Commentary: Quality vs. Quantity

 
“Before my diagnosis, I, like most people, would probably have said that living longer is the top priority. No question. Easy answer. But now I'm not so sure... another few months of feeling bad -- is that really the way I want to live? Is it worth it?”
 
 

The following essay is from the NPR My Cancer weekly podcast:

It's probably the toughest decision a cancer patient has to make. It's a question that most people don't ever expect to face — I know I didn't. And it really cuts to the heart of who we are and how we want to live. The question is: Quality vs. quantity... of life?

The treatments for cancer are not pleasant, to put it mildly. Surgery? That may be the easiest — you have it done, you heal, you move on. Not a lot of fun, but at least you can sort of see an end to the discomfort.

Radiation? I haven't had it, but it doesn't sound like much fun either.

And chemo? Definitely not fun. Debilitating, depressing, exhausting? and more. But you go through it because you hope that, if it doesn't destroy the cancer, then at least it will hold it at bay and buy you more time. And that's really what doctors are trying to do — buy you more time. There's usually very little talk of curing you of cancer — at least there wasn't for me. The only time it really came up was when my doctors told me not to expect a cure.

Instead, they want to do everything they can to prolong your life. Increasingly, cancer is treated as a chronic disease, like diabetes. Something you have, but that you can also live with. And that all sounds fine the first time you hear it. Even if there is no cure, this approach holds out the promise of longer life — maybe a much longer life. The hope is that cancer does not have to be a death sentence.

But after you've taken the drugs, or had the radiation, it may not be so attractive.

So it comes down to that one basic question: Would you rather have quality of life, or quantity? Is it worth it to live longer, even if the treatments that make that possible also make you miserable? Or would you rather have a better quality of life, even if that means a shorter life? I never expected to face a dilemma like that.

It's actually pretty simple though. There are two choices. Undergo treatment, feel miserable, but live another six months. (Is that time so precious that it's worth any amount of discomfort?) Or don't take the treatment, feel pretty good for a few months, but know that untreated, the cancer will probably kill you sooner.

If you had given me those choices before my diagnosis, I, like most people, would probably have said that living longer is the top priority. No question. Easy answer. But now I'm not so sure. I'm in no rush to die, believe me. But another few months of feeling bad — is that really the way I want to live? Is it worth it?

I don't know. And it's more complicated than just what I want. Is it fair to my friends and loved ones? Do I owe it to them to try to live as long as possible, no matter what the quality of that life is? Or is it more cruel to make them suffer through those painful treatments along with me? Is it selfish? Or is it my decision alone?

I go back and forth on this. Stopping treatment seems like a slow form of suicide. At the same time, having just taken a short break from chemo, the idea of not feeling sick is very appealing. But even if it means a shorter life?

I don't know how to answer this one. I hope that I won't actually have to make that decision any time soon, but I know that I will have to make it at some point. I wonder, when that time comes, if I will be wise enough to make the right choice.

 

Comments (Send a comment)

I don't think anyone who has not had the cancer experience realizes how difficult the treatment is and how frustrating it is to willingly make yourself ill each treatment. To know that the current manifestation of the disease has much less impact than the treatment is almost self-defeating. I used to tell myself you do what you have to do. But, I can see and feel that there is a point when I would possibly make the decision to stop. That the quality of life and, to be honest, the control of my life would be more important than the length of it. In cancer treatment, your life is given over to the disease and then to the specialists, their offices and the medical technicians. You know you've already lost control of your body because this growth had invaded it, but then the treatment and its mundane scheduling requirements take over. You're grateful, but you're also trapped each day by its necessities. The freedom to make a decision to stop and enjoy the time you have left under your own control is not admitting defeat but going out on your own terms. I don't know if your friends and loved ones would ever completely understand. Everyone looks for hope but we don't always get what we want.

