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Your goals, your care

How to Have a — Goals-of-Care Conversation With Your Doctor

A goals-of-care conversation feels like being told to give up. It is not that. It is a chance to tell your team what matters most to you — and to make sure every decision they make is shaped by that answer.

Medically reviewed by Dr. C. Raghavendra Reddy, Medical Oncologist, MBBS (Gold Medal) · DNB · DM (Medical Oncology, Gold Medal) · Last reviewed August 2026

  • Not the same as stopping treatment — Stopping a particular drug and stopping all care are two different things. You can stop one without stopping the other.
  • You are allowed to set limits — You can say that certain side effects are not acceptable to you. Your team cannot adjust the plan if they do not know this.
  • The conversation can happen more than once — What matters to you may change. You can ask for this discussion at any major turning point in your care.
  • It is about what you want — Your goals guide the decisions. The conversation is how you make that true in practice, not just in principle.
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A goals-of-care conversation is a discussion about what you want your care to achieve — not about ending treatment. Stopping a particular drug and stopping care are two different things. This conversation is how you tell your team what quality of life means to you, and what you are and are not willing to go through.

How do you prepare for a goals-of-care conversation?

  1. Write down what matters most to you

    Think beyond the medical. What do you want to be able to do? What would you find unbearable? Write it in your own words before the appointment — your team cannot act on what they do not know.

  2. Bring someone with you

    A family member or close friend can listen, take notes, and help you remember what was said. These conversations are hard to carry in memory alone.

  3. Ask your team to describe what is likely ahead

    Understanding what your illness is likely to do — and over what timeframe — helps you make decisions grounded in reality rather than hope or fear alone.

  4. Say what you are willing and not willing to go through

    You are allowed to say that a treatment's side effects are not acceptable to you. Your team cannot adjust the plan if they do not know this.

  5. Ask what care looks like if a particular treatment stops

    Stopping one drug or one line of treatment is not the same as stopping care. Ask specifically: if we stop this, what will you do to keep me comfortable?

  6. Ask to have this conversation again

    What matters to you may change. It is reasonable to ask for this discussion to continue at every major turning point in your care.

Does asking for this conversation mean giving up?

It does not. A goals-of-care conversation is about aligning your treatment with what you actually want — not about deciding to stop trying.

Stopping a particular drug and stopping care are two completely different things. You can stop a treatment that is causing more harm than benefit and still receive active, attentive care for pain, breathlessness, fatigue, and everything else your body is going through.

Many patients who have this conversation describe it as a relief — not because anything has been resolved, but because they have finally been heard.

What happens to your care when a treatment stops?

Care continues. The focus shifts from trying to change the course of the cancer to keeping you as well as possible for as long as possible.

That means active management of your symptoms — pain, fatigue, nausea, breathlessness — and support for your family. Palliative care, a specialist discipline focused on comfort and quality of life, can be given alongside cancer treatment, not only at the end of life.

Being clear about your goals makes this care more effective. Your team cannot prioritise what you have not told them.

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MBBS, DNB (Internal Medicine), DM (Medical Oncology)

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Dr. C. Raghavendra Reddy
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Dr. C. Raghavendra Reddy

MBBS(Gold Medal), DNB(General Medicine), DM(Medical Oncology)(Gold Medal)

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Words you may hear in a goals-of-care conversation

Goals of care
What you want your medical care to achieve — whether that is trying every available treatment, staying as well as possible for as long as possible, or being as comfortable as you can be at home.
Prognosis
What your illness is likely to do — how it may progress and over what timeframe. A prognosis is an estimate based on experience with many patients, not a certainty for any one person.
Advance care directive
A document that records your care preferences in advance, so your wishes are known if you cannot speak for yourself later. It covers medical decisions — it is not the same as a will.
Palliative care
Specialist care focused on comfort, symptom control, and quality of life. It can run alongside active cancer treatment from early in the illness, not only at the end.
Best supportive care
Treatment aimed entirely at managing symptoms and improving quality of life, without trying to control or shrink the cancer itself.
DNR / DNAR
A medical order recording your preference about resuscitation. It covers one specific decision — it does not mean that other care will stop.

Did you know?

Patients who receive palliative care alongside their cancer treatment — not only at the end of life — report better quality of life and in some studies have lived longer than those who did not.

