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What Hospice Care Means for CaregiversHospice care is patient- and family-centered care that focuses on relieving symptoms and increasing comfort and quality of life. The goal of hospice is to provide quality and compassionate care for those facing end of life. Hospice care can give you the information and support you need to provide the best care for your loved one. What Hospice Care Means for Caregivers: Detailed InformationThis information is meant to be a general introduction to this topic. The purpose is to provide a starting point for you to become more informed about important matters that may be affecting your life as a survivor and to provide ideas about steps you can take to learn more. This information is not intended nor should it be interpreted as providing professional medical, legal and financial advice. You should consult a trained professional for more information. Please read the Suggestions and Additional Resources documents for questions to ask and for more resources. Caregivers who have helped a loved one through the cancer journey understand how cancer changes the lives of everyone it touches. A caregiver goes through the physical and emotional ups and downs of the disease along with their loved one. A caregiver is there to listen, support, encourage, comfort and help in many different ways. As a caregiver, you are vitally important to the one you love. Hospice care allows a survivor with advanced cancer or other life-limiting illness to spend the remainder of his or her life comfortably and peacefully, surrounded by those they love. This is a very important time for everyone involved. This document provides an overview of hospice care and is meant specifically for caregivers. It describes common concerns and addresses how these services can be helpful to survivors, their loved ones, and all of the caregivers during advanced cancer. The information that follows includes:
What is hospice care? Hospice services are family-centered and are delivered by a team of specially trained and compassionate health care professionals and volunteers. They work with patients, loved ones and the caregivers to help ease the pain and stress that can occur during advanced illness. The term palliative care is often used to describe the type of care given in hospice programs. Palliative care emphasizes the total well-being of the survivor as well as that of loved ones and caregivers. The goal is to prevent, treat or eliminate discomfort whenever and however it appears. Hospice care gives patients and their loved ones a chance to make meaningful decisions that are respected. Hospice is not about giving up hope. An important goal is to help the patient to be free of pain to give the patient and his or her loved ones, friends and caregivers peace of mind and acceptance of life as it is. Some people are afraid to ask about hospice care for themselves or for a loved one. They may believe that choosing hospice care means giving up. However, these programs are not about giving up. Rather, they allow the patient and his or her caregivers to focus time and energy on quality of life. A hospice organization provides care through a team of professionals and volunteers who work closely with the patient and all of the caregivers and loved ones who want to be a part of this experience. Hospice care workers are trained to support the physical, emotional, spiritual and practical needs of all those who are supporting loved ones at the end of life. Hospice care is often provided in the patient’s home with a loved one, friend and/or hired caregiver managing day-to-day care. The professional hospice team makes regular visits to provide additional services. Hospice care services may also be provided in other locations such as:
When should hospice services be considered? Hospice care can be discussed at any time. Often, the discussion about hospice services takes place when the patient and his or her loved ones learn that:
Many physicians hesitate to bring up the subject of hospice because they do not want patients to think that they have given up. There may come a time when you think that hospice care should be considered, but are not sure how to start this conversation. If this is the case, a member of the health care team can help you define what options are available. Sometimes the patient is ready to consider hospice care before his or her loved ones are. In other cases, the family may want to start services. Often, the decision is made together by the patient and his or her loved ones. If you are struggling with the decision about hospice care, talk to a health care provider, oncology social worker, licensed counselor or member of a faith-based organization about your feelings and concerns. It is generally the patient’s right to make this decision unless he or she is unable to communicate. However, if a patient cannot communicate his or her wishes, a spouse or other family member may be asked to decide. The health care team or an oncology social worker can help you find out what hospice care is available in your community and how to arrange for it. In order to start hospice services, a physician must sign a “referring order” that certifies that the patient’s life expectancy is six months or less if the advanced cancer runs its expected course. If a person in hospice care lives longer than six months, hospice benefits can be continued if a physician states that the person’s life expectancy is still less than six months. How does hospice care work? Hospice care is flexible and can be molded to fit the different needs and lifestyles of patients and their caregivers. Care is primarily focused on making the patient as comfortable as possible when a cure can no longer be expected. Hospice services can include:
The different levels of hospice care include:
In some very advanced cases, the majority of hospice care is provided at home though the patient or loved ones choose that death occur somewhere else. Though this is likely to be a very difficult subject to discuss, it may be best to make a decision like this early enough so that everyone is comfortable with what occurs during the final days and hours. Who are the professionals that provide hospice services? Hospice care is a team effort. Caregivers work with trained health care professionals who will assist with the care of the patient as they guide the patient and his or her loved ones through the hospice care. The following table provides an overview of hospice professionals and their roles.
