I’m Ill-Opportunity9, and at 20 years old, I’m still trying to navigate life with herpes. I wasn’t diagnosed yesterday — I’ve had time to process it. I thought I had made peace with it, or at least as much as anyone can. But starting treatment? That was a whole new battle, one I wasn’t prepared for.

When I first took Valtrex, I thought it would finally give me some control. I expected fewer outbreaks, less pain, maybe even a sense of normalcy. I had read stories online, talked to doctors, and convinced myself that this little pill was my ticket to something better. Instead, my symptoms got worse—way worse.

Within days, my body felt like it was under attack. My eyes burned constantly, the pain radiating from behind them as if they were being scratched from the inside. My nose ached, congested and swollen in ways I never expected. And then there were the outbreaks. What was once manageable suddenly felt monstrous. The sores on my genitals became unbearable, flaring up worse than ever before. Every touch, every movement was a reminder that I wasn’t getting better — I was getting worse.

It felt like my body was punishing me for trying to help it. Each passing day became a test of endurance. I kept asking myself, *Is this normal? Is my body adjusting, or am I making a mistake?* I scoured forums for answers, but nothing reassured me. The fear crept in: *What if this is just how things are now? What if the treatment doesn’t work for me?*

No one talks about this part — the part where the supposed "cure" makes you feel like you’re losing. People tell you to “just take the meds,” to “trust the process,” but what if the process breaks you before it heals you? I tried to stay hopeful, but in my darkest moments, I wasn’t sure I’d ever win.

And that was the scariest part of all.

## **Valtrex: A Promise of Relief?**

When my doctor first prescribed Valtrex, I felt like a weight had been lifted off my shoulders. I had been battling this new, overwhelming diagnosis of herpes, and it felt like everything in my life was being defined by it. But here was the solution — something that could finally help me regain control. I imagined the outbreaks would stop, or at least become less frequent. I thought that maybe, just maybe, this tiny blue pill could be the key to feeling like myself again. I was desperate for anything that would bring back even a shred of normalcy.

I started at the prescribed 500 mg, and for the first time in months, I allowed myself to believe that things were about to get better. It seemed so simple, so straightforward — take the medication, and watch the symptoms fade. I had read about the success stories of others who were able to control their outbreaks with Valtrex, and I thought I’d be one of them.

But instead of relief, what I got was a nightmare. My symptoms, which I had hoped would ease, only got worse. It felt like my body was fighting back, as if it was punishing me for trying to heal. My outbreaks became more frequent, the sores more painful, and the constant itching was unbearable. To make things worse, the pain didn’t just stay in the usual spots. My eyes burned and itched, making it hard to even blink without feeling like something was stabbing me. My nose felt raw and sensitive, as if every nerve was on fire. And worst of all, the genital sores that had been manageable before now became excruciating.

I remember looking in the mirror, thinking, *This isn’t supposed to happen. This wasn’t the plan.* I had hoped for a quick fix, but instead, I found myself sinking deeper into a cycle of frustration and fear. The more I took the medication, the worse I seemed to feel. I couldn’t shake the feeling that I was doing something wrong, like maybe Valtrex wasn’t the miracle I had hoped for.

In those moments, I felt completely defeated. How could something that was supposed to help me make everything worse? How long would this go on? Was this just the way it was going to be from now on — forever trapped in a cycle of pain, confusion, and uncertainty?

## **A Treatment That Felt Like a Punishment**

Within days of starting Valtrex, I felt as if my own body had turned against me. What was supposed to be a solution quickly turned into a nightmare. The pain that had once been manageable now felt like an unrelenting force. My eyes, which had already been vulnerable due to my eye herpes, began to burn and itch incessantly. It was as if every blink was a reminder that I couldn’t escape the torment. The raw, uncomfortable feeling spread to my nose, which became inflamed and sensitive, making even breathing through it a painful experience.

But the worst of it was the genital sores. They flared up with a vengeance, becoming more painful and numerous than they had ever been before. Instead of the relief I so desperately needed, it felt like the fire was being stoked, not put out. It was as if each outbreak was fueled by the very medication that was supposed to stop them.

