End-of-Life Choice, Palliative Care and Counseling

Posts Tagged ‘Advance Directive’

Sep 25, 2012Wisconsin Medical Society Wants Planning for End of Life

By Guy Bolton
Milwaukee Journal Sentinel
September 20, 2012

The Wisconsin Medical Society is launching a statewide initiative to make advance care planning – including the sensitive and often difficult conversations about end-of-life care – a standard part of patient care.

The initiative – Honoring Choices Wisconsin – is modeled after a communitywide initiative in La Crosse that has drawn national attention as well as a similar initiative by the Twin Cities Medical Society in Minnesota.

The goal is for the state’s health systems eventually to have people on staff trained to help patients understand and document the care they would want if they could not make decisions themselves.

“We know the tragedy of not having these conversations,” said Tim Bartholow, chief medical officer of the Wisconsin Medical Society. More

Sep 21, 2012A Graceful Exit: Taking Charge at the End of Life

by Claudia Rowe
YES! Magazine
September 19, 2012

 

I was standing in my cubicle, a 24-year-old fact-checker envisioning a publishing career of glamor and greatness, suddenly shaking as I read the document my mother had mailed. It detailed her wish that I promise never to keep her or my father alive with artificial respirators, IV-drip nourishment, or anything else she deemed “extreme.”

I was horrified, and slightly angry. My mom was a 54-year-old literature professor who’d spent the 1970s eating whole grains and downing vitamins. She was healthier than anyone I knew. Why get so dramatic now? It seemed ghoulish, not to mention premature. But I scrawled my signature at the bottom of the page and shoved it into an envelope, my mother’s voice in my head, prodding me along.

As with the whole wheat and vitamins, my mother—back in 1990—was onto something long before it became conventional wisdom. But these days, Americans’ approach to aging and death is rapidly evolving, pushed both by the numbers and the grim reality behind them: In 40 years, there will be 19 million Americans over 85, all at high risk of losing the ability to care for themselves or dwindling away due to organ failure, dementia, or chronic illness. (The days of a sudden fatal heart attack are fading; by 2008, the death rate from coronary heart disease was down 72 percent from what it was in 1950.)

So while many seniors now live vigorous lives well into their 80s, no one gets a free pass. Eating right and exercising may merely forestall an inevitable and ruinously expensive decline. By 2050, the cost of dementia care alone is projected to total more than $1 trillion.

My mom’s decision to face her end came not from any of these facts, but from the nightmare of watching her own mother’s angry decline in a New York nursing home. “You’re all a bunch of rotten apples,” Grandma growled at visitors, the words erupting from her otherwise mute lips. And there she sat for three years, waiting to die. “Why can’t you just get me some pills so I can go?” she would sometimes wail.

The slide toward death was only slightly less awful for my father’s mother. Grandma Ada would greet me with a dazed smile—though it was impossible to know if she recognized the person standing in front of her wheelchair—before thrashing with involuntary spasms. An aide would come to restrain her, and then my dad and I would leave.

This cannot be right. This cannot be what we want for our parents—or ourselves. More

Aug 23, 2012Advance Care Planning: Take Charge of HOW You Die

By ABC News
ABC News
August 22, 2012

Did you know that 70 percent of Americans have thought about end-of-life preferences, yet only 29 percent have completed an advance directive? Did you know that while 70 percent of people say they would like to die at home, 70 percent die in hospitals?

At present, conversations about end-of-life wishes happen all too often for the first time in an ICU around a patient’s bedside, prompted by daunting questions such as, “If your husband’s heart would stop, do you want us to start it again?”

This is the last question someone wants to take responsibility for making for someone they love. Siblings disagree, decisions are delayed, and regrets over the things that should have been said surface.

All of this time the patient lies in bed in discomfort, with diminished quality of life, having procedures they may not have wanted, in a place they never wanted to die in. We all know that death is inevitable, but is this the kind of death you would hope for?

As a community, we need to grasp that although we do not have control over IF we die, we can take charge of HOW we die. Advance care planning is about making these wishes known to your loved ones. Anyone who has been at a bedside of a person who has passed away knows that death is not exclusively a medical event.

And so these conversations need to focus not only on preferences for medical treatments but also on values, what you consider quality of life, how comfortable you want to be, how you want to be treated, and what you want your loved ones to know. These conversations require time and thought and are truly most valuable when they occur when a person is healthy, before an illness or injury.

