Attention all CODAs! You're opinions are wanted!

We as CODAs are well versed in how similar we are. We share a lot of common experiences growing up with Deaf parents and all that comes with it. Yet, no matter how similar the experiences are, no matter how great it feels to hang around each other and share our stories, we are all still very different from one another. It’s not necessarily a good or bad thing, it just simply is what it is. It’s life, and we deal with it. There’s a lot of beauty in the diversity.
However, I feel that sometimes the differences aren’t always good things, and these are all just matters of opinions. For some CODAs, there are likely certain traits in other CODAs that make them cringe, and for other CODAs it’s something else. For me, it’s watching CODAs who act as if without them, their parents or other Deaf people would just crumble without their ability to take care of them. If you are reading this, a CODA, and are offended, well, I’m not necessarily sorry. I don’t mean ill will, it’s just something I don’t understand, and often times drives me crazy.
The reason it makes me nutty is this. How does a CODA go through life with Deaf parents, know their struggles in a hearing society, know their friends as well they know some of their own closest relatives, and still come out with this attitude of being the caretaker? Its obvious that many of us as CODAs have often had to interpret as children for our parents, or handle phone calls for our parents that children had no place handling, and all of the rest of the things we may have had to do at one time or another. I get that not all Deaf parents raise their hearing children the same as others, or that having siblings can help shape the different roles that particular set of siblings fall into. It’s logical to make the leap that from time to time we may feel like the caretaker, but let’s dig a little deeper. 
I think the part about it that really dumbfounds me is how it comes to be that CODAs who act this way seems to forget that their parents were around before them. Did they need you then? For my experience, at times I had to interpret, take calls, be the face that every hearing person spoke to when they realized I was the only one they could talk to (which often came with that attitude that I wasn’t just the only one they could talk to, I was the only intelligent one in the bunch). That last one always infuriated me to no end because I knew my parents were every bit as competent as any of the jerks I had to make nice to in front of my mom and dad. The only reason the situations occurred was the fact that audism existed, and obviously still does. But I also went to Deaf Club with my parents regularly. I often spent the night at their friends’ homes when we would visit. Thanks to my parents, I know who Deaf people are, and I know that if I wasn’t around to be that bridge for the Hearing, my parents would still have gotten done what they needed to get done, even if it would have been tougher and may have looked completely different.
I also know that some of our parents may play that role that they cannot do things themselves and they need us CODAs to fix it. My parents were from an older generation I saw it occasionally amongst them and their friends. Its just that when I try to see how some CODAs develop this attitude or arrive at the conclusion that they are the glue holding their parents lives together I become seriously agitated. I mean, did some of us, regardless of how intensely proud we are of our parents, how well we sign and everything else, just simply buy into the things that hearing people have said to us our whole lives? I don’t mean we actually deep down believe them, even if a good majority of it came from our extended family. I just wonder if all the years of those ridiculous comments, opinions, and observations somehow etched itself into some of us and became a part of our personalities? I just don’t understand it. 
It’s not easy to define CODAs, and it doesn’t help that it can be so difficult for us to define ourselves. I know I have that problem in a lot of areas of my life, and I want nothing more than to understand it better. Yet even with all that, I have never let myself believe that my parents would have perished or be significantly worse off without me there, and I know most of us as CODAs don’t feel that way. But it’s evident that some of us do, and when I see it, I want to put a pen through my eye or something much less gruesome and equally painful to distract me from it so I won’t say or do something stupid.
Does audism play a role in this? Could it be some type of CODA privilege that is being subconsciously enjoyed? I’m not sure of the answer myself, and would love to know everyone else's thoughts on the matter. Especially from any CODAs reading this.
One more thing. My opinion here doesn’t mean I hate CODAs who do act that way. I am disgusted with that attitude, and I may not like a fellow CODA because of it, but being CODA is belonging to something unique. I cherish that, and love every CODA brother and sister because of it. I just needed to vent, and even more so, want to have an open discussion about this so we can all understand each other better. CODA hugs and CODA love to you all!

Until next time,

R. M. 

CODA Advice?

Hello Everyone,

This post is not being done in ASL tonight. I may sign it in a video at a later date, but not now.

First things first. I am happy to be back. I meandered off of my path for a while. Call it cynicism, call it disinvestment of a sort, I'm not 100% sure myself, but I do know it was a mix of a number of things. I believe the catch-all, one word description is 'rut'. I have been in a long rut. I owe the timing of this return to two recent things. First, the website, si5s.org, is finally moving forward. Click the link to see what I mean. Second, in response to my enthusiasm about the first event, someone told me today that they miss my writing and want to read more. Do I really need further motivation? Not likely. So thanks are in order to Robert Augustus, for the drive to make si5s an integral part of Deaf culture, and to Dianne, you may only be one of a handful who regularly read these posts, but what you said earlier was taken to heart.

