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Chemotherapy is often called just "chemo." It involves taking strong drugs
that kill cancer cells. The drugs are most commonly taken by mouth or given
by injection into the bloodstream. Chemo drugs can damage both healthy cells
and cancer cells. Cells most likely to be injured are bone marrow, hair, and
the lining of the digestive tract from the mouth all the way to the
rectum or anus.
Side effects will depend on what kind of chemo drugs you take and how you
take them. The following are common side effects of chemo that can cause
eating problems:
- loss of appetite
- changes in taste and smell
- mouth tenderness or sores
- nausea
- vomiting
- changes in bowel habits
- fatigue
- low white blood cell counts with the increased risk of infection
You may not have these side effects from chemotherapy, but if you do, be
sure to tell your doctor or nurse. They may suggest medicines, daily
self-care practices, and changes in diet to lessen eating-related side
effects you are having. While you're getting chemotherapy, eating well can
help you to:
- feel better
- keep up your strength and energy
- keep up your weight and your body’s store of nutrients
- tolerate treatment-related side effects
- decrease your risk of infection
- heal and recover faster
Nutrition suggestions for people getting chemotherapy
Most people get chemo at an outpatient center. It may take anywhere from a
few minutes to many hours.
Plan ahead and bring a light meal or snack in an insulated bag or small
cooler. Find out whether there is a refrigerator or microwave you can use.
Make sure you eat something before getting your treatment. Most people
find that a light meal or snack before chemotherapy is well tolerated.
You may be very tired while getting chemotherapy. Fatigue (tiredness or
lack of energy) is very common during chemotherapy. Unless you are given
other instructions, eat a balanced diet that includes protein (meat, milk,
eggs, and beans, lentils, and other legumes) to help boost your energy. Other
suggestions to reduce fatigue are to prioritize your activities, doing the
most important ones when you have the most energy, and to balance rest and
activity so that it does not interfere with nighttime sleep.
Don't be too hard on yourself if side effects make it hard to eat. Try
eating small, frequent meals or snacks. Go easy on fried or greasy foods.
These can be hard to digest. On days when you are feeling well and your
appetite is good, try to eat regular meals and snacks. Be sure to drink
plenty of water or liquids (eight to ten 8-oz glasses) each day.
Don’t be afraid to ask family and friends for help with grocery
shopping and fixing meals. If you have no one to help you, think about having
meals delivered to your home or eating a meal at a community or senior
center. To learn more about meal delivery and other services, contact
us or call us at 1-800-ACS-2345 for
resources in your area. You might also try your county assistance groups,
area churches, and social services.
Some side effects of chemotherapy go away within hours of getting
treatment. If your side effects persist, tell your health care team. Prompt
attention to nutrition-related side effects can help keep up your weight and
energy level and help you feel better.
If you are having appetite problems, nausea or vomiting, diarrhea, sore
mouth or throat, dry mouth, trouble swallowing, or changes in the taste or
smell of food, please refer to these sections in this guide for information
on how to help manage these side effects.
If you are having trouble eating and have been following a special eating
plan for diabetes or some other chronic health condition, talk to your
doctor, nurse, or dietitian about how best to change your eating habits while
you are getting chemotherapy.
Be sure that your doctor or nurse knows about your side effects so they
can prescribe any needed medicines. For example, there are effective
medicines to control nausea and vomiting or to treat diarrhea.
For more information on managing side effects of chemotherapy, ask the
American Cancer Society about Understanding
Chemotherapy: A Guide for Patients and Families.
Revised 02/04/2008
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