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A few years ago,
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I was taking care of a woman
who was a victim of violence.
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I wanted her to be seen in a clinic
that specialized in trauma survivors.
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I made the appointment myself because,
being the director of the department,
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I knew if I did it,
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she would get an appointment right away.
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The clinic was about an hour and a half
away from where she lived,
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but she took down the address
and agreed to go.
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Unfortunately, she didn't
make it to the clinic.
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When I spoke to the psychiatrist,
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he explained to me
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that trauma survivors are often resistant
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to dealing with the difficult
issues that they face,
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and often miss appointments.
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For this reason,
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they don't generally allow the doctors
to make appointments for the patients.
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They had made a special exception for me.
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When I spoke to my patient,
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she had a much simpler
and less Freudian explanation
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of why she didn't go to that appointment:
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her ride didn't show.
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Now, some of you may be thinking,
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"Didn't she have some other way
of getting to that clinic appointment?"
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Couldn't she have taken an Uber
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or called another friend?
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If you're thinking that,
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it's probably because you have resources.
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But she didn't have
enough money for an Uber,
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she didn't have another friend to call.
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But she did have me, and I was able
to get her another appointment,
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which she kept without difficulty.
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She wasn't resistant,
it's just her ride didn't show.
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I wish I could say that this
was an isolated incident,
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but I know from running
the safety net systems
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in San Francisco, Los Angeles,
and now New York City,
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that health care is built
on a middle class model
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that often doesn't meet the needs
of low-income patients.
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That's one of the reasons why
it's been so difficult
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for us to close
the disparity in health care
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that exists along economy lines
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despite the expansion of health insurance
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under the ACA, or ObamaCare.
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Health care in the United States
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assumes that, besides getting across
the large land expanse of Los Angeles,
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it also assumes that you
can take off from work
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in the middle of the day to get care.
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One of the patients who came
to my East Los Angeles clinic
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on a Thursday afternoon
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presented with partial blindness
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in both eyes.
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Very concerned, I said to him,
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"When did this develop?"
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He said, "Sunday."
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I said, "Sunday?
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Did you think of coming sooner to clinic?"
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And he said, "Well, I have to work
in order to pay the rent."
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A second patient to that same clinic,
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a trucker,
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drove three days with a raging infection,
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only coming to see me
after he had delivered his merchandise.
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Both patients' care was jeopardized
by their delays in seeking care.
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Health care in the United States
assumes that you speak English
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or can bring someone with you who can.
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In San Francisco, I took care of a patient
on the inpatient service
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who was from West Africa
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and spoke a dialect so unusual
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that we could only find one translator
on the telephonic line
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who could understand him,
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and that translator only worked
one afternoon a week.
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Unfortunately, my patient
needed translation services every day.
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Health care in the United States
assumes that you are literate.
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I learned that a patient of mine
who spoke English without accent
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was illiterate
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when he asked me to please sign
a social security disability form
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for him right away.
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The form need to go
to the office that same day,
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and I wasn't in clinic,
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so trying to help him out,
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knowing that he was
the sole caretaker of his son,
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I said, "Well, bring the form
to my administrative office.
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I'll sign it and I'll fax it in for you."
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He took the two buses to my office,
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dropped off the form,
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went back home to take care of his son,
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I got to the office, and what did I find
next to the big "X" on the form?
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The word "applicant."
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He needed to sign the form.
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And so now I had to have him
take the two buses back to the office
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and sign the form so that
we could then fax it in for him.
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It completely changed
how I took care of him.
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I made sure that I always went over
instructions verbally with him.
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It also made me think about
all of the patients
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who receive reams and reams of paper
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spit out by our modern
electronic health record systems
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explaining their diagnoses
and their treatments,
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and wondering how many people actually
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can understand what's on
those pieces of paper.
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Health care in the United States assumes
that you have a working telephone
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and an accurate address.
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The proliferation
of inexpensive cell phones
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has actually helped quite a lot,
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but still my patients run out of minutes
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and their phones get disconnected.
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Low income people often have
to move around a lot by necessity.
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I remember reviewing a chart of a woman
with an abnormality on her mammogram.
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That chart assiduously documents
that three letters were sent to her home
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asking her to please come in for followup.
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Of course, if the address isn't accurate,
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it doesn't much matter how many letters
you send to that same address.
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Health care in the United States assumes
that you have a steady supply of food.
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This is particularly
an issue for diabetics.
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We give them medications
that lower their blood sugar.
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On days when they don't have enough food,
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it puts them at risk
for a life-threatening side effect
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of hypoglycemia, or low blood sugar.
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Health care in the United States assumes
that you have a home
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with a refrigerator for your insulin,
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a bathroom where you can wash up,
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a bed where you can sleep
without worrying about violence
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while you are resting.
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But what if you don't have that?
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What if you live on the streets,
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you live under the freeway,
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you live in a congregant shelter
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where every morning
you have to leave at 7 or 8 am?
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Where do you store your medicines?
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Where do you use the bathroom?
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How do you put your legs up
if you have congestive heart failure?
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Is it any wonder that providing people
with health insurance who are homeless
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does not erase the huge disparity
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between the homeless and the housed?