[Diabetes-talk] Emotions

dmgina dmgina at qwest.net
Thu Nov 6 16:00:36 UTC 2008


You have come to the rite list.
Talking about your concerns helps you get into perspective what you are 
learning to do.
Hope this helps.
Dar

----- Original Message ----- 
From: "K C" <kcc86 at hotmail.com>
To: "Diabetes Talk for the Blind" <diabetes-talk at nfbnet.org>
Sent: Wednesday, November 05, 2008 8:28 PM
Subject: Re: [Diabetes-talk] Emotions


> I'm writing this strictly off the cuff, so please forgive me if I'm just 
> complaining here.
>
> This week, my first, I just don't want to stick myself.  I don't know 
> anything, beyond the huge amount of support I've gotten from this list, 
> about controlling anything.  I don't have any symptoms, nothing to base 
> being in, or out of control on.  This week, I don't want to hear how 
> because my number is a mere 135, how it isn't any big deal.  Then in the 
> next breath, how I have to learn to consciously cause myself pain, put my 
> blood into a meter, and interpret numbers I don't even understand.
>
> I was talking with a dear friend earlier this evening, and I tried to 
> explain to him that in most cases you get time to deny, cry, scream, and 
> then accept the situation if you choose to.  After all, not choosing to 
> use a Cane because you don't want to admit going blind may cause you 
> personal pain, but you're not likely to get hit by the proverbial car. 
> But in this case, someone says you have Diabetes, so you've then been hit 
> by the car, and you have to get up, and do something about it, manage your 
> injuries right now!  This week I'm mixed between wanting to learn how to 
> use the meter, start my medication, and to just cancel the order all 
> together.  This disease is an unknown quantity, and this week I want to 
> keep it that way. But I can't.
> I hope it is all right for me to vent this way.  You all can let me know 
> if it isn't..
> K
>
>
>
> ----- Original Message ----- 
> From: "Ed Bryant" <ebryant at socket.net>
> To: "Diabetes Talk for the Blind" <diabetes-talk at nfbnet.org>
> Sent: Wednesday, November 05, 2008 11:31 AM
> Subject: [Diabetes-talk] Emotions
>
>
>> Hi Kijuana,
>>    As I promised, the following is some information about emotions.  In 
>> fact, this info is part of a story called "Emotions", which appeared in 
>> Voice of the Diabetic sometime back.
>>    If you have questions, please feel free to ask.
>>
>> Regards,
>> Ed Bryant
>> Understandably, most diabetes education materials focus on the physical 
>> aspects of the disease. This is appropriate. But the common emotional 
>> ramifications of diabetes need to be taken into account. An individual's 
>> emotional state may determine whether he/she prevails, or is felled by 
>> circumstances.
>>
>>
>>
>> Anger
>>
>> "Why ME?" We don't know what causes diabetes. Although we can manipulate 
>> statistics and use them to make predictions, we can't tell why a given 
>> individual gets diabetes, or any of its ramifications. And tight control 
>> helps, but it is no panacea.
>>
>> Folks used to believe that disability was the result of defective 
>> character. If you developed a disease, you had brought it on yourself; 
>> you were a "failure." We know better, but too many of us still judge 
>> ourselves harshly, blaming ourselves for "being weak." Diabetes is not a 
>> sign of weakness.
>>
>> "What did I do to deserve this?" Nobody gets diabetes, or ramifications, 
>> because they "deserve them." We don't know why one person gets it, and 
>> another does not. We have to do the best we can. Diabetes can be nasty 
>> and unpleasant, but it is not "diabolical." It is not a punishment.
