Hi, I’m Draper, I’m 29 and my journey hasn’t been an easy one. If you’ve ever felt like life has handed you one challenge after another, you might understand where I’m coming from. Growing up, I always felt a little different. Living with cerebral palsy meant I had to overcome barriers that most people don’t even think about—things like walking without drawing attention or proving my worth in a world that often measures people by their physical abilities.

But life had more in store for me. At 23, just as I was starting to figure out who I was, I received news that changed everything: a herpes diagnosis. It hit me like a ton of bricks. Suddenly, I wasn’t just someone trying to navigate life with a disability—I was also someone carrying a stigma I never asked for.

I’ve always tried to be honest and upfront with people. But being honest in a world that judges harshly can feel like standing in front of a firing squad. Relationships have always been hard for me, but this diagnosis made them feel impossible. The fear of rejection became something I carried every day, and there were times I wondered if love or acceptance was even in the cards for me.

Yet, here I am, sharing my story with you—not because it’s easy, but because it matters. If you’ve ever felt ashamed, afraid, or like giving up, know that you’re not alone. My story isn’t just about the challenges I’ve faced; it’s also about the resilience I’ve discovered along the way. It’s a story about learning to live with vulnerability and finding hope, even in the darkest moments.

Let’s dive in together.

## **How Did You First Find Out About Your Diagnosis, and How Did It Affect You Emotionally at the Time?**

I remember the exact moment my life took an unexpected turn. I received a phone call from a woman I’d been with, telling me I needed to get tested. Her tone was calm but distant, and she didn’t give me any details. At the time, I tried to stay hopeful, convincing myself that whatever it was, it could be easily treated. But deep down, I knew something wasn’t right.

Looking back, I realize she likely knew exactly what she had passed on to me. That thought alone brought a wave of emotions—anger, sadness, and a deep sense of betrayal. To make matters worse, this was only my second sexual experience, something that should have been simple and joyful. Instead, it became a defining moment that marked the beginning of a journey I never expected to take.

Finding out that I had herpes felt isolating. It was more than just a medical diagnosis—it was a label that carried stigma, judgment, and fear. I couldn’t help but wonder, “How will this change the way people see me? How will this affect my relationships?” It was overwhelming, to say the least.

## **What Has Been the Most Challenging Part of Living With Herpes, Especially in Relationships?**

Relationships were already hard for me long before herpes became part of my life. I was born with cerebral palsy, a condition that has always added an extra layer of complexity to how I connect with others. While my disability isn’t always visible unless I’m walking, it’s something I’ve always felt the need to disclose early. The truth is, being upfront about my condition has been a necessary but challenging process, one I’ve had to navigate carefully to avoid misunderstandings or disappointment.

When herpes entered the picture, things got even harder. It felt like I was piling one more reason for rejection onto an already daunting list. I could handle being seen as “different” because of my cerebral palsy, but adding the stigma of herpes? It often felt like too much to ask of anyone.

One of the hardest parts has been the way people react when I disclose my status. I’ve gotten used to seeing the shift in their expressions—sometimes there’s politeness, but more often, there’s a subtle withdrawal. I’ve tried to convince myself that this is just part of the process, but it doesn’t make it any easier. Every rejection feels like confirmation of my worst fears: that I’m asking for more than anyone is willing to give.

Still, I keep putting myself out there because I believe in being honest and giving others the choice to decide. But deep down, there’s always a part of me that wonders if I’ll ever find someone who sees beyond the labels to the person I really am.

## **How Has Disclosing Your Status Impacted Your Dating Experiences?**

Disclosing my herpes status has been one of the hardest things I’ve had to do. Every time I start talking to someone new, there’s this looming moment when I know I’ll have to tell them. I’ve learned not to wait too long because the longer I wait, the more it feels like I’m hiding something. So now, I disclose early—within the first few days of talking to someone.

In some ways, this approach has been better. I haven’t been accused of leading anyone on, which happened to me in the past when I waited too long. But disclosing early hasn’t exactly led to positive outcomes either. More often than not, the conversation ends shortly after I reveal my status. Sometimes, they’ll politely thank me for being honest, but I can usually feel their interest disappear.

What’s particularly hard is that I’ve been through this before, in a different way. Because my cerebral palsy isn’t immediately noticeable, I’ve always had to disclose that too, especially before meeting someone in person. I thought I was used to the discomfort of these conversations, but adding herpes to the mix has made it feel heavier. It’s not just about explaining my situation anymore—it’s about bracing myself for rejection, over and over again.

I keep hoping for the day when someone won’t lose interest, but it hasn’t happened yet.

## **What Led You to Change Your Approach to Disclosing Your Status?**

To be honest, there wasn’t a dramatic moment or shift that led me to change how I disclose my status. It’s something I’ve always felt was the right thing to do from the start. Not disclosing has never been an option for me because I couldn’t live with myself if I didn’t give someone the choice to decide. The idea of passing something on to someone unknowingly is something I would never want to carry on my conscience.

I’ve seen firsthand how not being upfront can harm others. Some of the people I’ve talked to have shared stories about being blindsided by a partner who didn’t disclose their own curable STDs. Those stories stuck with me and reinforced my belief that honesty is the only way forward.

I disclose early not because it’s easy but because it feels like the responsible thing to do. I don’t want anyone to feel misled or trapped. Even though it usually results in rejection, I’d rather face that than know I wasn’t fully honest with someone.