Sent by Chris | 3:30 PM ET | 07-03-2006

I was diagnosed with preliminary peritoneal cancer and will be operated on this Friday, July 7th. I can only tell you that although I go about my day as usual the fear inside me does not subside but, I do not know what I fear. Did I live a good life? Will I die at the operation table? Will chemo kill me? Is this a nightmare that I need to wake up from? It is not easy but, as you write, do I have a choice on what is going to happen to me in the near future? No! I have no control of what is happening inside of me and that is what scares me the most. All I can do is have trust in the doctors that are trying to heal me and be thankful for the life that I've had.

Regards, Frances

Sent by Frances Nichole Damas | 3:39 PM ET | 07-03-2006

This entry hit close to home as my family recently faced this issue. My dad passed away from lymphoma in April. Before that he had been losing feeling in his hand,and having trouble walking. He mentioned several times that he was more concerned about the quality of life then the quantity. He was lucky that once the illness progressed to the point where he was bedridden he only had two more weeks left. As a family member I feel that he would not have wanted to live longer, as there was no cure, and at peace with the fact that he went quickly. We all had quality time with him. For me as well, quality time with him at the end was more important then quantity.

Sent by Laura Levine | 3:41 PM ET | 07-03-2006

Leroy, Bless your heart, that's all I can say. Please know what to do when the time comes, and I am sure you will. When in doubt, like you are right now, do nothing. You will know what to do when it's time and it is obviously not right now.

Sent by Ruth White | 3:47 PM ET | 07-03-2006

Hi Leroy—

My wife and I asked ourselves some of the same questions you are asking. She had colon cancer that had spread to her liver. I always said that I was selfish — I wanted her to live as long as possible. But we talked a lot about quality of life, and I tried to be sensitive to her suffering. In the end, though, there wasn't much of a choice for us. She was 31 when she was diagnosed, and we were getting married in a month. We treasured our time together, and we wanted it to last as long as possible. We spent a lot of time on the couch watching TV, with her too tired to do anything else. But we also were able to make three trips to Europe in two years, and we had lots of fun times with friends and family.

As you have probably guessed by now, she died recently, on May 12. I have been comforted by the knowledge that we did everything we could to extend her life and to make that life as enjoyable as possible.

Thanks for this wonderful blog. I wish you all the best as you face the many, many questions and challenges ahead.

Sincerely,

Michael Workman

Here is a link to a story my wife wrote for the Baltimore Sun.

Sent by Michael Workman | 3:48 PM ET | 07-03-2006

Hello, Leroy:

Thinking about you (and all your compatriots fighting the good fight in whatever way works for them)on this Independence Day. May you be freed from pain and worry....have a great day today!

Sandra

Sent by Sandra Yudilevich | 11:26 AM ET | 07-04-2006

My husband died three years ago after living with cancer for over 5 years. I can't tell you how much this blog means to me. It really captures the reality of the issues faced. We searched hard for information that might give us some sort of insight into issues, options, feelings and decisions we faced. Your blog addresses these things with sensitivity and reality. It would have been great help to us, and is of great help to me. One of the worst complications of cancer is the isolation one feels at times as if it was just the two of us facing a crazy situation. There are no easy, rosy answers.

Sent by Linda | 11:27 AM ET | 07-04-2006

Thank you so much for this exceptional experience, Leroy. I read about this opportunity today in the Houston Chronicle and though I do not have cancer, my life has been and continues to be significantly touched by the cancer experience on a daily basis.

My most life-altering past experiences with cancer were my mother's struggle with lymphoma and my husband's battle with testicular cancer. Currently and during the past 18 years, my nursing practice has taken place in the hospice setting. So your quality vs. quantity dilemma is one that I'm very familiar with.

My mother died 25 years ago, and I remember when she said she wasn't going to take any further treatment! Though we didn't address it as quality vs. quantity, that was the issue. I wanted quantity and she acquiesced. She spent the final month of her life in the hospital, burdened with horrible side effects from the experimental treatment that she had agreed to take...for her family. Her entire mouth and esophagus was a battlefield of ulceration. How I wished I had listened to what she was trying to tell us. She wanted quality, and we didn't let her have it. I realized there wasn't any quality for her, when the presence of her only grandchild could no longer bring a sparkle to her eyes.

