i agree to all points you all mention
i my self also late blind person started enjoying blind life
only draw back i always felt is
when i was able to see much better  so many of my so called friends used to 
wait for half an hour just to mit me
when they used to get news i am coming to their area
now after total blindness
same people passed through me so silently  in order to avoid me even if they 
are in my area

----- Original Message ----- 
From: "niranjanraj urs" <[EMAIL PROTECTED]>
To: <accessindia@accessindia.org.in>
Sent: Monday, November 12, 2007 11:24 AM
Subject: Re: [AI] Reflections on Becoming Blind


The article is simply brilliant and touching. As a person sailing in
the same boat, I can really understand the meaning of every sentence.
For the sake of being honest. please let me share some of my inner
thoughts. Due to RP, when I started losing sight some 14 years ago, my
wife ,who is not highly accomplished, started reading for me. I used
to get annoyed and often abused her for the poor reading. I little
understood then about my own real position. Slowly, the thought that I
am blind has sunk into my mind. Today, it is only because of my so
called less accomplished wife that I have read volumes and volumes of
books(of course in Kannada), which I never would have read had I been
sighted. Becoming blind, today I can empathise more to sufferings than
when I was OK. Yes, every incident and happening has its own merit.
B.Niranjan Raj Urs

On 11/12/07, Subramani L <[EMAIL PROTECTED]> wrote:
> Fantastic story. After reading this, I wanted to forget about our agreed
> etiquette regarding on and off topics and wanted to express my feelings on
> this one.
>
> I think the whole thing sounds extremely honest and seem to reflect my own
> experiences of becoming blind from the same condition. When I reacted
> indifferently to my mom's suggestion that I must seriously consider gene
> therapy to restore my sight, she was shocked and couldn't understand how
> such an important thing as getting back my sight failed to evince a 
> serious
> response from me. I told her blindness has become my identity in the last 
> 15
> years and I am not all that comfortable shedding that identity. I told her
> it offered a fresh and a totally different perspective to life and so on,
> much on the same lines as Becky has described in her article, but the
> problem with the so-called able-bodied people is that they somehow fail to
> see the other side of things.
>
> Also, I don't know how many of you agree with me if I say this: when we 
> are
> blind, the world wants us to follow their weird and convoluted 
> understanding
> of morality. They, for instance, can't digest a blind person smoking. 
> Forget
> about the health implications of smoking or drinking, but most people 
> think
> it is utterly wrong as a habit for a blind person to smoke, even if he
> enjoys this activity with his sighted friends who are more than willing to
> light their cigarette for them or pour their drinks.
>
> As a smoker myself until three years ago, I used to learn from my sighted
> friends that I attracted disgusted looks from sighted strangers (who
> themselves would have gathered near that Tea shop to light a cigarette),
> whenever I smoked.
>
> As a teenager losing sight, smoking then was a way of gaining acceptance 
> in
> the mainstream world that never used to treat me on par. Only after
> realising the serious health implications as a thirty-something, did I 
> ever
> quit smoking and drinking. I am not recommending this to anyone as ways of
> gaining acceptance into the mainstream world, but am merely trying to 
> point
> out the weirdness in thinking among the able-bodied individuals in our
> society.
>
> Subramani
>
>
>
>
> -----Original Message-----
> From: [EMAIL PROTECTED]
> [mailto:[EMAIL PROTECTED] On Behalf Of LSanjay
> Sent: Saturday, November 10, 2007 12:03 PM
> To: accessindia@accessindia.org.in
> Subject: [AI] Reflections on Becoming Blind
>
>
>                         Reflections on Becoming Blind
>                              by Rebecca Atkinson
>                                 ************
>       From the Editor: On July 17, 2007, the Guardian, one of the most
> prestigious newspapers in the United Kingdom, published an essay by a 
> woman
> who is losing her sight from retinitis pigmentosa. In some ways her
> assumptions and experience of blindness depart startlingly from the
> American, or at least NFB, presumption that a trained blind person can
> travel as rapidly and cross streets as efficiently as sighted pedestrians.
> Yet by and large her experience and attitudes are healthy and articularly
> expressed. This is what she says:
>                                 ************
>       Rebecca Atkinson is going blind. An experimental therapy could offer
> her the chance to see again, but would she take it?