People kept telling me that sometimes things get worse before they get better, that my body was just adjusting to the medication. At first, I tried to believe that — tried to hold on to the hope that the suffering was temporary. But as the days stretched into weeks, the pain seemed to grow rather than subside, and I couldn’t help but question: *What if it never gets better? What if this is the reality I’ll have to live with?*

I was at my breaking point. I thought maybe the dose wasn’t enough, that increasing it might give me the relief I was desperate for. So, I doubled my dosage to 1000 mg, hoping for a change, praying that the pain would lessen and my outbreaks would begin to subside. But even after making that adjustment, nothing changed. The sores persisted, the pain remained, and the fear of never getting better loomed over me like a dark cloud. I felt trapped in my own body, unable to escape the suffering, helpless as the days dragged on with no sign of relief.

It was a cruel irony. Here I was, following the doctor's instructions, doing everything I was supposed to do, and yet the very medication meant to heal me was only intensifying my agony. I was lost, stuck in a loop of constant pain, uncertainty, and disappointment. It felt like a punishment rather than a treatment.

## **The Darkest Moments**

Herpes on my eye was more than just a physical symptom — it was a constant, suffocating presence. I couldn't even escape it in the one place where I had hoped to find some relief: sleep. Every time I closed my eyes, I was reminded of the relentless pain. The itching, the burning, the unbearable discomfort — it was all there, even in the quiet of the night. As I tried to rest, the thought of waking up to the same misery felt like a cruel joke. Sleep, which had once been my sanctuary, was now just another extension of my suffering.

Each day felt like an endless cycle of torment. I would wake up in the morning, exhausted from the lack of restful sleep, only to be confronted by the same symptoms that had tormented me the day before. My eyes stung with every blink, and I couldn’t escape the intense burning sensation that seemed to take over my entire face. It wasn’t just the physical pain that was overwhelming — it was the emotional toll of not knowing when or if this would ever end. The idea that this might be my new normal, that I could be stuck in this cycle forever, was almost too much to bear. It was like being trapped in a prison with no way out.

At my lowest, I started having thoughts I never imagined I would. In the midst of all the physical pain, I found myself thinking about the possibility of not waking up tomorrow. The thought of escaping the endless cycle of pain, the weight of the never-ending suffering, started to seem like a way out. It wasn’t just fear that I felt — it was an overwhelming sense of hopelessness. I wasn’t scared of the idea of not waking up. I was more scared of the fact that I couldn’t see a way forward, that there was no end in sight to the agony. I felt utterly powerless, as if I had no control over my own body or my own future.

Those thoughts were foreign to me, and they terrified me. The sadness was consuming. I wasn’t just dealing with the physical pain of the outbreaks — I was battling the mental and emotional toll that came with it. The constant uncertainty, the fear that I would never get better, was a weight I couldn’t shake off. I felt like I was sinking, and the medication that was supposed to help only seemed to make it worse. It was hard to see the light at the end of the tunnel when it felt like the tunnel was getting longer with every passing day.

## **Searching for Hope**

Desperation led me to the internet. I became obsessed with searching for stories of people who had been through what I was enduring. I needed to know that I wasn’t alone in this, that someone, somewhere, had felt the same pain and had made it through to the other side. I spent hours scrolling through forums, reading blog posts, watching videos. I desperately clung to every success story I found — hoping, praying that one of them would mirror my own experience and offer the hope I was starving for.

But every journey was different, and no matter how many success stories I read, I still felt alone. I wasn’t living one of those stories. The people in those posts had found relief, had moved on, had learned to live their lives again. They had made it through the worst of their outbreaks and had emerged stronger. I wanted that for myself, but it felt like an unreachable dream. I read about people who had taken Valtrex and experienced improvements within days, who talked about fewer outbreaks and less pain. That wasn’t my reality. My body seemed to reject the medication, and the suffering just kept escalating.

Every morning, I woke up with the faintest glimmer of hope — just enough to keep me going for a few more hours. I’d tell myself, “Today will be the day things start to get better.” But as the day wore on, the same patterns played out. The same burning sensation in my eyes, the same itching and pain in my nose and genital areas — it was like I was stuck in a loop. No matter how much I hoped or prayed for a breakthrough, I was met with the same reality. The same pain. The same fear. The same uncertainty.

