Hi, my name is Ahmed (not my real name). I’m a 28-year-old med student, and I recently found out I have HSV-1 and genital warts. Learning about these diagnoses changed my life in ways I never expected. It wasn’t just the medical reality that hit me—it was the emotional weight, the cultural stigma, and the fear of how it would affect my future.

What makes this harder is that I’m engaged to the love of my life. Telling her about my diagnosis was one of the most painful moments of my life. Her response left me questioning everything—my worth, my future, and whether I could ever be happy again.

I’ve struggled with guilt, shame, and even suicidal thoughts. But I’ve also realized the importance of sharing my story. For anyone else out there feeling isolated, I want you to know that you’re not alone. This is my story.

## Can you share more about how you first decided to get tested and what prompted that decision?

Before all of this, life was moving along smoothly. I was busy with med school and excited about my upcoming marriage. I had no reason to believe anything was wrong—I felt fine physically. But as part of routine health care, I decided to request a blood test, including an STI panel.

I didn’t think twice about it. I assumed everything would come back to normal, so when my doctor told me I had HSV-1, I was blindsided. I didn’t have any symptoms—no sores, no outbreaks. To me, this didn’t make sense. But the blood test was clear: I had the virus.

It was only after hearing this news that I started piecing things together. I thought back to times when I wasn’t careful when I let the heat of the moment cloud my judgment. Those decisions, which seemed insignificant then, suddenly carried so much weight.

## Can you share more about how you first decided to get tested and what prompted that decision?

When I first heard the words, “You tested positive for HSV-1,” it felt like a punch to the stomach. I walked out of the clinic in a daze, replaying the words over and over. I didn’t cry at first—I was too numb.

The emotions hit later like a tidal wave. I felt ashamed, guilty, and terrified. The shame came from knowing I hadn’t always made the best decisions. The guilt came from imagining how this could impact my fiancé. And the terror? That was the thought of a lifetime of stigma, rejection, and judgment.

Adding to the blow was the diagnosis of genital warts. Despite receiving all doses of the HPV vaccine, I had contracted a strain not covered by it. I couldn’t believe my luck—or lack thereof. It felt like I was being punished for my past mistakes.

## How has your diagnosis impacted your daily life and routine, especially as a med student?

Before my diagnosis, I had a clear path in life. I was focused on med school, working hard to build a future for myself and my fiancé. But after, everything felt different. I couldn’t concentrate in class, and my grades started slipping.

At home, I was a wreck. I stopped eating properly, lost interest in hobbies, and spent hours lying in bed. Every time I closed my eyes, my mind replayed my mistakes. I couldn’t escape the voice in my head that kept saying, “This is your fault.”

Socially, I pulled away from friends. I was too afraid they’d notice something was wrong and start asking questions. My life became smaller and smaller as I isolated myself.

The uncertainty was the worst part. Since HSV-1 can be asymptomatic, I didn’t know if I had it orally, genitally, or both. Not knowing how I could transmit the virus to someone else filled me with dread.

## What was the conversation with your fiancé like when you shared your diagnosis? How did you prepare yourself to tell her?

Telling my fiancée about my diagnosis was one of the hardest things I’ve ever done. It took everything in me to open up because I love her so much, and the last thing I wanted was to hurt her. I told her about my HPV diagnosis first, and to my surprise, she was understanding. She reassured me that HPV often clears up within a few years and that we could wait until it resolved before being intimate. Her support gave me hope that we could get through this together.

But when I told her about HSV-1, things became much more complicated. At first, she seemed okay, as she associated HSV-1 with oral herpes, which she considered manageable. However, I could sense a shift when she began to grasp the uncertainty surrounding whether I have it orally, genitally, or both. Because I’ve never had symptoms, I couldn’t give her a clear answer. The fact that HSV-1 can be transmitted during asymptomatic phases only added to her concern, and I started to feel the weight of my condition in a whole new way.

She made it clear that she could accept the risk of contracting oral herpes, but genital herpes was a line she couldn’t cross. Hearing her say that was devastating. It wasn’t just about the virus anymore—it was about the possibility that my condition might fundamentally alter our relationship. Her words echoed in my mind, resurfacing all the fears I’d been trying to suppress. I felt like my world was collapsing.

