Newly Diagnosed

If you or someone you know has recently been diagnosed with myelodysplastic syndrome (MDS), you may want to start reading here.

First, a few thoughts:

• All cases of MDS are not the same. The treatment that a friend or relative received may not be the best treatment for you. You may want to read about common treatment options to learn more. Your healthcare team can explain the options. They can talk with you about which combination is most likely to help you.
• A diagnosis of a serious illness can feel overwhelming. We have an experienced, compassionate team ready to help you adjust to what’s happening. You may want to read the section on support. You may want to join a support group, or talk to a social worker or chaplain. You also may find useful information in the Patient Education section of this web section.
• Ask someone you trust to go with you to doctors' appointments and tests. This person can provide emotional support. A friend or family member can also help by keeping track of questions you want to ask, taking notes, and doing research on your disease and treatment options.

You can also find out more about clinical trials and our multidisciplinary team. If you have not yet seen a doctor at the Seattle Cancer Care Alliance, you may want to read Your First Visit and Where Will I Be Seen.

If you are concerned about whether your health insurance will cover treatment at SCCA, click here for more information on insurance.

These SCCA resources are available to your family and friends as well.

March 2006