It felt like I was watching the world move forward while I stood still, trapped in a body that wouldn’t cooperate. I looked around me, and everyone else seemed to be going on with their lives, enjoying the things I longed for — freedom, normalcy, peace. But I couldn’t seem to catch up. I was drowning in this invisible illness that no one else could see, yet it controlled everything about my existence. I couldn’t even tell if the medication I was taking was helping or making things worse.

And so I kept searching, hoping to find someone who could tell me that it would get better. Someone who could explain how they made it through, how they pushed past the darkest days. But the truth was, it wasn’t just the medication I needed to understand — it was the reality that the path to healing was long and uncertain. That perhaps the search for a cure wasn’t as straightforward as I had hoped.

## **Was It Worth It?**

I kept telling myself that the pain I was enduring had to mean something. I kept telling myself that there had to be light at the end of this dark tunnel—that if I pushed through the worst of it, I’d eventually find relief. That the suffering, the sleepless nights, the burning pain and the constant fear of another outbreak, would eventually pay off in the form of something better — something manageable.

But as the days turned into weeks and the weeks into months, that hope started to feel like a fragile thread, ready to snap. What if I was wrong? What if all the pain, all the discomfort, all the moments I spent wishing for it all to end… what if they didn’t lead to healing? What if, instead, I was just learning to live with the struggle, learning to accept that my body would never feel the way it did before?

I still don’t have an answer. I wish I could say that all the pain was worth it, that the struggle was just a part of the healing process. But what if this is the reality? What if this — this constant, relentless pain, this uncertainty, this emotional rollercoaster — is the best it’s going to get?

The thought haunts me. It’s a cruel possibility that I can’t shake. I want to believe that things will get better, that somehow, I’ll find the peace I’ve been longing for. But in moments of clarity, I realize that I’m not sure anymore. I’m not sure if this is the point where I start to heal or the point where I learn to live with what I have. I don’t know if I’ll ever reach the place where I feel in control again.

And that uncertainty? It’s suffocating.

I don’t have an inspiring conclusion to offer, no promise of a happy ending that others so often cling to. I wish I could say, “Hold on, it gets better.” But the truth is, I’m still waiting for that answer. I’m still waiting for something that says, “Yes, it was worth it. Yes, the worst part led to something better.”

But what if the healing process isn’t linear? What if it’s just one long, uncertain journey where you’re forced to keep going even when you can’t see the destination?

I don’t know if this will ever feel truly manageable. I don’t know if I’ll ever be okay with this. But for now, I’m learning to keep going, even without the answers.

## **Living With the Unknown**

No one prepared me for this. No one warned me that the treatment, which was supposed to be my salvation, could feel more like a punishment. No one told me that healing isn’t always a straight line, that sometimes you’re forced to navigate a winding, jagged path full of setbacks. There’s no roadmap for this journey — no guarantee that the pain will eventually subside or that relief is just around the corner. The hope that a pill could fix it all quickly was shattered when it only made things worse.

The hardest part of this experience wasn’t just the physical pain, but the emotional toll — the weight of the uncertainty. That feeling of not knowing if what you’re doing will ever work, or worse, if it’s all in vain. I’m not just battling herpes, I’m battling the unknown. It’s the waiting game. The constant questioning: *Will I ever be okay?*

It’s easy to feel defeated when nothing is improving, when every day seems like a repeat of the last. But in those moments of doubt, I remind myself of one thing: I’m still here. I’m still fighting, even if the battle feels endless. And for now, that has to be enough.

I don’t know what the future holds. I don’t know if the pain will stop, or if I’ll ever feel like my old self again. I don’t know when, or if, things will truly get better. But I know that, despite everything, I’m still here. And sometimes, surviving in the face of overwhelming odds is the victory itself.

So I keep going, one day at a time, knowing that my journey is mine alone. I don’t have all the answers, but maybe, just maybe, surviving today is enough.

**Also Read: Jane's** [**<u>personal HIV story</u>**](https://www.shamelesspath.com/blog/std-stories/yes-i-have-hiv-yes-im-having-a-baby)

<p>I took Valtrex expecting relief, but instead, my symptoms got worse. Here’s my experience with unexpected side effects and what I wish I knew earlier.</p>

Valtrex: The Cure That Feels Worse Than the Disease

I took Valtrex expecting relief, but instead, my symptoms got worse. Here’s my experience with unexpected side effects and what I wish I knew earlier.