[nabs-l] Blindness is scary-how to teach otherwise while stillbeing compassionate
justin williams
justin.williams2 at gmail.com
Fri Oct 18 13:00:08 UTC 2013
Use positive affirmations. Try to find things that Dr. Jernagon or Dr.
Mauer said. Try to find out what she thinks is so terrible, then show her
how you or someone else surmounted the obstacle. Try to keep the negative
phrasing out. The more negative she is, the more likely she will be to lose
her sight, but don't tell her that. The more positive she is, the less
likely she is to lose her sight. Napoleon hill does a great job of
explaining this concept in his books. The more positive she is, the easier
it is to adjust. Keep in mind, at times, you just have to let someone go
through their stages of loss, and you can't stop them from doing serious
damage. Some of it is understandable, but she has not lost her sight yet,
so do your best to keep her positive. Remember, don't do yourself any hamr;
if it gets out of hand, then back off and take care of you.
-----Original Message-----
From: nabs-l [mailto:nabs-l-bounces at nfbnet.org] On Behalf Of Kaiti Shelton
Sent: Thursday, October 17, 2013 9:39 AM
To: National Association of Blind Students mailing list
Subject: Re: [nabs-l] Blindness is scary-how to teach otherwise while
stillbeing compassionate
Justin,
Your suggestion sounds interesting, but could you elaborate?
So far I'm reading it as try to get her to realize she still has vision
(correct me if I'm not understanding propperly). I think this could
potentially be good, but also could have negative effects. I don't want to
make her think I'm belittling her diagnosis by stressing that she hasn't
lost much. (she's lost some peripheral vision, but not enough to even keep
her from driving). But, she sees this as a major issue at least right now,
so I'm worried that if I put emphasis on the fact that she still has the
majority of her vision that she'll 1, lash out and take me as not being
supportive, and 2, really get confused on how to feel about things, more
than she already seems to be. She's not very open to talking about how she
feels about it now, other than saying it sucks. Emphasis is still being
placed on the vision issue rather than the other neurological symptoms.
But, I think after the initial shock and/or self-pitty has worn off, this
could be something that really works along witth showing her that blindness
isn't really crippling or something to be pittied. We'll have to see what
happens.
Thanks for your suggestion, and if you could clarify, if I'm reading it
wrong, I would appreciate it.
On 10/16/13, justin williams <justin.williams2 at gmail.com> wrote:
> See if you can get her to write positive affirmations which will
> affirm her in having sight. Try to get her to focus on those and read
> them everyday.
>
> -----Original Message-----
> From: nabs-l [mailto:nabs-l-bounces at nfbnet.org] On Behalf Of Kaiti
> Shelton
> Sent: Wednesday, October 16, 2013 9:23 AM
> To: National Association of Blind Students mailing list
> Subject: Re: [nabs-l] Blindness is scary-how to teach otherwise while
> stillbeing compassionate
>
> Hi all,
>
> The religious differences may be playing a role in my feelings of
> awkwardness too. Like her family members, my friend said in a sense
> that her vision was being attacked by the devel. I found this to be
> really interesting because it demonstrated a couple of things;
> although she knows this is all a brain issue rather than an eye issue,
> and she has other neurological symptoms including really bad
> headaches, she is focusing on the vision thing rather than the brain,
> which is actually the part of her body receiving the treatment. It
> also showed me how different religions impact perceptions of
> disabilities. I am Christian as well, but I do not think disabilities
> are influenced by religious things like that. Perhaps I am a little
> more scientific, but I see them as being genetic, accidental, or
> medically acquired such as through a virus or infection. She's deeply
> rooted in her faith though, and the belief that all good events are
> blessings and all bad ones are attacks is a part of that sect of
> Christianity. So, religion is playing a pretty big role too, and I
> failed to recognize that until yesterday. I'm learning that this is
> far more complicated for her than I even imagined, which really
> substantiates what Arielle said about it being very different from the
> experience of someone who has always had limitted vision in some
> capacity or another, and knows that they are either blind or will probably
be blind in the future.
>
> I'm just trying to wrap my head around all of this, because if I
> failed to consider the importance of religion in this I'm wondering
> what else I may be missing. Any thoughts on that? I want to be a
> little more aware of this issue not just for my friend, but also for
> other people should I come across this situation in the future.
>
> On 10/15/13, Elizabeth Mohnke <lizmohnke at hotmail.com> wrote:
>> Hello Kaiti,
>>
>> It sounds to me like your friend is working her way through the
>> normal grieving process that would occur for any type of loss in
>> life. For those who are not born blind, losing one's eyesight is
>> definitely a loss that needs to be grieved during the process of
>> coming to terms with blindness. I
>>
>> see this as no different as coming to terms with any other medical
>> condition
>>
>> that would significantly alter someone's life.
>>
>> I think you are being a good friend by simply trying to be there for her.
>> Although, you may want to try to talk about her feelings regarding
>> this situation if she is willing to discuss them with you. Perhaps
>> you could reassure her that having these feelings are normal for what
>> she is going through in her life right now. This suggestion comes
>> from what I wish other
>>
>> people could have given to me when I was first told that I had an eye
>> condition that would most likely cause me to become blind someday in
>> the distant future.
