“Everyone
has got to die, but I always thought an exception would be made in my case."
Author,
William Saroyan, on his deathbed.

 The
majority of us are not comfortable having conversations about the prospect of
end of life. Why is talking about care in the final stage of life so difficult? Perhaps, on an unconscious level we
think that if we ignore death, it will go away, or worse, if we do talk about
it we might jinx ourselves and bring it on.

In 2011,
people living in California were surveyed and the results were astonishing.

 Sixty percent say that making sure their families are not burdened by tough decisions about their care is "extremely important. However, 56% of Californians have not communicated their end-of-life wishes to the loved one they would want making decisions on their behalf.

 While a large majority of Californians (82%) say it is important to have end-of-life wishes in writing, only 23% say they have done so.

 Almost 80% say they definitely or probably would like to talk with a doctor about end-of-life care, but only 7% have had a doctor speak with them about it 

Read more: http://www.chcf.org/publications/2012/02/final-chapter-death-dying#ixzz2VdVg3Zjf

 How can take the fear out of this and
begin to have rich and meaningful conversations with those we care about and
those we care for? How can we begin to normalize the experience of approaching
difficult subjects? The California Conversation Project’s website has some
helpful tools that easily walk you through the process. http://theconversationproject.org/starter-kit/intro/

 It is important to recognize that
these conversations need to happen long before we are ill. Whether we are young
or old we need to begin the conversation, make our wishes known and write them
down. In healthcare we need to develop a comfort level in talking with people
about their wishes so that we can honor them.

 I invite you to watch this video of the
Jennings multigenerational family who gathered together to begin the conversation. This
was the catalyst I needed to complete my own advance directive. 

 

I hope you will gift your family and begin the
conversation with your loved ones.

 

~liz Sorensen Wessel

5 responses to “Days 158-159 The Conversation Project”

  1. Woody Wessel Avatar
    Woody Wessel

    “Always look on the brite side of life”. Its good to plan for your final hours {it stops people from arguing on when its time to pull the plug on you} just make sure you go out and Live Life while you can. We are all given just so many days and hours don’t waste them. The old say that youth is wasted one the young, I wonder if the dead say life is wasted on the living.

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  2. Maureen McDermott Avatar
    Maureen McDermott

    Thanks Liz for reminding us about those important questions in life. Let’s hope that the Conversations encourage people to share their hopes, plans and desires as well as the good things and meaningful experiences that have made them who they are. Thanks Woody for your encouragement to live life well as Jesus reminded us so well, “I have come that you may have Life and have it to the full.” (John 10: 10)

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  3. Stephanie Avatar
    Stephanie

    Ken and I tried to have The Conversation with his grandparents in their 70s around 1990, and it went over like a lump of lead. We heard later that they thought that we were trying to move them from their home into a rest home: the last thing we were thinking about! After I learned about “5 Wishes”, I used that as a tool to talk with my parents about their end of life wishes, and our Conversation is loving and ongoing. I think that with hospitals and health care workers routinely asking about advance directives, society is beginning to support these conversations. Mainstream videos such as this can be a big help. Thanks, Liz!

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  4. Erie Chapman Foundation Avatar

    Thank you for lifting up this issue in your essay, Liz. Perhaps, it will help move someone out there to begin a series of these discussions with someone they love.

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  5. Claire Wessel Avatar
    Claire Wessel

    Often those who have advanced directives neglect to actually inform their family that they have one (same goes for organ donors!). If it was important enough to make one, be sure to tell your family that you have one and where it is kept. If it is needed, the author will not be in a position to tell anyone where it is! My husband and I have talked often about what we would like to have happen if we were on life support or after we die but we do not have a will (even though that is ridiculously irresponsible with young children to care for!)

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