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.
At the time of this blog being published, I will be in route to Mexico in preparation for my weight loss surgery! ...It was finally time to put my health first and put my full faith in God!
What do you do when the life you want so desperately to forget collides with the life you've created? You feel.
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.
Mother's Day is never easy for me, because I don't have a relationship with my mother. She's not deceased, I just don't have a relationship with her, never really have to be honest.
Becoming a nurse taught me how to live with HIV.
Today I got the call that I have been not wanting to receive. I have known that my father has Alzheimer's, Dementia, and Parkinson's since May of 2020. It's been hard to make decisions for the person who I have felt caused me so much hurt.
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.
We all have baggage, we are carrying emotions we weren't meant to carry, and have allowed them to shape our identity!
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