>>
>> Elizabeth
>>
>>
>> --------------------------------------------------
>> From: "Kaiti Shelton" <crazy4clarinet104 at gmail.com>
>> Sent: Monday, October 14, 2013 12:33 AM
>> To: <nabs-l at nfbnet.org>
>> Subject: [nabs-l] Blindness is scary-how to teach otherwise while
>> stillbeing
>>
>> compassionate
>>
>>> Hi all,
>>>
>>> I am confronted with an interesting situation. A very close friend
>>> of mine may/may not have a neurological proglem which, if left
>>> untreated, could cause damage to the optic nerve and therefore
>>> blindness. I'm trying to be a good friend and be supportive,
>>> because what she's going through is definitely not comfortable or
>>> easy by any means, but she doesn't even have the test results or
>>> know of a treatment plan and she's already thinking about the what
>>> ifs associated
> with going blind.
>>>
>>> It's really difficult, because I realize that it is scary to think
>>> about; I probably would not be a happy camper if my vision
>>> drastically changed, and that's even with the knowledge that it
>>> could do so in a way that would further limit the sight I have/make
>>> me totally blind at any time if the right thing were to go wrong
>>> having been drilled into me since childhood. I would imagine that
>>> discomfort/annoyance would be at least ten-fold for a person who has
>>> spent nearly two decades as a sighted person, with little to no
>>> contact with a blind person until they met me in college. Yet, I
>>> feel somewhat awkward because I know that blindness is not the worst
>>> thing that could happen to a person by far, and that I've shown her
>>> by example that one does not need sight to do well in school, to
>>> cook and clean around an apartment, to have a job, or to be
>>> successful in general. I realize that seeing someone else do things
>>> differently and imagining yourself have to do them a different way
>>> is terrifying too, if I had to suddenly switch to using a foreign
>>> language or sign language to speak I'd definitely be freaking about
>>> the ramifications of being out of the loop, and perhaps that is what
this is like a bit.
>>>
>>> I'm just trying to think of ways that I can be supportive while
>>> still showing her that even if the worst does happen, things can be
>>> done---just differently. I feel like that is one of the best ways I
>>> can be supportive, because I have the knowledge about the subject
>>> that others around her do not, and since blindness has such a bad
>>> connotation, it is possible that those who don't know much about it
>>> are not helping the situation by panicking themselves. I'm trying
>>> to be empathetic as well, because although I have lost vision in
>>> chunks, I am probably the only person she knows who has experienced
>>> any form of vision loss, and there was a time in my younger teen
>>> years when I was terrified of losing all of my vision in which I had
>>> to put blindness into perspective and realize that much worse could
>>> happen to a person, too.
>>>
>>> So far I've been telling her to not freak about it is she doesn't
>>> even have test results yet, which I realize is much easier said than
>>> done but I thought it was the best I could do. I've also reminded
>>> her that even if she does have this condition there are treatment
>>> plans which could prevent vision loss, so even if she were to
>>> receive the diagnosis it is not a death sentence for her sight. I
>>> do not know what else I could do at this point but remind her of
>>> those things, since the rationalization seems to help for a while
>>> once she thinks through it.
>>>
>>> I would love to hear from people who have had similar experiences
>>> and/or lost sight later in life. If you are the latter and you knew
>>> there was a possibility of blindness before it happened what
>>> specific aspects about blindness bothered you the most? What, if
>>> anything, did others do that made you feel a little better about the
situation?
>>> What do you wish others would have done to help you? What would you
>>> suggest I do to help my friend? Did contact with other blind people
>>> help you durring that time? (The thing I'm worried about is her
>>> saying, "Well you can't empathize because you don't know what it's
>>> like," because in terms of having the sudden shock I do not, but
>>> everything else I do). Any thoughts?
>>> --
>>> Kaiti
>>>
>>> _______________________________________________
>>> nabs-l mailing list
>>> nabs-l at nfbnet.org
>>> http://nfbnet.org/mailman/listinfo/nabs-l_nfbnet.org
>>> To unsubscribe, change your list options or get your account info
>>> for
>>> nabs-l:
>>> http://nfbnet.org/mailman/options/nabs-l_nfbnet.org/lizmohnke%40hotm
>>> a
>>> il.com
>>>
>>
>> _______________________________________________
>> nabs-l mailing list
>> nabs-l at nfbnet.org
>> http://nfbnet.org/mailman/listinfo/nabs-l_nfbnet.org
>> To unsubscribe, change your list options or get your account info for
>> nabs-l:
>> http://nfbnet.org/mailman/options/nabs-l_nfbnet.org/crazy4clarinet104
>> %
>> 40gmail.com
>>
>
>
> --
> Kaiti
>
> _______________________________________________
> nabs-l mailing list
> nabs-l at nfbnet.org
> http://nfbnet.org/mailman/listinfo/nabs-l_nfbnet.org
> To unsubscribe, change your list options or get your account info for
> nabs-l:
> http://nfbnet.org/mailman/options/nabs-l_nfbnet.org/justin.williams2%4
> 0gmail
> .com
>
>
> _______________________________________________
> nabs-l mailing list
> nabs-l at nfbnet.org
> http://nfbnet.org/mailman/listinfo/nabs-l_nfbnet.org
> To unsubscribe, change your list options or get your account info for
> nabs-l:
> http://nfbnet.org/mailman/options/nabs-l_nfbnet.org/crazy4clarinet104%
> 40gmail.com
>
--
Kaiti
_______________________________________________
nabs-l mailing list
nabs-l at nfbnet.org
http://nfbnet.org/mailman/listinfo/nabs-l_nfbnet.org
To unsubscribe, change your list options or get your account info for
nabs-l:
http://nfbnet.org/mailman/options/nabs-l_nfbnet.org/justin.williams2%40gmail
.com
More information about the NABS-L
mailing list