So this post is a response to Erik Witteborg, who suggested a 'writing prompt'. He's good like that. This one made me think, and even now I don't fully know what I'm about to say. His prompt was this - If you can go back in time to meet your 10 year old CODA self, what advice would you give? This response should just be what it is. No conscious effort to be funny or serious. Thinking back to when I was 10, my parents reluctantly had to move to a town almost a two hour drive away from home. My father had landed a new job in the "Big City" of Bangor, Maine, so they sold the house and we moved. We eventually moved into an apartment complex, but first spent 6 long and grueling months with my mother's parents. The tension in the house was never lost on me. Worse than that, the town was considerably larger, and I had no friends there. This is the me that I would advise, so here goes.

Hey kid,

It's ok. Things look like shit right now, but it's ok. The first thing I want you to know is that it's ok to not want to be your parents interpreter. They don't like putting you in that position either, even if it seems like they just expect you to do it. Nevermind their friends who always tell you that you should grow up to be an interpreter. That's crap. Do what makes you happy. Mom and Dad will always be proud of that, and that's ok.

Second, don't stress out too much about the other kids at school. You know most of them won't even try to understand what having Deaf parents is like, and you DO know they will all ask you ridiculous questions about it. You can't hide it, and you may as well be straight with them. Don't forget to show your pride in them and in yourself. You don't know it now, but later you will begin to meet so many people with parents like yours, far many more than the ones you know now. You will call yourselves CODAs. I'm pretty sure many of them are calling themselves that now. Wear it like a badge, for it is you. It's ok to show them.

Third, don't back down when something needs to be said. You're gonna be great at this anyway, but don't hold back either way. Please do your best to remember to think about all sides of the situation. Family IS wrong for how they put Dad down, but someday they'll kind of get it, and that will be because you DIDN'T back down. It's ok, no matter how angry you get. Respect will come in the end. It's still ok.

Last, stop feeling guilty. You will take advantage of situations because you haven't found yourself yet. When you do, remember that was part of the process. Know that Mom and Dad understand this and won't hold a grudge. It's what kids do. Don't let that guilt remain there, even after Dad leaves this world. You don't need to tell him you're sorry. He gets it. He's proud of you no matter what because he believes in you. It's his legacy to you and when you're a man you keep that close to your heart instead of the guilt. Honor the legacy. Teach the world who Deaf people are, through you. The best thing you can do is leave this world better than you find it, and let's be honest, we've seen more than our fair share of shit. Way more. Honor the legacy and help clean it up. Teach the world, and they will begin to clean it up, too. Make it better for future generations. Believe you will see him again, and you will. You will see how proud he really is. Trust me, it's ok. It will always be ok.

__________

Well, there it is... and it's ok.

Until next time,

R. M.

Pride - an ASL Version

Hello everyone,

This is an ASL version of the English poem "Pride" from my eBook "Shadow Boxer & Other Poems". It's a look at a real relationship between a CODA and his deceased father. Please do not look at this ASL version as poetry. It really didn't come out that way at all. It's more like the ASL/Deaf version of spoken word or prose, and quite honestly, I'm not 100% sure how to define it myself. With that said, let's just say "it is what it is". If after viewing this you would like to read the English version, please refer to the 'My eBooks' tab at the top of the page. You can find the link to the book from there, and it is a free download. I hope you enjoy the video, and forgive my near 2 month absence from this blog (assuming any of you still check in, haha).

Until next time,

R. M.

"I am CODA, and I Know" Part One

For the ASL version, click here.

Hello Everyone,

This is the first post in the “I am CODA, and I Know” series. Recently I learned that some people informed Alan Abarbanell, or, Abababa (did I sign that right), that I used his poetry work in my blog. To be honest, I love his poem. He calls it a CODA anthem, and I agree. While my work is titled “I am CODA, and I Know”, and his poem is titled “We are Coda, and We Know”, I did borrow it because it’s perfect. I just wanted to share that with you all. I didn’t mean for there to be any commotion about it. To me, it’s a sign of respect. So we (Alan and I) discussed it, and he let me know that he is ok with me using his title. I am going to go ahead with this, so Alan “Abababa” Abarbanell, thank you!

Now this blog is focused directly on Noelle’s (Campbell) blog post “War With CODAs”. I looked it over, thought at length about it, and analyzed it. So now I’m going ahead, and setting this up in point-counterpoint style. Here goes...

(Noelle) “War With CODAs” 

I am not deaf. I am not a child of deaf adults (CODA), but most of my experience with CODA’s is as a friend of a parent who is deaf. I am generalizing a lot in this article, and it might be more of a rant than actual commentary, so be warned. 

Noelle, in this article you say that you make a lot of generalizations, and well, you really do, but it’s not necessary. Your warning disclaimer is done in poor taste. When you make an announcement in public like that and then add a disclaimer to it so you can be excused is inexcusable. 

(Noelle)

From the perspective of a parent, CODAs overwhelmingly come out of childhood as teenagers who want continual sympathy from both the hearing and deaf community.

