Top Tweets for #INvisibleProjectDisparities
A huge congrats to Sick Cells Ambassador Arelys Feliz for being featured in this edition of #INvisibleProjectDisparities. 🎉And thank you to @US_Pain for always centering the patient and caregiver voices.
Have you ordered your copy? https://t.co/Ux1qEIEIiO
#INvisibleProjectDisparities
“Another doctor walked in and asked why she was crying. The first doctor replied, in a mocking tone, ‘She thinks she has Ehlers-Danlos syndrome.’”
Read Annie’s story: https://t.co/XjCX8WN4kD
@annieelainey
#INvisibleProjectDisparities #NMHM2021
“The result is a vicious cycle: already marginalized and vulnerable communities may be made to feel they have nowhere to turn for adequate mental health care.”
https://t.co/W9qwb8a3xL #INvisibleProjectDisparities @ElisaFriedlandr
“Until 2020, the integration of #telehealth into the health care system had been frustratingly slow.” https://t.co/BtmEcRKFxE @PNWUHealth @endorfinrush18
#INvisibleProjectDisparities
“Often, health care providers don’t recognize how their own privilege and bias impacts the care they provide to people of color, people with disabilities, and other underserved individuals.”
https://t.co/UJqJh7nYn0 #INvisibleProjectDisparities @NHeLP_org #NMHM2021
"Over the years she’s watched colleagues who were unaware of her diagnosis disparage patients as 'drug addicts' and 'frequent flyers.'"
Read Heather’s story of life with #sicklecell: https://t.co/O7UoMCegPa
#INvisibleProjectDisparities #NMHM2021
Get tips for selecting health insurance & saving on out-of-pocket costs:
https://t.co/eTkVUrY5Yb @NPAF_tweets #INvisibleProjectDisparities
“For example, it is well documented that women are offered psychotherapy more often than men, who are more likely to be offered pain-relieving medications.”
https://t.co/bhEG7BiYfj #INvisibleProjectDisparities
@HealthyWomen @forgrace
"Lupus is most certainly not a death sentence, and Jasmine encourages anyone who was recently diagnosed to not see it as such."
Read her story: https://t.co/1G0oMeqr5A
#INvisibleProjectDisparities #NMHM2021 @LADAOrg
“The fight for equal rights isn’t all on your shoulders, and sometimes you might not have the time, energy, or financial resources to push back.”
Get tips for self-advocacy as a LGBTQ+ patient: https://t.co/e4fDgApBm1
#INvisibleProjectDisparities
My husband, disabled #chronicpain sufferer, has to deal with this kind of B.S. — it's shameful. Thank you for speaking up, Erica! #HealthAdvocacy #INvisibleProjectDisparities
"That’s the hard part about bias and health disparities, Erica says: you often have to look out for them, and most times you don’t realize they’ve happened until months or years later."
Read Erica’s story: https://t.co/2PWGYD3BO6
@achysmileblog #INvisibleProjectDisparities
"That’s the hard part about bias and health disparities, Erica says: you often have to look out for them, and most times you don’t realize they’ve happened until months or years later."
Read Erica’s story: https://t.co/2PWGYD3BO6
@achysmileblog #INvisibleProjectDisparities
The importance of a trained, medical interpreter cannot be overstated. https://t.co/XOJoX7AFSZ
@CMIcredential #INvisibleProjectDisparities #NMHM2021
“You have the right to believe my experiences or not. Just please don’t tell me, ‘It can’t be that bad.’ Because you don’t know how bad MS can get for me.”
Read Nicole’s story: https://t.co/P7mIRe8G9V @nclark140 @mssociety #INvisibleProjectDisparities #NMHM2021
“In fact, a 2016 study revealed that half of white medical trainees believe myths including: ‘black people’s nerve endings are less sensitive than white people’s’ and ‘black people’s skin is thicker than white people’s.’”
https://t.co/CYT9H1qOdq #INvisibleProjectDisparities
“The specialists she visited—all male—were acquaintances, and Elisa describes a ‘boy’s club’ atmosphere. ‘Like they’ve got each other’s backs. But they didn’t have my back, so to speak.’”
Read Elisa’s story: https://t.co/4DNvvO6rPr #INvisibleProjectDisparities @ElisaFriedlandr
“In health care, there is often an invisible power dynamic that favors providers and administrators. It can be difficult to navigate, especially for patients from already marginalized groups.”
https://t.co/MWazK7n0bv #INvisibleProjectDisparities
“I’m legally blind due to the fact they just dismissed me and my pain.”
Read Arely’s story: https://t.co/lSw8MujpiK
#INvisibleProjectDisparities
“You’re so inspiring!” https://t.co/Q8KaM5PPcs
#INvisibleProjectDisparities
We are kicking off our new INvisible Project by sharing an article each day!
Calvin Eaton, of Rochester, NY, lives with multiple painful conditions. But that hasn't stopped him from building a career he loves. Read his story: https://t.co/UZaDMSbCKR
#INvisibleProjectDisparities
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