Different Types of Hospice Care Services
In this article, I will outline key points my fellow hospice team members and I have observed in our day to day work.. I have worked over 12 years as a Spiritual Counselor in Hospice Care. Each person teaches me something, though it is I who is supposed to minister to them in the final moments. For my colleagues and I, working in hospice is an ongoing challenge and learning experience, that presents us with learning of the deepest kind – on a soul level. In this article, I share with you the perspectives of my colleagues and myself, at a Hospice Center in Northern, IN (USA). We work together as a team and here are some of the insights from my colleagues.
Hospice is not a place. It is a concept of care. Hospice staff go to people’s homes and extend care for the mind, body, and soul. Much of our work is to free people of physical pain, so a patient can be attentive to living until he/she dies. This is a time when many patients reflect on their life. This integration occurs naturally and is deeply embedded in the psyche/soul of an individual.
Much of the work we do at the end of life is transitional. We are supporting a dying patient as he/she moves into becoming more soul than body. It is a work that challenges and changes anyone who is touched by a person whom I like to say is “awakening into their most authentic self.”
Our Hospice President wanted me to remind doctors of the need to have appropriate points of referral to Hospice Care. Early referrals enable all the services of Hospice care to become established and integrate holistic care. In addition to physicians, hospice centers are comprised of volunteers, social workers, nurses, bereavement counselors, and spiritual counselors who work to establish care, creating the opportunity for patients and families to share their deepest concerns.
My co-workers in the social work department wanted me to share the importance of good listening. The patient is dying to everything he or she has ever known.. As he or she begins to die, they become very reflective, and may want to share their reflections with their caregivers.
Through these reflections, a patient gives meaning to their life. When we listen to a patient share their story, we are being invited into their soul. The tears that surface are symbols of love a person acknowledges and encountered during the course of his or her life.
My colleagues in Nursing wanted me to remind healthcare professionals to be liberal with medications for pain relief. It is vital to give a patient enough medication to keep him or her from being in pain. Hospice Nurses gauge this daily in their patients. The doctor/nurse team in palliative care is so important that one cannot underestimate the cooperation and good communication needed between health care team members to do what’s in the best interest of the patient.
When a patient’s pain is under control, the ability to focus on living creates hope in the midst of dying. This capacity to have quality of life in the midst of dying gives the patient a sense of control that disease takes away. Our ability to create this quality of life for a dying patient is a wonderful use of our medical capacities in order to bring healing comfort to those who need it.
The Bereavement Counselors on my team wanted to share with medical professionals the importance of taking time to understand and comfort family members, especially those who are care givers of the terminally ill. It is vital to the bereavement process that doctors and nurses take time to share with the caregivers that their loved one is dying.
Watch out for technical medical language – or jargon – when you speak with family members. It is not always understood, and in fact, has a way of blocking a sense of personal closeness that family members need, in order to fully participate in what their loved one is facing.
Intellectual understanding of a patient’s prognosis is important. In addition, a family member also needs to know that their loved one is personally cared for until he/she dies. Here, we enter into a realm of care that transcends the body. This is where we care for the souls of all the family members who are involved in a patient’s care. The way we care for the family system of a patient’s life during this point can promote or hinder the bereavement process.
My fellow Spiritual Counselor and I believes that our ability to be open to a patient’s personal faith is what leads to a sense of peace beyond death. Earlier I talked about the deepening awareness of soul, that dying people often experience. In addition, many of our patient’s have religious thoughts of God, as he or she understands God.
A person’s capacity to believe in a higher power that is beyond themselves is a vital part of the dying process. Here, a patient moves through merely what he or she has been taught about their Creator to a more intimate and direct experience of what is beyond concepts, labels, and formal religion.
Dying people have much to teach us about living. For many persons, facing the end of their life might be the first time they have confronted this topic. For others, it may be something they have thought about intellectually, but now have to confront it through experience. Regardless of what path people have taken to reach this point, for most every one, endings become a time for spiritual awareness.
My first Hospice patient taught me something I will never forget. She wanted me to sit in silence with her and pray meditatively. Our time together was filled with space: space to feel eternity reach through the dying experience and surround our inner selves with peace. This gave far more meaning beyond anything she or I could have ever comprehended in purely intellectual terms about dying.
Even to this day, I remember her words: “What matters in life IS NOT matter.” It was her way of telling me that there is more to life than what we see and touch. And as she neared the end of her life, it was the inner, spiritual aspect of life that was taking on a life of its own.
Regardless of your philosophy, if you are a health care provider who is dealing with the terminally ill, it becomes important to respect the idea of soul, even if you do not believe in it yourself. By soul, I do not mean something specific to a particular religion. I mean, rather, an awareness that can be experienced among persons of all paths and religions.
As professionals who care for those who are dying, it is vital we remember we are caring for a person’s soul and their body.
As part of the process of turning towards non-material things, a person begins to let go of the various roles he/she carried out in life. At such a time, the need to find meaning and hope beyond this existence becomes vital to the well being of a patient who is dying. As caregivers, the need to look through our eyes and no longer with them enables us to view our patients as more than a disease in dis-ease. It is here we connect with them soul to soul and forge an eternal relationship with them that will never die.
