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Normal Adjustment and the Adjustment Disorders (PDQ®)     
Last Modified: 05/20/2008
Patient Version
Table of Contents

Introduction
Normal Adjustment
General Factors Influencing Adjustment
Specific Influences on Adjustment
        Hearing the Diagnosis
        Cancer Treatments
        Post-Treatment
        The Return of Cancer
        Survivorship
Psychological and Social Distress
Screening
Psychological and Social Assessment
Psychological and Social Therapies for Distress
The Adjustment Disorders
Treatment
        Individual and Group Counseling and Psychotherapy
        Medications
Get More Information From NCI
Changes to This Summary (05/20/2008)
Questions or Comments About This Summary
About PDQ

Introduction

This patient summary on normal adjustment and the adjustment disorders is adapted from a summary written for health professionals by cancer experts. This and other credible information about cancer treatment, screening, prevention, supportive care, and ongoing clinical trials, is available from the National Cancer Institute. Most patients with cancer experience a variety of emotional responses, however, they do not have signs and symptoms of any specific mental disorder. Psychological and social distress can be experienced at many levels ranging from normal adjustment to adjustment disorders to major mental disorders (for example, major depressive disorder). This brief summary describes normal adjustment issues, psychological and social distress, and the adjustment disorders. (Refer to the PDQ summaries on Anxiety Disorders 1 and Depression 2 for more information.)

Normal Adjustment

Adjusting to cancer is an ongoing process in which the patient learns to cope with emotional distress, solve cancer-related problems, and gain control over cancer-related life events. Patients are faced with many challenges that change as the disease and its treatment change. Common periods of crisis and significant challenge include hearing the diagnosis, receiving treatment (for example, surgery, radiation therapy, and chemotherapy), completing treatment, hearing that the cancer is in remission, hearing that the cancer has come back, and becoming a cancer survivor. Each of these events involves specific coping tasks, questions about life and death, and common emotional problems.

Patients are better able to adjust to a cancer diagnosis if they are able to continue fulfilling normal responsibilities, cope with emotional distress, and stay actively involved in activities that are meaningful and important to them.

Coping is the use of thoughts and behaviors to adjust to life situations. A person's coping style is usually related to his or her personality (for example, always expecting the best, always expecting the worst, being shy or reserved, or being outgoing).

Coping strategies are thoughts and behaviors that are used in rare situations, for example, when one must change his or her daily routine or work schedule to adjust to the side effects of cancer treatment. Developing coping strategies can help a patient learn how to change problem situations, manage emotional distress, and understand why cancer has happened and what impact cancer may have on his or her life. Patients who adjust well are usually committed and actively involved in coping with cancer. They are still able to find meaning and importance in their lives. Patients who do not adjust well become less involved with coping, withdraw, and feel hopeless. Studies are looking at how different types of coping strategies affect the quality of life for cancer survivors.

Distress can occur when a person feels that he or she does not have the resources to manage or control the cancer. Distress experienced by patients who have the same diagnosis and are undergoing the same treatment may be very different. A doctor or health care professional can help the patient adjust to the treatment schedule and/or help the patient cope with treatment by, for example, providing medication for nausea.

General Factors Influencing Adjustment

Many individual differences affect how a patient adjusts to cancer. It is difficult to predict how a person will cope with cancer. The following factors influence how a patient adjusts to cancer:

  • The type of cancer, cancer stage, and chance of recovery.


  • The phase of cancer such as newly diagnosed, being treated, in remission, or recurrent cancer.


  • Individual coping abilities.


  • Whether or not the patient tends to focus on the most hopeful side of situations.


  • Friends and family available to support the patient.


  • The patient's age.


  • The availability of treatment.


  • Beliefs about the cause of cancer.


Specific Influences on Adjustment

Hearing the Diagnosis

The process of adjusting to cancer can begin even before hearing the diagnosis. Patients may experience normal levels of fear, worry, and concern when they have unexplained symptoms or are undergoing testing to determine if they have cancer. When a patient hears the diagnosis of cancer, many patients wonder, "Could I die from this?"

