If medical providers want to ensure adherence and linkage to care for people living with HIV, they will need to check their humanity.
Health, social, and psychological issues pummel people living with HIV on a daily basis, yet our community continues to not just survive, but to thrive.
A Minnesota HIV activist recounts her epic tale of overcoming not one, but two, diseases that can destroy us if we don’t accept—and treat—them.
Black communities have many reasons for mistrust of medical authorities. But getting vaccinated can help us get to a place where we can be together again, safely.
“I don’t know what healthy looks like anymore,” says Pato Hebert. “I know what I thought it was. I have fantasies of what it could be.”
The Americans with Disabilities Act prohibits providers from turning away patients based on their HIV status. When it happened to veteran HIV activist Mark Milano, he fought back.
Undetectable equals untransmittable (U=U) doesn’t mean the burden of staying HIV-free is solely on positive people.
“Because of my diagnosis and the struggle that I went through, coming to terms with it, I think it has made me a stronger person. I’ve actually accomplished things I never thought I would.”
Pride isn’t cancelled this year—in fact, it’s more inclusive than ever.
De Vonté Williamson writes about his journey of self-love and self-acceptance.