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Could I Have Lupus?
National Lupus Awareness Campaign
HHS Office on Women's Health
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Lupus
Publication Date: April 2009
The Many Shades of Lupus: Information for Multicultural Communities
If you have lupus, you probably have many questions. Lupus isn’t a simple disease with an easy answer. You can’t take a pill and make it go away. The people you live with and work with may have trouble understanding that you’re sick. Lupus doesn’t have a clear set of signs that people can see. You may know that something’s wrong, even though it may take a while to be diagnosed.
Lupus has many shades. It can affect people of different races, ethnicities, and ages, both men and women. It can look like different diseases. It’s different for every person who has it.
The good news is that you can get help and fight lupus. Learning about it is the first step. Ask questions. Talk to your doctor, family, and friends. People who look for answers are more likely to find them. This booklet can help you get started.
What Is Lupus?
Lupus is an autoimmune (AW-toe-ih-MYOON) disease. Your body’s immune system is like an army with hundreds of soldiers. The immune system’s job is to fight foreign substances in the body, like germs and viruses. But in autoimmune diseases, the immune system is out of control. It attacks healthy tissues, not germs.
You can’t catch lupus from another person. It isn’t cancer, and it isn’t related to AIDS.
Lupus is a disease that can affect many parts of the body. Everyone reacts differently. One person with lupus may have swollen knees and fever. Another person may be tired all the time or have kidney trouble. Someone else may have rashes. Lupus can involve the joints, the skin, the kidneys, the lungs, the heart and/or the brain. If you have lupus, it may affect two or three parts of your body. Usually, one person doesn’t have all the possible symptoms.
There are three main types of lupus:
- Systemic lupus erythematosus (eh-RITH-eh-muh-TOE-sus) is the most common form. It’s sometimes called SLE, or just lupus. The word “systemic” means that the disease can involve many parts of the body such as the heart, lungs, kidneys, and brain. SLE symptoms can be mild or serious.
- Discoid lupus erythematosus mainly affects the skin. A red rash may appear, or the skin on the face, scalp, or elsewhere may change color.
- Drug-induced lupus is triggered by a few medicines. It’s like SLE, but symptoms are usually milder. Most of the time, the disease goes away when the medicine is stopped. More men develop drug-induced lupus because the drugs that cause it, hydralazine and procainamide, are used to treat heart conditions that are more common in men.
- What Are the Signs and Symptoms of Lupus?
- What Is a Flare?
- What Causes Lupus?
- Who Gets Lupus?
- What Will the Doctor Do?
- Will I Get Medicine?
- How Can I Cope With Lupus?
- Hope Through Research
- Where Can People Find More Information About Lupus?
- Acknowledgments
Information Boxes
What Are the Signs and Symptoms of Lupus?
Lupus may be hard to diagnose. It’s often mistaken for other diseases. For this reason, lupus has been called the “great imitator.” The signs of lupus differ from person to person. Some people have just a few signs; others have more.
Common signs of lupus are:
- Red rash or color change on the face, often in the shape of a butterfly across the nose and cheeks
- Painful or swollen joints
- Unexplained fever
- Chest pain with deep breathing
- Swollen glands
- Extreme fatigue (feeling tired all the time)
- Unusual hair loss (mainly on the scalp)
- Pale or purple fingers or toes from cold or stress
- Sensitivity to the sun
- Low blood count
- Depression, trouble thinking, and/or memory problems.
Other signs are mouth sores, unexplained seizures (convulsions), “seeing things” (hallucinations), repeated miscarriages, and unexplained kidney problems.
What Is a Flare?
When symptoms appear, it’s called a “flare.” These signs may come and go. You may have swelling and rashes one week and no symptoms at all the next. You may find that your symptoms flare after you’ve been out in the sun or after a hard day at work.
Even if you take medicine for lupus, you may find that there are times when the symptoms become worse. Learning to recognize that a flare is coming can help you take steps to cope with it. Many people feel very tired or have pain, a rash, a fever, stomach discomfort, headache, or dizziness just before a flare. Steps to prevent flares, such as limiting the time you spend in the sun and getting enough rest and quiet, can also be helpful.
