KatieAdsila's blog

The lights have come out all over town, in the department stores, on the city lampposts, and in homes and yards across the country. How I used to love those lights, along with everything else that made the holidays festive: annoying dinners with family, shopping in crowded stores, and watching memorized Christmas specials… but it was still special.

It was a normal quiet Monday night when I got the first email. It was after eleven o’clock and I was winding down for the night while watching tv, who could be emailing me I wondered, pinkfoxxphoenix?? Who the hell is this?

I may never forget the night I got the email from Bruce Richman (founder and Executive Director of the Prevention Access Campaign U=U) asking if I would be interested in joining a campaign.

I love September, because it’s that time of year again, time for the end of summer conference on the sands of Fort Walton…Positive Living. I love this conference and look forward to going every year, because of all the HIV conferences, this one is special, let me tell you why by sharing my experience with Positive Living that began four years ago.

Touchdown… I finally land in Huntsville International Airport at 10:00 pm. I felt like it was two in the morning and I walked all the way to Huntsville from Orlando on foot. I was exhausted, but what...

I'm sitting here thinking about an upcoming conference that I'll be attending in the next few weeks, thinking about my schedule, my expectations and anticipations, but mostly about the people I'm...

I remember being in the seventh grade living on Cape Cod in the early 80's, and the fear of AIDS that gripped society at the time. Stigma was a monster in those days, greater than the Boogeyman under...

I'm still a very young advocate, having just gotten into HIV advocacy a year and a half ago, but I'm no newbie to depression. As a transgender individual I've lived with deep and debilitating clinical...

I first heard the Undetectable equals Untransmittable message in 2016 and it changed everything about how I felt about myself. I was diagnosed in June of 2000 so that’s 16 years of living in the dark...

Long Term Survivor day is coming up soon, a day when we celebrate the longevity, the courage, the strength and especially the wisdom of those who have lived with the disease for many years, through...