Showing posts with label Audism Fighting Federation. Show all posts
Showing posts with label Audism Fighting Federation. Show all posts

Wednesday, September 11, 2013

Thank You Keith and Wink, New AFF Member


Hello Everyone and welcome,

Today I want to announce something. You know my roster? Really there’s only one name on the AFF roster. Today I get to announce there’s a new name to add to it. Her name is Norma Boots. She provided the subject for my previous post. She had been reading a book when she came upon a comment the author wrote that was negative toward deafness. She looked up the author’s contact information and sent her a direct email. The author responded, becoming a discussion. Norma stayed strong and positive and did a lot to help the author understand Deaf culture. That’s the point of the AFF - to help eradicate Audism - that.
So the two of then discussed what name she wanted. My name is the CODA Kidd, with 2 d’s, because it looks more like a wrestler’s name. So we both thought on it and came up with ideas, but when we shared them we didn’t like them. So we did it again and man, what a waste. Finally, she had come up with one. She is the “Paladin of Justice”, but I prefer to sign “Justice” like this (the sign for equality as opposed to the one that relates to “court”). That’s cool! Her name is The Paladin of Justice! Yeah! So now it can be added to the roster, meaning there are now two people. I’m waiting for more, so who’s out there? Come on, I’m ready!

Recently my wife and I went to Brewer, Maine, for the Keith Wann and Wink show. I bought tickets for myself, my wife, niece, sister, (my mother), and my aunt. She is very special to me. Both of my parents are Deaf. No one on my mother’s side of the family ever really signed, and it was the same for my father’s side of the family, with one exception - his sister (my aunt). My father was the oldest of his siblings while my aunt was the youngest. There’s about 15 years separating them. So when she was a kid, somewhere between 4 and 6 years old, my father taught her ASL. He would show her the alphabet and some signs. She started to pick it up, and then just took off with it. That’s what makes her unique in their family - she is the only one who signed. Very nice. So we brought everyone to the show.
The first performance was the comedy show, which was Wink followed by Keith. It’s such a good experience, but I had seen the same show twice before in Boston and New Hampshire. Despite that, the show was still awesome. Anyways, during the break we looked around at the school the show was held in. It’s an elementary/middle school. The same aunt I just mentioned works there, and has her classroom upstairs on the second floor. She’s the special ed teacher, so it was cool to have her show us her room and the upstairs. 
When we came back down, I noticed my mother hanging around and chatting with the other Deaf people there. It was a very good time. It was so nice to see everybody, so many old faces I remember, but I couldn’t recall most of their names. It’s the CODA curse, maybe (what do you think?) because when you’re a little kid at the Deaf Club meetings with your family and you see all of the adults, and play with all the other CODA children, you get to know their faces, all of them - strong remember. But names? My god, I was just a little kid. I didn’t remember any names because no one ever spoke them. You can’t pick it up if it’s not mentioned - but their faces? Oh yes they’re etched in my brain. It was really nice to see so many people. 
Keith’s comedy performance was the same routine until the very end, where he added a sort of “thank you” to everyone who came. He wanted to show everyone, it’s hard to explain, really. It was beautiful of course, and it bent my heart. To be honest, it did draw a tear from my eye, but it’s ok, I am still a man here, alright? He performed a song and I don’t know its name, but it sounded a lot like country. The words on their own were very powerful, about each person having a candle representing their spirit, and how we should be responsible for finding those whose candles are out, go to them and help them by showing our own light, in hopes theirs will ignite. It was really how he signed it and told the story, though. It was so powerful to see this on stage and realize it was just like watching a music video, like the ones you see on MTV or other stations. When you watch a video, it has its story in English words, but the video itself tells a story, too, just like a movie does. Keith’s performance was just like that - a music video.
I just sat there, jaw on the floor in awe of what I was seeing. So Keith, I just want to say “thank you”. That performance really touched my heart, and that was a wonderful experience, so thank you.
