Letter from Doctor to Patients with Chronic Illness

Thanks to JC Colyer for sharing this very inspiring message of a "Letter from Doctor to Patients with Chronic Illness" as written by Dr. Rob on July 14, 2010, in BEING A DOCTOR, BEST OF, JUST STUFF KIND OF THINGIES, PERSONAL MUSINGS.

It reads:

Dear Patients:

You have it very hard, much harder than most people understand. Having sat for 16 years listening to the stories, seeing the tiredness in your eyes, hearing you try to describe the indescribable, I have come to understand that I too can’t understand what your lives are like. How do you answer the question, “how do you feel?” when you’ve forgotten what “normal” feels like? How do you deal with all of the people who think you are exaggerating your pain, your emotions, your fatigue? How do you decide when to believe them or when to trust your own body? How do you cope with living a life that won’t let you forget about your frailty, your limits, your mortality?

I can’t imagine.

But I do bring something to the table that you may not know. I do have information that you can’t really understand because of your unique perspective, your battered world. There is something that you need to understand that, while it won’t undo your pain, make your fatigue go away, or lift your emotions, it will help you. It’s information without which you bring yourself more pain than you need suffer; it’s a truth that is a key to getting the help you need much easier than you have in the past. It may not seem important, but trust me, it is.

You scare doctors.

No, I am not talking about the fear of disease, pain, or death. I am not talking about doctors being afraid of the limits of their knowledge. I am talking about your understanding of a fact that everyone else seems to miss, a fact that many doctors hide from: we are normal, fallible people who happen to doctor for a job. We are not special. In fact, many of us are very insecure, wanting to feel the affirmation of people who get better, hearing the praise of those we help. We want to cure disease, to save lives, to be the helping hand, the right person in the right place at the right time.

But chronic unsolvable disease stands square in our way. You don’t get better, and it makes many of us frustrated, and it makes some of us mad at you. We don’t want to face things we can’t fix because it shows our limits. We want the miraculous, and you deny us that chance.

And since this is the perspective you have when you see doctors, your view of them is quite different. You see us getting frustrated. You see us when we feel like giving up. When we take care of you, we have to leave behind the illusion of control, of power over disease. We get angry, feel insecure, and want to move on to a patient who we can fix, save, or impress. You are the rock that proves how easily the ship can be sunk. So your view of doctors is quite different.

Then there is the fact that you also possess something that is usually our domain: knowledge. You know more about your disease than many of us do – most of us do. Your MS, rheumatoid arthritis, end-stage kidney disease, Cushing’s disease, bipolar disorder, chronic pain disorder, brittle diabetes, or disabling psychiatric disorder – your defining pain - is something most of us don’t regularly encounter. It’s something most of us try to avoid. So you possess deep understanding of something that many doctors don’t possess. Even doctors who specialize in your disorder don’t share the kind of knowledge you can only get through living with a disease. It’s like a parent’s knowledge of their child versus that of a pediatrician. They may have breadth of knowledge, but you have depth of knowledge that no doctor can possess.

So when you approach a doctor – especially one you’ve never met before – you come with a knowledge of your disease that they don’t have, and a knowledge of the doctor’s limitations that few other patients have. You see why you scare doctors? It’s not your fault that you do, but ignoring this fact will limit the help you can only get from them. I know this because, just like you know your disease better than any doctor, I know what being a doctor feels like more than any patient could ever understand. You encounter doctors intermittently (more than you wish, perhaps); I live as a doctor continuously.

So let me be so bold as to give you advice on dealing with doctors. There are some things you can do to make things easier, and others that can sabotage any hope of a good relationship:

Don’t come on too strong – yes, you have to advocate for yourself, but remember that doctors are used to being in control. All of the other patients come into the room with immediate respect, but your understanding has torn down the doctor-god illusion. That’s a good thing in the long-run, but few doctors want to be greeted with that reality from the start. Your goal with any doctor is to build a partnership of trust that goes both ways, and coming on too strong at the start can hurt your chances of ever having that.
Show respect – I say this one carefully, because there are certainly some doctors who don’t treat patients with respect – especially ones like you with chronic disease. These doctors should be avoided. But most of us are not like that; we really want to help people and try to treat them well. But we have worked very hard to earn our position; it was not bestowed by fiat or family tree. Just as you want to be listened to, so do we.
Keep your eggs in only a few baskets – find a good primary care doctor and a couple of specialists you trust. Don’t expect a new doctor to figure things out quickly. It takes me years of repeated visits to really understand many of my chronic disease patients. The best care happens when a doctor understands the patient and the patient understands the doctor. This can only happen over time. Heck, I struggle even seeing the chronically sick patients for other doctors in my practice. There is something very powerful in having understanding built over time.
Use the ER only when absolutely needed – Emergency room physicians will always struggle with you. Just expect that. Their job is to decide if you need to be hospitalized, if you need emergency treatment, or if you can go home. They might not fix your pain, and certainly won’t try to fully understand you. That’s not their job. They went into their specialty to fix problems quickly and move on, not manage chronic disease. The same goes for any doctor you see for a short time: they will try to get done with you as quickly as possible.
Don’t avoid doctors – one of the most frustrating things for me is when a complicated patient comes in after a long absence with a huge list of problems they want me to address. I can’t work that way, and I don’t think many doctors can. Each visit should address only a few problems at a time, otherwise things get confused and more mistakes are made. It’s OK to keep a list of your own problems so things don’t get left out – I actually like getting those lists, as long as people don’t expect me to handle all of the problems. It helps me to prioritize with them.
Don’t put up with the jerks – unless you have no choice (in the ER, for example), you should keep looking until you find the right doctor(s) for you. Some docs are not cut out for chronic disease, while some of us like the long-term relationship. Don’t feel you have to put up with docs who don’t listen or minimize your problems. At the minimum, you should be able to find a doctor who doesn’t totally suck.
Forgive us – Sometimes I forget about important things in my patients’ lives. Sometimes I don’t know you’ve had surgery or that your sister comes to see me as well. Sometimes I avoid people because I don’t want to admit my limitations. Be patient with me – I usually know when I’ve messed up, and if you know me well I don’t mind being reminded. Well, maybe I mind it a little.
You know better than anyone that we docs are just people – with all the stupidity, inconsistency, and fallibility that goes with that – who happen to doctor for a living. I hope this helps, and I really hope you get the help you need. It does suck that you have your problem; I just hope this perhaps decreases that suckishness a little bit.

Sincerely,

Dr. Rob

I love this. Thanks.

Very nice. I want to send my doctor a nice card after reading this. I honestly appreciate her very much. Thank you for this.

Thank you for posting this.

While I admire Dr. Rob's honesty, gotta say this is one of the more depressing things I've read in awhile. It sounds like his advice is to just put on the little '50s era housewife attitude. Keep the myth of doctor-as-god alive, don't let them know how much you know, don't ask for too much at any one visit. "At the minimum, you should be able to find a doctor who doesn't totally suck." Sucks 85% is OK? 70% suckage all right? "You don’t get better, and it makes many of us frustrated, and it makes some of us mad at you." This is OK?? I guess the terminology that "the patient has failed three biologics" isn't going away any time soon.

I will forever be grateful to the orthopedic hand specialist who looked at my hand, looked me in the eye, and told me he had never seen anything like this before and that he wanted to look some stuff up and talk to others before doing anything. That's a man who is secure enough to admit he doesn't have instant answers. Then there's my mother's ophthamologist. She has severe macular degeneration. He tells her that there are treatments in the pipeline, even if nothing is available right now. He likes her, he respects her, he knows how devastating it has been for her to lose her vision, even if he can't "fix, save, or impress" her.

All I want for Christmas is a rheumatologist who has patience, who doesn't blame the victim, who isn't looking for praise or deification. One who knows the field, and isn't rude or dismissive. At a few hundred bucks a visit, is that too much to ask?

This is so true! It was not until I let the Doctor lead and diagnose while getting my concerns heard' that I got the diagnosis and treatment that I needed. I am glad that Dr. Rob had the courage to write this letter; it is well said and covers everything we think, feel and act as patients. Also Thank You for being so candid. I think we put doctors on a pedestal and then when they don't meet our grand expectations we get upset and disappointed. This was a great reminder for all of us.