BS! I myself have never tried to get any pity from either the Deaf or Hearing communities. Now some teenage CODAs will seek that out from the Deaf and hearing, but remember, it’s because they are TEENAGERS. It doesn’t matter if they are Deaf or hearing, both look to avoid any consequences from their parents or something like that. That generally is not a CODA specific thing. 

(Noelle)

I have seen teenaged CODAs refuse to sign to their parents in public, which makes communication a pure bitch for someone who can’t turn their hearing on and off. I know how hard it is to raise a teenager, I have two that are grown and two well on the way to teenagehood, but CODA’s add the additional complication of language barriers.  

Huh? What language barriers? Are you referring to refusal to sign in public? Come on! Most teenagers regardless of being Deaf or hearing (or CODA) won’t talk to their parents when they are mad at them. That is a tendency of many teenagers. That really isn’t a “CODA” thing.

(Noelle)

Teenage CODA’s to their deaf parents, are EMO without the clothes and make up. Imagine ALL your children walking around in skinny black jeans, black dyed hair, listening to mopey music and putting safety pins in their ears, or eyebrows, etc. That is what a CODA looks like from the perspective of a deaf parent, even if they look and act completely normal to you and me - the hearing people. 

In all my experiences being around Deaf parents, none of them have ever complained that their kids were EMO. NEVER. Some of them may even dress up a bit goth in all black, but they don’t continually gripe about it. They don’t complain about it any more than hearing parents of hearing children who act EMO/goth. 

(Noelle)

As adults CODA’s can be even more annoying. They either make a complete break from Deaf Culture, or become a zealot intent that everyone be as ‘immersed’ in ASL when learning as they were. 

Statement untrue! Did some of us break from Deaf Culture? Sure. Did all of us? No way. And you say that CODAs wish to force everyone to learn ASL through immersion and constant exposure? We as a whole do not say that. I have been teaching ASL to hearing people for 9 years, and yes, I really believe that the best approach to learning ASL, for most people, is through consistent immersion in ASL. But think about that. They are in class once a week for 2 hours at a whack. There needs to be constant signing during those times because hearing people don’t necessarily have friends or partners to practice with, so they have little to no opportunity, and therefore it’s important that in class this is the focus. But at times some (my students) have needed to use voice because despite all my best efforts to explain things in ASL, some of it still goes over their heads. So I usually hold the last ten minutes or so of class as a “voice on” time to discuss what was confusing them so that they can understand what it means. It helps them moving forward to gain a better understanding and be able to improve their voice off sign. All of us just don’t think that way, some (hearing) people need it spoken, too. 

(Noelle)

When I was learning ASL, it wasn’t the CODAs (who could hear and understand me) that taught me, it was the deaf and some very tolerant hearing interpreters. The children of deaf adults often do go into interpreting, though many shun it because they were forced into the position as interpreter for their parents. I understand the later perspective as a hearing wife of a deaf husband. When we go out, I am interpreter.

You need to understand something. Many of us CODAs did feel forced to interpret for our parents, but not just for them. We had to interpret for all the hearing people out there, too. The every day constant of fielding ignorant questions from the hearing can become very frustrating after a while. And with the influence of our Deaf parents’ frustrations with hearing people upon us, wow, it is true that some of us CODAs make generalizations and complain about it. I mean, what do you expect? You’re upset with CODAs because they refused to teach you sign? You really need to think about your own ignorance and limitations in your lack of understanding CODAs and their backgrounds. Instead of making generalizations of CODAs, why not respect our differences? You don’t understand us, so just respect that and leave it be. 

(Noelle)

In my experience both in and out of the deaf community, CODAs that become interpreters are remarkably intolerant of people who are trying to learn ASL. Because they are so immersed in Deaf Culture they are automatically deferred to on all issues deaf that interpreters don’t want to address with the deaf. Here’s an example: Kieth Wann is famous in the deaf community as a Comedian. He is a CODA. Recently he engaged in a crusade to stop hearing people (mostly teenagers learning ASL on their own or at school) from posting ASL music videos. Music videos translated into ASL are ADORED by the deaf. Even the bad attempts they will tolerate as a ‘good try’ because there are so many good ones. He didn’t bother to ask his parents if they liked ASL videos - and he doesn’t respond to people who disagree with them, he just puts up a straw man argument about how he is trying to preserve the language.

That’s funny, because most of the Deaf people I know view amateur posts in ASL (Hey look! I know how to sign!) as a disappointment. Their awkward signing has many mistakes, and other hearing people tune in thinking ‘Oh cool! They’re signing! I can do that too!’, and that it’s somehow fluent sign they are seeing. Then they go ahead and copy that, making all the mistakes they just saw and didn’t realize. It’s not fluent sign. It’s spreading incorrect language to more hearing people, and that’s not right. Leaving that aside, did you approach Keith Wann yourself and ask him if he ever discussed ASL music videos with his parents? How do you know there wasn’t ever a conversation about it? Do you honestly, HONESTLY think the three of them never talked about it? Keith also said that he is trying to keep the language safe, and preserved, and he’s right in that. If amateurs keep posting these videos online, more hearing people who are thinking about learning ASL will be looking there, too, thinking these videos are (examples of) fluent sign. They’re really watching awkward signing rife with mistakes and grammatical errors, and that’s what will spread out amongst the hearing. If that happens, Deaf people will still be alright within their community, but all these hearing people will think they are doing correct ASL when it’s really not. I have a suggestion. All the amateur ASL students and beginning signers should have a disclaimer in the video’s description and title stating that “I am not a fluent ASL signer. I am a beginner.” Let us all know that. That’s fair because anything posted on the internet is ‘public’, meaning all of us should sense an inner responsibility to inform the viewers. Posting these without any disclaimer is irresponsible. So there you go.