I speak with patients and families on a daily basis who are struggling with the issue of quality vs. quantity. Encouraging each to speak with honesty, but always advocating for and empowering the patient. It should be the patient's choice...not the doctor's, not the family's, not the priest's, not the friends', and not the co-workers'.

There are many beautiful and wonderful experiences that can take place, if and when loved ones can "align" with the person who is dying. These experiences won't eliminate sorrow or tears by any stretch of the imagination, but they can give us something consoling to hold onto while dealing with our grief.

I'm passionate about providing information that will allow for informed decisionmaking. Anything less diminishes an individual's dignity.

Sent by Ruth | 11:44 AM ET | 07-04-2006

I recently began treatment again after my latest recurrence of small bowel cancer (carcinomatosis). The first two times I went through chemo I thought I did pretty well ? a few days of discomfort, followed by a fairly predictable period of feeling better. This time, I have few "days off" from the discomfort. I cannot work as I cannot predict how I'll feel each day. I've begun asking those questions: how many good days must I have to make treatment tolerable? 3 days out of every 2 weeks? 5 days? I haven't answered that question yet, but at the moment, with only 3 or 4 good days in each cycle, it doesn't feel like I can manage this for a long time. And yet, with two college age daughters, I can't ignore the quantity side of the equation either. As with all aspects of the cancer experience, there is no road map to lead the way ? just a daily grappling with life's tough questions.

Best to you-

Barbara Close

Sent by Barbara Close | 12:30 PM ET | 07-05-2006

Thank you for talking about the really hard things about cancer. It's too easy to tippy toe around the subject and then we miss saying and feeling the things that come from having a friend or family member with this life-robbing disease.

Sent by Barbara | 12:33 PM ET | 07-05-2006

Animal experimentation cannot be accurately extrapolated to humans i.e. Vioxx, yet it continues causing a waste of taxpayer money and non-ending animal cruelty. Superior alternatives exist! I might suggest that there are inmates on death row who may wish to redeem themselves with society by allowing experiments and/or drug tests on themselves. Never against their will, however!

Sent by Joan Mutcheer | 4:19 PM ET | 08-28-2006

Send a Comment

Comments are reviewed and edited by NPR prior to display. All comments will be read, but not all will be posted.







 (privacy policy)

NPR reserves the right to read on the air and/or publish on its Web site or in any medium now known or unknown the e-mails and letters that we receive. We may edit them for clarity or brevity and identify authors by name and location. For additional information, please consult our Terms of Use.




   
   
   
null


 
E-mail this page Print this page
 
 
 
Leroy Sievers

Leroy Sievers

Blogger

 
 
 

Leroy Sievers in the Ted Koppel Documentary

A Ted Koppel documentary focuses on his friend Leroy Sievers' "My Cancer" blog and the response it evokes.

 
 
 

About 'My Cancer'

My Cancer will be updated Monday through Friday with posts and commentaries from Leroy Sievers. A journalist for more than 25 years, Leroy has worked at CBS News and ABC News, where he was the executive producer at Nightline. You can follow his story through this blog, his weekly podcast and his monthly series on Morning Edition.

 
 

Discussion Guidelines

Read the discussion guidelines for our blog.

 
 

My Cancer Podcast

MY CANCER PODCASTDownload Leroy Sievers' radio commentaries and exclusive audio segments in the My Cancer podcast.



» Get the Podcast

 
 

Subscribe to 'My Cancer' via E-mail

Enter your email address to receive daily updates from this blog:



Delivered by FeedBurner

 
 

Search 'My Cancer'

Search for the word(s):
 
 

Contact Leroy:

If you'd like to write Leroy and the My Cancer staff privately, please use our e-mail form.

 
 
 

Related News Feeds

 
 

Browse Topics

Services

Programs