Ditto what you said Louise. I found this really demotivating.

I have been with a dr. who was frustrated I wasn't getting better, couldn't focus on more than one problem at a time, like the doc. in this letter describes. I fired her and found a rheumy who I know, and he knows, can't fix me, but CAN work with the tools we have to improve my situation.

Louise said:

While I admire Dr. Rob's honesty, gotta say this is one of the more depressing things I've read in awhile. It sounds like his advice is to just put on the little '50s era housewife attitude. Keep the myth of doctor-as-god alive, don't let them know how much you know, don't ask for too much at any one visit. "At the minimum, you should be able to find a doctor who doesn't totally suck." Sucks 85% is OK? 70% suckage all right? "You don’t get better, and it makes many of us frustrated, and it makes some of us mad at you." This is OK?? I guess the terminology that "the patient has failed three biologics" isn't going away any time soon.

I will forever be grateful to the orthopedic hand specialist who looked at my hand, looked me in the eye, and told me he had never seen anything like this before and that he wanted to look some stuff up and talk to others before doing anything. That's a man who is secure enough to admit he doesn't have instant answers. Then there's my mother's ophthamologist. She has severe macular degeneration. He tells her that there are treatments in the pipeline, even if nothing is available right now. He likes her, he respects her, he knows how devastating it has been for her to lose her vision, even if he can't "fix, save, or impress" her.

All I want for Christmas is a rheumatologist who has patience, who doesn't blame the victim, who isn't looking for praise or deification. One who knows the field, and isn't rude or dismissive. At a few hundred bucks a visit, is that too much to ask?

Louise and Marietta, I totally get what you are saying! For me, however, the letter was a reminder that my doctors are human, emotional and fallible and that as a patient, I can get better care if I try to take that into account. That said, there are some docs who are asleep at the switch and don’t do their jobs. That’s a different story all together, and they deserve to be fired. (I fired my first rheumy too, Marietta, and I wrote her a long and detailed letter explaining why I did so.)

Wow, I really admire your honesty Dr Rob, thank you so much for giving us insight into your world. As a sonographer I deal with about 15-20 patients per day and I can see where you are coming from. As a patient newly diagnosed with chronic disease I feel I automatically turn into this needy patient looking for answers. I feel I can relate to my patients more now.

The look into the mind of a dr. is awakening. There are 2 sides to every story. As a nurse, I went into the field to soothe, aid, teach, and hopefully alleviate the patients issue. I embrace educated patients and their family members. It makes my job a whole lot easier. I am not at all comparing myself to a dr. right now, but when I get a pt or family member who is constantly challenging me, the treatment plan, education, care, doubting me, etc. I put up a wall. I don't want to, or consciously do it, but I know I do. I think this excerpt is a great look into the thoughts of the M.D. whether they are valid or not. It's not right or wrong that guide them, it's their perception of us, are we open to them even treating us. Are they just another jerk that we have to forget about and move on? There are many dynamics involved, including prejudices on both sides. I praise my maker for my rheumy because we have MUTUAL respect for each other, and he listens to me. He's compassionate when he needs to be and firm when he needs to be. I count myself very lucky. I'm glad I read this storys.

I ditto Seenie's comment: I love this. Thanks.

Frances

Thank you...I have felt this for many years....comforting to hear a doctor's affirmation.

I saw my rheumy yesterday - he's an amazing, doc who actually listens to me and treats me as individual, unique PsA patient. I thanked him for all these qualities - he smiled, shook my hand and said I made his day - he said that several times. He said he rarely has a patient thank him. the good ones need encouragement as we need it.


Frances thanks for sharing this...I think sometimes when I see my rheumy I have so much to check out I forget to notice what a great job he does...
Frances said:

I saw my rheumy yesterday - he's an amazing, doc who actually listens to me and treats me as individual, unique PsA patient. I thanked him for all these qualities - he smiled, shook my hand and said I made his day - he said that several times. He said he rarely has a patient thank him. the good ones need encouragement as we need it.