Preventing a Flare
- Learn to recognize that a flare is coming.
- Talk with your doctor.
- Try to set realistic goals and priorities.
- Limit the time you spend in the sun.
- Maintain a healthy diet.
- Develop coping skills to help limit stress.
- Get enough rest and quiet.
- Moderately exercise when possible.
- Develop a support system by surrounding yourself with people you trust and feel comfortable with (family, friends, etc.).
What Causes Lupus?
We don’t know what causes lupus. There is no cure, but in most cases lupus can be managed. Lupus sometimes seems to run in families, which suggests the disease may be hereditary. Having the genes isn’t the whole story, though. The environment, sunlight, stress, and certain medicines may trigger symptoms in some people. Other people who have similar genetic backgrounds may not get signs or symptoms of the disease. Researchers are trying to find out why.
Who Gets Lupus?
Anyone can get lupus. But 9 out of 10 people who have it are women. African American women are three times more likely to get lupus than white women. It’s also more common in Hispanic/Latino, Asian, and American Indian women.
Both African Americans and Hispanics/Latinos tend to develop lupus at a younger age and have more symptoms at diagnosis (including kidney problems).
They also tend to have more severe disease than whites. For example, African American patients have more seizures and strokes, while Hispanic/Latino patients have more heart problems. We don’t understand why some people seem to have more problems with lupus than others.
Lupus is most common in women between the ages of 15 and 44. These are roughly the years when most women are able to have babies. Scientists think a woman’s hormones may have something to do with getting lupus. But it’s important to remember that men and older people can get it, too.
It’s less common for children under age 15 to have lupus. One exception is babies born to women with lupus. These children may have heart, liver, or skin problems caused by lupus. With good care, most women with lupus can have a normal pregnancy and a healthy baby.
Diagnosis: How Do You Find Out If You Have Lupus?
- Medical history – Telling a doctor about your symptoms and other problems you have had can help him or her understand your situation. Your history can provide clues to your disease. Use the checklist at the end of this booklet to keep track of your symptoms. Share this checklist with your doctor. Ask your family or friends to help you with the checklist or come up with questions for your doctor.
- Complete physical exam – The doctor will look for rashes and other signs that something is wrong.
- Laboratory testing of blood and urine samples – Blood and urine samples often show if your immune system is overactive.
- Skin or kidney biopsy – In a biopsy, tissue that is removed by a minor surgical procedure is examined under a microscope. Skin or kidney tissue examined in this way can show signs of an autoimmune disease.
What Will the Doctor Do?
Go see a doctor. He or she will talk to you and take a history of your health problems. Many people have lupus for a long time before they find out they have it. It’s important that you tell the doctor or nurse about your symptoms. This information, along with a physical examination and the results of laboratory tests, helps the doctor decide whether you have lupus or something else.
A rheumatologist (ROOM-uh-TALL-uh-jist) is a doctor who specializes in treating diseases that affect the joints and muscles, like lupus. You may want to ask your regular doctor for a referral to a rheumatologist. In some cases, a dermatologist, a doctor who specializes in treating diseases that affect the skin, may be involved in diagnosis and treatment. No single test can show that you have lupus. Your doctor may have to run several tests and study your medical history. It may take time for the doctor to diagnose lupus.
Will I Get Medicine?
Remember that each person has different symptoms. Treatment depends on the symptoms. The doctor may give you aspirin or a similar medicine to treat swollen joints and fever. Creams may be prescribed for a rash. For more serious problems, stronger medicines such as antimalaria drugs, corticosteroids, and chemotherapy drugs are used. Your doctor will choose a treatment based on your symptoms and needs.
Always tell your doctor if you have problems with your medicines. Let your doctor know if you take herbal or vitamin supplements. Your medicines may not mix well with these supplements. You and your doctor can work together to find the best way to treat all of your symptoms.
How Can I Cope With Lupus?