How do we move our culture from avoiding the topic to embracing it? Multiple approaches need to be taken. Many are already in process. As a nation, every April 16 we celebrate National Healthcare Decisions Day. On and around this day community groups, churches, healthcare institutions, and other gathering spots are encouraged to host community programming on starting the conversation.

The media is starting to change — think of the recent movie “The Descendants,” the coverage of Randy Pausch’s last few months, and the upcoming “Death and Dying” series.

These and other thought provoking stories could easily be used as conversation triggers. A wealth of information is available on the internet as well as on advance directives, starting the conversation, frequently asked questions, etc.

In health care, the responsibility for this discussion needs to rest on both the PCP and the patient. Our PCPs need to not only ask us if we have an advance directive — a legal document setting forth your decisions about end-of-life care — but also educate us on why it’s so important to do one now. The right time and place to hear this from a medical provider is during a “well visit,” not in the hospital.  Checking to see that a patient has an advance directive should be as normal as checking their list of current medications.

Because the conversation can even be difficult for physicians, as educated consumers we have a responsibility to initiate it as well. The comfort level with having the conversation will increase as it becomes more commonplace; this is how real culture change happens.

Margaret Mead said, “Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has.” 

Don’t wait for the culture change to start the conversation; start it today.

Aug 17, 2012The Next Steps: How to Start Your End-of-Life ‘Conversation’

By Dr. Shari Barnett
ABC News
August 16, 2012

You have started to think about what you would want for the end of your life, but where should you start?

Fortunately, there are several resources to which you can refer to help you start your own conversation, including those that will help you decide what questions you should ask yourself and what choices you or your family will be faced with at the end of life.

Initiate the Conversation

The Caring Conversations Workbook, published by the Center for Practical Bioethics, is a great place to start. This workbook will help you ask yourself questions that will be important for your decision-making process. It will help you explore your feelings about certain scenarios and provide you a place to start collecting your thoughts.

Another resource, produced by the American Bar Association, is its Tool kit for health care advanced planning. This collection of 10 simple tools to help you and your family have an end-of-life conversation can also help you explore, refine and voice what is important to you at the end of life.

Get Your Documents in Order

These resources can help get you started in preparing the documents you need to secure your end-of-life plans.

There are three major terms you should know when you are trying to communicate your wishes to your loved ones and your health care team.

Advanced directive: It refers to any document that gives instructions about your health care. Your advanced directive is often made up of a living will and durable power of attorney for health care.

Living Will: Your living will is the section of your advance directive that states your wishes regarding the medical treatments you would want if you were terminally ill, permanently unconscious or in the end-stage of a fatal illness.

Durable Power of Attorney of Health Care (or Health Care Proxy): Your durable power of attorney for health care is person (or proxy) who will make medical decisions for you if you can no longer make them for yourself. You should give the proxy instructions for how to make these medical decisions in your living will and also discuss these topics with all of your loved ones, but especially your proxy. Your proxy is supposed to communicate to the health care team what you would want in the event you can no longer do so.

Choices like these can be demanding on not just person who is setting up the living will but also on the family member or friend who will be called on to act as a health care proxy or agent.

Act as a Health Care Proxy or Agent

There are resources for the health care proxy or agent, as well. The American Bar Association has produced guide on how to serve as an effective advocate for a loved one.

Start the Process Online

There are many resources to help you establish an advance directive online. Mydirectives.com (mydirectives.com) can also help you establish a Web-based universal advance digital directive for free. The directive can be digitally signed, is encrypted and stored so it is available to you any time you might need it.

The American Bar Association has an online form to establish a universal durable power of attorney for health care that can be used in 45 states. The ABA has also compiled a list of resources by state.

The Caring Conversations Workbook can help you establish a durable power of attorney as well as an advanced directive.

Jul 20, 2012Making decisions for loved one’s final days

By Warren Wolfe
Star Tribune
July 19, 2012

Sue Schettle has spent the past three years coordinating an ambitious campaign to help Minnesotans make better end-of-life medical choices. As CEO of the Twin Cities Medical Society, she’s seen how often big decisions go wrong at difficult moments.

Then she found out that her sister, who almost died from complications of emphysema 18 months ago, had made a big decision of her own: She had designated Schettle to be her “health care agent” to decide on proper care in case she is unable to speak for herself.

“This is very different from talking with other people about the benefits of planning for the end of life,” said Schettle, 47, as she visited her sister, Pam Lyons. “This is real, and it’s personal.” More