Afterwards was the second performance by Wink, entitled “My Father’s Gift”. It wasn’t really a comedy, but a more serious look at his parents, who are Deaf. It was really interesting to see at the beginning of his performance how he explained his parents’ backgrounds growing up (the family dynamic, what kinds of schools they went to, etc). I noticed it was very similar to my family. His father and mine both went to schools for the Deaf when they were 5 years old, so they got to be around other deaf children the entire time, signed, and interacted. The contrast was interesting to see that his mother and my own, when they were of age for school, were both sent to public schools by their own parents, with nothing more than some hearing aids and a push out the door with the hopes they would learn to speak. I’m pretty sure Wink’s mom was in the public school system through graduation. My mother was in public school until about 12 or 13 years old. Her parents noted that her improvement was insignificant, so they felt it was perhaps best to send her to a school or the deaf, and she finally got to go. To see how their stories were similar was really cool, and helped me to relate even more. 
He told the story of how his parents had met, how his father had fallen in love with her, and that was a beautiful story. Later on they had a baby girl (Wink’s older sister). Wink was the second child. In his performance he became both of his parents. The story truly broke my heart, but knowing how he survived, well, I have to say that his story, compared to Keith’s ASL song, it’s like this. Keith’s brought a tear to my eye. However, Wink’s story had me removing my glasses to wipe the many tears from my face and looking around to make sure no one saw me. That. 
The story was so powerful, seeing those Deaf have so much inner strength, love and everything else you could mention. It was during that time (part of the story) that his father’s strength was the solitary reason for Wink being born. Now as an adult this is how Wink thanks him. It really is his father’s gift.
I want to sum up here. Keith’s performance really touched my heart. Wink’s was so powerful, not only did it touch my heart, but at the same time, it ripped it open, and then healed it to be even stronger because of what happened in that story. His father’s strength, the love for his family, for his wife, that whole thing - wow - that - really made me feel inspired. It’s really a wonderful story about “Deaf Can”, “Deaf Strong”, and “Do Deaf Need Hearing People? No!” That was impressive. We CODAs carry around a “Deaf heart” inside of us, and that story touched mine, making such an impact that it will be in my mind and heart forever. That’s what I want to say, to Wink, “Thank you. I want to let you know that seeing your performance, your comedy show, and other experiences I’ve had with you whether it was the interview or just hanging out, you’ve left a mark on my life, and that’s a true inspiration for me. Thank you. To Keith, thank you as well. Both of you guys are awesome!
So all this rambling about the show and how it affected me by breaking my heart, mending it, yada yada, does have a purpose. I want all of you - those of you who haven’t yet seen Wink and Keith perform - to go online, right now. Well that’s just dumb of me, you guys are already watching this vlog (or reading this blog). So let’s do this. When this video (or blog) is finished, I want you to go to keithwann.com or winkasl.com. It doesn’t matter which one you go to, just search their page for a tour schedule. If you find that they are coming to your area, by all means, please, don’t be patient, and certainly don’t wait. Grab those tickets. Bring your friends and your family, everybody. Bring them all and watch the show. I know your hearts will be impacted the same way mine has been. 
Until next time,

R. M. 

Saturday, July 20, 2013

From Ignorance to Audism -- and a New AFF Member!



Hello everyone,

Today’s post started with a Facebook message from a fellow CODA by the name of Norma, who has agreed to let me share this experience with you. Here is her initial message:

Hi Fraser!!! How are you??? Sorry to bother you, I know you’re a busy guy, but I think I need your input on something. I was reading a book and twice the term “deaf and dumb” was used. Not as a reference to a Deaf person, but referring to an emotional state (rendered deaf and dumb). Even though I knew what the author meant, it still bothered me. (The book was published last year, and the setting is modern day-cell phones, tablet computers, etc). Then I find out the author has a child that wears hearing aids, so now I’m even more stunned she would use that term---even in an emotional context…Am I over reacting???