(Noelle)

      All languages evolve - ASL faster than most because it is so young and so heavily influenced by modern culture. You have just as much luck trying to stop it from changing as you do stopping kids from using textspeak in Facebook posts. Instead of encouraging people - as they had in the past when they weren’t whiny little man-childs - they belittle their efforts to learn the language.

Again, huh? You think ASL is evolving faster than other languages? How do you know? Do you have any research proving this? That is a biased opinion, and really ignorant to make such a statement in public. And you think that all of us CODAs refuse to encourage hearing people to learn ASL and sign? You really know nothing about us. Most CODAs want hearing to learn ASL because it’s more beneficial, far more respectful to our parents, and better communication all around. Plus, we (CODAs) won’t feel so (as you put it earlier) ‘forced’ (to be interpreters).

(Noelle)

It isn’t as if ‘poor language’ use is unique to ASL. My Abuelo would get very terse with me for my poor Spanish skills, but he never made fun of my accent or my efforts when I actually used Spanish with him because he wanted me to speak to him in the language he was most comfortable with. This is the problem with CODA’s. They aren’t ‘most’ comfortable with ASL, they grew up FORCED to speak it. And I understand, almost universally, at one point or another in their young life, they resented having to use it when it made them stand out. But really, how is this different from being a Muslim who wears a hijab, or a Sikh who wears a turban? How is it different from being black in a white community or white in a black community? Everyone has their burdens, but while a black person might be able to get sympathy from one or the other race he is ‘forced’ to live in/with, he can rarely get sympathy from both cultures. That isn’t true for a CODA.

Honestly, I am ‘most’ comfortable with ASL over English because it is my first language. I didn’t feel forced to learn sign any more than any hearing child feels forced to use the language their hearing parents use. Its a pretty equal scenario. I wasn’t FORCED. You can think about it in two different ways. One being ‘forced’, and one being ‘it is what it is’. There is a big difference there. Any time I had to use sign in a situation that put all eyes on me was never an experience I hated, because in every one of those situations my parents were always proud of me. I never resented their pride in me. 

(Noelle)

I go to a deaf branch of the LDS church because it is easier for my husband to socialize with the deaf and use ASL.  I am his interpreter there, but I am also a Sunday School teacher supervising the CODA’s in Primary (ages 3-11).  When we discussed doing songs in ASL for a program so the deaf parents could understand, the interpreter brought up a concern that the CODA’s don’t like being put in a position where they HAVE TO sign.  I countered with “so what?”  The hearing kids don’t like to be put in a position where they have to sing for parents.  I made the case that the program wasn’t being put on for the kids, it was for the parents to see how much the kids had learned, and the deaf parents wouldn’t know how much they had learned if they refused to sign it.

Whoa, first off, if the interpreter that said that to you is a CODA, then fine. If that interpreter isn’t a CODA then they have no experience or background with it, making them just as clueless as you are. Are you really taking their word for it? That’s a bit messed up. It’s true that most people, regardless of being hearing, Deaf, or CODA, don’t like being ‘forced’ to do anything. It’s natural. It goes back to my previous point, so let me elaborate some more. When I was in 4th grade, my school was putting together a show for all the parents to come and see. I was to stand on stage and sign two of the songs. Whew! At that time, my family had just moved to town, so the school was only few months old to me, and I hadn’t made many friends yet, just one or two. There was a part of me that was uncomfortable having to do this and hated the idea. (That part of me) didn’t want to do it. But did I have any resentment or regret for doing it? No. I saw my parents watching me sign away on stage and I could see the pride in their faces. That was a really positive experience because it really built my character. 

(Noelle)

The interpreter wasn’t a CODA, but being a terp, she knew all the sad sob stories of CODA’s.  Every kid has a sob story.  I bet even Donald Trumps pampered princess could tell us some sob stories that would evoke the utmost sympathy from us.

Come on! These repeated generalizations are so ridiculous and unnecessary!

(Noelle)

If our goal in life is to get sympathy, no one has it down better than CODA’s.  But if the point of life is to learn, grow and move on from your experiences, then many CODA’s have some serious growing up to do.  In the end, my experiences have shown that CODA’s (even my own who act decidedly CODA when I’m not around or when they think I’m not around) are just as troublesome, beautiful, heart-wrenching and redeemable as any child.  It’s just trying to get through those struggles with them (or watching them happen to friends) that’s the hard part.

