Posts Tagged With ‘ Barbara Karnes ’

We think of grief as mourning, of our emotional reaction to a loss. The tears, the “I miss her so much,” the sadness she is no longer with you. Grief is sadness. For some, it may be a relief that someone or something is no longer a part of our life.  We don’t just grieve for those we care about. We grieve for people we are challenged by also. Another component when experiencing the death of someone close to us is learning how to live without that person. The component that extends beyond the emotional and into the physical, day to day life experiences. The adjusting to a new way of living,... Continue Reading

Where does someone go who doesn’t have anyone to care for them as end of life approaches? Most people, when told they can’t be fixed, believe they will stay at home, alone if necessary, and die in their own bed. Unfortunately, as death approaches none of us will be able to take care of ourselves. There will come a point when we will need assistance. We probably won’t even be aware we need assistance, but we will. The above question, “Who will take care of us when we can’t take care of ourselves?” is  part of the current medical/ social dilemma facing Americans today. The first thought... Continue Reading

For many people, nursing facilities have become their home. It is therefore reasonable that Hospice services be available in facilities. BUT care in a facility is not the same as care in the home. Here are some of the differences—and challenges. Nursing facilities’ focus, by regulations, is to keep people alive. All the care is concentrated on living the best possible life under the circumstances. Yet, most people in nursing facilities are there because of health challenges or aging that has made independent living unsafe. These people will die in the facility. I know that sounds harsh, but... Continue Reading

Sometimes our patients and families don’t want to hear the words “hospice” or “end of life care.” I have been asked, “should we use words that are more sensitive?” I don’t think so; I don’t think we need to use other words to be more sensitive to end of life issues. This seems to be a problem today with physicians and healthcare workers. Don’t use the “d word.” Address treatments but don’t say “There is nothing more we can do.” Everybody dies. Our bodies are programmed to die. From the moment we are born we begin to die, yet... Continue Reading

We talk about a Durable Medical Power of Attorney and how important it is to make our end of life wishes known. If we don’t legally make our wishes known in writing and generally notarized, healthcare professionals will make those decisions for us.  Those decisions will be to try to start our heart when it stops beating. (The chances of this procedure being successful if there is a life threatening illness or we are age compromised are slim.) Medical providers will generally listen to the “loudest protester” as to what care is to be given. Generally that loud voice is shouting to do everything... Continue Reading

It has been almost six months since my husband of 62 years died. As an end of life educator I have taught about loss and grief, and even written a booklet about it. BUT what I didn’t really understand were the emotional thoughts and feelings of grief. I couldn’t and didn’t understand because I had not walked in those particular shoes yet. Now I have. I’ve shared thoughts with you during this grief journey. My thinking is if I am feeling a particular way, then others must also. SO, here is what I have experienced recently that would appear “wrong.” I think others must have felt this... Continue Reading

If you look at a person from a healthy perspective you see the need for food, sleep, and socialization. We eat to live. Sleep to revitalize. Interact with others for stimulation.  If the body is preparing to die, the reverse is the norm. We gradually stop eating. We begin sleeping more. We begin withdrawing from worldly interests. All of these patterns are part of the normal life progression. However, most people don’t think of the dying part as normal. They have been led to believe that something pathological is happening. Our body is programmed to die. We are born. We experience, and then... Continue Reading

Dear Barbara,  What suggestions do you have in overcoming the changes we see in hospice and healthcare today? It doesn’t look like it did 20 years ago. How do we maintain balance while keeping patients centered?  Hospice originated outside of the medical model. It met needs the medical establishment did not. Gradually, ever so slowly, hospice agencies have been absorbed into that medical model and the original concept has morphed into a business. With any business, money becomes an important factor. With hospice outside of the medical model, in the hands of not-for-profits, it struggled... Continue Reading

Dear Barbara, We have heard the terms “compassion fatigue” and “caregiver burnout.” Today, after covid, it is being called “beyond burnout.” What are your thoughts about this? Doesn’t it feel like the world has sped up? Everything is so intense these days. That energy affects us all on many levels. Our minds and our feelings are constantly being touched with so much negative energy, world wide. When you add to the external happenings our own individual challenges and you have “beyond burnout.” What do you do about it? I’m not sure there is much we can... Continue Reading

Being in a relationship is about sharing and compromise. It is “let US do this, what do YOU think?” When a person is alone, not in a relationship, they can do what they want; there is no sharing or compromise. I hadn’t thought of that before because I didn’t have to. Now that I am only responsible for myself, I only have to figure out “what do I want?” The interesting thing for me is I’m not used to knowing or doing exactly what I want even though I thought I was. This is another aspect of grief I didn’t know until now that I am living it. Who am I if I am only one? What have I... Continue Reading