal and bond on the need to communicate with each other regardless the preferred mode of communication method. You may have people, for example, who know how to sign (e.g. SEE, ASL, PSE, BSL, FSL), those who do not know how to sign and do not want to sign, those who prefer to talk and listen only, or those who prefer to use cued speech with their talking. Each person has his or her own personal value when it comes to their hearing loss whether it’s a Deaf-centric one or not. Deaf-centric value does not take center stage on Deaf Village but is seen as an equal among other values that deaf and hard of hearing people share.

No one aggregator site is an island.

This latest incident about DeafRead (and here) reminded me of a time when people began abandoning Deafnotes several years ago for a variety of reasons. Former members began to design their own online forum websites and the net result was a noticeable shift by those who felt uncomfortable or disgusted to join these new forums. Others left and joined new forums because moderators were less heavy-handed and more neutral on allowing new members more freedom to discuss various deaf or non-deaf related topics. This includes less fear of getting booted or locked out of a discussion forum for political or apolitical reasons. The reasons for leaving or joining other deaf or hard of hearing website forums are many but in the end there are now more deaf and hard of hearing related forums that it was several years ago. And today we see many Deaf, deaf and hard of hearing related forums.

Now, for the aggregator business it is a niche business by catering to a particular subject for blogs to be aggregated. And there are just a few of them right now. But just because an aggregator website has a niche subject such as deafness to choose their blogs from, it isn’t necessarily enough sometimes. There can be this perception issue in regard to an aggregator site by those who run it. A perception by those on the outside who may see one aggregrator site as a wholly Deaf-centric and Deaf-controlled aggregator site that mostly aggregates Deaf blogs rather than a site that promotes true diversity while trying to fullfill and keep to the loyalty factor to their mostly Deaf bloggers.

And then we have those damning myths or half-truths where parents of deaf/hh children, older deaf/hh people and the late deafened from young kids who have lost their hearings to older adults who may view Deaf people as living in an insular Deaf bubble world. And why would they see that? Well, it only takes a few examples to help propagate those myths or even half-truths (and some cases wholly true) on a continuing basis where bloggers may end up on not wanting to be associated with a particular blog/vlog aggregator website simply for that reason whether it's true or not. It's the perception and the various myths, half-truths and truths that drive their decisions.

Take one particular example of a Deaf leader who represents the editors or moderators that help run an aggregator site. The leader may claim the “diversity” mantle by pointing to the fact that there are many aggregated blogs from bloggers who are deaf, Deaf, hard of hearing, deaf/blind, cochlear implant users, late deafened, deaf and blind, cuers, or those who wear hearing aids while each of them have a different and preferred method of communicating. And that would be fine. But then this picture gets a little skewed and wanting when, for example, the leader refuses to include subtitles in his/her own video blog but signs only. Now, would the average person believe this Deaf leader’s claim of diversity when he/she refuses to add subtitles in the first place on the basis of not destroying the “purity” of ASL signing? Since there are 30 million people with hearing loss you’d have about 3% of that population that can understand ASL well enough but to actively engage to exclude the rest of the population is not a sign on acceptance or the embracement of diversity in totality. Lead by example is the heart of this question.

All this becomes a Deaf-centric, Deaf-loyalty issue and not about the firm belief on diversity when it gets down to the core issue of communication access for all. This is what Deaf Village, a blog aggregator site, is set out to do and that is to embrace diversity, promote tolerance, provide common sense ideals in regards to communication access and the proper respect to bloggers who do share those common core beliefs.

Granted, this is a long discussion on “diversity” but it was necessary to put these thoughts down. I am sure there are millions of deaf and hard of hearing people who will share the exact same sentiments as mine. There is no doubt about that. We don’t strive to live in a bubble or insular world but to become a world where everyone can be a part of by welcoming one and all. After all, we all share the one common theme and that would be hearing loss and communication access.