>                                 ************
>       Earlier this year doctors at Moorfields Eye Hospital, London, began
> the world's first gene therapy trials to treat twelve patients who have
> Leber's congenital amaurosis, a condition that causes progressive sight
> loss. Following successful animal trials (said to have restored the vision
> of blind dogs so they could navigate a maze without difficulty), it is
> hoped that the technique, which involves injecting working copies of 
> faulty
> genes directly into the retina, will prove equally effective when carried
> out on humans. The results will not be made public for a year, but, if the
> technique works, scientists hope it could eventually be used to treat a
> wide range of inherited sight disorders affecting up to 30,000 visually
> impaired people in the UK and potentially millions more worldwide.
>       The first viable treatment for blindness is twinkling on the 
> horizon,
> and, as one reader said on a national newspaper message board discussing
> the trials, "The possibility of being able to give improved sight to 
> people
> with visual impairments is a great development for the human race."
>       But what of the people we seek to repair? Those who have been born
> blind and those, like me, who are losing or have lost their vision. Is 
> this
> what we have been waiting for? Is it "a great development for the human
> race," or a step forward in the eugenic quest for an über race, free of
> imperfection and rid of the unease about disability that nestles quietly 
> in
> society's pocket?
>       For the past thirteen years I have been losing my sight, due to a
> genetic and incurable condition called retinitis pigmentosa (RP). RP 
> causes
> the photoreceptive cells on the retina to die off, causing, in my case,
> tunnel vision. I liken it to looking at the world down the middle of two
> toilet rolls. My central vision remains intact, but where once was
> peripheral vision, now float only my thoughts. In time these loo rolls 
> will
> shrink to knotholes and then pinholes and then possibly nothing.
>       In the early years after my diagnosis, blindness remained a 
> repulsive
> and terrifying concept. Every year I would visit the doctor, and he would
> say the same thing--that I must live and plan my life with the certainty
> that blindness was inevitable. And so, slowly over time, that is what I
> learned to do.
>       But now the advent of gene therapy has pushed open a chink in the
> door. Disabled people have long asked themselves the hypothetical "would
> you be cured if you could?" question. Now for the first time there is a
> chance, albeit very small, that maybe one day I might actually get my 
> sight
> back. Hurrah, you cry. I must be thrilled.
>       Actually I am a bit confused. It is easy to assume that all visually
> impaired people will be hammering down the doors should gene therapy prove
> successful. But to say this is to assume that a blind life is lesser and
> that all blind people really want to be sighted. They don't.
>       The first blind man I ever met, who also happened to be my boss at
> the time, is one of them. I recently asked him if he would have gene
> therapy if he could. No, came his reply. Because, he tells me, regaining
> sight is more than just seeing again. There are issues of identity and
> culture at stake too. "As the blind-from-birth son of blind parents, I am,
> in part of my soul, defined by my blindness," he explains. "It directly
> equates to ethnic or racial origin. If you give a black person the choice
> to be white, there may well be significant advantages in such a deal: more
> access to better jobs; freedom from the shackles of ignorant prejudice; in
> short, a step closer to equality. But I'd bet most would turn the offer
> down flat."
>       But what if, unlike my old boss, you haven't always been blind? What
> if, like me, you grew up with full vision and have seen all the cliché-
> ridden things that those born totally blind are pitied for never having
> seen--the sunset, your own reflection, the look in your lover's eyes. What
> if your soul is sighted, and then you go blind? You will cry and wonder
> why. You will hope and pray. You will wish it would all go away. But the
> longer your sight has been on the slide, the more it seeps into every 
> crack
> of your psyche until one day you are no longer the "sighted person" who
> can't see anymore. Somehow, strangely, in the dead of night your identity
> has rolled over in bed, and you wake up and get out the other side a
> "visually impaired person," and it feels like part of you.
>       It doesn't happen overnight, and perhaps it doesn't happen to all 
> who
> sail the strange seas of sight loss with me. But for me there came a point
> when impending blindness was no longer my alien, but my friend. I had had
> my time as a sighted person. I had seen the world through my eyes. Now it
> was time to touch it and smell it and hear it. When you lose your vision,
> you have to relearn the sorts of things that will allow you to survive on
> the planet, such as crossing the road without being flattened. Next you
> must tackle the real problem and learn to deal with the attitudes of 
> others
> as they morph around you. Misconceptions start to spout from even your
> oldest friends' mouths because negative attitudes about blindness permeate
> us all. You are about to cross over into the dark side and see what
> wriggles and writhes on the underbelly of society. Folk will see you as 
> the
> sufferer, the pitiful, the afflicted, the subhuman--that's you, yes, you.
> If you use a cane or a dog, people will stare as you walk down the street.