Receiving a diagnosis of cancer can cause expected and normal emotional distress. Some patients may feel disbelief and ask, "Are you sure you have the right test results?" Most patients feel they are unable to think clearly. They may feel numb or in shock, or as if "This can't be happening to me." Many patients may not understand or remember important information that the doctor gave them about the diagnosis and treatment options. Patients should have a way to review this information by having someone with them at appointments, requesting that the session be taped, or by requesting a second appointment to ask the doctor questions and go over the treatment plan. As the patient gradually accepts the reality of the diagnosis, he or she may begin to experience depression, anxiety, lack of appetite, inability to sleep, poor concentration, and varying degrees of inability to function in daily activities. There can be high levels of stress for newly diagnosed patients awaiting surgery. Extra professional support to help deal with problems such as fatigue, insomnia, and depressed mood can be helpful during this time. When the patient receives and understands information about treatment options, he or she may gradually feel more hopeful and optimistic. Eventually, patients develop ways to cope and to adjust to the cancer diagnosis.

Cancer Treatments

When cancer treatment begins, patients may experience fears about painful procedures, unwanted side effects (for example hair loss, nausea and vomiting, fatigue, pain), and interruptions to normal activities and responsibilities (for example being unable to work). Patients who can weigh the discomforts of short-term loss against the benefits of long-term gain (for example living longer) and decide, "It's worth it" usually adjust well. Questions that patients may ask during treatment include, "Will I survive this?"; "Will they get it all?"; or "What side effects will I experience?" As these questions arise, patients will learn to adjust with them. Developing ways to cope with specific problems (for example fatigue, transportation to treatment, and work schedule changes) is helpful.

Post-Treatment

Completing cancer treatment can cause mixed feelings. It may be a time of celebration and relief or a time of increased anxiety with awareness that the cancer could return once the treatment is stopped. Patients who can balance their positive expectations with the realities of ongoing fears adjust well. Many patients experience increased anxiety and fear of the cancer returning as they have less frequent contact with their physician. Other adjustment concerns include living with uncertainty, resuming previous responsibilities, and being overly concerned about health. During remission, patients often experience normal anxiety and worry as the dates of regular follow-up appointments with their oncologist approach with the possibility that the cancer has returned.

A study of women with early-stage breast cancer suggests that patients who have more physical symptoms and side effects during treatment are more likely to have distress following treatment.

Normal adjustment to post-treatment and remission may involve using the following coping strategies to help control normal emotional distress:

  • Being honest with one's emotions.
  • Being aware of one's feelings and able to express them to others.
  • Having a nonjudgmental acceptance of one's feelings and a willingness to work through these emotions.
  • Having support from others who are willing to listen and accept.

Patients who can express a wide range of both positive and negative emotions usually adjust well.

The Return of Cancer

Changing from a treatment plan that focuses on curing the cancer to one that provides comfort and relief of symptoms can cause extreme anxiety. Patients may experience shock, disbelief, and denial followed by a period of significant distress (for example, depressed moods, difficulty concentrating, and frequent thoughts of death). Normal adjustment may include periods of sadness and crying, feelings of anger at God or a higher power, periods of withdrawal and isolation, and thoughts of giving up. Patients gradually adjust to the return of cancer over a period of weeks by changing expectations from curing to healing. Healing is a process of "becoming whole again" by transforming one's life in many ways in the face of death. It is very important that the patient maintain hope throughout this process. Patients who believe that pain and suffering can be controlled will have hope for future quality of life. Those who believe they are loved and cared for will have hope in future relationships. Religion and spirituality are very important in helping patients maintain hope.

