
Alexandra Power-Hays, MD
@DrPowerHays
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Same username on Blue Sky. Find me there! Sickle Cell Doc & hematologist fighting for our pts, locally and globally 🌍
Joined September 2019
Did your hospitals #AntiRacism pledge include efforts to help #SickleCellWarriors?. If not, you've got more work to do!.💪🏿💪🏾💪🏼. @PTMcGann & I outlined some steps to get you started. #PHOdocs #hematopoieticjustice #SickleCellAwarenessMonth #MedTwitter.
nejm.org
As medical leaders around the United States issue statements denouncing racial injustice and calling for the dismantling of racism, we must ensure that these pledges translate into durable improvem...
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RT @AmerAcadPeds: Pediatricians do not profit off vaccines. In fact, most pediatricians either break even or even lose money when they offe….
nytimes.com
Experts said the health secretary’s remarks send a dangerous message: Don’t trust your physician.
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Does anyone out there have any recommendations on a good course for the mandatory 8 hour DEA training? . Ideally a course that will help me to take better care of people in pain #meded #chronicpain #sicklecell.
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RT @GeauxGabrielle: Everybody is gonna feel this. But with all my heart, I am so sorry for rural disabled children. Especially in the south….
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Wasn't there an Executive Order on Day 1 to restore freedom of speech and end government censorship?. "Government censorship of speech is intolerable in a free society".
🚨BREAKING. From a program officer at the National Science Foundation, a list of keywords that can cause a grant to be pulled. I will be sharing screenshots of these keywords along with a decision tree. Please share widely. This is a crisis for academic freedom & science.
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RT @PeteButtigieg: Despicable. As families grieve, Trump should be leading, not lying. We put safety first, drove down close calls, grew Ai….
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RT @RepJasmine: If Trump doesn't reverse course, millions could lose healthcare, food assistance, childcare, and even emergency services.….
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3rd principle: Ujima, we take care of our own. Grateful that our amazing community of leaders has decided to raise money and collect coats for our #sicklecellwarriors this year! 🙏🏽.
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I just set up my Blue Sky account. Hoping to recreate the supportive and educational community of #sicklecell advocates, nerdy academics, blue dots prepared to care for our world, and anyone willing to share pet photos. Same username, find me!💙.
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RT @dukesickle: Dr. Ivey sharing his experience with SCD, nearly dying from ACS and starting on hydroxyurea, a game changer for him in 1996….
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RT @CodyGathersMD: PICU boards studying today. Someone tell me why out of all the practice questions I did, the only child living in a fost….
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RT @BarackObama: Don't wait – check your state's voter registration deadline today and make sure you're registered and ready to vote. And t….
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The above photo is old. Thanks to input from our patients & excellent leadership from @JPCincyOnc and Dr. Ware, oncology and hematology now have their own staffing and units with art and photography that is representative, diverse, and welcoming to all (more on that another day).
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This story is especially important for #PHOdocs and pediatric hematology/oncology divisions in September, which is for some reason both #ChildhoodCancerAwarenessMonth & #SickleCellAwarenessMonth
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It's not a competition of which diseases are worse, but I want these options for her and other #sicklecellwarriors as well. I sat back down.
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My heart sank. Do I tell her that #sicklecelldisease is just as hard? That its more painful? Still life-threatening? And life-long. Do I tell her that thanks to incredible advances, most children w cancer will be cured? That almost all will have access to life-saving treatments?.
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A different type of hand-on-the-door doctor story:. Recently a #sicklecellwarrior was admitted for pain. She was new to me & when I checked on her in the afternoon we talked about school, friends, tik tok. Not medicine. A few moments of calm during a busy week as a new attending.
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