Who should consider being a caregiver during advanced cancer? Becoming a home caregiver for someone who may be dying can come suddenly or after many years of battling cancer. Caregiving can be extremely rewarding, but also very demanding. Take time to look within yourself and think about your personal strengths and limitations. Caregiving is a 24-hour-a-day, 7-day-a-week job. As a caregiver, asking for and accepting assistance from others may be hard to do—but it will probably be needed. Keep in mind that you will be giving others the opportunity to serve and feel good about themselves for doing so. Talk with reliable family members, loved ones and friends about specific tasks and when and how they can help. Develop a schedule and contact list of those helpers you trust. Keep track of all the information necessary to stay in touch with these helpers. Caregiving requires a time commitment. The amount of time and energy needed to provide care for someone is not easy to predict. Sometimes a rotation schedule with other family members and loved ones is helpful. However, caregiving can be very demanding at times, so you may have to take time off from your job at some point. Serving as a home hospice caregiver is covered by the Family Medical Leave Act (FMLA), which protects an individual’s job standing and benefits during unpaid leave of up to 12 weeks. Not all companies are required to offer this benefit, so discuss the FMLA with your employer. You can also talk with your employer about caregiving demands and how you can meet them through changes at work such as:
What is the best way for caregivers to work with the hospice staff? Caregivers and loved ones are a vital part of the hospice team. The hospice staff will be there every step of the way to help provide this care. Some tips for working well together include:
The hospice staff should respectfully listen to you and respond quickly at any hour of the day or night. This includes making home visits at any time to address symptoms or issues that develop. Be sure you keep the 24-hour emergency number for hospice in a visible place for all caregivers and loved ones. Loved ones and caregivers work with the hospice staff to keep the patient as comfortable as possible. The hospice personnel may help set up a space in the home for ease of care. They arrange for equipment and supplies that are needed to care for the patient such as:
A caregiver will usually be responsible for keeping track of many kinds of information. This includes setting up and maintaining a recordkeeping and organizing system that will help to make life as a caregiver easier. Some people are able to organize all of these tasks and schedules by themselves, but many people need help. Hospice staff can help assist to set up an organizational system that will work for you. Serving as a caregiver during hospice care can be a very loving and fulfilling experience. Many who have worked with hospice programs describe the experience as the most meaningful and rewarding work they could have done. However, there may also be unexpected challenges that come with this experience. Caregiving for a loved one who is dying can be very different than caring for someone who has a chronic (ongoing) illness. A patient with advanced cancer usually has a variety of symptoms that caregivers try to manage, and care needs will probably increase slowly over time. Caregivers must take care of themselves or they will not be able to care for the patient when he or she may need the most care. Some ways to make caregiving easier include:
What are the responsibilities of a caregiver during advanced cancer? Hospice staff can be called 24 hours a day to answer questions. They are also available to make in-home visits at any time of the day or night to address pain or other issues that might develop. The hospice team will work with the patient and family to create a care plan that is based on specific needs. The care plan includes a schedule of visits from the hospice team members, and it will be changed as needs change. Many memories are created during the hospice journey. Keep this in mind as plans are made for end-of-life care. The following is a typical example of scheduled home hospice visits:
Every caregiving experience is unique. However, caregivers may be required to provide a variety of care tasks including: Physical care Research shows that families find personal care to be the most physically and emotionally challenging aspect of caregiving. For some families this is satisfying and rewarding. For those who are not comfortable providing this care or need extra help, hired private home health aides can help caregivers. Hospice does not pay for such private care, so these are out-of-pocket expenses for the survivor and/or family. If possible, find people to perform different tasks that the patient is comfortable with. Also, talk with family members and friends to determine who is comfortable performing tasks such as:
Emotional care
Practical care
What types of assistance are available from hospice programs? Hospice services can help with everything from insurance and other financial matters to routine chores. Some hospice organizations provide light housekeeping as part of their covered services. The hospice staff will provide information about things to do to keep the patient comfortable. Needs will change over time, and hospice will help you understand and watch for these changes. If you have any questions, you can contact a member of the hospice staff at any time. A hospice social worker can help with many practical concerns such as:
Caregivers also need breaks (respite) to avoid physical and emotional exhaustion. Respite care services can provide this type of relief for caregivers for up to five days. Hospice benefits pay for the patient to be cared for outside the home (at a nursing facility or other residential care facility) during respite care for the main caregiver. During this time, the caregiver can visit the patient. Talk with the hospice staff as soon as possible about arranging for this type of break because respite care may not be available immediately. Why are advance directives important for hospice patients? Advance directives can be provided to family and physicians to advise them of a patient’s care preferences. They include a Living Will, a Medical Power of Attorney, and a Do Not Resuscitate (DNR) order. Ask the health care team or hospice staff to talk with you about the benefits and risks of each type of directive. Hospice programs do not require these directives. However, they support the right of patients to make their own decisions about care. Advance directives give patients the control and legal ability to state how they want to be cared for and who they want to make decisions for them if they ever become unable to communicate their wishes. These directives specify the types of medical support wanted by the patient including the use of feeding tubes, breathing machines, and provision of cardiopulmonary resuscitation (CPR). Advance directives are prepared at the patient’s request and must be signed by him or her before they are given to the health care team. The patient decides what will be included in each document. If he or she becomes unable to clearly communicate his or her wishes for care, certain family members can complete these documents on the patient’s behalf. If advance directives have not been completed at the time of hospice admission, and the patient would like to complete them, the staff can help to arrange for and finalize these documents. Each option will be clearly explained so that the patient can make informed decisions. Advance directives and DNR orders can be changed or cancelled by the patient at any time. Advance directive forms that are approved for your State can be downloaded at www.caringinfo.org How can hospice staff and caregivers help manage pain? As a loved one’s illness progresses, caregivers may spend a lot of time and energy trying to manage symptoms that keep changing. People living with advanced cancer may experience many different symptoms. The hospice staff will tell you what changes or symptoms you need to watch for. Remember that all difficult symptoms can be relieved either somewhat or completely, so be sure to ask your hospice team for help. Different medications are often given around the clock to relieve symptoms. Sometimes, treating one symptom can cause others to appear. Caregivers will be observing and discussing changes with the hospice staff while working to relieve physical discomfort the patient may have. Some people experience little or no pain at the end of life. For others, pain may be constant and intense. Pain that cannot be relieved at least a little bit is rare. Hospice physicians and nurses are experts in using the most advanced pain control methods available. The hospice nurse will advise about what symptoms to track and discuss with the hospice staff. Use a notebook to write down and describe in detail such things as symptom changes, including different levels of pain, new symptoms, responses to treatments and other changes as instructed by hospice staff. Pain medications are generally taken by mouth, usually on an around-the-clock basis to control the pain and prevent new pain from appearing. If swallowing becomes difficult, medicines may be given in various other ways including in small amounts of concentrated medicine under the tongue or inside the cheek, by suppository, by skin patch, or through a feeding tube (if there is one). Breathing and relaxation exercises may also be used when appropriate What types of emotional and spiritual support are available to caregivers? Being a caregiver can affect you both physically and emotionally. You may have trouble sleeping, which can lead to fatigue. The fatigue, in turn, can make negative feelings worse and even result in your own depression. Caregivers or loved ones who become emotionally overwhelmed may be helped by the hospice social worker or by a referral to a therapist. Patients and their loved ones are welcome to talk about how you are feeling with the hospice nurse, social worker and chaplain. Because caregiving is such a big job, caregivers need to take care of themselves to avoid becoming exhausted. In some cases, home care may not be possible. Try to be clear in your own mind what loved ones and caregivers want to do and are realistically able to do. Then work with the hospice staff to develop a plan for what is best for everyone involved. Take care of yourself during this time, and try to avoid worrying about what you think you should do--or what other people might expect you to do. What emotions are common for loved ones and caregivers? When hospice care is started, many caregivers and loved ones feel overwhelmed by the fact that the end of life may be near for someone they love. There may be many types of emotions, both expected and unexpected, that come and go unexpectedly. Over time, there may be a realization that the patient is not going to get better despite your best care. This may bring feelings of frustration, anger, sadness, grief and loss. During advanced cancer, the final months, weeks and days are likely to be very emotional for everyone. Some people are able to use their remaining time together to grow closer. They celebrate the life they have shared by talking, laughing, telling stories and being open about their feelings--perhaps as never before. Everyone deals with dying and death differently. There is no wrong or right way. As you deal with advanced cancer, it is important to allow yourself to express your sadness, grief and acceptance with your loved ones and others you trust. These types of symptoms are common and part of the process that both the patient and caregivers go through. The following emotions are common to those dealing with advanced cancer:
It is very difficult to determine what another person is thinking or feeling. However, most emotional changes are accompanied by physical changes that should be watched for and discussed with the hospice staff, including:
Keep in mind that pain problems can lead to or worsen emotional issues for patients. Certain medications can sometimes cause emotional symptoms to occur. The hospice nurse will help you understand what to do to keep the patient as comfortable as possible Ignoring feelings can be harmful. Expressing and sharing them can be freeing. Find someone to talk with and cry with--someone who will just listen and not judge you for how you are feeling. Do what is right for you, and trust yourself to know what you need. You may find comfort in talking with the hospice chaplain, your own spiritual advisor, or an oncology social worker or other counselor. Caring for a loved one who is nearing death can be an important time of growth for caregivers. It may also help with the grieving process after death. The experience can bring a deep sense of joy and satisfaction in having helped to make a loved one’s last days happier and more peaceful. The final phase of your loved one’s cancer journey may be the most intense experience of your life. As a caregiver, you have provided a very loving gift by making sure that the person you love dies with peace and dignity. Hospice provides families and loved ones with bereavement support free of charge for one year after a death. During this time, the program may stay in touch through letters and phone calls on a regular basis. Many hospices offer grief support groups and some offer individual counseling. Some hospice programs offer special memorial services for those who have lost loved ones. How are hospice care services paid for? Most health insurers have a hospice benefit that pays for all or most of the costs associated with the types of hospice care listed below. This means that families usually pay very little, and often nothing, for this end-of-life care. Some costs are not covered by insurers when hospice care is given in a retirement or nursing facility such as rent, meals and routine care services provided by the facility. Hospice benefits typically pay for:
Insurers that provide a hospice benefit include:
If the patient does not have or qualify for any form of health insurance, some hospices may still be able to provide services at little or no cost. Talk with several hospice organizations to find out what is available. If outside help is hired, such as home health aides, prepare a list of duties so the workers will know exactly what you expect of each of them. Hospice does not pay for the services of private professionals that you hire. This document was produced in collaboration with: Betty R. Ferrell, PhD, RN, FAAN, Cancer Survivorship Consultant Caroline Huffman, LCSW, MEd, Survivorship Program Manager, Lance Armstrong Foundation Jennifer Zieger, MPH, Pancreatic Cancer Action Network Works cited: American Cancer Society. When the Focus Is on Care: Palliative Care and Cancer. Eds. Kathleen M. Foley, MD et. al. National Consensus Project for Quality Palliative Care. Clinical Practice Guidelines for Quality Palliative Care. May 2004. “Choosing a Hospice.” NHPCO.org. 2005. National Hospice and Palliative Care Organization Caring Connections Program. “All About Hospice: A Consumer’s Guide.” Hospice-america.org. 2005. Hospice Association of America. “Hospice Care.” PLWC.org. 2005. People Living With Cancer. “What Does Someone Dying Need?” Hospicenet.org. 2005. Hospice Net. “The Hospice Choice” MMHospital.org. 2005. Marietta Memorial Hospital. “Knowing What to Expect Helps You Help Your Care Recipient” Caregiving.com. 2005. Caregiving.com. Byock, Ira R. “Hospice and Palliative Care: A Parting of the Ways or a Path to the Future?” Journal of Palliative Medicine 2 (1998): 165-176. What Hospice Care Means for Caregivers: SuggestionsThe suggestions that follow are based on the information presented in the Detailed Information document. They are meant to help you take what you learn and apply the information to your own needs. This information is not intended nor should it be interpreted as providing professional medical, legal and financial advice. You should consult a trained professional for more information. Please read the Additional Resources document for links to more resources. Things to consider before becoming a caregiver:
The hospice staff visits the home only several hours a week. You will be responsible for your loved one’s care for the rest of the time. Be sure you are able and willing to provide this care. Ask yourself the following questions:
How to find a hospice provider: Questions to ask prospective hospice providers:
Recordkeeping and Organization Tips for Caregivers Caregivers need to keep track of many types of information. Hospice staff will help you develop an organization system that works for you. Here are some ideas that may help you get started.