## **Have You Encountered Any Positive or Unexpected Reactions When Disclosing?**

I wish I could say that I’ve experienced positive reactions, but honestly, that hasn’t been the case so far. Most of the time, people thank me for telling them, which I suppose is better than outright judgment. Occasionally, someone will share their own story—usually about a time when they were in a similar situation with a partner who didn’t disclose their curable STD.

Hearing those stories does make me feel like I’m doing the right thing by being upfront. It’s a small reminder that honesty, even when it’s difficult, matters. But aside from those rare moments of understanding, there’s a consistent pattern: people politely retreating, their interest fading soon after I disclose.

I know that reactions could vary depending on the person, but in my experience, no one has truly stayed. It’s hard to keep hoping for a different outcome when rejection feels like the norm.

## **What Kind of Support (If Any) Did You Seek After Your Diagnosis, and Was It Helpful?**

After my diagnosis, I tried to take steps that I thought would help me cope and prepare for the future. One of the first things I did was start daily suppression medication. I figured that if I could show a future partner I was already doing everything I could to reduce the risk of transmission, it might help ease some of their concerns.

At the time, I was already in therapy, and that helped a little too. My therapist provided a space where I could talk about my fears and frustrations without feeling judged. Still, even with professional help, there were—and still are—days when the weight of everything feels overwhelming. It’s not just the diagnosis itself; it’s the stigma, the fear of rejection, and the constant question of whether anyone will accept me as I am.

Even though the medication and therapy helped, they didn’t erase the emotional toll. I’ve realized that while support can make things a little easier, it doesn’t make the challenges disappear entirely.

## **Are There Specific Misconceptions About Herpes That You Wish More People Understood?**

One of the most frustrating parts of living with herpes is dealing with the stigma. The condition itself isn’t nearly as bad as the way people perceive it. The stigma feels far worse than the physical reality of having herpes.

Most people don’t seem to realize how common herpes is or that many people who have it don’t even know they’re carrying the virus. The misinformation out there is staggering, and it often leads to harsh judgment and rejection. I wish more people would take the time to do their own research instead of jumping to conclusions or writing someone off because of a diagnosis.

What bothers me most is how people react as if herpes is a reflection of someone’s character. It’s not. It’s a medical condition, and it doesn’t define who I am or the kind of person I strive to be. I wish more people understood that it’s manageable and that a diagnosis doesn’t mean someone is reckless or irresponsible.

## **What Advice Would You Give to Someone Newly Diagnosed or Struggling to Disclose Their Status?**

If I could sit down with someone newly diagnosed, I’d tell them that it’s okay to feel overwhelmed at first. It’s a lot to process, and it’s natural to have fears and doubts. The best piece of advice I can give is to take things one step at a time. Start by talking to your doctor about suppression medication. It’s not a cure, but it can help reduce the chances of passing the virus to someone else and make the physical symptoms easier to manage.

When it comes to disclosing, I won’t pretend that it’s easy—it hasn’t been for me. But honesty is the best approach. The earlier you tell someone, the better, even though rejection might come with it. It’s not about sparing your feelings; it’s about giving the other person the respect and choice they deserve.

Also, try not to let the stigma get to you. I know that’s easier said than done, but remember, herpes is just a medical condition. It doesn’t change your worth or the person you are. If you’re struggling, find a support system, whether it’s a therapist, a close friend, or even online communities. You don’t have to go through this alone.

## **Has Living With Herpes Taught You Anything About Yourself or How You Approach Relationships?**

Living with herpes hasn’t been the kind of life lesson anyone asks for, but it’s taught me a lot about vulnerability and resilience. It’s made me more aware of how I approach relationships, forcing me to be honest about who I am from the very beginning. I’ve learned to have difficult conversations, even when they’re uncomfortable, and to face rejection head-on, which isn’t something I ever thought I’d get used to.

It’s also shown me how important it is to value the right kind of connection. I’ve come to realize that anyone who can’t look past a medical condition isn’t someone I could build a meaningful relationship with anyway. That doesn’t make rejection hurt any less, but it’s a small comfort to know that the people who leave weren’t meant to stay.

On the flip side, living with herpes has reminded me just how much strength I have. Some days, it feels like I’m carrying the weight of the world, but I keep showing up for myself. It’s not about winning every battle—it’s about continuing to try, even when it feels hopeless.

## **What Message Would You Want to Share With Others in the Community Who Might Feel Discouraged?**

To anyone out there who feels discouraged, I want you to know that you’re not alone. I know how easy it is to feel isolated when you’re dealing with something as stigmatized as herpes, especially when it feels like rejection is a constant part of the journey. But your diagnosis doesn’t define you. It’s just one part of your story, not the whole narrative.

The world can be harsh, and people’s reactions can sting, but there’s a strength in being honest and vulnerable. Every time you disclose your status, you’re showing courage, even if it doesn’t feel like it. You’re giving others the choice to accept you for who you are, and that’s something to be proud of, no matter the outcome.

If I could share one piece of advice, it would be this: Don’t let the stigma rob you of your worth. You are more than a diagnosis, and there are people out there who will see you for everything you are. It might take time, and the road might feel lonely, but your honesty, kindness, and courage matter.

**Also Read: 22-year-old male's personal** [**<u>HPV story</u>**](https://www.shamelesspath.com/blog/std-stories/living-with-hpv-trust-betrayal)

<p>Facing stigma after an HSV-2 diagnosis? My story of battling mental health challenges and finding self-acceptance offers hope and inspiration.</p>

Living With Cerebral Palsy, Herpes & Rejection

Living with cerebral palsy & herpes, Draper shares struggles with stigma, rejection, & dating while embracing honesty, resilience, & self-worth.

Living With Cerebral Palsy, Herpes & Rejection

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