Again, I’ll go back to my previous point. I didn’t hate doing these things, and I never sought sympathy from anyone while growing up. I’m very proud to be a CODA. If there’s one thing I’ve learned form my experience growing up it was this: the thoughts and opinions of all you bigots out there don’t really matter. It’s nothing I really need to see again and again. 

You said that if the goal of life is to learn, grow and move on from our experiences, well then, that is just good advice. It really is. Perhaps you should follow it yourself. Your making these generalized comments (about CODAs) in a public forum. Think about what’s happening. You have a responsibility, too. Your statements ARE your responsibility. Do you remember a man from decades ago called Jimmy the Greek? Well, instead of me taking time to explain who he was, you can Google it yourself, then you’ll understand what I mean.

Until next time,

R. M. 

Response to "War with CODAs", at Least the Beginning, Anyway...

Having technical difficulties with video uploads. You can view the ASL version of this post at https://www.youtube.com/watch?v=sYnS1lwyzDI

Hello everyone,

Recently my attention has been on an ongoing issue. I want to respond to it, but I need to take time and think about how I should respond. A little while ago, on Facebook, someone in my circle of friends posted a link to a blog post. The woman who wrote it is hearing and is married to a deaf-blind man. The post is titled “War with CODAs”. When I saw that, I thought to myself, “War with CODAs? Who am I at war with?” 

I admit it’s true that I have an agenda because one of my goals is to help hearing people with no Deaf experience understand what Deaf people are like, how they live, and what struggles they go through. What I hope is that they will develop a measure of respect that will change their perspective, and maybe that will help reduce Audism. So maybe I do have some adversaries worthy of going to war with, but I really don’t feel that way.

“War with CODAs” was written last year. However, it’s only been recently that people have really taken notice of it. I saw many responses posted by CODAs who were irate at being insulted in this way. I don’t feel any different about it myself. I am a CODA, and I was insulted, too. I don’t want to yell at this person, and I want to be fair, so I thought about what I should do. After reading the post again I wondered if she had other posts related to Deaf and/or CODAs. So I checked through the blog and I found quite a few. I read them all. And I noticed something common popping up in every post. 

I feel like her attitude, after reading her commentary, shows that she doesn’t really understand Deaf culture. She’s really ignorant of this. Some of the other comments made me feel as though she is a deep-rooted Audist. You know, sometimes it’s not so easy to separate Audism from ignorance, but I will give it a try.

So my plan is to start at the beginning of this with the “War with CODAs” post and evaluate it. I will discuss those comments that exemplify her ignorance and Audist attitude. From there I will move on to the next post, and the next one, in chronological order, and do the same type of evaluating.  I’m going to call this series “I am CODA, and I Know”. I don’t say this to mean “Hey! Look at me, a CODA who knows everything!” My point is to use my experience growing up in two worlds, hearing and Deaf. The cultures are different, but I am involved in both of them. I am going to use this unique experience as my viewpoint, but do so in an objective manner. 

One thing I do want to say to the woman who wrote the post is this; “Just so you know, I read your blog posts, and noted how many times you said things like ‘I’m just ranting’, or ‘I’m just expressing my opinions’, or even ‘My blog only has like 40 followers, so really not very many people read this, it’s no big deal.’ That’s ok, I guess. You DO have a right to free speech, but at the same time, you DO have a responsibility. Yes, you do. When you make generalized comments that stereotype different groups of people on a blog, you’ve also made it open to the public. Imagine if you will a time long ago when there wan’t any real technology. There was no internet, but there big printing press machines. So you decide to print up an article declaring that all Deaf people act the same and insult you, and therefore should just go away, and that all CODAs are a bunch of little whiners and ‘Damn! What’s wrong with all of you?’ So then you take that printed article and bring down to town square, where you proceed to find a post (maybe a light post, perhaps, or something suitable) and tack it up by its corners. Well everyone who sees it is going to come walking by and see it. Some will be curious and read it, only to be seething with anger by the end of the article, and will end up coming to your house, knocking on your door just top say ‘Hey! What’s up!? What’s your problem?, etc etc. Now you’re going to act surprised and be angry with them? That’s straight up not fair. You know that hearing people have a saying... ‘People who live in glass houses shouldn’t throw stones’.” I think that sums it up well.

The next post will be up soon and will address “War with CODAs”. 

Until next time,

R. M.

RM Interviews Keith Wann - SuperCoda

Hello Everyone,

I want to say first that I apologize for not having a video of my interview with Keith Wann. I stated previously that all English blog posts in the future would have a corresponding ASL vlog to go with it. The interview began last year and slowly completed a few weeks ago, all via email, so unfortunately no video was taken. With that in mind, I want to say a few things about Keith before the interview. 

