A deaf hostage has been released six months after her husband was killed when she was seized by Somalian pirates in Kenya.
Judith Tebbutt, 56, is believed to be profoundly deaf in both ears and a hearing aid wearer. A ransom in excess of $1million was raised by family and friends and then paid to the pirates to secure her release.
This BBC news report quotes her as saying: “I’m just happy to be released and I’m looking forward to seeing my son who successfully secured my release. I don’t know how he did it, but he did, which is great.”
Speaking to ITV News upon her release, she said: “I am very relieved to have been released. Seven months is a long time and under the circumstances with my husband passing away… made it harder. There were some very hard psychological moments… but I got through it. So I’m really relieved.”
By Charlie Swinbourne, Editor
deaf news uk
Tali
March 22, 2012
Profoundly deaf? There are pictures of her talking on the phone http://www.telegraph.co.uk/news/worldnews/africaandindianocean/somalia/9159362/Judith-Tebbutt-to-fly-home-today-after-ransom-paid.html and they said she was allowed phone calls.
I highly doubt she is profoundly deaf. Probably slightly hard of hearing which is nothing really. A bit like someone who needs glasses to see properly 100%.
Editor
March 22, 2012
There’s been mixed reports, perhaps ‘partially deaf’ is a better description, that’s what the Mirror have described her as: http://www.mirror.co.uk/news/uk-news/judith-tebbutt-british-hostage-freed-767770
Either way, we’re glad this Deafie has been freed!
Tali
March 22, 2012
Hopefully it will re-ignite the debate of what and who is “deaf”! Most people in this country have some kind of defect in their eye sight and they are wearing glasses whether they are long sighted or short sighted. Are they partially blind? I myself, without my glasses, cannot see a thing literally – I have very bad eyesight. With glasses, I can see very well, almost 100%. Shall I call myself “partially blind”? Absolutely not!
Editor
March 22, 2012
I’m not sure I’m a fan of that debate.
For a start there’s a big difference between what glasses do to your eyesight and what hearing aids do to your hearing. It’s not anything near 100%, and hearing aid wearers don’t get 20/20 hearing.
For me, one of the most damaging things that partially deaf people can be told is that they (or I should say ‘we’ as I am partially deaf) don’t qualify as ‘deaf’ in some way. Of course I recognise that there are different types of deaf people and we have a lot of descriptions for that, but on another level, it’d be nice to feel like we’re all accepted along with our differences, we can all feel like we have a link, can belong to the community, and contribute together as deaf people.
Tali
March 22, 2012
I get your point entirely.
When there is national media images of Judith talking on the phone whilst being “deaf” – its just confusing really and the ramifications are that the profoundly deaf suffer for it – because everyone expects us to talk on the phone and do everything like a hearing person! Even the Government thinks we are capable on our own now and that there is no need for benefits (PiP)!
At the end of the day, there is appalling PR when it comes to defining hearing loss and deafness. What can we do about it? Anyone has any ideas?
Tracey Ball in KY
March 22, 2012
I’m in the USA, Kentucky to be exact, and I am newly deaf. I really don’t know how I am categorized in the deaf community other than “not a part”. I don’t know how it works in the UK but in the States the deaf are a very tight group. I understand this but at the same time don’t understand why all deaf people have to be “categorized”. Why can’t we all be accepted for what we are?
I was diagnosed improperly with type 2 diabetes in 2005. Long story short, I was really a type 1 however wasn’t diagnosed until 2 years later and after much illness. In January 2007 I started losing hearing and 2 sets of hearing aides later, in may of 2007, I was completely deaf. I hear nothing – it’s as though my head is plugged. I no longer hear myself inside so in the last 6 or so months have started losing speech clarity. I am just now, through Kentucky Vocational Rehabilitation, getting tutoring lessons in ASL Sign Language. Communication is very hard for me and I guess this all qualifies me as a newbie!
I have worked hard all my life, owned my own business, then suddenly my world was turned upside down. Now I stay at home almost in hiding because I can’t communicate. I am NOT ashamed of my new life. I accept my deafness and I can see first hand how miserably the deaf are treated in certain instances. I too have been treated horribly. However, deafness is a disability in a hearing world. We are not disabled the way hearing people would have us be. We just have to communicate in alternate ways-not in “hearing” ways. Hearing people are ignorant of the ways of Deaf Culture. Like any culture on earth, unless you seek understanding, you will not be informed. Having been on both sides now for 6 years and at the age of 55 I wonder why there is such a gap for this, now my, culture? I’m sure that further categorizes me for not understanding. I have read intensely about Deaf Culture and who started sign language and how it became uniform in the States.
All this said, I think it is wrong to categorize this poor woman. She has a hearing loss. Is it profound? Who cares? All I can do is feel sympathy not outrage because she isn’t deaf enough. How deaf do you have to be for acceptance? I am beyond profoundly deaf and am still not accepted so I say to myself get out your big girl panties and accept that many, many people in this world could care less about your situation. It’s true…right? You can try to change ignorance but it’s hard. I think by harping on my situation, or poor old deafies, you just further widen the communication chasm between cultures.
