Living with genital herpes can take a deep emotional toll—one that isn’t always visible from the outside. For many, the diagnosis brings a wave of distress that extends far beyond physical symptoms. The weight of stigma, secrecy, and fear can quietly erode confidence and alter the way individuals see themselves and their relationships.
The psychological burden of herpes often matches, or even exceeds, its physical impact. Feelings of shame, anxiety, and isolation are common and can affect self-esteem, emotional wellbeing, and interpersonal connections. These struggles may be especially intense for individuals with limited access to support or care, who may feel they have no one to confide in or turn to.
Among the emotional responses that can arise, depression is both common and frequently overlooked. It may show up gradually, fueled by ongoing stress about outbreaks, fear of rejection, or a sense of being permanently flawed. Without acknowledgement and support, these feelings can deepen, creating a cycle of distress that affects daily life and overall health.
This article aims to help individuals living with herpes recognize the signs of depression and understand that what they’re feeling is valid—and treatable. Through awareness, support, and appropriate care, it’s possible to restore a sense of control and reconnect with hope.
Why Herpes May Contribute to Depression
A genital herpes diagnosis doesn’t happen in a vacuum. It arrives in a cultural context where misinformation and judgment still linger, often distorting how people see themselves and how they expect others to respond. The emotional fallout isn’t just about managing a virus—it’s about navigating a landscape of stigma, anxiety, and self-doubt that can take a heavy toll on mental health.
The Weight of Stigma and Isolation
Stigma remains one of the most potent drivers of psychological distress in people living with herpes. It reinforces harmful stereotypes and breeds silence, often leaving individuals feeling ashamed or alone. This sense of secrecy can make it difficult to seek support or even talk openly with friends or partners, fueling a cycle of isolation. Many begin to internalize these societal judgments, which chips away at self-esteem and can create or worsen symptoms of depression.
For women in particular, stigma has been shown to correlate with a marked decline in perceived quality of life. The emotional impact goes far beyond embarrassment—it touches deeply on how one views their value, their attractiveness, and their right to intimacy.
Chronic Stress and Disclosure Anxiety
Even beyond stigma, herpes can create a constant undercurrent of stress. Recurring outbreaks are often unpredictable, which can make daily life feel uncertain. Many live in fear of the next flare-up or worry about how and when to disclose their diagnosis to a new partner. This kind of ongoing emotional pressure can become exhausting, especially when compounded by anxiety about rejection or misunderstanding.
Disclosure, in particular, presents a uniquely difficult challenge. Fear of judgment can lead some to withhold the information altogether, which only increases stress and emotional burden. The more intense the fear, the harder it becomes to form new connections, leading to further isolation and—over time—depressive symptoms.
Self-Worth and the Erosion of Identity
Herpes doesn’t just affect the body; it can quietly unravel how someone sees themselves. People often describe feeling “damaged” or “unlovable,” especially in the early stages after diagnosis. These feelings aren’t irrational—they stem from the very real messages that society sends about sexual health, purity, and desirability. Internalizing that negativity can make it difficult to maintain a healthy sense of identity or trust in relationships.
Negative self-image is more than just insecurity—it’s a validated part of the herpes experience that has been closely linked to depression. When individuals begin to see themselves through the lens of a diagnosis, rather than as a whole person, their emotional resilience can weaken. Without support or affirmation, those feelings may deepen into long-term distress.
Together, these factors—stigma, stress, and self-perception—create an emotional climate where depression can easily take root. But understanding this connection is the first step toward interrupting the cycle and finding a path to healing.
Recognizing Signs of Depression
Depression can show up in quiet, insidious ways—especially when layered over the emotional weight of a herpes diagnosis. It doesn’t always look like deep despair. Sometimes, it feels like emotional flatness, physical exhaustion, or the slow fading of joy from everyday life. Being able to identify the signs is a critical step toward getting the help you deserve.
Emotional Red Flags
At the emotional level, depression often brings a heavy, persistent sense of sadness or hopelessness. These feelings may not be tied to any specific event, and they often linger despite efforts to “think positively” or “snap out of it.” For some, the sadness is less about crying and more about a constant emptiness—a numbness that makes it hard to connect or care.
Irritability is also common, especially for younger individuals or those under chronic stress. Frustration over small inconveniences may feel outsized or hard to control. Alongside these feelings, a deep sense of guilt or worthlessness can take hold. These thoughts often feed on the stigma and self-doubt that may already be present, especially for someone adjusting to life with herpes.
Physical Warning Signs
Depression isn’t only emotional—it can weigh heavily on the body, too. Fatigue is a major symptom, with many individuals feeling drained even after a full night’s sleep. Physical energy dips, and routine tasks may start to feel overwhelming.
Changes in sleep patterns—whether it’s difficulty falling asleep, waking early, or sleeping too much—can also be clues. Appetite shifts are another common sign. You might notice sudden weight loss or gain, or simply a lack of interest in food altogether.
Then there are the aches and pains. Depression is frequently linked to unexplained physical discomfort, like headaches, stomach trouble, or muscle tension, even when no medical cause is found.
Behavioral Shifts
Perhaps the most telling signs of depression are found in behavior. People often begin to pull away from friends, partners, or social spaces, not out of choice, but because connecting feels too hard or meaningless. You might cancel plans more often or stop returning messages—not because you don’t care, but because you don’t feel up to it.
Motivation fades. Things that once felt fulfilling—work, hobbies, relationships—can start to seem pointless or exhausting. This loss of interest in daily pleasures is known as anhedonia, and it’s a hallmark of depression.
