# Dr. Carl Kjellstrand /AKF

**URL:** <https://forums.homedialysis.org/t/dr-carl-kjellstrand-akf/675>\
**Category:** HD For Professionals\
**Created:** [February 21, 2006, 7:50am UTC](https://forums.homedialysis.org/t/dr-carl-kjellstrand-akf/675 "2006-02-21T07:50:03Z")\
**Posts on this page:** 3\
**Page:** 1

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**Author:** ![Jfwag](https://forumcdn.homedialysis.org/letter_avatar_proxy/v4/letter/j/3e96dc/32.png) [@Jfwag](https://forums.homedialysis.org/u/Jfwag)\
**Post date:** [February 21, 2006, 7:50am UTC](https://forums.homedialysis.org/t/dr-carl-kjellstrand-akf/675/1 "2006-02-21T07:50:03Z")

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I am so happy that HDC has posted in their update that the American Kidney Fund is to bestow its highest honor on Dr. Carl Kjellstrand. I will never forget when I read one of his “statements” so early on in my dialysis career. Below is what was read and to me at least it was very profound.  
That’s not to mention what the AKF did for my spouse and me at one of the lowest points in our lives. The AKF is a great resource.  
Below is something that I find very influential and moving when “debating” home dialysis at the time. He made a difference.

Dr. Carl Kjellstrand

DIALYSIS IN THE USA

In recent medical studies, it has come to light that people receiving  
dialysis treatment for kidney failure in Europe experience, on average,  
better health with fewer complications and longer life expectancy than do  
their American counterparts. There are a number of possible reasons for this  
discrepancy, such as differences in patient populations and in treatment  
procedures, but the most significant seems to be the difference in the  
respective goals of treatment.  
In Europe, the goal of dialysis is rehabilitation. Patients are expected  
to do well and to return to normal lives, and their doctors are not satisfied  
until they do. In the United States, however, the goal often seems to be  
merely to keep patients alive, without any serious ongoing attention to  
rehabilitation or quality of life. Might this great difference in intentions  
and expectations be the deciding factor in the difference in outcomes?  
Bernie Seigel, M.D., Deepak Chopra, M.D., and others, have written about  
the influence that expectations of doctors and medical staff have on patient  
outcomes. Their thesis is that since patients tend to conform with their  
doctor’s expectations, performing up to, or down to, those expectations, it  
is a doctor’s solemn responsibility to convey as positive and hopeful an  
outlook as possible to assure the most beneficial outcome. A recent study in  
Clinical Psychology Review on the ‘placebo syndrome’ clearly shows that  
belief in a particular outcome can be as strong a determinant as any  
medication. Indeed, is it really any surprise that low expectations lead to  
less than optimal outcomes?  
Dialysis in the USA has become by default a kind of limbo, and the  
experience of patients, while fraught with difficulty, is rarely allowed full  
expression or resolution. Instead, patients are expected to be ‘nice’ while  
being treated as little more than items on an assembly line. The prevailing  
attitude of doctors and staff at many clinics is that of denial: that the  
situation is so bad that it must not be dealt with. The corporate owners,  
usually far removed from the clinics, tend to make treatment decisions based  
on short-term profitability, often to the short-term and long-term detriment  
of their customers well-being. Although patients become inured to the idea  
of having to dialyze, and would be more than happy to get on with worthwhile  
lives, they are held back by a system that regards them as permanent invalids  
with one foot in the grave.  
It seems that aversion to the idea of dialysis is the stumbling block  
preventing further investigation of solutions to dialysis-related problems.  
The common perception is that dialysis is an awful burden which it is  
impossible to do anything about. Great pains are taken to impose this view  
on the patients, with regular negative reinforcement: in combination with  
the treatment, it is an effective form of brainwashing. This defeatism  
inevitably colors treatment decisions, and leads to a poorer quality of life  
for all concerned.  
I don’t think that kind of mentality is appropriate in any medical  
situation. There may be no cure per se for kidney failure, nor is there a  
cure for blindness, amputation, paralysis, or brain damage. However, the  
general trend in all these other cases is to overcome the disability and  
return the person to a full and worthwhile life, regardless of the obstacles.  
What makes dialysis so different? Is it the machine? Is it the blood?  
What is it? I think it is a self-fulfilling prophecy.  
The time is overdue to re-examine our priorities and re-establish the  
dialysis program on a solid basis of the optimization of the quality of life  
of each individual dialysis patient. When that becomes the standard of care,  
we will also see the optimization of outcomes: patient satisfaction,  
rehabilitation, and longer, healthier, more productive lives. That is what  
the system was intended to produce, and that is what we are paying for.  
Let’s do what it takes to make it so.

April 15, 1994

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**Author:** ![system](https://d16rlmixcfjfyh.cloudfront.net/original/1X/5d85dacb7e76ee0f7b162785afa5f129bc0805ad.png) [@system](https://forums.homedialysis.org/u/system)\
**Post date:** [March 1, 2006, 5:50pm UTC](https://forums.homedialysis.org/t/dr-carl-kjellstrand-akf/675/2 "2006-03-01T17:50:12Z")

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> [@Jfwag](#):
>
> …He made a difference. …

Thanks for the post. IMO, there is no higher accolade. Making things better, making a difference, should be the goal for all of us.

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**Author:** ![Beth\_Witten\_MSW](https://forumcdn.homedialysis.org/user_avatar/forums.homedialysis.org/beth_witten_msw/32/541_2.png) [@Beth\_Witten\_MSW](https://forums.homedialysis.org/u/Beth_Witten_MSW)\
**Post date:** [March 1, 2006, 6:11pm UTC](https://forums.homedialysis.org/t/dr-carl-kjellstrand-akf/675/3 "2006-03-01T18:11:00Z")

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And he is continuing to make a difference, by the way. He is truly a terrific advocate for quality care for patients. He is one of the rare people who speaks his mind even if what he says is not “politically correct” or exactly what everyone else in the renal community is saying. He is an “outside the box” thinker. In my opinion, we need more people like him in healthcare today. I am one of his many fans.