Early on after my first few blog posts I quickly realized that one of my goals was to give insight to hearing people about the Deaf community. As a CODA, I am very familiar with Deaf culture and my local Deaf community. I am still and always will be a part of it. One of the things I know is that most hearing people don’t get it. Please don’t take offense to that if you are one of those hearing people because it’s not your fault. You just never had any experience with it. But if you read these posts and get something meaningful from them, then I have accomplished that goal. This is where Keith Wann comes in. He is a CODA like me and very involved in his Deaf community. 

Anyone who has seen one of Keith’s performances, or watched any of the plethora of videos he has online can tell that ASL and Deaf culture are huge parts of his life. Through his work he is doing the same thing I am, and reaching a much bigger audience, I might add. He does it in his way, through humor, performing, and storytelling. I have been watching him now for several years and wondered if I could convince him to take time to let me interview him. So, I found him on Facebook and sent him a message, asking him for an interview. His exact response was this - “sure thing! I would be honored - let me know what I need to do!”

Well over the last year we have finally completed this thing. Keith is a very busy person who wears many hats, and almost all of those hats involve Keith giving his time to others. Whether through performing/touring, his ASL radio program (which I just learned is no longer airing), his work with LegalShield, or with his family, he is giving everything he has of himself to other people, and that’s an invaluable contribution to humanity. I have a very deep respect for him, especially after meeting him recently. Anyways, I’ll end my ramble here and get on with the interview. Here goes....

RM: Are both of your parents Deaf?

Keith: Yes.  My mother became deaf at the age of three - german measles and pneumonia.  My biological father is hearing, (we) never met.  The man who I call dad who raised me was born deaf.

RM: As a CODA, and knowing other CODAs, we have all had some similar experiences growing up. Could you speak of these and how they affected your childhood?

Keith: I believe having similar experiences allowed me to have more empathy as a person later in life. I could hear someone and even if I didnt have that same experience I could understand that was their world and what they experienced.  For me this came as a lesson to me at the CODA Conference Hawaii 2004 - when I was asked to get on stage and do a bit of my show.  I said sure!  and then I was asked to voice and not sign...which blew me away...I always sign my show.  Then I was told there were codas in the audience that didnt know sign language so I had to be accomodating to them.  I was floored... I thought all codas had the same experience as me, deaf and ASL.  Lesson learned. For those that did have the same experience I always feel that kindred spirit.  The stories I do in my show are not all mine - they are OUR stories.

RM: What is your funniest Deaf related experience or story growing up?


Keith: Can't really name one - made a career out of sharing millions of the childhood stories - I do remember my parents buying me a radio and telling me to listen and learn to talk - they didnt know about the dial tone and didnt teach me either, so I listened for days to a station that played country that wasnt exactly on the dial - so the static was louder then the music.  Week later (an) older coda came over, and saw the radio and gave me the "lesson".

RM: What got you into, and when did you start doing ASL storytelling/comedy?


Keith: I was just flapping my hands as an interpreter and one night after bombing the gay and lesbian comedy festival since at that time I had no background in teabagging and tossing salads I decided to try out for a local asl improv group.  From there we traveled up and down the state of california until one night we were asked to each do a 10 minute solo from our childhood - my first story was the unplugging the vacuum story and the rest is history.

RM: I think it's safe to say that Peter Cook is considered one of the best ASL storytellers today. What is it like to work with him?


Keith: I still cannot believe that Peter is my personal mentor. He is such an inspiration and support that I now try to be with others that I work with. He has set the bar for ASL performing.  To have him treat me like an equal and ask my opinion on how he should change his story is an awesome feeling. To be able to travel with him and see how he thinks, how he treats people, and to see how genuine he is about life, I am one of the luckiest people. He became a close friend, was the pastor at our wedding. His work ethics is outstanding and something all of us need to strive for!

RM: What is the one piece of work you are most proud of?


Keith: Anything that one person takes away and it changes them. I can be proud of one particular piece but it might be for another reason, a simple statement, sign, or story that another person takes and it changes them. Gary Sanderson gave me a gem early in my career and he wasnt aware of it, and I was so happy I was able to talk to him years later and thank him for it. I had someone approach me a year later after one of my shows and say "thank you for pulling my sister up on stage (a silly improv asl song I do) - I am deaf and she is hearing and after you involved her she jumped into ASL and now we have regular sister -sister conversations without mom having to interpret." I get those kind of thank yous all the time and that is what I am most proud of.

RM: Tell us what Audism is in your own words.


Keith: Seems to be if a deaf person can talk they feel they are higher in the pecking order since they are 'closer' to hearing.

RM: Describe your ASL radio show.

Keith: A way for the hearing world to hear more about our ASL world.

RM: What is your biggest fear?

Keith: That I go blind.

RM: What can we expect from Keith Wann in the future? 


Keith: More behind the scenes stuff and ASL children's book literature - my 10 years of being America's funniest ASL comedian has been a great ride and I have no problems helping the next generation of ASL performers like Wink and Austin Andrews have their 10 years...there is plenty of room for 100 more ASL coda performers - My show was never about me, but us.

RM: Is there anything that you would like to let the readers know?