Survivorship

The adjustment from completing cancer treatment to a long-term survivorship is a gradual process that extends over many years. Some common problems reported by cancer survivors as they face the future include fear of the cancer coming back, lasting physical effects such as tiredness, problems sleeping, and concerns about sexual function. Most patients adjust well and some even report benefits of having cancer such as a greater appreciation of life, changes in life values, and stronger spiritual or religious beliefs. Patients who do not adjust well usually have more medical problems, fewer friends and family who provide support, fewer financial resources, and problems with psychological adjustment unrelated to the cancer.

Psychological and Social Distress

Most patients experience some level of distress, however, only a small percentage receive help. Distress is an unpleasant emotional, psychological, social, or spiritual experience that interferes with the patient's ability to cope with cancer treatment. Patients may experience a range of feelings from normal sadness and fear to deep depression, anxiety, panic, or isolation. These feelings can interfere with a person's ability to relate to family, friends, coworkers, and others during the normal routines of daily living. This is called social distress.

Screening

Health care professionals may have patients complete questionnaires periodically to identify the need for referral to a mental health professional. Key times that distress may become disabling include the time of diagnosis, during cancer treatment, at the end of a long course of treatment, during remission, when the cancer returns, or when beginning palliative care. Patients who are experiencing mild distress may benefit from a referral to a self-help group. Patients who are experiencing moderate to severe distress may require a referral to a mental health professional such as a psychiatrist, psychologist, social worker, or pastoral counselor.

Psychological and Social Assessment

It is important that patients understand the benefits of talking with a mental health professional about their concerns and worries. A patient can expect the health professional to:

  • Listen closely to his or her concerns.
  • Show an interest in his or her experiences with cancer.
  • Ask about his or her family, friends, and other persons who provide support.
  • Ask how he or she has been adjusting to the cancer.
  • Encourage him or her to continue using coping strategies that are successful.
  • Suggest other coping strategies to address his or her concerns.

Patients will be encouraged to continue counseling or psychotherapy as needed.

Psychological and Social Therapies for Distress

Recent studies of psychological and social therapies have shown benefits for cancer patients. These therapies are defined as non- drug treatments offering psychological and educational support, such as:

These therapies may be combined in different ways for various lengths of time, in both individual and group formats. To date, these therapies have most commonly been studied in white, middle-to-higher income American women with breast cancer, though they are currently being studied in more patient groups. Cancer patients who receive such therapies show positive benefits compared to those who do not, including lower levels of depression, anxiety, and disease-related symptoms, as well as improved immune system functioning and health habits like exercise. The size of these benefits and how they affect patients' recovery will need more study.

The Adjustment Disorders

Adjustment disorders include behaviors or moods more extreme than expected in reaction to a cancer diagnosis, treatment, recurrence or side effects. These behaviors or moods may result in significant problems in functioning with family, friends, and at work. An adjustment disorder usually begins within three months of the first signs of distress, for example a cancer diagnosis. Some patients may develop a chronic adjustment disorder because they experience multiple causes of distress, one right after another (for example, the cancer diagnosis, the start of treatment, side effects of treatment, completion of treatment, and returning to work). Chronic adjustment disorders may become a more serious mental disorder (for example major depression). This is more common in children and adolescents than in adults.

Treatment

Individual and Group Counseling and Psychotherapy

Treatment that focuses on the patient's thoughts, feelings, and behaviors may be used to relieve emotional distress in individual patients or groups. The following are examples of these techniques:

Medications

Counseling or psychotherapy should be tried before medication. If the patient does not improve with short-term psychotherapy or develops a more severe mental disorder, such as depression, the doctor will then prescribe the appropriate medication. (Refer to the PDQ summaries on Depression 2 and Anxiety Disorder 1 for more information.)

Get More Information From NCI

Call 1-800-4-CANCER

For more information, U.S. residents may call the National Cancer Institute's (NCI's) Cancer Information Service toll-free at 1-800-4-CANCER (1-800-422-6237) Monday through Friday from 9:00 a.m. to 4:30 p.m. Deaf and hard-of-hearing callers with TTY equipment may call 1-800-332-8615. The call is free and a trained Cancer Information Specialist is available to answer your questions.