My response was a follows: 

nope, not at all. I'm offended by that. Its likely that the author meant it in the same vein as someone using the word "retarded" to describe an idiot. However, the fact this author has a hard of hearing child may suggest they are straight up oralist. Its a likely dynamic with a HoH child, even more so than with a deaf child. I think it stuns most of us who have a clue about Deaf, because we have a clue about Deaf. I think our problem is that sometimes we don't remember that most people out there don't have any experience with Deaf, and when we see that they might have had some and still say things like that, it seems to us to be unfathomable. Either way, it's Audism, and how offended you are should be influenced by whether it was inherently hateful or just said out of a lack of awareness and sensitivity. Do you mind if I use this in a blog post?

Norma later filled me in a bit more about the details of this incident that I would like to share with you, so here you go:

Here’s part of the sentence I read in the book   “…was on the verge of being rendered deaf and dumb by the paralyzing…”  It definitely triggered something in me, even in that context. I contacted the author thru her website. I wanted to take the opportunity to share Deaf awareness and educate her on audism. We exchanged several emails (that’s how I found out about one of her kids has 30% hearing, and I too picked up on the vibe that she’s probably raising the child orally). She was extremely sweet and kind, she apologized profusely from the bottom of her heart, she agreed with all of my viewpoints, she does NOT believe deaf=dumb.... she talks about being in the head of this particular character.  In one of her emails she said “I agree, I think there are certain words or sayings that trigger certain responses in everyone. And you are right, the term “deaf and dumb” does not bother me – in the context in which I meant it. I can absolutely see it coming across as something else, which I promise you, I didn’t mean. Yes, I would completely take offense if the words were used together to describe a deaf person as being dumb. I took a step back when you emailed and completely understood how that would sound if you weren’t right there in my head witnessing how I felt Tag was feeling. He was completely overwhelmed which affected his cognitive abilities because of his reaction. Like I said, I completely understand…

smh, WHAT!!!! I was blown away by this, but at the same time this was the email from her that finally put the puzzle pieces together for me. You said “Its likely that the author meant it in the same vein as someone using the word "retarded" to describe an idiot”  …that makes sense to me. The conclusion I came up with was she’s comparing the traits of an overwhelmed hearing person to the traits of a deaf and dumb person. In my last email to her I stated this to her and attached the following two pics…she has not replied back to me. HA!! If you are ok with this and think it’s appropriate, I would love to send her your blog when you finish it. I told her (twice), that I was anxious to discuss this topic with other Codas.
Looking foward to your thoughts on this!!!  YOU ARE AWESOME!!!

Again, my response:

oh wow, it's mainly out of ignorance, but also carries little regard to how offensive it can truly be. It's a typical reaction to first finding out you offended someone, or a group of people, I think.... Thank you for this Norma, this is awesome stuff, and kudos to you on confronting her in a non offensive way. That takes a lot of guts, and it hopefully plants a seed in her mind the next time she intends to use that phrase...

Norma’s next email to me was this: 

“kudos to you on confronting her in a non offensive way. That takes a lot of guts”…hahaha, actually it’s the exact opposite for me, I fear confrontations!!! and I was totally shocked when she replied to me, I honestly thought my email would just sit somewhere or get deleted. My goal was to try to get her in a calm and respectful discussion and fortunately she responded the same way. She has absolutely no control over how I react to words in her book, that’s on me. Does that make sense???? I was trying to figure out why this was a trigger for me, and she helped me figure it out, even though I don’t think she liked my results. *smile*  I want to share some more of her words with you.