You need to find out what works best for you. You may find that a rheumatologist has the best treatment plan for you. Other health professionals who can help you deal with different aspects of lupus include psychologists, occupational therapists, dermatologists, and dietitians. You might find that doing exercises with a physical therapist makes you feel better. The important thing is to follow up with your health care team on a regular basis, even when your lupus is quiet and all seems well.
Dealing with a long-lasting disease like lupus can be hard on the emotions. You might think that your friends, family, and coworkers do not understand how you feel. Sadness and anger are common reactions.
People with lupus have limited energy and must manage it wisely. Ask your health care team about ways to cope with fatigue. Most people feel better if they manage their rest and work and take their medicine. If you’re depressed, medicine and counseling can help.
Also,
- Pay attention to your body.
- Slow down or stop before you’re too tired. Learn to pace yourself. Spread out your work and other activities.
- Don’t blame yourself for your fatigue. It’s part of the disease.
- Consider support groups and counseling. They can help you realize that you’re not alone. Group members teach one another how to cope.
- Consider other support from your family as well as faith-based and other community groups.
It’s true that staying healthy is harder when you have lupus. You need to pay close attention to your body, mind, and spirit. Having a chronic disease is stressful. People cope with stress differently. Some approaches that may help are:
- Staying involved in social activities
- Practicing techniques such as meditation and yoga
- Setting priorities for spending time and energy.
Exercising is another approach that can help you cope with lupus. Types of exercise that you can practice include the following:
- Range-of-motion (for example, stretching) exercise helps maintain normal joint movement and relieve stiffness. This type of exercise helps maintain or increase flexibility.
- Strengthening (for example, weight-lifting) exercises help keep or increase muscle strength. Strong muscles help support and protect joints affected by lupus.
- Aerobic or endurance (for example, brisk walking or jogging) exercises improve cardiovascular fitness, help control weight, and improve overall function.
People with chronic diseases like lupus should check with their health care professional before starting an exercise program.
Learning about lupus may also help. People who are well-informed and take part in planning their own care, report less pain. They also may make fewer visits to the doctor, have more self-confidence, and remain more active.
Women who want to start a family should work closely with their health care team; for example, doctors, physical therapists, and nurses. Your obstetrician and your lupus doctor should work together to find the best treatment plan for you.
Hope Through Research
Scientists are working to find out what causes lupus and how it can best be treated. Here are some of the questions they are trying to answer:
- Who gets lupus and why?
- Why are women more likely to get lupus than men?
- Why are there more cases of lupus among certain racial and ethnic groups?
- What goes wrong in the immune system and why?
- What genes play a role in lupus?
- How can we fix an immune system that isn’t working well?
- How can lupus symptoms best be treated?
The National Institutes of Health (NIH) supports research on health and disease. The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) supports research on the bones, connective tissue, joints, muscles, and skin. These are the parts of the body that can be affected by lupus. Research supported by NIAMS is looking at these issues:
- Scientists have demonstrated that people with lupus who test positive for certain antibodies are more likely to have severe flares and that taking prednisone can prevent flares in many individuals.
- Proteins have been identified in the urine of lupus patients that can indicate the type and severity of kidney disease they have. A simple blood test based on this finding could help patients avoid painful and costly kidney biopsies.
- Certain genes make some people more likely to have serious complications, such as kidney disease. NIAMS researchers have found a gene linked to a higher risk of lupus kidney disease in African Americans. Changes in this gene keep the immune system from removing harmful germ-fighters from the body after they’ve done their job. Other genes may also play a role.
- Lupus is more common in women than in men. Researchers are looking into the role of hormones and other male-female differences.
- One NIAMS project is testing a new drug that scientists hope will have milder side effects than standard treatments. Another study is testing a combination of two medicines. One is a standard drug and the other is a new drug. Scientists hope that the combination will be more effective and cause fewer side effects.
Where Can People Find More Information About Lupus?