Keith: I look forward to learning, growing, and sharing more with our ASL Community.

I was saddened to learn recently that the Keith and Wink ASL Radio Show is no longer happening. Its concept was great and its delivery medium was original, to say the least. Hopefully the good people of Florida got a lot out of it. Awareness of the Deaf community among hearing people is, in my opinion, the best way we can fight Audism. Power to the Deaf and ASL!

The above picture is (hopefully obvious) myself and ELF with Keith at his show in Cambridge, MA. The other performers, "Wink" Windell Smith, Jr., and Gregg Spera, both put on exceptional performances. They had us laughing all night long. I was able to make a connection with Wink, and we set aside some time before their next show in Manchester, NH (April 26) to do a video interview. That post should be coming within the next month. It could be a while. I need to go back through and translate all the signing for the hearing people who don't know ASL. Once that is more finalized I will let you all know of a date for that post, so keep checking back!

I want to personally thank Keith for the time he gave to this interview and the inspiration he has been to many of us. Don't stop performing. People need to know, and laugh about it, too! Find him at keithwann.com, and watch any of his many videos on youtube. It's great stuff!

Until next time,

R. M. 

Si5s.org and its Relation to Deaf Education

Hello everyone,

The following is a video I made several months ago. I decided to post it under the "ASL Vlogs" tab, and the following is a translation in English. 

I’m curious... has anyone in this group seen the book ASL Write? I think that’s the name... well the website is si5s.org. A Deaf man invented a writing system that matches ASL. I checked out the website, and it was pretty cool. 

I work in deaf ed, so I approached my boss and showed her the website. She looked it over and agreed that the school should order the book. I’m still waiting for it to arrive. My plan/goal is to read through all of it when it gets here. I want to know if it really matches up with ASL. 

If it does, I want to know if other Deaf people have looked it over or if any of you have. My gut feeling is that it’s truly important for deaf education to have an ASL writing system. Currently Deaf around the world have no writing system and kids don’t know of one. But if they knew, if they could learn it, then wow... ASL, signed language, that would feel more, really - no, that’s the wrong sign - LEGITIMATE. 

The proof would be right there. Just like with spoken language, English speaking and writing, Spanish speaking and writing, German speaking - and well, writing, and signing and writing... they would be equal. I feel that would be a good self-esteem booster for Deaf people. That would be one thing. The second thing would be more media access through writing. It would be possible for them. 

Let me think of other things. Well really, I know that in American deaf education, there’s a huge focus on learning to read and write English. It’s important, but English is really a second language for Deaf people and not the first one. So, I know some Deaf people who have spot on English reading and writing skills, but most that I know, whether they are children or adults, reading and writing skills in English are shaky at best. So my thought is that if Deaf people have a writing system of their own that matches ASL, well wow... they would have a fully accessible writing system. For Deaf people, there’s limited to no access to spoken language, and therefore access to its writing system is limited to none, as well. 

It makes me feel like this - how can we expect them to learn to read and write a language without full access to it? But writing in ASL would provide full access. That means that learning to write a fully accessible language first would allow skills to be transferred to the second written language, and wouldn’t that mean more successful results for the second one? 

My theory is yes, if there is a strong foundation in reading and writing ASL, then there would be an improvement in reading and writing English, too. They would both benefit. What do you guys think?

R. M. 

A Wonderful Night With Three Great Performers

Hello everyone,

It has been forever since I have posted anything on this blog. Much of what has been taking my attention away from writing is finally over, which gives me some much needed free time. So this post is me spending some of that time so I can share with you a wonderful experience that ELF and I had about two weeks ago.

Ever since I heard the term CODA, it gave me a sense of belonging to something. For the most part, that tie is to Deaf people. Deaf people who use ASL, but mostly my family, my parents’ Deaf friends, and the many Deaf friends I have made here in the Boston area. There is another tie, just as strong and as unique to my tie with Deaf people. It’s the tie to other CODAs, and it’s uniqueness comes from our common shared experiences. 

It’s because of these ties that I have become increasingly interested in ASL performances. Most everything I have seen has been via the internet, watching ASL poems, storytelling, and comedy routines. One of my favorite performers has been Keith Wann. Any CODA reading this likely knows exactly who I am talking about. He may be one of the funniest performers I have ever seen. It’s been a dream to see him perform live, and two weeks ago I finally got to when he came to perform at Harvard University. 

The first surprise came after ELF and I parked the car in a local garage and began walking towards Sever Hall where the show would be. On our way down Quincy Street I had noticed and pointed out to ELF two Deaf women just ahead of us on the sidewalk. We had no idea where Sever Hall was, but knew they were on their way there, so we decided to follow them. In about another 200 feet, one of them got into a car, and the other one turned around to make her way to the same vehicle. That’s when I recognized her face. As a young child, my family spent a lot of time with hers. Her father and my father were good friends all through school. 

