I almost quit after the section on “Racial Categorizations in the United States” b/c it oversimplifies & inaccurately recounts the history of census racial designations.
(No “Black” or “Native” in the 8/2/1790 census, btw. Indigenous ppl were first counted in the 1860 census)
Many weren’t “white” until coming to the US & many immigrated to access “whiteness”
The US census can’t be used to demonstrate the merits of race as a proxy for biology or ancestry - white is a group for the non-Black/non-othered & includes Northern European & North African folx
The authors then refer to ethnicity as a way to capture “common values, cultural norms”
The oversimplification is offensive. Hispanic/Latino is not a monolithic grouping of people. The authors even show in (figure 1) how different ancestry can be *within* this ethnic group.
That difference in ancestry translates to VERY different cultures in terms of food, customs, & even language. Sociopolitical relations also translate to different ways that people are treated based on the precise origins of their Hispanic identity.
Anyway-not going to pick the whole thing apart- the authors are basically like: race/ethnicity is an epidemiologically important variable and we shouldn’t toss it.
But no one has actually argued that people should stop studying racial differences and inequities
We’ve argued that we should study race w/ the same scientific rigor & scrutiny as other variables-that we should explicitly define race like we do other exposures & avoid overstating what data show about a cohort chopped up into Black/White/Other using poorly defined criteria
We’ve argued against using race as a proxy for a stereotyped composite of socioeconomic exposures. Want to studying how housing, or personal experience of racism or income or zip code impacts health? Then, Beloved, THOSE are your exposure variables, not race.
We’ve argued that when designing studies or framing discussion of data, researchers shouldn’t selectively ignore prior research/writing from @DorothyERoberts and others that debunks race biology & demonstrates genetic variation within racial/ethnic groups
We’ve argued for research that addresses (not just describes) health disparities
Maybe we could also abolish the convention of reporting racial inequities as a deficit in the historically “othered” populations?
Centering whiteness as the “normal” against which all else is compared reinforces the falsehood of the supremacy of whiteness.
It warps perspective & leads to blaming the culture & genes of minoritized people for illness. Problematic if the goal is equity & anti-racism, no?
Where we currently report “Black people have less survival compared to white people for X disease” what if we discussed the pathology that influences *excess survival* - hoarding of privilege, power, access, & resources?
Would we-by using traditionally excluded/othered populations as the reference -be less inclined to search for polymorphismes of uncertain significance to explain major racial inequities?
Would we be better positioned to avoid research w/ intrinsically racist hypotheses?
So the “reckoning” : are y’all really trying to be anti-racist or are y’all just playing?
Cuz if you’re really trying to be anti-racist & dismantle structural racism & all the things that are oft said these days, it’s kind of an all or nothing thing.
No sprinkle of racism is acceptable-it’s all bad. It’s all got to go-not slowly, but expeditiously.
Nah fam, we’re not keeping racist hypotheses b/c the outcome might be net good for some.
Being sick is bad enough - fatigue, pain, shortness of breath. I imagine that to be a member of the majority caste in this country is to be able to just be sick. To be able to focus energy on getting well and maybe (because medical capitalism) how to pay.
There is so much more on the minds of Black patients - considering if the hospital you go to will treat you well (or at all). To have to, in the midst of the emotional and cytokine storm of infection, muster strength to fight for adequate care. To trade rest for diligence.
Last night while researching frailty scores, I vividly remembered being paged at 2am by the paging operator to call a patients family member while I was working in the ICU (back in the day when I did such things 😅)
Things were calm - and I figured a patient family member paging in the middle of the night was probably important - so I called:
“Is this Dr. Weeks?”
“Yes”
“you may not remember me, but I’m ___ you took care of my dad a few months ago and I wanted to talk about his paperwork.”
Now this was curious. This patient died but my mind is a Rolodex of patients I’ve pronounced so I remembered this family well.
“How can I help you?”
“Well I noticed in the admission note you wrote and the discharge summary you listed “failure to thrive” as the chief concern.”
I try to be thoughtful about what I write/say because words matter. I don’t always get it right, but this is a hill I am willing to die on.
*clears throat*
🗣 We don’t need to fix Black people’s mistrust. We need to fix medicine’s lack of trustworthiness. #COVID19#CovidVaccine
It isn’t enough to “remember Tuskegee.” The Tuskegee Syphilis Study ran from 1932- 1972. There’s segregation and disregard for humanity happening in the here and now.
40+ years after Tuskegee ended & 50+ years after “whites only” signs came down and hospitals are still segregated spaces! There are hospitals where it is rare to find a Black patient or provider.
Transparency involves being honest abt who/what you are.
So it’s probably less benevolence driving the consideration to prioritize minorities & more interest convergence. Minorities r disproportionately impacted by the virus & are a large portion of essential low wage workforce
It is in the interest of Black people to take a vaccine that could curb community spread of a virus that is killing us AND it is in the interest of a country that wants to get back to “normal” to not have a workforce that isn’t sick/vulnerable & overcrowding hospitals.