Meningioma: Questions to Ask the Doctor

Approved by the Cancer.Net Editorial Board, 07/2015

ON THIS PAGE: You will find some questions to ask your doctor or other members of your health care team, to help you better understand your diagnosis, treatment plan, and overall care. To see other pages, use the menu on the side of your screen.

Talking often with the doctor is important to make informed decisions about your health care. These suggested questions are a starting point to help you learn more about your care and treatment. You are also encouraged to ask additional questions that are important to you. You may want to print this list and bring it to your next appointment, or download Cancer.Net’s free mobile app for an e-list and other interactive tools to manage your care.

Questions to ask after getting a diagnosis

  • What type of meningioma do I have? Is it benign or cancerous?

  • What is the grade of the tumor? What does this mean?

  • How many patients with this type of tumor do you treat each year?

  • Do you attend expert meetings to discuss complicated tumor cases? What kinds of specialists attend such meetings?

  • Can you explain my pathology report (laboratory test results) to me?

  • Will an experienced neuropathologist review my pathology slides?

  • Is any special genetic testing needed? If so, can you describe this testing to me?

  • Do my family members have a higher risk of developing meningioma? 

  • Do you have reading material that would help me understand my disease?

Questions to ask about choosing a treatment and managing side effects

  • What are my treatment options?

  • What clinical trials are open to me? Where are they located, and how do I find out more about them?

  • What treatment plan do you recommend? Why?

  • What is the goal of each treatment? Is it to eliminate the tumor, help me feel better, or both?

  • When should I start treatment?

  • Should I get a second opinion?

  • Where will my treatment take place? Are there CNS tumor centers of excellence that you recommend?

  • Who will be part of my health care team, and what role does each person have?

  • Who will be coordinating my overall treatment?

  • What are the possible side effects of this treatment, both in the short term and the long term?

  • How will this treatment affect my daily life? Will I be able to work, exercise, drive, and perform my usual activities?

  • Could this treatment affect my sex life? If so, how and for how long?

  • Could this treatment affect my ability to become pregnant or have children? If so, should I talk with a fertility specialist before treatment begins?

  • If I’m worried about managing the costs related to my medical care, who can help me with these concerns?   

  • What support services are available to me? To my family?

  • Do you work with a social worker that assists patients with a CNS tumor?

  • Do you know of a local support group for patients with a CNS tumor?

  • Who answers patient questions when you are unavailable?

  • Whom should I call for questions or problems?

  • Is there anything else I should be asking?

Questions to ask about having surgery

  • What type of surgery will I have?

  • How long will the operation take?

  • How long will I be in the hospital?

  • Can you describe what my recovery from surgery will be like?

  • What are the possible long-term effects of having this surgery?

Questions to ask about having radiation therapy or chemotherapy

  • What type of treatment is recommended?

  • What is the goal of this treatment?

  • How long will it take to give this treatment?

  • What side effects can I expect during treatment?

  • What are the possible long-term effects of having this treatment?

  • What can be done to relieve the side effects?

Questions to ask about planning follow-up care

  • What is the risk of the tumor returning? Are there signs and symptoms I should watch for?

  • What long-term side effects or late effects are possible based on the treatment I received?

  • What follow-up tests will I need, and how often will I need them?

  • How do I get a treatment summary and survivorship care plan to keep in my personal records? 

  • Who will be coordinating my follow-up care?

  • What survivorship support services are available to me? To my family?

The next section in this guide is Additional Resources, and it offers some more resources on this website beyond this guide that may be helpful to you. Or, use the menu on the side of your screen to choose another section to continue reading this guide.