Language Matters
The American
Diabetes Association has released multiple statements on language and it’s
important to remember that language matters I would encourage you to erase some
words and phrases from your practice.
Erase These
Diabetic
Diabetes causes
Fail/Can't as a
clinical marker
'You' |
Empower These
Person with diabetes
(PWD)
Diabetes-RELATED
complications
Physiology focus
'WE' |
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One
such word is diabetic. This
word does not speak about
the patient--it speaks about
the disease. Instead we
should refer to a diabetic
as a 'person with diabetes'.
Another acceptable moniker
is 'the diabetes community'.
Diabetic retinopathy and
other diabetic complications
can be referred to as
'diabetes-related
complications'. After all,
people who do not have
diabetes still get
neuropathy, nephropathy,
retinopathy, and other
opathies. Too often I hear
clinicians tell patients,
"If you can’t lose the
weight by yourself then
we’ll start this
medication", or "if we fail
to lower your blood sugar to
our goal then you’re going
to need to do this". That’s
really unacceptable because
it implies to the patient
their entire picture is
somehow under their control.
And this is many times not
true! This is going to lead
to the patient getting
discouraged and feeling
judged. And they could start
wanting to avoid clinical
encounters and their
medications because they
feel that they are being
medicated as punishment for
not reaching their goals.
Instead, maintain a
physiology focus, "if
modifications to both your
diet and exercise don't
improve your insulin
sensitivity to the point
where your body is able to
self-regulate, then we'll
need to use pharmacologic
support. The medication will
help your body to do what it
needs to do to make sure
you’re healthy. If your body
is not able to produce
sufficient insulin on its
own then we'll need to
supplement that with
injected or inhaled
insulin".
And, finally,
let's talk about 'you-based' phrasing. When we talk about what you need
to do or what you’ve done in the past, it can come off as very judging
and blaming. A better way to communicate is to use 'we' statements such as, we
are going to work to reach this goal, or we’re going to see if this medication
works well for you and, of course, we’re going on this journey together. That
gives the ongoing message that this is a team approach that whether or not we
get the desired clinical outcomes.
Isolation - The Silent Symptom of Distress
One
particularly important area to screen for is isolation. Isolation can portrayed
in several ways: avoiding parties, not going out to eat, expressing anger at
others for their food choices, feeling distress at being connected or
disconnected from their care team or supports, or even not being able to use
food as a coping mechanism.
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Ask patients
what they avoid due to their diabetes
Encourage
patients that it is ok to have “moments of mess”
Encourage long-term perspectives on management
Screen for
anxiety, compulsivity and depression |
Ask your
patients what they avoid due to their diabetes and let them know that it’s OKAY
to have moments of unstable
blood sugars (for instance, during
holiday meals
with families). Let them know that it’s okay
as long as it’s not
an everyday occurrence. Encourage them to keep a long-term
view of their progress and remind them that it’s all about building healthy
sustainable lifestyles.
A major factor
in the burden diabetes on our mental health is the added number of decisions
that must be made.
A 2014 Stanford
University study found that the average person with type 1 diabetes makes more
than 180 diabetes specific decisions per day! That’s on top of what they’re
having to do as a part of their normal routine. Other statistics measure the
amount of mental energy put into diabetes management. The findings being similar
to that of a part time job--and many of our patients already have full-time
commitments like jobs
or
school. These decisions include things like medication
dosing, blood glucose monitoring, dietary choices, physical activity
adjustments, safety concerns, side effects from medications, hyperglycemia or
hypoglycemia prevention, and financial concerns.
Decisions,
Decisions!
Reduce the # of
diabetes encounters/ decisions in an effort to reduce the burden of care
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Anything we as
caregivers can do to reduce the number of decisions a patient has to make is
going to reduce their burden. Helping the patient to figure out how to reduce
the number of times they have to check their blood sugar throughout
the day, or reducing the number of medication dosages, or maybe combining
correction and meal time boluses, or lumping together medication schedules so
that they take medications only in the morning and at night. Also, helping
patients find healthy strategies and working out a viable implementation
schedule—writing
them in
a calendar or (better yet) a scheduling app so that they can just get alerts
when they need something.