I would love any and all responses..
Tali
March 23, 2012
Hi Tracy,
The origins of my discussion was not really about Deaf Culture. Either your in it (sign language) or out of the deaf culture (mainstream). It is more of an discussion about the label “deaf”.
I have my concerns because now, thanks to hard of hearing people like Judith Tebbutt (which are the majority of deaf people in this country) act almost like an hearing person and whenever a person with a little bit of hearing loss is portrayed in the media talking on the phone , it makes hearing people – whether they are general public or government, think that profoundly deaf people like myself are expected to be 100% like hearing people and not entitled to any disability benefits (in the forthcoming disability benefits changes).
It gets even harder because when applying for jobs and the like people are a bit surprised at my slightly poor speech because they probably all know someone who is hard of hearing and “seems to speak quite well and talk on the phone!”
Tracy, I am sorry to hear about your story. Have you thought about Cochlear implant? To me it seems very successful when implanted on babies born deaf, or in those who recently lost their hearing.
Being born deaf myself and now almost reaching my thirties – I am not sure if a cochlear implant will benefit me.
Tracey Ball in KY
March 23, 2012
Hi Tali! Thanks so much for your response. I understand your point but I guess what I was trying to relay is that it is our disability but THIER ignorance; that is to say “people who don’t get it or understand”. Deafness has many, many levels of impairment. I am obviously the worste case because I get nothing. I never understood deafness myself until this happened to me and I had a moderately deaf grandmom, her sister was deaf, my dads sister was profoundly deaf and my dad is profoundly deaf. Who should better understand than me? But I didn’t until it hit home. I agree there needs to be more awareness but deafness is as old as time. Do you really think we can make a difference? How? What can WE do that all our ancestors have yet to accomplish? This article we are basing our conversation on is a normal reporting. It’s ignorance, “they” don’t get it. They won’t get it unless they are touched by it. Maybe the woman in question asked to be portrayed this way not understanding the impact it would have on the Deaf community. Or maybe the reporting was done by someone totally ignorant of the desired impression the deaf community wishes to have conveyed regsrding it’s culture. Who knows….
I too was completely deaf but had perfect speech. I looked for work after selling my business and was not successful. Even with good speech employers don’t want the added burden of accommodating a deaf worker. Then if you have mottled speech as you and I obviously do, it further complicates matters. Honestly I think people don’t listen hard enough and have the patience to try and understand what we say. Therefore we are brushed aside or painted with a broad stroke. We no longer exist. I would think many disabled persons in all other areas feel much as we do on some level.
My perception regarding the deaf in the States is that expecting to be supported by the government is not a good thing. This then indicates a resolve that deaf people are indeed disabled. I collect my benefits from Social Security that I paid into the system since I was 15 and started working. This is not a gift or handout though because I paid the money in. Deaf people don’t want to be seen or represented as disabled because we aren’t. We just can’t hear. I suffer the backlash of this because I feel I am disabled because of my age, 55, my health due to diabetes and the unlikelyhood that a cochlear implant would be successful on me. If I were 20 years younger I would maybe go for it but not now. So I guess in a way I have imprisoned myself.
I am learning sign but as we know that is just the very beginning in the journey we share. Sign is just scratching the surface. I sometimes use this analogy regarding people who want to learn sign and can hear: “teach me how to speak enough Chinese so I can order from the menu in a Chinese restaurant. Now I know how to speak Chinese”. People think if they know basic sign they can relate to the deaf – how absurd!
I am just seeking understanding. I do not stand in judgement of anyone for any reason. I try to educate people wherever I go as I think my story, though it maybe more common than I think, is a unique telling of the much different path we, the deaf, must take and the things that the hearing take so much for granted. Although I am struggling to do this I try. You spoke out on this site so you tried. Maybe that’s all we can do.
Tali
March 23, 2012
Hi,
Thank you so much for your fantastic comments. You are 100% correct what you said that hearing people just will never “get it”.
I have heard many deaf people do not want to claim benefits as they don’t see themselves “disabled”. I may be profoundly deaf and I definitely don’t see myself disabled, but I believe I am entitled to funding to pay for support such as interpreters. Disability benefits here is not that much about ranging from £20 to £40 a week for deaf people (depends how “lucky” you are when you get the claim assessed). So after about a month of disability, I can finally have some money to pay for an lipspeaker for ONE social event a month. (here interpreters can charge like £30 an hour!). Now that is under threat with the forthcoming disability benefits changes.
I do not sign – brought up in a hearing family etc – not really in the deaf culture etc – and its so hard to learn sign language – ive tried and failed. I don’t know why. So everything is at the mercy of my lipreading and speaking skills. I find it hilarious when people all of sudden when finding out I am deaf start signing and I have to inform them that I don’t know sign and watch their disappointed crestfallen faces!