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Visibility vs. Fear: What Happened When I Wore "I Am HIV+" in My Own Community

Submitted on Apr 1, 2026 by Godsbabi
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A Girl Like Me blogger Godsbabi.
Photo courtesy of author

Last night, I attended my first social event within the HIV community. I went in hopeful—open to connection, understanding, and a sense of belonging.

What I didn't expect was conflict.

I chose to wear something intentional: a shirt that read "I am HIV+." For me, it wasn't fashion—it was purpose. It was a quiet but bold declaration that I am not ashamed, that I am still here, and that I refuse to hide.

But my presence—and my visibility—sparked a strong reaction.

Another woman became visibly upset. She raised her voice and expressed that what I was wearing represented everyone at the event, and that it could put people in danger. She said something that stayed with me: that people are killed over things like that.

And she's right.

There is still very real fear surrounding HIV. There is still stigma, discrimination, and in some places, danger. For many, privacy is not just a preference—it is protection.

But there is another truth that exists alongside that fear.

Silence is what allowed stigma to survive this long.

For me, wearing "I am HIV+" is not about speaking for anyone else. It is not about forcing visibility on those who are not ready. It is about reclaiming my own narrative. It is about choosing to stand in the light instead of shrinking in the shadows.

Before my diagnosis, I searched for someone who looked like me—someone who didn't fit the stereotypes, someone who would say, "This can happen to you, too."

I couldn't find her.

 

We often talk about awareness, but awareness requires visibility. It requires real faces, real voices, and real stories.

 

And that absence is part of the problem.

We often talk about awareness, but awareness requires visibility. It requires real faces, real voices, and real stories. It requires people who are willing—when they feel safe and ready—to say, "This is my truth."

The LGBTQ+ community faced similar tensions in their fight for acceptance. Visibility was once seen as dangerous, controversial, and even irresponsible. But over time, it became one of the most powerful tools for change.

I believe we are at a similar crossroads in the HIV community.

There are those who need privacy to feel safe—and that must be respected.

And there are those who choose visibility to create change—and that must also be respected.

Both can exist.

But one cannot silence the other.

I left that event with mixed emotions—hurt, but also more certain than ever about my purpose.

Because if my visibility makes someone uncomfortable, it may also make someone else feel seen.

And that is worth everything.

HIV is no longer the story it once was. With proper care, people living with HIV can live full, healthy lives.

But stigma?

Stigma is still very much alive.

And I refuse to carry that.

I am not representing everyone.

I am representing myself.

And for someone out there searching the way I once did—that is enough.

— Marie Niles
Founder, Bee HIV+ Foundation
"Together, We Thrive"

Submitted by Red40something
2

This is a thought provoking blog, and thank you for your transparency in sharing. When walking into advocacy spaces I think many of us assume that the default is safety in visibility. I too have made people uncomfortable by wearing HIV themed shirts in spaces that are not explicitly designated as such. I could see the other person point though as a nurse having worked in a clinic where both people living with and without HIV got care. For many, true safety is found in invisibility and fitting in.

This is definitely a situation where there is no clear answer and my reaction has become to choose the path that offers the least harm to the most people. (In medicine- first do no harm)  For example a conference about HIV i would wear my gear, for local meetings or spaces that aren't broadly advertised as being HIV friendly or in spaces where it might be "mixed company" I might wear something a little more subtle like a ribbon or pin over a tee - but honestly- there is NO WRONG way for you to do you and walk in your truth!  

Appreciate your voice and advocacy! 

Submitted by Godsbabi
0

We should all be able to wear what we are comfortable wearing. I choose to wear HIV Awareness clothing everywhere we go unless it's a more formal event.   We did a morning Yoga event and then a Bowling escapade that evening.  I don't comment on peoples choice of religious shirts, pride clothing, or anything regarding any other illness (Ie cancer/mental health/autism).  I would never put anyone is a position to implicate them or expose their status, but to esentiall be attached at my first community event was very hurtful.

Submitted by Red40something
1

I should have said this first-- I'm sorry you went through that. Feeling like you are being attacked when you expected support is a lot to process. The only other thing I can say to it (and its not an excuse!) is that the stigma and shame of HIV run deep and eveyone deals differently. I do hope you remain encouraged and continue your advocacy journey. 

Submitted by Godsbabi
1

You’re so sweet!! Noting will stop my advocacy, but your words of encouragement and support mean everything!! I recognize that I am relatively new with my diagnosis. I don’t begin to know what it’s like being diagnosed years ago!! I am navigating this the best way I know how and I’m 100% certain that I’ve made a difference in people’s lives. I will not allow one bad experience cause a detour! I turn my pain into purpose and I’m doing GODS work. I’m thankful for this platform as it also shares awareness to other women that have experienced more stigma and have more fear - let’s have Grace with each other.  I’m trying to raise awareness by VISIBILITY not just amongst those infected, but to a world of others just like I use to be!!! 

Submitted by TrulyBlessed
1

I absolutely support you wearing what you want. I would wear a shirt stating my diagnosis. If people can wear shirts saying U=U I can wear a shirt stating I’m positive. After living with this diagnosis for over 20 years now I put a face to it. Godsbabi (sis) Im so dam proud of you. Thank you for being brave, courageous and being you. I love you sis keeping advocating and educating beautiful ❤️

Submitted by Godsbabi
1

I wish I could just reach out and hug you through this BLOG !!! Thank you 🙏  this took a psychological toll on me and your words of encouragement were just what I needed!!

Submitted by TrulyBlessed
1

You have made a big impact in my life and so many others. It took me awhile to be comfortable speaking out and sharing my diagnosis. You have made an impact from the start and I absolutely admire and respect you for that. We should never shame a person for speaking. That is anger misplaced. I love you and thank you for being you ❤️

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