NIH Information Sources
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National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Information Clearinghouse
National Institutes of Health1 AMS Circle
Bethesda, MD 20892-3675
Phone: 301-495-4484
Toll Free: 877-22-NIAMS (226-4267)
TTY: 301–565–2966
Fax: 301-718-6366
Email: NIAMSinfo@mail.nih.gov
Website: http://www.niams.nih.govNIAMS, a part of the NIH, leads the Federal Government research effort in arthritis and other diseases that affect the muscles, bones, joints, and skin. NIAMS supports research and research training throughout the United States, as well as on the NIH campus in Bethesda, Maryland. The NIAMS Office of Communications and Public Liaison provides health and research information for the public through the NIAMS Information Clearinghouse.
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Clinical Trials at NIH
Toll Free: 800-411-1222
Website: http://clinicaltrials.govClinical trials are medical research studies to see whether new treatments are safe and effective. These studies help doctors learn how people respond to medicines or other new or improved treatments. This Web site provides patients, families, and the public with an easy way to get information about clinical trials. Links to the people who are recruiting participants for each study are also provided.
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MedlinePlus
Website: http://medlineplus.gov/
The National Library of Medicine’s Web site for consumer health information
Department of Health and Human Services (HHS) Online Resource
The following Web site can help you find additional sources of information about lupus:
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HealthFinder
Website: http://www.healthfinder.gov
The HHS site for consumer health information
Other Organizations
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American Academy of Dermatology (AAD)
P.O. Box 4014
Schaumberg, IL 60618-4014
Phone: 847-330-0230
Toll Free: 866-503-SKIN (7546)
Fax: 847-240-1859
Website: http://www.aad.orgThe academy is the national organization for dermatology. It is dedicated to achieving the highest quality of dermatologic care for everyone. It can also provide referrals to dermatologists.
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American Academy of Orthopaedic Surgeons (AAOS)
6300 North River Road
Rosemont, IL 60018-4262
Phone: 847-823-7186
Toll Free: 800-824-BONE (2663)
Fax: 847-823-8125
Email: pemr@aaos.org
Website: http://www.aaos.orgThe academy provides education and practice management services for orthopaedic surgeons and allied health professionals, including those who treat children. It also serves as an advocate for improved patient care and informs the public about the science of orthopaedics. The orthopaedist’s scope of practice includes disorders of the body’s bones, joints, ligaments, muscles, and tendons. For a single copy of an AAOS brochure, send a self-addressed stamped envelope to the address above or visit its Web site.
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American College of Rheumatology (ACR)
1800 Century Place, Suite 250
Atlanta, GA 30345-4300
Phone: 404-633-3777
Fax: 404-633-1870
Website: http://www.rheumatology.orgThe American College of Rheumatology (ACR) is an organization of doctors and associated health professionals who specialize in arthritis and related diseases of the bones, joints, and muscles. The Association of Rheumatology Health Professionals, a division of ACR, aims to enhance the knowledge and skills of rheumatology health professionals and to promote their involvement in rheumatology research, education, and quality patient care. The association also works to advance and promote basic and continuing education in rheumatology for health professionals who provide care to people with rheumatic diseases.
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American Autoimmune-Related Diseases Association, Inc. (AARDA)
22100 Gratiot Ave.
East Detroit, MI 48021
Phone: 586-776-3900
Toll Free: 800-598-4668
Fax: 586-776-3903
Email: aarda@aarda.org
Website: http://www.aarda.orgThe American Autoimmune-Related Diseases Association (AARDA) is a nonprofit voluntary health agency dedicated to bringing a national focus and collaborative effort to the more than 100 known autoimmune diseases through education, awareness, research, and patient services. By collaborating with the National Coalition of Autoimmune Patient Groups (NCAPG), AARDA supports legislative advocacy for autoimmune disease patients. AARDA provides free patient education information, physician and agency referrals, forums and symposia, and a quarterly newsletter.