“… I want to clarify something. These words in my term do not go together as in deaf = dumb, but rather their senses were completely overwhelmed…I completely understand your response to the terminology and I want to apologize if in any way it was expressed that the two words related to one another. I definitely agree with your entire email and I apologize from the bottom of my heart if you believe I was referring to the hearing impaired in a negative way. I assure you that I was not. Thank you so much for taking the time to send me the email…

Thank you Fraser for validating my feelings. It makes me feel better. Not sure if offended is the right word for me personally, but I’m sad that she doesn’t “get it”, or maybe she does now, and that’s why she hasn’t replied back to me. I hope the pics I sent her didn’t offend her; I chose them very carefully for a reason. I wanted to show her the Deaf part in me. The word “peace” for her- regardless of our difference of opinion, and the robot for her child. Surely, even oralists can’t be offended by the ILY handshape, right??!!

My response to this:

true, but she may only be an unwitting oralist (she is and she doesn't know it). Either way, it does boil the whole thing down to ignorance a lack of awareness, and thats enough for me to blog about. I put her in the category of people who would likely benefit from Deaf awareness education, and not just a hateful person who will never get it....

To sum this up, ignorance leads to not so good things. In this case, it led to Audism, and Norma spoke out against it. I am proud of her for doing so. I know many CODAs who spend their entire lives frustrated with all the hearing people that ask the same questions and make the same comments over and over about being Deaf, sign language, etc. It’s tedious for most of us, I think. I know it certainly has been for me, and  thankfully ELF tends to take up the rebuttal (if you will) when I am asked those things now. That’s her contribution to helping end Audism. It’s too frustrating for me to go that route at times, but I find it much easier to talk about in these blog posts.

I believe we all (Deaf, CODAs, Interpreters) have a responsibility to educate and spread awareness about Audism, and what it means to be Deaf. There are plenty of ways to do so that all vary in the amount of involvement. Norma, for example, chose to confront the author of the book she’d read. I write blogs. Many interpreters do answer questions from hearing people regarding Deaf culture. Many Deaf people are politically active, or perform for hearing audiences about their lives and their observances. Some of us just perform what we think is entertaining, and through that the world gets to see how normal and equal Deaf people truly are. 

My point is this -- I don’t mean that all of us as CODAs need to do these great big things in order to achieve this, but I want all of you reading this to understand that if you do feel a responsibility to do something, please find an avenue to do so which works for you, no matter how little or how great the amount of your life you give to it. It’s how we can give back to our parents, and help squash out most of the ignorance that leads to Audism.

Norma, here’s to you and your effort! Cheers!

Until next time,

R. M.

P. S., I need to add one more thing. Norma, you saw an incidence of Audism and you went right and challenged that person. Wow that was brave! You know what you did means? Yea, you’ve become an Audism fighter! So now you can join the roster. Just so you know, you can come up with your own name, you know, like a good nickname, kind of like a wrestling name. You think about it and let me know, and I’ll add it to the blog roster. Congratulations, and thank you!

Wednesday, August 22, 2012

100 Followers!!! Call to Fight Audism from the AFF!

Hello to everyone,

This is just an in-between reviews post. Today marks a milestone for me, as The Fraser File now has 100 followers! I'd say that's pretty good in less than a year's time. I want to thanks every one of you who have decided to follow the blog. Not sure how many continually read it, but that's ok. I'm getting enough comments from time to time to make this a worthwhile venture.

I guess the next question is, how do I celebrate this? Well, back when I reached either 20 or 25 followers, I held a giveaway of my ebook, Allesandra's Bequest, to five people. The only thing I have done this far is send messages to vintage books and KindleMom, who are my 99th and 100th followers. I have no way of knowing who was number 100, but as a thank you to them I have offered free copies of the same book.

So for the rest of you, I want to do something a little more interactive. You see the AFF logo on the right hand side of the blog? Previously I had stated that if anyone finds an Audism related ad on my page and reports it to me, I would make them the latest Superstar on the AFF roster, proving your worth as an Audism Fighter. It's a take-off of my a guilty pleasure of mine - professional wrestling. Also, check out The Frog's (his album cover at the bottom of the page is a link) album, T3RD, and hear his song "Professional Wrestling".

Ok, got off track there for a second. What I have noticed is that I have yet to see an Audism related ad since I started blocking them. I assume that so far, no one else has seen one. I could be wrong, but I go with what I have in front of me.