Chat online

The NCI's LiveHelp® 3 online chat service provides Internet users with the ability to chat online with an Information Specialist. The service is available from 9:00 a.m. to 11:00 p.m. Eastern time, Monday through Friday. Information Specialists can help Internet users find information on NCI Web sites and answer questions about cancer.

Write to us

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NCI Public Inquiries Office
Suite 3036A
6116 Executive Boulevard, MSC8322
Bethesda, MD 20892-8322

Search the NCI Web site

The NCI Web site 4 provides online access to information on cancer, clinical trials, and other Web sites and organizations that offer support and resources for cancer patients and their families. For a quick search, use our “Best Bets” search box in the upper right hand corner of each Web page. The results that are most closely related to your search term will be listed as Best Bets at the top of the list of search results.

There are also many other places to get materials and information about cancer treatment and services. Hospitals in your area may have information about local and regional agencies that have information on finances, getting to and from treatment, receiving care at home, and dealing with problems related to cancer treatment.

Find Publications

The NCI has booklets and other materials for patients, health professionals, and the public. These publications discuss types of cancer, methods of cancer treatment, coping with cancer, and clinical trials. Some publications provide information on tests for cancer, cancer causes and prevention, cancer statistics, and NCI research activities. NCI materials on these and other topics may be ordered online or printed directly from the NCI Publications Locator 5. These materials can also be ordered by telephone from the Cancer Information Service toll-free at 1-800-4-CANCER (1-800-422-6237), TTY at 1-800-332-8615.

Changes to This Summary (05/20/2008)

The PDQ cancer information summaries are reviewed regularly and updated as new information becomes available. This section describes the latest changes made to this summary as of the date above.

Changes were made to this summary to match those made to the health professional version.

Questions or Comments About This Summary

If you have questions or comments about this summary, please send them to Cancer.gov through the Web site’s Contact Form 6. We can respond only to email messages written in English.

About PDQ

PDQ is a comprehensive cancer database available on NCI's Web site.

PDQ is the National Cancer Institute's (NCI's) comprehensive cancer information database. Most of the information contained in PDQ is available online at NCI's Web site 4. PDQ is provided as a service of the NCI. The NCI is part of the National Institutes of Health, the federal government's focal point for biomedical research.

PDQ contains cancer information summaries.

The PDQ database contains summaries of the latest published information on cancer prevention, detection, genetics, treatment, supportive care, and complementary and alternative medicine. Most summaries are available in two versions. The health professional versions provide detailed information written in technical language. The patient versions are written in easy-to-understand, nontechnical language. Both versions provide current and accurate cancer information.

The PDQ cancer information summaries are developed by cancer experts and reviewed regularly.

Editorial Boards made up of experts in oncology and related specialties are responsible for writing and maintaining the cancer information summaries. The summaries are reviewed regularly and changes are made as new information becomes available. The date on each summary ("Date Last Modified") indicates the time of the most recent change.

PDQ also contains information on clinical trials.

A clinical trial is a study to answer a scientific question, such as whether one method of treating symptoms is better than another. Trials are based on past studies and what has been learned in the laboratory. Each trial answers certain scientific questions in order to find new and better ways to help cancer patients. Some patients have symptoms caused by cancer treatment or by the cancer itself. During supportive care clinical trials, information is collected about how well new ways to treat symptoms of cancer work. The trials also study side effects of treatment and problems that come up during or after treatment. If a clinical trial shows that a new treatment is better than one currently being used, the new treatment may become "standard." Patients who have symptoms related to cancer treatment may want to think about taking part in a clinical trial.

Listings of clinical trials are included in PDQ and are available online at NCI's Web site 7. Descriptions of the trials are available in health professional and patient versions. Many cancer doctors who take part in clinical trials are also listed in PDQ. For more information, call the Cancer Information Service 1-800-4-CANCER (1-800-422-6237); TTY at 1-800-332-8615.