Since that conversation, I’ve been struggling to find hope. I spend a lot of time lying in bed, crying and replaying everything in my head. The idea that I might lose her because of this is unbearable. I’ve tried to tell myself that genital-to-genital transmission of HSV-1 is rare, but even the smallest chance feels overwhelming. I didn’t have the strength to go into detail about the risks, especially when I’d already struggled so much just to reveal my diagnosis.

The hardest part is knowing how much I love her and how badly I want to build a life together. I’ve dreamed of marriage, having children, and growing old with her, but now all of that feels so fragile. I’m terrified of losing her, and the thought of finding someone else who might accept me feels impossible.

Her reaction has made me question so much about myself and my future. I can’t help but think about the mistakes I made in the past—reckless decisions that seemed harmless at the time but now feel like they’ve ruined everything. I admit I’ve made mistakes, and I’m paying for them in ways I never imagined.

Still, despite everything, I don’t blame her for how she feels. She deserves to make choices that are right for her, and I respect that. But her reaction has left me feeling lost, like I’m trapped in a situation I can’t fix. It’s been an emotional rollercoaster, and some days, I don’t know how to move forward.

## As someone from a Muslim background, how has your cultural and religious identity influenced how you feel about your diagnosis and your ability to seek support?

Being Muslim adds layers of complexity to my story that are difficult to put into words. In my culture, STIs aren’t just seen as medical conditions; they’re viewed as moral failings. The assumption is that if you’ve contracted an STI, you’ve made poor choices and strayed from the righteous path. It’s as if your diagnosis is a reflection of your character, not your health.

I grew up hearing these beliefs. They were unspoken but always present—a heavy, invisible weight. When I got my diagnosis, those ingrained judgments turned inward. I felt like I’d failed in every possible way: as a person, as a son, and even as a Muslim. I couldn’t stop thinking, What will my family say if they find out? What will my community think? Will I ever be seen as worthy again?

The thought of anyone in my community discovering this terrifies me. The reactions I imagine—judgment, pity, whispers behind my back—are unbearable. In our world, people don’t always try to understand the medical realities. Instead, they focus on how you’ve “brought shame” to yourself or your family.

Because of this fear, I’ve kept everything to myself. I haven’t sought support from people I know, even though I desperately need it. I feel trapped in silence, caught between the need to heal and the fear of stigma. It’s a lonely place to be, but I’m slowly learning that my worth isn’t defined by others’ opinions—or my diagnosis.

## You mentioned feeling suicidal at times—what has been your coping mechanism during these dark moments, and have you sought any professional help or support groups?

I wish I could tell you that I’ve handled everything with grace, but the truth is, I’ve struggled more than I ever thought possible. There were nights when I lay in bed, staring at the ceiling, wondering if it would be easier to just disappear. The pain felt so heavy, like a weight pressing down on my chest, making it hard to breathe.

I felt like I had no way out. I kept thinking, My life is ruined. My fiancé deserves better. My family would never understand. It was hard to imagine a future where I could be happy or at peace.

What kept me going during those moments was love. Love for my fiancé and the dream of a life we could build together. Love my future as a doctor and the idea that I could help others who might feel as lost as I did. I reminded myself that giving up would mean never seeing those dreams come true.

Writing also became a lifeline for me. I started journaling, pouring all my thoughts and fears onto paper. It helped me make sense of the chaos in my mind and gave me a way to release the emotions I’d been bottling up.

I also turned to online forums. Reading the stories of others who’d been through similar experiences was like finding a light in the darkness. Their words reminded me that I wasn’t alone and that things could get better. Knowing that strangers cared and understood gave me the strength to keep going.

I’m not completely healed—far from it—but I’m taking things one day at a time. I’ve learned that it’s okay to feel broken as long as you don’t let those feelings define you.

## What are your biggest fears for your future, both personally and professionally, as you navigate this chapter of your life?

The uncertainty about what lies ahead is one of the hardest things to deal with. I have so many fears that sometimes it feels overwhelming.

My biggest fear is losing my fiancé. She means everything to me, and the thought of her deciding she can’t handle the risk of being with me breaks my heart. I keep wondering, If she leaves, what then? Will I ever find someone else who can accept me for who I am?

In my culture, finding a partner when you have an STI feels almost impossible. The stigma is so strong that many people would reject you outright without even trying to understand. I can already hear the whispers and the judgment from my community if this ever came to light.

