After I got my diagnosis, I automatically started to apply what I knew, to ask questions, to better understand. You might not believe it, but we're still so far behind in terms of information.
Automáticamente después de saber mi diagnosis empecé a usar mi conocimiento, a hacer preguntas, a informarme porque, aunque no lo creas, todavía estamos muy atrasados en cuestión de información.
I understand mental health is a big issue in today's society, but what happens when the mental health of the provider is at stake here. What should we do?
Many may be able to relate that diagnosis day is rarely filled with happy memories. As time goes on, we cope and come to terms with our diagnosis and live out our bad ass lives, but there's still always that reminder.
Becoming a nurse taught me how to live with HIV.
When searching for support groups, I found friends of all ethnicities. However, I didn't find many from my Asian community... I encourage others to talk openly about living with HIV.
As we commemorate National Women and Girls HIV/AIDS Awareness Day 2024, I can't help but reflect on my journey over the past decade, filled with challenges, resilience, and ultimately, triumph
No tienes que pasar por tener VIH o SIDA solo. Incluso si no los tienes, puedes crear tu propia familia extendida.
You don't have to go through having HIV or AIDS alone. Even if you don't have them, create your own extended family.
El estigma es más mortífero que la enfermedad en sí, y el conductor principal del estigma del VIH, en mi opinión, es la iglesia.
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