>>
>>
>>
>> Denial
>>
>> "It will never happen to ME!" Social workers and psychologists are very 
>> familiar with the problem of denial, the conviction that in spite of the 
>> facts, the rules do not apply in this particular case. The ramifications 
>> of diabetes do not manifest immediately, but the more time spent with 
>> high blood sugars, the greater the likelihood of future eye, kidney, and 
>> nervous system complications. The diabetic who seeks to prove that he or 
>> she is "exempt," and "gets away with it," short term, is only increasing 
>> the likelihood of down-the-line problems. The literature is full of 
>> stories by folks who were "non-compliant" in their youth, but saw the 
>> error of their ways about the time their vision began to fail. Denial is 
>> a common problem, and one that should be addressed right along with the 
>> need for conscientious self-management.
>>
>> "NO! I'm not BLIND!" Sight loss brings its own denial. There are people 
>> who won't use their canes, or learn Braille, or even stop driving, 
>> because they cannot admit they are going blind. Some delay learning 
>> adaptive skills with, "It's only temporary; I'm sure my sight will come 
>> back!"
>>
>>
>>
>> Fear
>>
>> "What am I going to do? I won't be able to..." While some folks deny 
>> they'll ever be affected, others swing to the opposite extreme. These 
>> diabetics pay close attention, read the reports, and work diligently, but 
>> for them, there are demons under the bed, and every bullet has their name 
>> on it. Too many folks are convinced that a diagnosis of diabetes, or the 
>> need to start injecting insulin, or blindness, or kidney failure, or any 
>> of the other possible complications, means the cessation of life as they 
>> know it.
>>
>> It doesn't. With proper adaptive equipment and training, blind diabetics, 
>> those losing vision, even those coping with multiple ramifications, such 
>> as blindness, amputation, and kidney failure, can maintain or recover 
>> independence, and remain (or become!) fully productive participants in 
>> mainstream society. Fear, or the use of fear to encourage diligent 
>> compliance, is counter-productive, as we shall see below.
>>
>>
>>
>> Burnout
>>
>> "I'm tired of it!" Diabetes self-management is a discipline, seven days a 
>> week, from now until doomsday. There are no reprieves, no opportunity to 
>> take breaks, and short of a pancreas transplant, there is yet no cure. 
>> There is only the routine, day after day after day.
>>
>> Some folks thrive. Presented with the facts, the need for multiple 
>> monitoring and insulin injections, one young man said, "Of course I will! 
>> I want to stay healthy as long as possible!" He was, and is, ready. 
>> Others find the prospects daunting.
>>
>> A lifetime of dietary restrictions, regular exercise, blood glucose 
>> testing, and multiple injections or oral medications can become wearing, 
>> especially after a number of years with the condition. Some folks get 
>> tired of it; others come to hate "doing it because they must." Still 
>> others stop believing their own welfare is "worth the fuss." This is 
>> "burnout," psychological rebellion against one's duties.
>>
>> When burnout leads to non-compliance, it is a recipe for trouble. Why do 
>> some folks "burnout" and not others?
>>
>> The answer is attitude. The folks who thrive, who make the best of a less 
>> than perfect situation, are like savvy poker players who, dealt a 
>> doubtful hand, play it for all it's worth. Often these folks outperform 
>> the ones holding the aces! It's not the cards you're dealt; it's how you 
>> play the game.
>>
>> "Positive attitude" can mean so many different things, but here it means 
>> a wholehearted belief in one's own capacities, and determination to 
>> overcome all obstacles, regardless of how long it takes. If you don't 
>> believe in yourself, even the small hills can look impassable.
>>
>>
>>
>> Loss of independence
>>
>> "How can I face my friends? How can I get anything done? I can't DO 
>> anything!" Too many folks respond to disability, or other trauma, with 
>> the "wounded animal response"-flight to solitude, to "lick one's wounds." 
>> Up to a point, this is part of the grieving process, the mourning for 
>> what must be let go. When it passes, rehabilitation can begin.
>>
>> But some folks "get stuck" there. Some independent, self-reliant people, 
>> high achievers, can be more traumatized by their own "incapacity" than by 
>> their actual physical loss. The belief: "I have lost something, and am 
>> now less than I was," discourages action. This can occur with most any 
>> incapacity, but is not uncommon in cases of sight loss.