Glossary Terms

activities of daily living
ADL. The tasks of everyday life. These activities include eating, dressing, getting into or out of a bed or chair, taking a bath or shower, and using the toilet. Instrumental activities of daily living are activities related to independent living and include preparing meals, managing money, shopping, doing housework, and using a telephone. Also called ADL.
adjustment disorder (uh-JUST-ment dis-OR-der)
A condition in which a person responds to a stressful event (such as an illness, job loss, or divorce) with extreme emotions and actions that cause problems at work and home.
anxiety (ang-ZY-uh-tee)
Feelings of fear, dread, and uneasiness that may occur as a reaction to stress. A person with anxiety may sweat, feel restless and tense, and have a rapid heart beat. Extreme anxiety that happens often over time may be a sign of an anxiety disorder.
appetite (A-peh-tite)
A desire to satisfy a physical or mental need, such as for food, sex, or adventure.
biofeedback
A method of learning to voluntarily control certain body functions such as heartbeat, blood pressure, and muscle tension with the help of a special machine. This method can help control pain.
breast cancer (brest KAN-ser)
Cancer that forms in tissues of the breast, usually the ducts (tubes that carry milk to the nipple) and lobules (glands that make milk). It occurs in both men and women, although male breast cancer is rare.
cancer (KAN-ser)
A term for diseases in which abnormal cells divide without control. Cancer cells can invade nearby tissues and can spread to other parts of the body through the blood and lymph systems. There are several main types of cancer. Carcinoma is cancer that begins in the skin or in tissues that line or cover internal organs. Sarcoma is cancer that begins in bone, cartilage, fat, muscle, blood vessels, or other connective or supportive tissue. Leukemia is cancer that starts in blood-forming tissue such as the bone marrow, and causes large numbers of abnormal blood cells to be produced and enter the blood. Lymphoma and multiple myeloma are cancers that begin in the cells of the immune system. Central nervous system cancers are cancers that begin in the tissues of the brain and spinal cord.
chemotherapy (KEE-moh-THAYR-uh-pee)
Treatment with drugs that kill cancer cells.
chronic (KRAH-nik)
A disease or condition that persists or progresses over a long period of time.
clinical trial
A type of research study that tests how well new medical approaches work in people. These studies test new methods of screening, prevention, diagnosis, or treatment of a disease. Also called a clinical study.
cope (kope)
To adjust to new situations and overcome problems.
coping skills (KOH-ping skilz)
The methods a person uses to deal with stressful situations. These may help a person face a situation, take action, and be flexible and persistent in solving problems.
counseling (KOWN-suh-ling)
The process by which a professional counselor helps a person cope with mental or emotional distress, and understand and solve personal problems.
cure
To heal or restore health; a treatment to restore health.
denial (deh-NY-ul)
In psychiatry, a state in which a person is unable or unwilling to see the truth or reality about an issue or situation.
depression (dee-PREH-shun)
A mental condition marked by ongoing feelings of sadness, despair, loss of energy, and difficulty dealing with normal daily life. Other symptoms of depression include feelings of worthlessness and hopelessness, loss of pleasure in activities, changes in eating or sleeping habits, and thoughts of death or suicide. Depression can affect anyone, and can be successfully treated. Depression affects 15-25% of cancer patients.
diagnosis (DY-ug-NOH-sis)
The process of identifying a disease, such as cancer, from its signs and symptoms.
disorder (dis-OR-der)
In medicine, a disturbance of normal functioning of the mind or body. Disorders may be caused by genetic factors, disease, or trauma.
distraction
In medicine, a pain relief method that takes the patient's attention away from the pain.
distress (dih-STRESS)
Extreme mental or physical pain or suffering.
drug
Any substance, other than food, that is used to prevent, diagnose, treat or relieve symptoms of a disease or abnormal condition. Also refers to a substance that alters mood or body function, or that can be habit-forming or addictive, especially a narcotic.
early-stage breast cancer (ER-lee stayj brest KAN-ser)
Breast cancer that has not spread beyond the breast or the axillary lymph nodes. This includes ductal carcinoma in situ and stage I, stage IIA, stage IIB, and stage IIIA breast cancers.
