Category Archives: right to die

Value of Life and the Infinte Doctor

Grandpa, dad and I walked hand in hand.
Grandpa, dad and I walked hand in hand.

As I have thought about the subject a lot lately, I keep coming back to what seems like a conclusion.  We all wonder how to value life, and most of us swear we have an answer.  As a patient, a father of special needs children, and a patient advocate my conclusion seems simple compared to the many theological based answers I run across.

I think the value of life is determined solely by the desire one has to live it.  I came to this conclusion thinking about what Dr. Weis whom I met with the American Board of Internal Medicine, wrote about two ways to perform the role of a doctor.  The first is as if every visit has a finite interaction duration with a predefined beginning and end.  If the doctor comes into the room, diagnoses the patient and goes about ordering/performing/giving the care which has the highest likelihood of prolonging life, then the doctor has performed the best care possible.  This is measurable/finite doctoring (sort of, if we can agree on the most effective care possible).  The doctor came in, diagnosed the condition necessitating the visit, and treated it.  That is the end of the doctor’s role in a finite model.  I note this is the current model most of our insurance uses to pay for treatments.

The second way to perform the role of a doctor is to look at the patient as a whole.  What do they want to do, and how is their condition preventing this?  Will solving the nominal cause of the visit allow the patient to resume their life as they desire?  What is it that drives them and keeps them going?  What is the patient’s answer to life’s most important question, “For what or whom do you live?” If the doctor can allow them that part of their life which they value, should not that be the goal?  Notice however in this model, the role of the doctor doesn’t end when the patient is treated for the reason they came into the visit.  In this model, the role of the doctor continues for as long as the patient values some part of their existence.  This is the infinite doctor’s role, for it has no defined end point at the time the doctor sees the patient.  It ends with a lack of desire or ability to experience what the patient values in his or her life.

As I have interacted with patients, I find many who have experiences like mine where they overcome expectations because they have something which they value in their lives.  I see patients who spend their time helping others, and the desire to do so gives them fortitude beyond what should be expected.  I see kids who want desperately to play with their family, and that gives them strength to push on long after they should have needed to stop.  If we take the time to know what we or the patients really want out of this life, I suspect we may go down very different roads than the road of trying to preserve life for as long as possible.

I note treatment under these two models can have some profoundly different outcomes.  Now think about under which model of a doctor’s role you want to be cared?

This came to a head for me last month.  My dad had been in the surgical intensive care unit for months.  It became clear he was never going to be able to get back to the parts of life he loved.  He wasn’t going to be able to go out boating and drinking with friends at the marina.  He wasn’t even likely to be able to go read a book by the water for a long time, even if things went optimally.  Yet through infection after infection and surgery after surgery he held on.  Why?  I strongly suspect he persevered because he never wanted to leave my step-mom alone.  He loved her the way we all hope to be loved.

Still, on a Friday after months in the hospital she told him it was OK to let go, and what he wanted became clear before she even left the building.  If life’s most important question is “For what do you live?” clearly his love and concern for her was his answer.  He tore off the oxygen before she even got to her car.  They put it back on him, but through the weekend it became clear he was done.  He died on the Monday after family said our good byes and stopped all medication save those comforting him.  He valued knowing his wife was OK enough to endure whatever came his way, and when reassured she was, his decision was life was not worth the discomfort. He was lucky enough to be treated at a  hospital where the ultimate goals of maintaining and preserving life meant more than a heartbeat.

I don’t doubt for a second the entire team of medical professionals at the University of Maryland Medical Center worked to preserve a chance for him and our family to return to a life with meaning.  What’s more, when that chance passed, they respected the wishes of our family to let him go and not insist on medical treatment unlikely to add value to his or our lives.  For them, I am thankful.

For my dad, we will all miss your self deprecating humor. With your passing, we will miss thousands of smiles, Hawaiian shirt sightings, deep conversations and opportunities to enjoy great food and drink. May you forever travel happy knowing you are loved.

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Are You Strong Enough to Let Go?


The feel of not to feel it,
When there is none to heal it
Nor numbed sense to steel it. – Keats
I have thought of this quote off and on since I first ran across it on an MS World forum.  As I have dealt with loss of sensations and increased pain, as odd a pairing as I ever expect to run across, I have wondered if I would ever want to die.  Thus far, no pain has induced me to consider it, but this article is a scary look at what kind of strength is required for people to follow their loved one’s requests.  Words to paper, even with witnesses, will not allow for seemingly needed release without the strength of those who left behind.
A Life-or-Death Situation
After reading the article early in the week, two quotes from the article resonate with me still:
“He still wants to believe the mind is everything. But he has learned that no mind can fly free of a useless body’s incessant neediness.”
and
“Pain eats away at your soul.”
The article was one of the saddest I have read in a long time.  In it, an ardent defender of the right to die, Margaret Pabst Battin (Peggy), deals with her husband after an accident.  Despite his living will, writing of a farewell letter and even an “attempt” to let go, she has kept him alive saying it is not his time.  
In the end, I cannot help but think she is a hypocrite.  For somebody who advocates for so many to have the right to die, she seems to hold control of her husband’s fate despite his previously expressed desires.  In fairness, how many of us have the strength to let our loved ones die?  Maybe it is how the article is written, but she does not seem to believe in allowing him to choose to die.  Maybe she will let him think he has that power, but only for a moment.  Worse in my eyes, is the telling him after that she would have revived him.  Is it not enough to have to live that way without a loved one taking away from him even the appearance of control over his fate?  The control freak in me would hate the life I breath with the loss, one I already fear.
Clearly, he does not want Peggy to suffer.  With that, I suspect she fools herself thinking he would voice his thoughts second-guessing her.  These decisions are hard enough for all involved.  I know I would never voice my second-guessing of J in the same situation…though I would still hope she would follow through with my wishes…With evidence, she had not done so once, twice or even more, still I would hope for a better outcome the next time, especially if she said she would let me go.  In the end, I would hope she comes to recognize my will when she is ready enough to follow it as promised.  To do otherwise would seem a cruelty.  It is a hard enough burden to leave for those behind, the having to choose the hour of passage of a loved one.  The second-guessing of acts done in love and grief would seem a harshness to me, unworthy of the love motivating the acts.
I will always remember the last words I heard my grandma say.
“Please don’t make me cry.”

further interview of author on NPR:  http://www.npr.org/2013/07/25/205455599/for-bioethicist-with-ailing-spouse-end-of-life-issues-hit-home

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