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Understanding End-of-Life Care Key to Making Shared Decisions with Your Family

October 18, 2012 by Emmi Solutions

Featured Guest Blogger: Susan R. Dolan RN, JD

Susan R. Dolan RN, JD

Susan R. Dolan RN, JD

You plan for weddings, births, and vacations, in order to have the best experiences possible. Similarly, the best way to plan for a good death, with end-of-life care that honors your life and wishes, is to gather information ahead of time, determine and document your wants and needs, and discuss your wishes with those closest to you.

To make decisions about your end-of-life care requires information and clear communication, from fact-finding and gathering advice from experts, to discussing your wishes with loved ones. The better you understand your options, the more prepared you become—the more you and your loved ones will benefit.

 Planning for a good death: Gather information ahead of time, Determine and document your wants and needs, Discuss your wishes with those closest to you

You can start with a simple checklist:

  • Gather information from reputable sources and websites. A few suggestions include Caring Connections, a program of the National Hospice and Palliative Care Organization and the Hospice Foundation of America provides a variety of information, resources, and tools.
  • Take the initiative to open conversations about your end-of-life choices with your loved ones, health care agents (the person you have appointed in your power of attorney to make decisions on your behalf), doctor, and lawyer.
  • If you have a serious health issue, take someone with you when you visit your doctor. Write down questions in advance and take notes at the doctor’s visit.
  • If you have questions about end-of-life care, call a local hospice for a free consultation.
  • Make sure everyone understands your wishes. Take a copy of your advance directive (power of attorney for healthcare/living will) with you whenever you are admitted to a healthcare facility. Check with your doctor to make sure a copy of it is in your medical record.
  • If you become seriously ill, ask the doctor to explain your diagnosis, treatment options (including benefits and burdens), and expected outcomes. Make sure the doctor understands your goals for care. If you meet resistance, seek a second opinion.
  • If you become hospitalized and you have questions about whether to initiative a “Do Not Resuscitate” (DNR) order, ask to consult with a member of the palliative care or hospice team. If you have a DNR and live at home, display it in a prominent place, such as on front of your refrigerator, for easy access—especially if paramedics are called to your home.

Information and communication are crucial to excellent planning at any stage of life. For end of life care, these two keys can make the difference in living—and dying—well. Take the time to plan and prepare now.

 

About the Author

Susan R. Dolan RN, JD, is cofounder and executive director of Angels Grace Hospice located in Bolingbrook, Illinois and coauthor of The End of Life Advisor: Personal, Legal and Medical Considerations for a Peaceful, Dignified Death, a winner of the 2009 American Journal of Nursing Award. See http://www.angelsgracehospice.com.

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Posted in Chronic Condition Management, Disease Management, EHR, End-Of-Life, Events, Health Literacy, informed consent, Medical Home, Patient Communication, Patient Education, patient engagement, patient experience, Patient Safety, Patient-Centered Care, Shared Decision-Making | Tagged Communication, End-of-life care, health, Health care, Health literacy, Hospice, Hospice Foundation of America, Palliative care, Patient Education, patient engagement, Patient Experience, Patient Safety, Shared Decision-Making | 3 Comments

3 Responses

  1. on October 19, 2012 at 12:20 am lkafle

    Reblogged this on lava kafle kathmandu nepal.


  2. on October 31, 2012 at 8:01 am The 2012 Health Literacy & Shared Decision Making Series: A Recap « Engaging The Patient

    [...] Susan Dolan asked why we’ll plan for a wedding or a birth, but we often fail to plan for the end of our [...]


  3. on November 2, 2012 at 5:21 am kathy kastner (@KathyKastner)

    Thanks for this! One thing to note: often we patients/real people don’t know enough to know the right questions. I’ve charted my journey to better understand options and their consequences on www,BestEndings.com
    Kathy



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  • About this blog

    Both news and opinion, Engaging the Patient is brought to you by Emmi Solutions and is designed to connect healthcare leaders with peers who are making patient engagement a reality.

    This is a place where high profile healthcare experts write about their work and their goals. Our topics might vary from day to day but our focus remains constant. We believe patients are the biggest untapped resource in healthcare and we are searching for ideas and stories of new, innovative ways to make patient engagement a reality every day.

    If you have questions or would like to be one our featured guest bloggers, drop us a line.

    Some comments or opinions expressed on the blog may not reflect those of Emmi Solutions, LLC

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