Slipping Into the Shoes of a Hospice Patient
Barbara Karnes, RN
Author of GONE FROM MY SIGHT aka: "the hospice blue book", NHPCO Hospice Innovator Award, End of Life Educator
Dear Barbara,
How does a person feel as a hospice patient? ?Everyone is waiting on them, they are unable to do things for themselves. They have to wear diapers and probably don't want to be a problem for caregivers. Often, their well-meaning loved ones stay for long visits when they want to rest.
I don’t think there is a “one size fits all” answer here. I can only guess, not having been in that situation yet. What stands out for me is that whether we are facing the end of our life or have a serious illness or some sort of debilitation, how we react and respond is going to be according to our personality. It is going to be how we have faced other challenges and life situations.
Challenging life situations generally don’t change how we react or respond to others. Our personality traits are mostly just intensified.
So — if I am a very private person, I will probably have a challenge accepting all of the attention. If I’m an extrovert, then interacting with others can be helpful. You see where I am going with this. Look at the person, their personality, how they would react if they were well and that is probably what they are thinking and how they would want to be treated now. But even more so.
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The one way of addressing these questions in the months before death is to ask, How do you feel about all this company? Do you want to talk about all the changes that are occurring?? It is important to give the person as much control over their living, their wants, their idea of comfort as possible within the circumstances of their inabilities. And that requires talking about the changes and how their life is unfolding.
The above applies to people before their labor begins. Once they are weeks from death , this world and its activities, its protocols, its people, and its interactions lose their importance. The focus is now on leaving.?
The person is sleeping most of the time and seems confused and “other worldly.” I don’t think they are thinking about themselves or what their wants or needs are.
Something More… about Slipping Into the Shoes of a Hospice Patient
The more the caregiver knows what to expect during the dying process of their special person, the more calm and sacred the months, weeks and days will be for everyone. Having the end of life guideline series bundle at the bedside for caregivers, friends and visitors to read and refer to will be a huge help.
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5 天前Dignity is huge. I experienced this when my father was passing. He did not like to depend on anyone, but at this point he needed help. Finding small ways to give them the help they need without making them feel bad, embarrassed or like they have no choice makes all the difference. The situation is tough for everyone involved but especially for the person we are there to take care of.
Hospice Nurse at Arkansas Hospice
1 周Thanks for sharing
Chief Executive Officer at Kirva Hospice;- a joint partnership with Jewish Family Services & Beth Sholom Senior Living
1 周Thanks for sharing
Employee and Volunteer at Sharp HospiceCare
1 周I work in our hospice homes. Often I see many family and friends come to visit our patients. We try to explain to them their loved one needs time to rest. Our message isn’t always well received.
Nurse Practitioner—Retired
2 周The patient should do what they can for as long as they can. Diapers are Depends or pull ups. Bibs are clothing protectors. Let them have choices when safe and appropriate.