> People will assume you are more lacking in intelligence than your sighted
> counterpart. People you have never met before will ask if you want
> children, and if you do, they will ask if the kids will have the same
> condition that you have, and whether that is right or wrong. Welcome. Your
> reproductive autonomy is in the docks of the moral courts of the nation's
> minds.
>       So if this underbelly is so wretched, surely if the time comes when
> the doctors are looming forth with a needle containing the working version
> of my faulty gene and heralding the promise of a new day, one with a 
> bright
> sunset and me at the wheel of a fast car, I'll take it, right? Anything to
> escape? No.
>       Saying yes to seeing again, even for someone who wasn't born blind,
> isn't easy. The repercussions would ripple beyond my eyes into my
> friendships, my work, my relationship. Would I retain the unity I have 
> with
> my disabled brethren if I could see? Or would I have different friends, 
> the
> type who fall by the wayside now because they are not aware or empathetic,
> or are too aesthetically obsessed? Would I lose the friends with whom I
> have nothing in common but who remain in my phone book because they get 
> the
> blindness thing? And would it be right to dump them just because I can see
> and don't need their empathy anymore? If I stepped into the pool of 
> "normal
> people" again, where would my identity go? The kernel of who I am has been
> sucked into a new body; now it would have to be sucked back into the old
> one. And what of my relationship? Would we stay together, or would I run
> off to do all the things I never got to do before? There is a high rate of
> separation among couples where one person gets a guide dog for the first
> time. Why? Because suddenly they can do things on their own again. This 
> new-
> found independence shifts the balance and cracks appear. If this can 
> happen
> with a dog, think what could happen with a pair of fully working eyes and 
> a
> car.
>       Going blind isn't a smooth ride, though. It comes down and squishes
> you under an insurmountable weight of grief and disbelief. It is limiting
> and frustrating and changes the way you do many of the things you used to
> enjoy--now you must dance with the light on and drive from the back seat.
> But like the affirmation of near death, it affects more than just your
> physicality. It gives you a unique perspective. It is a grand experiment
> that most don't get to try: to observe as your brain rewires and watch as
> the human body adapts in infinite ways. When my vision began to get worse,
> I bumped into everything in my path because I was still careering down the
> pavement at the speed of someone who could see. As my mind caught up with
> my eyes, I changed the way I walked, with more caution and less speed, and
> the perpetual bumping and tripping stopped. Losing your sight is not like
> just shutting your eyes.
>       The loss is so gradual that, as one sense dies, others grow. 
> Suddenly
> you can smell the world and sense when someone is standing out of your 
> line
> of vision. Your brain grows on the inside, and things on the outside start
> to matter less. I get to live my life twice over, in two different bodies
> (the sighted one I used to have and the partially sighted one I now have),
> and with that comes the privilege of spying on the world and its
> intricacies from multiple vantage points. It's a cliché to say that
> disabled people are nicer. It is incorrect, in fact. But for me vision 
> loss
> has made me more empathetic and more openminded. I have to take so often
> that I give more freely. When you rely on friends to take you down Oxford
> Street or a stranger to get you across the road, you think more 
> consciously
> about what you give back and battle with the feeling that you need them
> more than they need you.
>       But, strangely, I am happier like this than if I had carried on down
> the middle lane to mediocre city, never having seen or felt real loss and
> known how to appreciate the good things around me. I have met people I
> would never have met had I been sighted, and we have been joined together
> by the common bond of disability (and there is no glue that sets as hard 
> as
> that squeezed from the pores of a minority). When part of your body starts
> to die, you feel what it is to be human. You wake up from the slumber of
> being just another idiot with an iPod because you are forced to work out
> the bigger questions. Or at least ask them. Why am I here? Why is this
> happening? You are alert to the immediacy and fragility of your life. You
> know that the choices of the modern age do not and can not extend into
> every realm of your life. You can't choose to see (at least not yet). This
> is it. The upshot? You live in the moment. You settle for your lot and 
> love
> it.
>       The concept of sight loss as a positive thing is an elusive one. It
> is hard to grasp when you have experienced it, and even harder to grasp
> when you haven't. It is not something I would have chosen, but it is not
> something I wish hadn't happened.
>       Would I like to stop it getting worse? Yes, because I'm only human
> and, sometimes I lie awake worrying how I'll cope when it's all gone. But
> would I like to have gene therapy and see perfectly again? Five years ago
> I'd have said yes. Now I'm not sure, because if this experiment of going
> blind has taught me anything, it is that what you lose in one place, you
> gain elsewhere, and while a blind life is different from a sighted life, 
> it
> is not lesser. And ultimately it is better than having no life at all.
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