>>
>> An adult type 1 diabetic, for example, may have been self-managing for 15 
>> years or more, before retinopathy put an end to a sight-based lifestyle. 
>> Some folks, with positive attitude, good instruction and proper adaptive 
>> equipment, make a smooth transition. Others wilt.
>>
>> It's a question of attitude again, so many times. An individual is 
>> accustomed to being in charge, to caring for self and others, and to 
>> being "a productive member of society." In his or her mind, loss of sight 
>> means the end of their capacity to continue doing so. Feeling diminished, 
>> feeling ashamed, the individual withdraws from society, and stays "out of 
>> circulation." Belief in his/her incapacity has become a self-fulfilling 
>> prophecy.
>>
>> These people are not lazy. They are not "slackers," taking a long 
>> vacation from responsibility. They are in emotional agony, grieving for 
>> losses they don't know how to replace. These people need to be shown 
>> their options. They need to hear of (or from!) others like themselves, 
>> who have looked the demon of self-doubt in the eye and moved forward 
>> anyhow. They need support groups and rehabilitation professionals who 
>> will respect their self-doubts-and then show them how to overcome them. 
>> Some might declare, "You can't teach attitude!" but what you can do is 
>> show such a person their options, show them others who have "done it 
>> themselves," and then get out of the way.
>>
>>
>>
>> The Cure
>>
>> Nothing about diabetes, or blindness, or any other disability, diminishes 
>> a person's human-ness. Loss of sight, or of a limb, or of mobility and 
>> independence, does not make one "incomplete." There are no "part-people" 
>> out there-we're ALL fully complete, real people.
>>
>> But it hurts to have to give something up. We are not oxen, facing our 
>> traumas with placid equanimity. Fear and pain are perfectly logical 
>> responses. Some folks will pass smoothly through the stages of grief, and 
>> be ready to learn the necessary adaptive skills. Most will need the 
>> support of their fellows and the positive examples of their predecessors, 
>> and will need to have their feelings validated. Passing this hurdle, they 
>> are ready for, and fully capable of, independent self-management and full 
>> participation in the mainstream.
>>
>> The presence of emotional issues is not a sign of weakness, but of 
>> humanity. Any holistic approach to health takes a person's 
>> mental/emotional state into account, right along with their specific 
>> physical ramifications. We are individuals, and we heal in our own way.
>>
>>
>> ----- Original Message ----- 
>> From: "K C" <kcc86 at hotmail.com>
>> To: "Diabetes Talk for the Blind" <diabetes-talk at nfbnet.org>
>> Sent: Tuesday, November 04, 2008 4:23 AM
>> Subject: Re: [Diabetes-talk] I'm a silent Diabetic
>>
>>
>>> Thank you for the welcome.  Actually I have only just gotten information 
>>> about even ordering a meter yesterday.  My state rehab is recommending 
>>> the Prodigy auto code meter?  What is the difference between that one, 
>>> and the voice?  I receive Medicate, and Medicare, all parts.  In 
>>> general, can you get new testing strips for these special meters at your 
>>> local pharmacy, or do you have to order them always from Prodigy.  And 
>>> lastly does your list offer emotional support?  I'm still in shock, and 
>>> am scared to death... Before last Thursday I didn't even know I had 
>>> this. Thank you all.
>>> Kijuana
>>>
>>>
>>> ----- Original Message ----- 
>>> From: "Ed Bryant" <ebryant at socket.net>
>>> To: "Diabetes Talk for the Blind" <diabetes-talk at nfbnet.org>
>>> Sent: Monday, November 03, 2008 3:42 PM
>>> Subject: Re: [Diabetes-talk] I'm a silent Diabetic
>>>
>>>
>>>> Hi Kijuana,
>>>>    I am glad you have joined our Diabetes talk list.  There are 
>>>> probably several ways we can assist you, but first it sounds like your 
>>>> blood sugars are too high, so that should be an immediate goal to get 
>>>> the sugars down.
