Geez!! Anyone else feeling really really tired, exhausted and unmotivated?! I have been for awhile, and I can't even blame covid although it certainly hasn't helped. I was talking with a coworker...

Have you ever battled with HIV fatigue and/or depression and felt very alone in your own sadness? A particular scene appeared in front of my vision: I was sitting behind my friend Karuna on her...

I recently decided to get the Covid vaccine. When it first started being administered I decided I was going to wait to see what happened to everyone else who got it. I didn't trust it. I felt it was...

I have a least favorite question when it comes to HIV. It annoys me. It didn't always, but over time due to folks' reactions and overheard statements, it gets on my damn nerves. "May I ask you...

Most of us long term survivors living with HIV virus are not doctors or nurses, but have impacted and helped improve the wellbeing of newly diagnosed persons. Fifteen years ago, a neighbour came to my...

My name is Jonique (John-Neek), I am a single mother of two smart and amazing HIV-negative boys. I was born and raised in New Haven, Connecticut.

My lovely people, can you explain to me why white people coming to Africa are quickly called "experts", but people of African descent in Europe are often called "refugees, migrants, or illegals"...

Hi all, as an aging member of our community I have seen and dealt with a lot of issues. Yesterday during a group conference call regarding health and aging with HIV, I learned that a drug I took for...

It’s hard to believe that we’re coming up on the 40 th anniversary of the first reports of what would come to be known as HIV. My personal journey with HIV began in 1994 when my sister, Ellen, was diagnosed with AIDS—with under 100 T-cells. It was a devastating diagnosis for my family, and the after-effects (including the degree to which her disease was accepted, or not, by those around her, and what she did with that) have had a long-lasting impact on me.

I've had this virus nearly 11 years now and not long after diagnosis, I made it public. I'm sure a lot of those reading can relate and understand my frustration.