fatigue
A condition marked by extreme tiredness and inability to function due lack of energy. Fatigue may be acute or chronic.
follow-up
Monitoring a person's health over time after treatment. This includes keeping track of the health of people who participate in a clinical study or clinical trial for a period of time, both during the study and after the study ends.
hypnosis
A trance-like state in which a person becomes more aware and focused and is more open to suggestion.
imagery (IH-mij-ree)
A technique in which the person focuses on positive images in his or her mind.
immune system (ih-MYOON SIS-tem)
The complex group of organs and cells that defends the body against infections and other diseases.
insomnia
Difficulty in going to sleep or getting enough sleep.
medication (MEH-dih-KAY-shun)
A legal drug that is used to prevent, treat, or relieve symptoms of a disease or abnormal condition.
mental health
A person’s overall psychological and emotional condition. Good mental health is a state of well-being in which a person is able to cope with everyday events, think clearly, be responsible, meet challenges, and have good relationships with others.
National Cancer Institute
The National Cancer Institute, part of the National Institutes of Health of the United States Department of Health and Human Services, is the Federal Government's principal agency for cancer research. The National Cancer Institute conducts, coordinates, and funds cancer research, training, health information dissemination, and other programs with respect to the cause, diagnosis, prevention, and treatment of cancer. Access the National Cancer Institute Web site at http://www.cancer.gov. Also called NCI.
nausea
A feeling of sickness or discomfort in the stomach that may come with an urge to vomit. Nausea is a side effect of some types of cancer therapy.
oncologist (on-KAH-loh-jist)
A doctor who specializes in treating cancer. Some oncologists specialize in a particular type of cancer treatment. For example, a radiation oncologist specializes in treating cancer with radiation.
palliative care (PA-lee-uh-tiv...)
Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of palliative care is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease, and psychological, social, and spiritual problems related to a disease or its treatment. Also called comfort care, supportive care, and symptom management.
panic (PA-nik)
Sudden extreme anxiety or fear that may cause irrational thoughts or actions. Panic may include rapid heart rate, flushing (a hot, red face), sweating, and trouble breathing.
pastoral counselor (PAS-tuh-rul KOWN-suh-ler)
A person who is trained to give spiritual and mental health advice.
PDQ
PDQ is an online database developed and maintained by the National Cancer Institute. Designed to make the most current, credible, and accurate cancer information available to health professionals and the public, PDQ contains peer-reviewed summaries on cancer treatment, screening, prevention, genetics, complementary and alternative medicine, and supportive care; a registry of cancer clinical trials from around the world; and directories of physicians, professionals who provide genetics services, and organizations that provide cancer care. Most of this information, and more specific information about PDQ, can be found on the NCI's Web site at http://www.cancer.gov/cancertopics/pdq. Also called Physician Data Query.
physician
Medical doctor.
prevention (pree-VEN-shun)
In medicine, action taken to decrease the chance of getting a disease or condition. For example, cancer prevention includes avoiding risk factors (such as smoking, obesity, lack of exercise, and radiation exposure) and increasing protective factors (such as getting regular physical activity, staying at a healthy weight, and having a healthy diet).
psychiatrist (sy-KY-uh-trist)
A medical doctor who specializes in the prevention, diagnosis, and treatment of mental, emotional, and behavioral disorders.
psychological (SY-koh-LAH-jih-kul)
Having to do with how the mind works and how thoughts and feelings affect behavior.
psychologist (sy-KAH-loh-jist)
A specialist who can talk with patients and their families about emotional and personal matters, and can help them make decisions.
psychotherapy (SY-koh-THAYR-uh-pee)
Treatment of mental, emotional, personality, and behavioral disorders using methods such as discussion, listening, and counseling. Also called talk therapy.
quality of life