I’m also terrified about how this will impact my career. I’ve worked so hard to get into med school, but lately, my mental health has been taking a toll on my studies. I’ve been losing focus, and it’s hard to find the motivation to keep going some days. What if I can’t keep up? What if I let this defeat me?

And then there’s the question of children. I’ve always wanted to have a family, but now I’m scared. Will I ever feel safe enough to have kids without worrying about passing on my conditions? Will I ever forgive myself if I do?

These fears are constant, but I try to remind myself that the future isn’t written yet. There’s still time to build the life I want, even if it doesn’t look exactly how I imagined.

## What has been the most surprising or unexpected part of your journey so far in dealing with both HSV-1 and HPV?

When I started this journey, I thought I understood everything about STIs. As a med student, I’d learned about the science—the facts and figures, the transmission risks, the treatments. But what I didn’t expect was how much shame and self-judgment I would feel.

I always thought I was someone who approached things rationally. But when it came to my own diagnosis, all that logic flew out the window. I couldn’t stop blaming myself. I kept thinking, You’re a future doctor—how could you let this happen? It surprised me how much harder it is to face something when it’s personal, not just academic.

Another surprise was the kindness I found in unexpected places. When I turned to online forums, I didn’t know what to expect. Would people judge me? Ignore me? Instead, I found support, empathy, and understanding from strangers who knew exactly what I was going through.

Their words gave me hope when I felt hopeless. They reminded me that I’m not alone and that there’s still so much compassion in the world, even if it doesn’t always feel that way.

## If you could go back in time, is there anything you would do differently regarding your sexual health, or do you see this experience as a learning moment?

If I could go back in time, there are so many things I’d do differently. I’d take my sexual health more seriously and make smarter choices. I wouldn’t let the heat of the moment cloud my judgment, and I’d prioritize using protection every single time. Looking back, I realize how careless I was at times, thinking that nothing bad could happen to me. I know now that those moments of recklessness have lasting consequences.

I also wish I’d been more proactive about educating myself. As a med student, I should’ve known better, but there’s a difference between knowing the science and actually applying it to your life. I was too focused on the present and didn’t think about the potential long-term effects of my decisions.

At the same time, I try to see this as a learning moment. It’s painful, yes, but it’s also taught me lessons I’ll carry with me forever. I’ve learned to value honesty, both with myself and with others. I’ve learned that taking care of your health is a form of self-respect, and it’s something you owe to yourself and the people you care about.

This experience has also made me more empathetic. I used to think STIs were something that happened to “other people,” but now I know it can happen to anyone. It’s taught me not to judge others for their mistakes because we’re all human, and we all make them.

If I could go back and change things, I would in a heartbeat. But since I can’t, I’m choosing to move forward with these lessons and use them to build a better, more informed future. It’s the only way to find peace and keep growing.

## What message would you want to share with others who might feel isolated or overwhelmed after receiving an STI diagnosis?

If you’re reading this and you’ve been diagnosed with an STI, please know this: You are not your diagnosis. It doesn’t define who you are or what you’re worth.

It’s easy to let shame and fear take over, especially when society bombards us with stigma. But remember, you’re still the same person you were before. You’re still capable of love, happiness, and a fulfilling life.

Take things one step at a time. It’s okay to feel scared or overwhelmed—that’s normal. But don’t let those feelings stop you from moving forward.

Find support wherever you can. Whether it’s through therapy, friends, family, or online communities, there are people who care and want to help. Don’t be afraid to reach out—it can make all the difference.

And most importantly, don’t give up on yourself. Your story isn’t over, no matter how dark things may seem.  You are stronger than you think, and you are worthy of love, acceptance, and happiness. Never forget that.

**Also Read: Young soldier's** [**personal molluscum contagiosum story**](https://www.shamelesspath.com/blog/std-stories/fighting-shame-in-a-military)

Ahmed, a Muslim med student, shares his journey facing stigma with HSV-1 and genital warts. Discover his struggles with shame, guilt, and hope for acceptance.

Engaged and Diagnosed: Stigma as a Muslim Med Student

Facing stigma as a Muslim med student with HSV-1 & genital warts, Ahmed shares his struggles with shame, guilt, and the hope for acceptance and healing.