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You don't have to. You. Don't. Have. To. No tienes. Tu n'as pas. I can't repeat it enough. You do not have to take everything that comes to you. Not everything you find is yours to pick up and not...

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Have you ever heard a doctor, advocate or friend say "you probably know someone living with HIV and you just don't know it"? People hiding in plain sight. I've said that to people. It's a way to get...

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If you can read this, or let someone read it to you, and you are sexually active – and you don't know your status or the status of your partner(s), you are at risk for HIV. Yes, YOU TOO! Woman, man...

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I recently "came out" with my HIV status on Facebook even though I've been quietly doing the advocacy thing in the background for a while now. Caring for my patients, using my writing, some small...

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I attended the virtual USCHA conference this year put on by NMAC, supported by too many sponsors to name and I want to start by saying this: I love us. "Us" as in the HIV community.

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As a woman, I know what it feels like to be invisible. As a Black woman that feeling is sometimes intensified. It gets juxtaposed with occasionally being the person everyone is looking at, but not really seeing.

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One of the most powerful things a patient said to me was "Just because I hear you doesn't mean I understand what you're saying". His regimen was changing because he had some resistance and I was doing...

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This month marks my 9th year of living with HIV. Wow. Wait, this month marks my 9th year of living with HIV? I had to write it again because who would ever have thought I'd be here? The wild part is...

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I'm going to go out on a limb and assume something. Don't get mad if I'm overstepping or overstating. I know it doesn't apply to everyone, but it's common enough. It's just a little something that I...

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I filled out a questionnaire today. It was about wise words that I would offer to someone newly diagnosed with HIV. It's interesting to me to see how my perspective has changed over the years and how it's stayed the same.

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