Addressing inequities in the treatment and diagnosis of psoriasis
A panel of BIPOC patients discusses their their difficulties in getting a psoriasis diagnosis.
Transcript
Traditionally, Black people don't have psoriasis. So for years, I went improper treatment, wrong diagnosis.
And as a young girl, having these lesions on their skin is just not pretty in addition to it being painful and uncomfortable.
[MUSIC PLAYING]
It's so important for us to be having this conversation today, as we know that racial health disparities exist. We also know that psoriasis has shown
to have a greater impact on the quality of life of Black and Brown patients than white patients and that some dermatologists feel less confident diagnosing
psoriasis in darker skin tones. What were your presenting symptoms and how long did it take before you actually
got your diagnosis? With psoriasis, there is a mental component
that brings about the anxiety, the depression, the stress, which you will see physically, but sometimes you can't see it.
And when I was on those medications, you couldn't see that I was really hurting inside and that I really just felt like a shell of myself.
What were the characteristics of the doctors that finally you felt comfortable with this type of person listening to you, hearing you,
and trusted their diagnosis and their treatment? Most of the dermatologists were white men.
Constantly going to them and getting improper treatment, improper care, medicine that just doesn't work, it shapes the way
that I interact and I engage with health professionals moving forward. Sometimes [INAUDIBLE] say, I have this degree, this degree,
this knowledge-- I shouldn't have to sell myself like a lemon and pitch something to get--
just courtesy. It wasn't until I found a female Black doctor
that I felt seen-- felt seen, felt heard.
When your life is on the line, it's just-- for years, I operated as a shell of myself.
What are some of the questions that you would point them to to say, these are some of the things that you should ask a provider?
If you are going to a doctor that is not a person of color, I would ask about their experience with darker skin.
A lot of the-- for psoriasis, for example, a lot of the creams will bleach my skin. Talking to the nurses is something
that I would do as well because they will give you a lot of insight on what is going on and which doctor you should probably go to,
a lot of research on Google. And then whatever medical questions that you have,
have your notebook, have your phone. And if your doctor cannot answer those questions,
they don't need to be your doctor. You should not leave that office with any unanswered,
anything unsaid. You should leave the office feeling secure in what the steps are moving forward.
You can challenge in a nice way if you feel you've been misdiagnosed or under-diagnosed or whatever. You don't want to skim over things.
You want to jot down everything. Sometimes when I have appointments, I go home and have questions. I go back. I go through the portal.
Wherever it is, you want to keep a line of communication open and see how receptive they are to you challenging a more
in-depth look at things, not even in an aggressive manner, but in an informed manner. I'm showing up for myself, and that is your obligation
and your duty as well. [AUDIO LOGO]
psoriasis
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