The overall enjoyment of life. Many clinical trials assess the effects of cancer and its treatment on the quality of life. These studies measure aspects of an individual’s sense of well-being and ability to carry out various activities.
radiation therapy (RAY-dee-AY-shun THAYR-uh-pee)
The use of high-energy radiation from x-rays, gamma rays, neutrons, protons, and other sources to kill cancer cells and shrink tumors. Radiation may come from a machine outside the body (external-beam radiation therapy), or it may come from radioactive material placed in the body near cancer cells (internal radiation therapy). Systemic radiation therapy uses a radioactive substance, such as a radiolabeled monoclonal antibody, that travels in the blood to tissues throughout the body. Also called radiotherapy and irradiation.
recurrence (ree-KER-ents)
Cancer that has recurred (come back), usually after a period of time during which the cancer could not be detected. The cancer may come back to the same place as the original (primary) tumor or to another place in the body. Also called recurrent cancer.
recurrent cancer (ree-KER-ent KAN-ser)
Cancer that has recurred (come back), usually after a period of time during which the cancer could not be detected. The cancer may come back to the same place as the original (primary) tumor or to another place in the body. Also called recurrence.
relaxation technique
A method used to reduce tension and anxiety, and control pain.
remission
A decrease in or disappearance of signs and symptoms of cancer. In partial remission, some, but not all, signs and symptoms of cancer have disappeared. In complete remission, all signs and symptoms of cancer have disappeared, although cancer still may be in the body.
screening (SKREEN-ing)
Checking for disease when there are no symptoms. Since screening may find diseases at an early stage, there may be a better chance of curing the disease. Examples of cancer screening tests are the mammogram (breast), colonoscopy (colon), Pap smear (cervix), and PSA blood level and digital rectal exam (prostate). Screening can also include checking for a person’s risk of developing an inherited disease by doing a genetic test.
side effect
A problem that occurs when treatment affects healthy tissues or organs. Some common side effects of cancer treatment are fatigue, pain, nausea, vomiting, decreased blood cell counts, hair loss, and mouth sores.
social support (SOH-shul suh-PORT)
A network of family, friends, neighbors, and community members that is available in times of need to give psychological, physical, and financial help.
social worker
A professional trained to talk with people and their families about emotional or physical needs, and to find them support services.
spirituality (SPIR-ih-choo-A-lih-tee)
Having to do with deep, often religious, feelings and beliefs, including a person’s sense of peace, purpose, connection to others, and beliefs about the meaning of life.
stage
The extent of a cancer in the body. Staging is usually based on the size of the tumor, whether lymph nodes contain cancer, and whether the cancer has spread from the original site to other parts of the body.
supportive care
Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of supportive care is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease, and psychological, social, and spiritual problems related to a disease or its treatment. Also called palliative care, comfort care, and symptom management.
surgery (SER-juh-ree)
A procedure to remove or repair a part of the body or to find out whether disease is present. An operation.
survivor (ser-VY-ver)
One who remains alive and continues to function after overcoming difficulties or life-threatening diseases like cancer.
survivorship (ser-VY-ver-ship)
In cancer, survivorship covers the physical, psychosocial, and economic issues of cancer, from diagnosis until the end of life. It includes issues related to the ability to get health care and follow-up treatment, late effects of treatment, second cancers, and quality of life.
symptom
An indication that a person has a condition or disease. Some examples of symptoms are headache, fever, fatigue, nausea, vomiting, and pain.
therapy (THAYR-uh-pee)
Treatment.
vomit
To eject some or all of the contents of the stomach through the mouth.


Table of Links

1http://cancer.gov/cancertopics/pdq/supportivecare/anxiety/Patient
2http://cancer.gov/cancertopics/pdq/supportivecare/depression/Patient
3https://cissecure.nci.nih.gov/livehelp/welcome.asp
4http://cancer.gov
5https://cissecure.nci.nih.gov/ncipubs
6http://cancer.gov/contact/form_contact.aspx
7http://cancer.gov/clinical_trials