End-of-Life Comfort Care The following are some things you can do to keep your loved one comfortable during end-of-life care. The hospice staff can provide more information to you about providing physical care and emotional support.
When your loved one is no longer able to communicate:
Caring for the Caregiver While you are taking care of your loved one, you will need to take care of yourself as well. If you become physically or emotionally exhausted, you will be less able to help your loved one. Do things to take care of yourself in the different areas of your life such as:
What Hospice Care Means for Caregivers: Additional Resources
The resources listed below provide more detailed information and support services to help you with hospice care. Please read the Detailed Information and Suggestions document for more information and questions to ask. LIVESTRONG SurvivorCare Program
LIVESTRONG SurvivorCare offers assistance to anyone affected by cancer, including the person diagnosed, loved ones, caregivers and friends. The program provides information about treatment options and matching to clinical trials or treatments in development. Counseling services and assistance with financial, employment and insurance issues are also available. To provide these services, LIVESTRONG SurvivorCare has partnered with several organizations including CancerCare, Patient Advocate Foundation and EmergingMed. American Cancer Society
The American Cancer Society (ACS) offers information about many of the challenges of cancer and survivorship. You can search for information by cancer type or by topic. ACS provides a list of support groups in your area. You can join online groups and message boards. Some information on the website is available in Spanish, Chinese, Korean and Vietnamese. ACS specialists can answer questions 24 hours a day by phone or email. National Consensus Project for Quality Palliative Care
The National Consensus Project (NCP) is a joint effort among four organizations: the American Academy of Hospice and Palliative Medicine, the Center to Advance Palliative Care, the Hospice and Palliative Nurses Association, and the National Hospice and Palliative Care Organization. These groups worked together to develop the Clinical Practice Guidelines for Quality Palliative Care available for free download). They are now working to increase awareness of palliative care and to raise public understanding of the need for such care. Through the NCP Website, survivors can learn more about what palliative care is, as well as how these organizations are working to advance the quality of palliative care. National Hospice and Palliative Care Organization
This organization offers information about pain management, advance directives, caregiving, grief, and choosing a hospice facility. Publications cover topics such as planning and communicating end-of-life wishes. Financial planning information includes ways to pay for hospice care. You can request information about your state’s laws and requirements for advance directives. The site also helps you find hospice programs in your community. Some information is available in Spanish. U.S. Institutes of Health - National Cancer Institute (NCI)
The National Cancer Institute’s website provides accurate information about the challenges cancer can bring. You can search for information by cancer type or topic. You can find information about treatment, financial and insurance matters. You can also learn how treatments in development work and search for a clinical trial in your area. This site also has a good dictionary of cancer terms, drug information and other publications. Cancer information specialists can answer your questions about cancer and help you with quitting smoking. They can also help you with using this Web site and can tell you about NCI's printed and electronic materials. The knowledgeable and caring specialists have access to comprehensive, accurate information on a range of cancer topics, including the most recent advances in cancer treatment. The service is confidential, and information specialists spend as much time as needed for thorough and personalized responses. Quality of Life and Palliative CarePalliative care is any type of care that is meant to relieve the symptoms or problems caused by cancer or other diseases. Although this type of care was once more commonly associated with end of life, the goal of palliative care is to relieve physical, emotional and practical concerns at all stages of illness. Understanding what palliative care is and how you can get this type of care can help you improve your quality of life at any stage of survivorship. Quality of Life and Palliative Care: Detailed InformationThis information is meant to be a general introduction to this topic. The purpose is to provide a starting point for you to become more informed about important matters that may be affecting your life as a survivor and to provide ideas about steps you can take to learn more. This information is not intended nor should it be interpreted as providing professional medical, legal and financial advice. You should consult a trained professional for more information. Please read the and Additional Resources documents for questions to ask and for more resources. The term palliative (pronounced PAL-yah-tiv) is used to describe health care that is meant to relieve the symptoms of a disease rather than to cure it. It focuses on comfort and quality of life. Cancer treatments are designed to cure or control cancer. Palliative care can be given at the same time as treatments or at any time after a cancer diagnosis. Life during and after cancer treatment may require ongoing care and attention to help you feel your best in every area of your life. Palliative care focuses on the total well-being of a patient. It respectfully addresses and treats physical, emotional, social, spiritual, and financial needs from the time of diagnosis through the end of life. This document describes how palliative care can improve the overall quality of life. The information will help you:
Who can benefit from palliative care? Palliative care may be appropriate and beneficial at any stage of the cancer journey including for those survivors who:
Some health care professionals may think of palliative care only as the care given to those nearing end of life. This is because, in the past, the term palliative care was focused on hospice care and improving the physical comfort of survivors nearing the end of life. It also included addressing the emotional and spiritual needs of the patient and his or her loved ones. While palliative care still includes hospice and end-of-life care, it now also includes care for people at all stages of life-altering illnesses. What you call this type of care is not as important as getting the care you need. Your health care team may not use the term palliative care to describe post-treatment services. Other terms may be used to define this type of care such as whole-person care, comfort-oriented care or supportive care. What guidelines exist for palliative care? Palliative care focuses on preventing, treating, reducing or removing discomfort whenever and however it appears. The quality of life is given more importance than focusing only on the length of life.The personal satisfaction of the patient with how he or she feels and lives defines quality of life. Getting the help you need for any concern you have will help you create a high quality of life. The National Consensus Project (NCP) for Quality Palliative Care has created a set of accepted professional guidelines that define palliative care and provide guidance to health care professionals. You can download a copy of the most current set of guidelines by visiting http://www.nationalconsensusproject.org. The NCP guidelines are meant to help relieve suffering and provide support for survivors to enjoy the best possible quality of life at all stages of living with cancer. They focus on preventing, evaluating and treating pain and other physical, emotional and spiritual concerns. These guidelines address specific areas of care including physical, psychosocial, cultural, spiritual, ethical and legal. The goal is to provide patient and family-centered care by putting survivors and their loved ones first while addressing and respecting individual needs and wishes. Who provides palliative care services? Palliative care generally involves a team approach that can include the services of a variety of health care and other professionals for physical, emotional, spiritual and practical concerns. These services may be delivered in and continued across various settings at different times. This is known as continuity of care. These settings can include the following:
The followng tables cite the types of professionals who provide services and an overview of their roles. Physical Well-Being
Always check with your health care team before starting any approach that includes a change in physical treatment such as exercise, massage or physical therapy, medication, herbs and vitamins. Emotional, Social, Spiritual Well-Being
Assistance with Practical Concerns
When might palliative care be needed? Palliative care may be given during treatment and at any time after. The needs of survivors change over time, and no two will have exactly the same experience. Some may complete treatment and continue life with few or minor changes. Other survivors might face physical or emotional challenges that begin immediately or many years after treatment. Palliative care is appropriate whenever you need it–now or in the future. You have the right to ask for the help you need throughout your survivorship at any time during your cancer journey. At the time cancer is diagnosed and during treatment, palliative care may include:
After cancer treatment, palliative care can provide:
End-of-life palliative care provided by hospice may include:
Various types of palliative care are available to address individual needs. Work closely with your health care team to learn what options may be appropriate for you. The following is a partial list of palliative care options you and your health care team may decide to explore in various areas of your life:
