Ever since I came out of the closet for the second time with my diagnosis I made a promise to myself that I would be vocal, to anyone who’d listen, about my life as a gay man and living with HIV.
Essentially, I had practice coming clean about situations in my younger years when I talked with friends and schoolmates about my adoption from a foster home in Colombia. I thought nothing of it, but what always amazed me was how fascinated people were with my story. As I grew older I realized it wasn’t so much my adoption that they were interested in hearing, rather the passion I exuded in my words.
It’s always great to get my listeners to laugh when I told them I was adopted and I happened to be on sale that week and went by the name, “Baby Number 5.” Of course I was joking! From there on I knew that I loved to make people laugh…even over a touchy subject like HIV. I never stop talking about my beginning HIV story and where I am now, but recently I returned my energies back towards gay rights in our country - something I hadn’t cared much about since I began with HIV. Now I advocate for both the rights of positive people and gay people.
I’ve endlessly told my HIV story and spoke about my background on many websites, including my own blog site and in particularly, Robert Breining’s POZ I AM site where individuals recently diagnosed can find a safe haven. Now that it’s been over two years since my diagnosis I’ve acquired the skill to summarize my limited experience (time-wise) with HIV in a couple of paragraphs. That way it leaves the dialogue open for people to reach out to me for further details.
I was diagnosed January 21, 2010. I went into a severe depression that only took a downward direction when I was told that it was in my best interests to start medications right away given my low T-cell count at the time. I began my regimen March 27, 2010 and was declared undetectable with a growing T-cell count by June. I was lucky and once I knew that there was nothing to worry about I disclosed my status to my parents one hot July evening at home. Following that, I went viral with a YouTube video that disclosed my status to friends, relatives, co-workers and strangers. The video continues to get recognition and praise for the most part and can be found at the end of this post.
My video skills have since improved, but I’ll never forget how nervous I was when I filmed it. It took almost a whole day to get my words right. One can probably pick up on the fact that I stuttered with my words, trying to get all my feelings out in ten minutes (I thought it would be my only video.) Needless to say when it was published my Facebook page, my cell phone and email FLOODED with responses from all my connections of life. They cried and admired, making sure I was okay and that I wasn’t dying. Talking to everyone as if I was a doctor explaining how my HIV isn’t killing me, I quickly realized that I made a breakthrough with my words and began a stepping stone for people’s idea of HIV. Sky was the limit for me from that point on. This coming August that video will be two years old.
So there you have it, my HIV history in a speedy nutshell. I’m not one for living in the past as I have a mind to just look at the road ahead- bumps and smooth terrain alike- with a little more knowledge and experience under my belt.
I’m at a place in my life where I meet people in bars or social events and I talk about my HIV like it’s an everyday thing - because it is, in retrospect. I know disclosing isn’t as easy for everyone, but I’d like to think my one voice will encourage others to come out, negative and positive, and talk about HIV. Besides, I’m tired of being a third class citizen - second because I’m homosexual and third for being an HIV positive homosexual. And don’t get me started on HIV-positive women in this country as my heart will always have a place for them.
The reason I bring this up is because I’ve transitioned my HIV story from being recently diagnosed to living with HIV. I’m stealing the “So What, Now What?” slogan. I live in America where the news and media is lately saturated about our President’s support for gay marriage. Sure, I’m happy to hear about his support, but I’m one of those people that want to see action. After all it is an election year in our country and isn’t timing just everything? What happens if one day my body’s virus takes a turn for the worse and my partner at the time is unable to see me in the hospital?
With my “so what, now what” attitude and my HIV in a healthy check I reassembled my fight for gay rights that I put on the backburner since January 21, 2010. I’m still hopeful that more and more of our states and provinces will approve equal rights for all. This will be quite a year in our country with the election, the mass hysteria over gay rights and the International AIDS Conference being held this summer in Washington, D.C. The President won’t be able to hide then when he’s asked why America has a waiting list for medications and treatment for even one individual too many and what he plans to do about it.
I can’t wait when a few decades down the road I’m writing the memoir of my life and I make jokes at the fact that I remember a world that opposed gay marriage and people feared HIV. Those were the days. However, that future I set will only be a reality if more people like me come out from the shadows and scream about their HIV.