I waved her down and introduced myself. Before I could finish spelling my last name, her face lit up in surprised recognition and she immediately began to relay it through the car windows to her friends inside. The group turned out to be her husband, who had been a more recent fishing buddy of my father’s, her mother whom I haven’t even seen since childhood, and another couple who were also good friends with my parents and hers. They had made the four hour drive from Bangor, Maine to Boston just for the show. We had a great conversation on the way to the hall and while waiting inside before the show began. 

It was great catching up with all of them, and before I knew it, one of them expressed his thoughts to me on my father, his good friend, and what it meant for him to miss him. His little speech on this caused me to choke back some nearly uncontrollable tears on the verge of crashing down in front of everyone. It was a very thoughtful gesture, and I’ll never forget his words. Loosely translated, he said that he really missed my father, would always remember his laughter, and pointed out that I must miss him dearly. That’s when the flood came for me, and as I was nodding yes he hugged me out of nowhere. I hadn’t seen this man since my father’s funeral service over five years ago, and I’m pretty sure we didn’t even hug then, but it was a very welcome thing nonetheless. I mean, where else can one find such a small community closeness? For me, there isn’t really any other place that lives up to that Deaf community standard. 

Well, anyways, after that it wasn’t long before we were allowed into the lecture hall for the show. It was a small audience, maybe about 100 people or a few more. It turned out to be a great show. I was surprised to see one Gregg Spera perform an opening act (very good one-of-a-kind performer, by the way) before another man named Wink performed. If you’re familiar with Keith’s work then you may recognize Wink as well. They have been working together for some time now on an ASL radio show in Florida. The show broadcasts over the radio for the hearies and podcasts on the internet for all the ASLers. Wink is a CODA as well, and his stand up routine had me laughing almost constantly. 

When Keith went up to perform it was no different. The man is incredibly funny, and between the two of them I identified with so many CODA experiences. Everything they said and did was funny, but to relate to it so well just made the laughter all the more special. I really felt at home, so to speak. After the show ELF and I hung around to meet them, and to our surprise we were invited to hang out with them at a local restaurant. 

This second surprise was something I couldn’t turn down, despite how late it was and the fact that ELF and I had to be up early the next morning. So we threw caution to the wind and had ourselves a good time. I do want to say that Keith seems like an incredible guy, and he was very down to earth. We just hung out and ASLed for a couple of hours, occasionally attracting the attention of hearies trying to figure out what all this hand-flying around stuff was all about. One guy literally stopped outside a window to look in on us with his mouth wide open. Well whatever, I’m used to that, I suppose. 

What turned out to be an amazing evening of surprises had just one more for us  after we parted ways. Keith and Wink returned to their hotel room, Gregg went home, and the other person who was there led us back to the path to our garage. Enter surprise number three; the garage was locked and the security doors down. No way in or out while raining in late March at twelve-frickin-thirty in the morning. So we did the only thing we could do - I called a friend out of bed to come pick us up and bring us home. Thankfully he answered the call. It even turned to snow for a short time before he finally made it there to pick us up. 

It didn’t damper the experience at all, however. It was quite a stamp to put on at the end of the day, but we had a great time. The only thing that made it better that it already had been was the fact that not at any single moment did ELF need anything interpreted. She has come such a long way, and I am so proud of her.

There is one other piece of news that I wish to share with you all. About one year ago, I contacted Keith Wann in the meager hopes that he would agree to do a blog interview. Well, he agreed to it on the spot, and that was a wonderful surprise. I mean, the CODA Brothers didn’t respond at all, and here was this guy ready to go. So I sent him some questions via email, and over the course of the past year, we finally found time to complete the thing. I will be posting this interview 28 days from now, on May 5th. Not sure by what time, but look for future posts either here or on facebook. If I decide on something, it will be mentioned either here or there. 

Until next time,

R. M.

Come on App Store, really?

Hello to everyone,

Long time, no time. My apologies. There will be some more book reviews coming, but not until sometime in November.

I am posting this via my mobile app. Not sure how to entirely use this, but as long as text will post, the blog will happen. I was looking at certain mobile apps that teach people American Sign Language. There were some made by people I recognize from DVD programe, etc. Others just looked flat-out awful. For the most part, I have to say I'm disappointed with what's out there.

One app description actually claimed that American Sign Language is a language for people who cannot speak or hear. My first thought was "Really? Only for those who can't speak or hear?" So, from one perspective it came off as this is something for those who are disabled. I don't know, it must just be the CODA in me, but that's a ridicuklous statement. If that's their approach and understanding to Deaf people and ASL I am scared to see what's inside.

This did get me thinking about other things, though. First, I need to do something to put something correct about ASL and Deaf awareness in the app pool. I'm thinking its about time I learn to develop my own apps and get them out there. This needs to happen. The current available apps for the most part, are giving Deaf culture and ASL a bad reputation. So I'm going to try and bend the curve the other way. Besides, the next best thing to a Deaf person making a good quality ASL app is to have a native ASL signing CODA do it. Perhaps there can be an app for other things, too. Time to brainstorm!

Until next time,

R. M.