This garden, created by award-winning designer Matthew Childs, serves as a powerful symbol of the progress made in the fight against HIV since the 1980s.
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.
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?
I know I'm not that old; I'm only 51. I'll be 52 in July, but still I can't help but start thinking about what my legacy will be. How will I be remembered when I'm gone?
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.
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.
On a recent episode of TheBody's Instagram Live series “At Home With,” The Well Project executive director Krista Martel talks with Charles Sanchez about what our organization is up to.