How can you talk with your health care team about palliative care? Start by finding out if your health care team can provide palliative care service. If you have not yet started cancer treatment, ask about treatment options and what side effects and late effects are possible. Ask if there is anything they can do to help you prevent or prepare for possible adverse effects. Anytime, during or after treatment, it is important to let your health care team know how about your feelings and concerns. They can help you with your symptoms or refer you to a professional specialist for help that is right for you. This document was produced in collaboration with: Betty Ferrell, R.N., Ph.D., Cancer Survivorship Consultant Works Cited National Consensus Project for Quality Palliative Care. Clinical Practice Guidelines for Quality Palliative Care. Second Edition, March 2009. Quality of Life and Palliative Care: SuggestionsThe suggestions that follow are based on the information presented in the Detailed Information document. They are meant to help you take what you learn and apply the information to your own needs. This information is not intended nor should it be interpreted as providing professional medical, legal and financial advice. You should consult a trained professional for more information. Please read the Additional Resources document for links to more resources. Keep a written record of all of your symptoms and concerns. During and after treatment, be aware of the changes in your day-to-day physical and emotional health. Keep your health care team informed about changes that affect your overall well-being and ability to go about your daily routines. Telling your health care team about all of the physical and emotional symptoms you are experiencing is very important to getting the right health care. However, describing your symptoms and concerns can be difficult. Writing this information down before your health care team visit can help you organize your thoughts and make sure that you talk about important information. Ask your health care team about palliative care for different areas of your life such as: Physical concerns Before cancer treatment
During cancer treatment
After cancer treatment
Emotional concerns
Practical concerns
Quality of Life and Palliative Care: Additional ResourcesThe resources listed below provide more detailed information and support services to help you with palliative care. Please read the Detailed Information and Suggestions document for more information and questions to ask. LIVESTRONG SurvivorCare Program
LIVESTRONG SurvivorCare offers assistance to anyone affected by cancer, including the person diagnosed, loved ones, caregivers and friends. The program provides information about treatment options and matching to clinical trials or treatments in development. Counseling services and assistance with financial, employment and insurance issues are also available. To provide these services, LIVESTRONG SurvivorCare has partnered with several organizations including CancerCare, Patient Advocate Foundation and EmergingMed. American Cancer Society
The American Cancer Society (ACS) offers information about many of the challenges of cancer and survivorship. You can search for information by cancer type or by topic. ACS provides a list of support groups in your area. You can join online groups and message boards. Some information on the website is available in Spanish, Chinese, Korean and Vietnamese. ACS specialists can answer questions 24 hours a day by phone or email. National Consensus Project for Quality Palliative Care
The National Consensus Project (NCP) is a joint effort among four organizations: the American Academy of Hospice and Palliative Medicine, the Center to Advance Palliative Care, the Hospice and Palliative Nurses Association, and the National Hospice and Palliative Care Organization. These groups worked together to develop the Clinical Practice Guidelines for Quality Palliative Care available for free download). They are now working to increase awareness of palliative care and to raise public understanding of the need for such care. Through the NCP Website, survivors can learn more about what palliative care is, as well as how these organizations are working to advance the quality of palliative care. National Hospice and Palliative Care Organization
This organization offers information about pain management, advance directives, caregiving, grief, and choosing a hospice facility. Publications cover topics such as planning and communicating end-of-life wishes. Financial planning information includes ways to pay for hospice care. You can request information about your state’s laws and requirements for advance directives. The site also helps you find hospice programs in your community. Some information is available in Spanish. U.S. Institutes of Health - National Cancer Institute (NCI)
The National Cancer Institute’s website provides accurate information about the challenges cancer can bring. You can search for information by cancer type or topic. You can find information about treatment, financial and insurance matters. You can also learn how treatments in development work and search for a clinical trial in your area. This site also has a good dictionary of cancer terms, drug information and other publications. Cancer information specialists can answer your questions about cancer and help you with quitting smoking. They can also help you with using this Web site and can tell you about NCI's printed and electronic materials. The knowledgeable and caring specialists have access to comprehensive, accurate information on a range of cancer topics, including the most recent advances in cancer treatment. The service is confidential, and information specialists spend as much time as needed for thorough and personalized responses. |
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