In the U.S., I was trained to do everything for my patients—to think about all the possible diseases, diagnose the appropriate illness, and treat accordingly. I was spoiled into thinking that with enough resources, tests, and consults we can uncover an answer to even the most difficult clinical questions, and treat (and fix) the problem. I was taught to never give up. Here, I am learning very different lessons. I am learning that with limited resources comes limited capacities. I do not have specialists on consult, and I can’t send everyone to the university hospital four hours away if I have questions. But more importantly, I have to respect the desires and limitations of my patients. Families here face decisions that most people in the US are lucky to avoid—to save one child or feed the rest; to spend everything they own to travel to a hospital where their child will most likely die, or take them home to be with their family.
Today, I had to respect the wishes of a father who could not spend another month with no income and a family to support. He looked at me this morning and, via a translator, said “thank you…thank you for all your work to try to help my daughter. I know that she may die, and I am very sad. But I need to go home.” And without a diagnosis, without an answer, without succeeding in helping his daughter, I went against my American instincts and let her go.
This last blog was gut wrenching
ReplyDeleteOne thing that I teach people when talking about hospice and palliative care for the elderly is traditional medicine (not just in America) equates death to failure.
You are not dealing with the elderly, you are dealing with a young child who could have had potential elsewhere.
there is a time that people chose quality over quantity and that is what this father chose for his child in taking the baby home.
Love,
Dad