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Arthritis Foundation
P.O. Box 7669
Atlanta, GA 30357-0669
Phone: 404-872-7100
Toll Free: 800-283-7800
Website: http://www.arthritis.orgThe Arthritis Foundation is devoted to supporting arthritis research and providing educational and other services to individuals with arthritis. The foundation publishes a free pamphlet on rheumatoid arthritis and a magazine for members on all types of arthritis. It also provides up-to-date information on research and treatment, nutrition, alternative therapies, and self-management strategies. Chapters nationwide offer exercise programs, classes, support groups, physician referral services, and free literature. The foundation also has free information about lupus, scleroderma, and other autoimmune and rheumatic conditions on its Web site.
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Lupus Foundation of America (LFA)
2000 L Street, N.W., Suite 710
Washington, DC 20036
Phone: 202-349-1155
Toll Free: 800-558-0121
Fax: 202-349-1156
Website: http://www.lupus.orgThe Lupus Foundation of America is a national nonprofit voluntary health organization dedicated to finding the causes of and cure for lupus; and to providing support, services and hope to all people with this condition. The LFA and its network of nearly 300 chapters and support groups conduct programs of research, education, and advocacy.
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SLE Lupus Foundation
330 Seventh Avenue, Suite 1701
New York, NY 10001
Phone: 212–685–4118
Toll Free: 800-74-LUPUS (745-8787)
Fax: 212-545-1843
Email: lupus@lupusny.org
Website: http://www.lupusny.orgThe SLE Foundation supports and encourages medical research to find the cause and cure of lupus, and improve its diagnosis and treatment. It also provides a wide variety of services to help people with lupus and their families. In addition, this voluntary organization conducts a broad-based public education program to raise awareness of lupus, and increase understanding of this serious chronic autoimmune disease.
Symptom Checklist
Print out this page and use it to make notes to take to your doctor. Put a check mark beside the symptoms you have. Note when you experienced them.
Symptom | ![]() |
Where? | When did you first notice? | How often? |
Recent dates? |
---|---|---|---|---|---|
Example: Rash | ![]() |
face and chest | 2 years ago | Once or twice a month | 9/17, 10/8, 10/23, 11/15 |
Red rash or color change | |||||
Painful or swollen joints | |||||
Unexplained fever | |||||
Chest pain with deep breathing | |||||
Unusual hair loss | |||||
Pale or purple fingers or toes | |||||
Sensitivity to sun | |||||
Other |
Do You Have Lupus or a Related Condition?
You may be able to help scientists learn more about these conditions.
For information about research projects near your home, call
NIAMS
301–495–4484
You could make a difference!
In Appreciation
NIAMS thanks the following people and organizations for their contribution to this project:
Arthritis Foundation Metropolitan Washington Chapter, Lupus Foundation of Greater Washington, Lupus Foundation of America, Barbara Mittleman, M.D., Clifton A. Poodry, Ph.D., Laura Robbins, D.S.W., Cheryl Contreras, M.P.I.A., Patricia Fraser, M.D., M.P.H., M.S., Lori Harrison Port, M.P.H., and Bobbie Drake-Saucer.
Special thanks go to our focus group participants and patients with lupus who reviewed this publication and provided valuable input.
The mission of the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), a part of the National Institutes of Health (NIH), is to support research into the causes, treatment, and prevention of arthritis and musculoskeletal and skin diseases; the training of basic and clinical scientists to carry out this research; and the dissemination of information on research progress in these diseases. The National Institute of Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse is a public service sponsored by NIAMS that provides health information and information sources. Additional information can be found on the NIAMS Web site at www.niams.nih.gov.
This booklet is provided by the National Institute of Arthritis and Musculoskeletal and Skin Diseases in cooperation with the Arthritis Foundation Metropolitan Washington Chapter.
This booklet is not copyrighted. You can make copies of it and give out as many as you want.
For more copies, contact
-
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Information Clearinghouse
National Institutes of Health1 AMS Circle
Bethesda, MD 20892-3675
Phone: 301-495-4484
Toll Free: 877-22-NIAMS (226-4267)
TTY: 301–565–2966
Fax: 301-718-6366
Email: NIAMSinfo@mail.nih.gov
Website: http://www.niams.nih.gov
NIH Publication No. 09–4958