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Living as a Myelodysplastic Syndrome (MDS) Survivor

Myelodysplastic syndromes (MDS) can be treated, and some people can live with them for a long time, but they are often hard to cure. Because of this, many people with MDS might never be ¡®finished¡¯ with treatment completely.

People with MDS often go through periods of treatment when needed (such as when they¡¯re having symptoms), with periods of rest in between. Different treatments might be used at different times, including both drugs and supportive care.

Learning to live with cancer that doesn¡¯t go away completely can be stressful. See Managing Cancer as a Chronic Illness for more about this.

Follow-up care

It¡¯s important to tell your health care team any time you notice new symptoms, especially if they might be signs of an infection or a bleeding problem. Be sure you know what to look out for, and when (and how) to contact your health care team.

Whether or not you're being actively treated for MDS, your doctors will still want to watch you closely, so it's very important to go to all your follow-up appointments.

Exams and tests

How often you need to see your doctors will depend on things like the type of MDS you have, how fast it¡¯s growing and if it¡¯s causing symptoms, if you¡¯re currently getting treatment (and what type of treatment you¡¯re getting), and other factors.

During follow-up visits, your doctors will ask you about symptoms, examine you, and will probably order blood tests. They will continue to watch for signs of infection or bleeding, possible progression of the MDS to leukemia, as well as short-term and long-term side effects of treatment. This is a good time for you to ask your health care team any questions you need answered and to discuss any concerns you might have.

Almost any cancer treatment can have side effects. Some might not last long, but others might. Don¡¯t hesitate to tell your care team about any symptoms or side effects that bother you so they can help you manage them.

Keeping health insurance and copies of your medical records

It¡¯s very important to keep health insurance. With a chronic disease like MDS, your treatment may never really be over. You don¡¯t want to have to worry about paying for it. Many people have been bankrupted by medical costs.

At some point after your treatment, you might find yourself seeing a new doctor who doesn¡¯t know about your medical history. It¡¯s important to keep copies of your medical records to give your new doctor the details of your diagnosis and treatment. Learn more in Keeping Copies of Important Medical Records.

Can I lower my risk of the MDS progressing?

If you have MDS, you probably want to know if there are things you can do to reduce your risk of it progressing, such as exercising, eating a certain type of diet, or taking nutritional supplements. At this time, not enough is known about MDS to say for sure if there are things you can do will help. 

Adopting healthy behaviors such as not smoking, eating well, getting regular physical activity, and staying at a healthy weight may help, but no one knows for sure. However, we do know that these types of changes can have many other positive effects on your health, including helping you feel better.

About dietary supplements

So far, no dietary supplements (including vitamins, minerals, and herbal products) have been shown to clearly help lower the risk of MDS progressing. This doesn¡¯t mean that supplements couldn't be helpful in other ways, though.

Dietary supplements are not regulated like medicines in the United States ¨C they don¡¯t have to be proven effective (or even safe) before being sold, although there are limits on what they¡¯re allowed to claim they can do.

If you¡¯re thinking about taking any type of nutritional supplement, talk to your health care team. They can help you decide which ones you can use safely while avoiding those that might be harmful.

Getting emotional support

Feeling depressed, anxious, or worried is normal when MDS is a part of your life. Some people are affected more than others. But everyone can benefit from help and support from other people, whether friends and family, religious groups, support groups, professional counselors, or others. To learn more about this, see Coping and Living Well During Cancer Treatment.

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Developed by the ÃÛÌÒ´«Ã½ Cancer Society medical and editorial content team with medical review and contribution by the ÃÛÌÒ´«Ã½ Society of Clinical Oncology (ASCO).

 

National Cancer Institute. Myelodysplastic Syndromes Treatment (PDQ?)¨CHealth Professional Version. 2022. Accessed at https://www.cancer.gov/types/myeloproliferative/hp/myelodysplastic-treatment-pdq on July 18, 2024.

National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines?): Myelodysplastic Syndromes. Version 2.2024. Accessed at https://www.nccn.org/professionals/physician_gls/pdf/mds.pdf on July 18, 2024.

Sekeres MA, Platzbecker U. Myelodysplastic syndromes/neoplasms (MDS): Overview of diagnosis and management. UpToDate. 2024. Accessed at https://www.uptodate.com/contents/myelodysplastic-syndromes-neoplasms-mds-overview-of-diagnosis-and-management on July 18, 2024.

 

 

Last Revised: November 21, 2024

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