ASCO and ESMO both now recommend early integration of palliative care as standard practice, not a last resort.

Source: ASCO and ESMO guidelines on integration of palliative care in oncology

Questions families ask most

What if I am not ready for this conversation?

You do not have to be ready. You can ask for more time, ask to come back to it, or simply say you are not ready yet. No single appointment has to settle everything. What matters is that your team knows enough about your situation to give you care you can live with — not that you resolve every question at once. If a doctor raises it and you feel overwhelmed, it is completely reasonable to say: I need more time to think about this. Can we talk again next week?

What if my family wants to keep trying every treatment, but I want to focus on comfort?

This is one of the hardest situations in cancer care, and it is more common than families admit. Your wishes about your own body carry the most weight legally and ethically — but that does not make the conversation with your family easier. A social worker, palliative care specialist, or counsellor can help facilitate that conversation without you having to carry it alone. Tell your oncology team that the tension exists; they have helped many families through exactly this.

Will my doctor think I am giving up if I raise this?

No. An oncologist who hears you ask about your goals of care is not hearing defeat — they are hearing a patient who is engaging seriously with their situation. It is also information your team genuinely needs to care for you well. If the conversation feels unwelcome or dismissive when you raise it, that is worth noting. You are entitled to seek a second opinion or ask to speak directly with a palliative care specialist.

Can I change my mind after this conversation?

Yes, at any point. A goals-of-care conversation is not a contract. What you say today is a statement of where you are now — and where you are can change as your illness changes, as new treatments become available, or simply as your own priorities shift over time. Tell your team when something changes. They follow your lead, not the other way around.

What does this conversation actually look like in practice?

It usually begins with your doctor summarising where things stand medically, then asking what you understand and what matters most to you. You may be asked questions like: if things get harder, what would be most important to you? or: what are you most worried about? There is no script you need to follow. You can ask questions, stay quiet, cry, or say you do not know. Your team's job in that room is to listen, not to lead you toward a particular answer.

Should I write an advance care directive before speaking to my oncologist?

You do not need one written before the conversation — the conversation can actually help you know what to put in one. An advance care directive is most useful when it reflects what you already understand about your illness and your options. If your oncologist has already explained the likely course of things, that is a good foundation to start from. Your team can also refer you to a social worker or counsellor who helps patients complete one.

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Common questions

Frequently asked questions

What is a goals-of-care conversation in cancer treatment?

A goals-of-care conversation is a discussion between you, your family, and your medical team about what you want your care to achieve. It covers what matters most to you, what you are and are not willing to go through, and what care should look like at each stage of your illness. It is not the same as deciding to stop treatment — it is a way of making sure every decision your team makes is shaped by what you actually want.

Who usually starts a goals-of-care conversation?

Either your doctor or your family can raise it. Your oncologist may suggest it when a treatment plan is changing, when a line of treatment has not worked, or when your illness has progressed significantly. You can also ask for it yourself at any point — you do not have to wait to be invited. Saying 'I would like to talk about what I want from my care going forward' is enough to open it.

Does having this conversation mean I will not receive active treatment?

No. Many patients have goals-of-care conversations while they are still on active treatment, and the conversation does not change the treatment plan unless that is what you decide together. It is about making sure the treatment you receive is treatment you actually want — not about limiting or removing your options without your agreement.

Is palliative care only for people who are dying?

No, and this is a misunderstanding worth correcting early. Palliative care is specialist support focused on symptoms, side effects, and quality of life. ASCO and ESMO both recommend starting it alongside cancer treatment, not only when curative options are exhausted. At CION, palliative support is part of your care, not a last resort added at the end.

Can I ask for this conversation to be held in my own language?

Yes. You are entitled to have a medical conversation in the language in which you think most clearly. Ask your care team for an interpreter or for a team member who speaks your language. If that is not available at the time, ask for the conversation to be scheduled when it can be. A goals-of-care conversation conducted through misunderstanding is not a goals-of-care conversation.

What if I am asked to sign a document I do not fully understand?

Do not sign until you understand it. Ask what the document does, what it does not cover, and what happens if you do not sign it. You have the right to take time and, if you want, to take it home and return with a family member or trusted person. No decision in a goals-of-care conversation should feel forced.

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