As a dying patient begins to let go of their personality, an identity with something within him/her begins to emerge. This emergence is a calm awareness that has been with him/her their whole life. It is the part of us not attached to the experiences of the world. It is an identity with an aspect of us that transcends even death itself. In some ways, this perspective on dying enables the one who is dying to awaken into eternal life.
There are many definitions of the word soul. But most everyone agrees that it refers to something unseen, and yet we know exists. Inside us is a landscape of the soul. It is the part of us that knows without a doubt that an experience is true without having a tangible experience of it. This part of us guides us through some of life’s most difficult circumstances. It gives us hope beyond our present circumstances transcending us from self-centered awareness to life-centered awareness. This part of us is the same part a dying person begins to identify with at the end of their life giving them a sense of peace beyond anything he/she has been able to conceive to this point in life.
As the dying person makes their journey towards his or her end, and beyond, he or she is engaging in one of life’s most sacred journey. As the spiritual aspects of a person unfold along this journey, it becomes a chance for others to learn from them. As a health care provider, you are in a unique position, not only to comfort people as they make this final journey, but to also learn from and be deepened by your patients.
The spiritual awareness that can develop within you as a result, of the peace that grows in a dying person can be a lesson that you carry with you, and share not only with other hospice patients, but all of your patients, family and friends.
Sam Oliver, author of, “God a Logs on Living and Dying”
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Question by rive_gauche79: Is hospice care only for those who are dying?
My mother has advanced breast cancer and is currently receiving treatment. She has not been given an estimated life expectancy or been told that there is nothing else that can be done for her. However, the doctor who recently treated her with radiation suggested hospice for her because I am her sole caregiver and am in need of help. Is hospice appropriate for her situation? I am not ready to give up treatment (chemo); however, I don’t want her to suffer through chemo that isn’t going to work.
Best answer:
Answer by Belie
Hospice isn’t for those that are dying, it’s for those that cannot receive the best treatment at home and would be better off staying in a hospital environment where they can monitor her around the clock.
What do you think? Answer below!

May 15th, 2011 at 5:00 am
To accomplish so much with so little is incredible. Puts ‘western’ healthcare spending in perspective – very moving story. May it inspire all who watch it.
May 15th, 2011 at 5:26 am
To qualify for hospice, a doctor must say that the patient has an estimated 6 months or less to live. That doesn’t mean they won’t live longer, and hospice will continue to pay. My father had Parkinson’s Disease, and was put into hospice, and it was a life-saver for my step-mother.
May 15th, 2011 at 6:15 am
hospice care is for those who need LOTS of care like your mom. This is too big a job for you and the doctor recognizes that. Take it with gratitude.
Your mother should be the one who decides if she wants more or less chemo. Not you.
If it’s advanced cancer she is very ill and needs all the help she can get. She will also be aware of how much “trouble” she is and will be grateful to have help for you to tend to her.
At some point the doctor will know if the chemo is buying her any comfort or time. If it is of no use he will know. If it is not shrinking the cancer it is not working. He should check at appropriate times. You can ask him how often that will be done. It might be checked thru blood tests. Or xrays.
You are carrying a heavy load and could do with help. Try to get out and feed your soul. Get fresh air and some exercise which will ease some of your tension. You aren’t responsible for your mom, you are there to help but you need help too.
It is hard I know. My mom died of lung cancer.
It is wise she has not been given a time frame. The doctor has not given up. So don’t you.
xxxxx
May 15th, 2011 at 6:31 am
We are all dying, and yeah a hospice is just somewhere that can provide better care than most other places.
May 15th, 2011 at 6:49 am
It is. you don’t need to give up hope or treatment (chemo). Hospice is there to assist you and for the patient to be comfortable.Hospice help allows you to be a better care provider. This means that you can relax, sleep or attend to your responsiblities and your life. I’m sure that you have things that must be done everyday without being worried that your mom is alone or that she will need or want something while you are taking care of yourself and or your family. Even though she is ill, you still have to deal with everyday issues that affect you.
May 15th, 2011 at 7:29 am
i am very sorry to hear this. cant imagine how hard it must be for you. hospice care tends to be for those who want a home situation. like their own room and more relxed visiting hours etc. with the care and medicine that they cant always recieve at home. also can be used for respite where they can go for a short while to give sole carers like you, a little break. and you can join them. its just to help you aswel. hope things work out for the best.
May 15th, 2011 at 7:33 am
It certainly could be. The doctor does have to say the patient has less than 6 months to live, but many patients live much longer than this. How does your mom feel about continuing the treatment? I think one of the reasons the doctor may be suggesting this is that chemo isn’t helping her. Hospice provides care, but of a different sort. It’s emphasis is in palliative treatment of symptoms to make the person more comfortable and usually to stay at home. They also can provide the equipment, medication and staff to check on her, teach you what to do and provide some direct care in the home. It can be a Godsend to people who would rather be at home with a better quality of life.