If you have found your way to this website and are reading this article, you or a loved one are probably dealing with serious illness. Open and honest communication with your physician is vital to your well being, regardless of the stage of this illness. But sometimes discussions may be less than satisfying or productive, and you may feel like it’s the healthcare provider who drives these talks rather than you—the one who needs answers. Your appointments occur within the constraints of the doctor’s available time, and yet the days of your life may be limited. It may feel like you’re on an uneven playing field. Of course, it is the physician who has the knowledge and skill, but it is you who are sick.
The fact that you are ill is out of your control, but you can regain some control by being clear about what you need from the healthcare provider. Both of you can commit to thoughtful listening and speaking. You can be on equal ground, and you can work effectively together when the truth is spoken and heard.
There is no set script for dealing with illness or confronting difficult choices about care. Your life is unique. Being sick is the latest chapter in a life story that is all your own, and navigating the illness journey will look a lot like the way you have handled other transitions. The issues raised and questions suggested in this article are comprehensive, but all of them may not be for you; choose what best works for you. Some people need detail and seek vast amounts of information about their disease, treatments, and outcomes. For them, the unknown is scarier than the most worrisome facts. Others may decide they can function best without knowing what seems frightening.
Frank discussions with those closest to you can help you sort out what feels right. But bear in mind that healthcare decisions are best made with good information, so shutting out the unpleasant can make life more difficult for you and family members in the long run.
Thinking Ahead About Your Values
Preparing for meaningful talks with your doctor begins early in critical illness and starts at home. It’s time for a conversation with yourself about the road ahead. You may have some ideas about what you need from your doctor… for how much you want to know.
To guide your introspection and family discussions, here are some questions for you to evaluate on your own so you can share them with your doctor later:
- What do I most value in my life?
- What makes a good day for me, a meaningful day?
- Is it important for me to be cared for at home?
- Do I want someone to be with me for doctors’ appointments, to be a second set of ears and to be familiar with my case to support my decision-making?
- What is an acceptable outcome, and what am I willing to endure to achieve it?
- If I don’t want my life prolonged with extraordinary measures, what do I consider “extraordinary?” (If you have an advance directive for the healthcare of a living will, you may have already considered this.)
- If I find that my disease is not reversible, what would a “good death” look like for me?
These are all things that your physician will need to understand. Your faith and spiritual values may impact your answers, and you may want to talk with your spiritual advisor about this.
Keeping the Devil Out of the Details
When you make your appointment, tell the receptionist you need extra time for discussion, and do so every time you need an in-depth talk. If you want someone with you for appointments, ask that person to come along and take notes. This will help you listen more attentively.
During this first expanded meeting, you will want to confirm your confidence that this is the right doctor for you. Review the logistics of the doctor-patient relationship. The office manager may answer some of the questions, or the practice’s website may give you guidance.
- What hospital do you use? Do you use a hospitalist (a physician who is contracted to manage your care if you are hospitalized)?
- Are you comfortable with second opinions?
- Can I see you the same day if I need to?
- When I call with a question, who will return my call, and how soon? Is there a best time to call?
- How do you handle insurance? Will you bill the insurer or me?
- I am giving you permission to speak openly to ________ about my case. (You may need to put this permission in writing.)
- I want to be sure that there is one person who is in charge of my case; who is that person?
- Who else should be kept informed, and will you do that?
- Do you have a working relationship with a nutritionist, therapists for occupational or physical therapy, and support services for my family and me?
- I would like to keep copies of my operative notes, pathology reports, and tests so if I’m ever in a situation requiring emergency help, I can provide the needed information. Can I get these from your office?
- I have an advance directive for my healthcare decisions, and it also identifies my proxies. Please keep a copy, I will want to review it if my condition changes.
If you are satisfied with these “housekeeping” details, move ahead with candidly expressing the values you’ve considered at home, as discussed above. For this first visit and others, be sure to write down your questions, or the things you want your doctor to know, before the appointment. It’s a good idea to share that list with the person accompanying you so nothing will fall through the cracks.
Talking About Your Diagnosis
- (If you have cancer:) What type of cancer do I have, and what is the current stage and grade? What do these terms mean?
- How many patients have you had with my diagnosis and history?
- What is the expected course of my disease?
- Is it reversible?
- If not, can my life be extended? By what means, and how successful is that for people in my condition?
- How long can I expect that extension to continue?
- What lifestyle changes should I consider?
- Can you recommend some other reliable resources (written, online) for learning more about my diagnosis?
- Are there any clinical trials for my condition? If so, do you have access to these trials?
Tell your doctor promptly if you are anxious or depressed. You may have an initial depressive reaction to your diagnosis, and as you receive treatment, medications or the disease process may also cause depression. It can be treated, so speak up.
When a Treatment is First Discussed, or Additional Treatments and Tests are Considered
- What, specifically, does this treatment do?
- Why do you recommend this treatment instead of another?
- Does this treatment cure me, change the course of the disease or slow it down?
- What would success look like?
- How many patients like me have you treated this way, and what was their experience?
- What percentage of patients like me get better from this treatment, and for how long?
- Will this treatment help me be more active in the future?
- Will it make me more comfortable in the future?
- When can I expect to feel some results?
- What should I expect during this treatment—physically, mentally, emotionally?
- What percentage of patients receiving this treatment are disabled by its side effects?
- Tell me what symptoms you want me to promptly report to you.
- Would a palliative care consultation, to work with you on managing my symptoms, be helpful? Is there a palliative care physician you’ve worked with?
- I want you to tell me if you would choose this treatment for yourself or a loved one.
- What would happen if I didn’t have to this treatment?
- Do I need this test? Will it tell us something we don’t already know?
- Will the results of this test change my treatment? What if I don’t have this test?
- When will I have results, and will you call me?
If you are interested in participating in any relevant investigational treatments or clinical trials, let the doctor know.
If/When Treatments No Longer Have the Desired Effect
Re-visit a discussion of “extraordinary measures.” You may have thought about what they mean to you, be they tube feedings, ventilators or CPR. What about IV fluids or antibiotic mediations? Be sure that you and your doctor have the same understanding.
A number of states now endorse POLST—Physician Orders for Life-Sustaining Treatment. POLST documents your wishes as a standard medical order; it can travel with you if you change care settings. Whether you have an advance directive or not, POLST is a new and valuable way to transform your wishes into a tool, signed by your doctor, that can be acted upon.
If palliative care was not considered earlier and your symptoms have become more troubling, ask about it again. If you have not already talked about the following, this is the time for further discussion:
- Will you tell me when hospice is the best option for me? I want the benefits of hospice comfort care and support for my family.
- If you are not sure about hospice for me, will you talk to a hospice clinician about it?
- I want to discuss my feelings about alertness vs. sleepiness when we treat my pain.
- I’d like to talk again about what is most important to me so we can be sure you understand what I want.
Source: American Hospice Foundation: americanhospice.org