>>>>    Your doctor may  have already had you do a lab called hemoglobin 
>>>> A1C, which gives you your average blood sugar for a two or three month 
>>>> period.
>>>>    It sounds like you are testing your blood glucose levels, but there 
>>>> is a fairly new blood glucose monitor out, which is pretty easy to use 
>>>> for someone who is blind or has low vision.  It is called the Prodigy 
>>>> Voice and can be ordered from:
>>>> Homecare Supply of America
>>>>
>>>> Big Sandy, TX
>>>>
>>>> 800-333-1412
>>>>
>>>> Meter: $89.95
>>>>
>>>> Container of 50 strips: $21.95
>>>>
>>>>    If you have Medicare they will pay for the meter and a few strips, 
>>>> but they will only purchase you a new meter, I believe, every three 
>>>> years.
>>>>
>>>>    If you have Medicaid, they will help with a glucose meter, but they 
>>>> can be difficult to work with.  They are run state by state while 
>>>> Medicare is nation wide.
>>>>
>>>>    If you need to use Medicaid, please let us know, and I am sure you 
>>>> will receive help from this list.
>>>>
>>>>
>>>>
>>>> Regards,
>>>>
>>>> Ed Bryant
>>>>
>>>> ----- Original Message ----- 
>>>> From: "K C" <kcc86 at hotmail.com>
>>>> To: <diabetes-talk at nfbnet.org>
>>>> Sent: Monday, November 03, 2008 9:12 AM
>>>> Subject: [Diabetes-talk] I'm a silent Diabetic
>>>>
>>>>
>>>>> Hello, everyone.  My name is Kijuana.
>>>>> On Thursday the 30th of October I was diagnosed with Diabetes after
>>>>> Uterine surgery on the 23rd of October.  I had no idea I had it.
>>>>>
>>>>> I'm so scared!  I have never had to stick myself to test my blood 
>>>>> sugar or
>>>>> anything else.  I know a little about it because I have had personal 
>>>>> friends
>>>>> who have
>>>>> suffered major complications from this disease, and some of them have 
>>>>> died.
>>>>> Logically I know it is something people live with, and control 
>>>>> everyday. I
>>>>> also understand that it is a very common illness.  It's just that it 
>>>>> has
>>>>> never been a part of my daily life.
>>>>>
>>>>> I don't know how to act, or react now.  Because I have no symptoms I 
>>>>> don't
>>>>> know how to eat differently or anything else.  Over the past few days 
>>>>> I have
>>>>> continued to do like I always have, but the numbers on the blood tests 
>>>>> say
>>>>> different.  Its silence scares me more than if I had some weird 
>>>>> symptoms,
>>>>> went to my Doctor, and was diagnosed then.
>>>>>
>>>>> How do you deal
>>>>> with the days, weeks, and months after diagnoses emotionally?  They'll 
>>>>> be a
>>>>> lot of education I'll get in the coming weeks on diet, life style 
>>>>> changes,
>>>>> etc.  But what I really need right now is those who're living with 
>>>>> this
>>>>> disease to share their experiences with me so I can put my feet on 
>>>>> some kind
>>>>> of ground.  Thank you for reading all this.  I feel totally 
>>>>> disoriented. My
>>>>> state services for the blind leave a lot to be desired, so my 
>>>>> councilor
>>>>> doesn't even know where to begin as far as purchasing a meter, testing
>>>>> supplies, etc.  Any help will really be appreciated.
>>>>> Kijuana
>>>>>
>>>>>
>>>>
>>>>
>>>> --------------------------------------------------------------------------------
>>>>
>>>>
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>>>>>
>>>>
>>>>
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>>>
>>>
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>>>
>>>
>>
>>
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>
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