So here's the deal. If you find an act of Audism anywhere on the internet (should't be difficult if you are actively looking for it), leave a comment with a link to the website. I will break down all the horrible Audist aspects within it, and place you on the AFF roster, complete with cool wrestling nickname! This is also in addition to finding an Audism related ad on this site. As an additional thank you and in celebration of reaching 100 followers, the first 5 Superstars added to the AFF roster will also receive a copy of Allesandra's Bequest for free!

Again, thanks for following the blog everyone! I want to make one last comment about the petition from change.org that you can see on the right hand side of this page. The petition is intended to help stop St. Martin's Press from publishing Kristin Henson's Super Smutty Sign Language book. I have posted on this before, and it's Audist for sure! The petition needs 10,000 signatures to go forward. Initially this petition got a lot of signatures, but has slowed down immensely over the last few weeks. If you haven't done so, please sign it. If you have any friends that would like to help the cause, get them to sign it to. Clicking the ad on this page will link you to where you can sign the petition for yourself. The more signatures means the louder the voice will be telling St. Martin's Press and Kristin Henson herself that this book is offensive to culturally Deaf people everywhere. As CEO of the AFF, I urge you to sign the petition! Hahaha!

Until next time,

R. M.

Saturday, August 11, 2012

Audism Experiment and Book Review Update: Red Leaves and the Living Token by Benjamin David Burrell

Hello everyone,

I wanted to update all of you in regards to the Audism Experiment posts, which were done to show how Audism is such a deep seeded part of every day life by seeing what happened with content related ads presented by Google AdSense. I have looked into options for blocking those sites that promote Audism and/or that are Audist in nature (my apologies if Audi car ads still show up). What I found is that I can block whole categories of ads.

So what I decided upon for now was to block everything health-related. The medical profession is one of the worst Audism offenders out there, and it seemed that most, if not all, of my Audism related ads were from that group type.

I understand that this will likely be far from a fool-proof plan, and that more Audist ads will leak their way onto the page. I will be regularly checking the site myself for these ads, but more sets of eyes are better than just mine, so I need the help of all of you readers. Anyone who informs me of an Audist ad on my page will be forever memorialized on this blog for all readers to see as an "Audism Fighter". Just imagine, you could kind of be a superhero, with unheard of fame (seriously, there's only 96 followers right now)! Still cool in a nerdy sort of way if you ask me, though, and I'd be proud to put your name up. I should make an Audism Fighter logo to go with it. It could be something like a badge for everyone who makes the page! Cue symmetrical H-As repeating away from my maniacal laughing Joker face! It can be combined with my favorite guilty pleasure, professional wrestling! Instead of TNA or the old WWF, it can be called the AFF - the Audism Fighting Federation! We can all be superstars with great nicknames! Mine can be "R, The Mallet, Fraser", otherwise known as "The Audism Smasher" (kind of like what Gallagher did in his stand up routine). Or how about "The CODA Kidd"? That would be so cool! My finishing move could be boxing someone's ears to make them go Deaf! BWAHAHAHAHA!

I do have one other update. This in regards to Benjamin David Burrell's novel, Red Leaves and the Living Token. After posting my recent review, he contacted me and gave me some new excerpts that is currently being added into the book as a revised newer addition. I had an opportunity to read through them, and they helped to round out the story in certain small areas of the book. I wouldn't consider it enough to change my review of the book, but I am very excited to read book 2 of the series now. previously I had been trying to weigh the book as it was with what I hoped would be a better writing effort shown in the sequel. The fact that Burrell went out of his way to show me these excerpts tells me that he is very serious about his writing, which is all the proof I need to know that he has a good upside in his future writing career. At some point I will be purchasing book 2 of this story, and I have a gut feeling I won't be disappointed.

Please remember to report any Audism related ads that you might come across on my page. The AFF will soon be on the map!

Until next time,

R. M.