Recognizing these symptoms doesn’t mean labeling yourself or rushing to a diagnosis. It’s about tuning into what your mind and body are telling you—and understanding that these experiences are valid, common, and treatable.
Unique Challenges of Depression in Individuals with Herpes
While depression alone is complex, its interplay with a herpes diagnosis brings added layers of emotional strain. The stigma, secrecy, and misunderstandings surrounding herpes don’t just complicate day-to-day life—they also shape how depression is experienced, expressed, and addressed.
Shame and the Silence It Breeds
One of the most difficult aspects of managing depression in the context of herpes is the compounded weight of shame. Many individuals describe feeling fundamentally flawed or “contaminated” after their diagnosis. This internalized stigma often pushes people to keep their status a secret, not just from potential partners, but from friends, family, and even healthcare providers. The desire to protect oneself from judgment is understandable—but it can also lead to deeper emotional isolation.
When someone is struggling with both shame and secrecy, reaching out for help becomes harder. That lack of openness, in turn, can prevent them from receiving emotional or medical support when they need it most. Over time, the psychological burden increases, feeding into a cycle of distress and disconnection.
The Isolation of Disclosure Anxiety
Fear of rejection is a powerful emotional barrier. Many individuals delay or avoid disclosing their herpes status altogether, worried about how others might respond. This apprehension isn’t just rooted in personal insecurity—it’s shaped by real experiences and a cultural atmosphere where herpes is still widely misunderstood.
Avoiding disclosure may feel protective in the short term, but it often leads to greater emotional distance in relationships. The effort of hiding a significant part of one’s health can be exhausting, and the resulting disconnection can deepen feelings of loneliness. For some, this persistent fear of being “found out” or judged can become a major contributor to depressive symptoms.
When Symptoms Feed Anxiety
Another underrecognized challenge is how people interpret their physical symptoms. During an outbreak or even when feeling unwell in general, the anxiety tied to herpes can flare up quickly. Some may misread normal physical sensations as signs of worsening illness, or worry that others will notice something is wrong. This hyperawareness can lead to elevated stress, which not only affects emotional health but may also trigger more frequent outbreaks.
It’s also common for the emotional impact of herpes to feel disproportionate to the clinical reality. The stigma, not the symptoms themselves, often shapes how someone experiences their diagnosis. When the emotional narrative around herpes is dominated by fear, rejection, and shame, depressive episodes can deepen, regardless of how mild or infrequent the outbreaks may be.
These unique emotional dynamics don’t mean someone is overreacting—they point to a deeper truth: depression connected to herpes isn’t just about mood. It’s about the invisible weight of navigating a stigmatized condition in a society that rarely makes room for honest, compassionate conversations.
Practical Steps to Manage Depression
While depression linked to a herpes diagnosis can feel overwhelming, it’s important to know that support and relief are possible. Managing mental health is not about “fixing” something broken—it’s about nurturing the emotional strength to live fully, even in the presence of challenge. Healing happens in many forms, and these strategies can help create space for that process to unfold.
Building Emotional Resilience
Resilience isn’t a fixed trait—it’s something that can be built with intention and practice. Mindfulness techniques and cognitive-behavioral tools, for example, have been shown to reduce depressive symptoms by helping individuals notice and reframe unhelpful thought patterns. These approaches cultivate emotional regulation, making it easier to respond to stress with clarity rather than overwhelm.
Everyday self-care matters, too. Small but consistent actions—like getting quality sleep, maintaining a nourishing diet, and moving your body—can anchor emotional wellbeing. When life feels unpredictable, routines can offer stability and a gentle sense of control.
Equally important is how we speak to ourselves. Practicing self-compassion and affirming your worth—even when it feels difficult—can counteract shame and self-stigma. For those navigating the emotional weight of herpes, reminders that you are not defined by a diagnosis can be powerful steps toward healing.
Seeking Professional Help
Professional support can make a meaningful difference, especially when it comes from someone who understands the unique emotional layers that come with chronic health conditions like herpes. Therapists trained in sexual health or psychosexual counseling are equipped to help individuals work through shame, rejection fears, and distorted self-perceptions.
Therapies like cognitive-behavioral therapy (CBT) and dialectical behavior therapy (DBT) are especially effective. They offer structured, evidence-based ways to reduce depressive symptoms while improving emotional regulation and resilience.
It’s also essential to feel safe with your therapist. If you’re living with herpes, working with a provider who is nonjudgmental and stigma-aware can build the trust needed for real healing. Don’t hesitate to ask potential therapists about their experience with chronic illness or sexual health—open communication at the start can set the tone for a more supportive therapeutic relationship.
Medication and Clinical Support
For some, therapy alone may not be enough. When depression is persistent, severe, or affecting daily life, antidepressant medication can be a valuable part of treatment. Choosing this path doesn’t mean weakness or failure—it means prioritizing your health.
Unfortunately, stigma still surrounds the use of psychiatric medications. Education and compassionate conversations can help shift this narrative. Understanding how these medications work—and acknowledging that they’re tools, not life sentences—can help reduce fear and improve treatment engagement.
If you’re considering medication, an honest conversation with your healthcare provider is a good starting point. Talking openly about your symptoms allows them to assess what support is most appropriate and ensures you feel seen—not just as a patient, but as a whole person.
Managing depression isn’t about eliminating every difficult feeling. It’s about building the skills, support systems, and compassion needed to navigate them. And you don’t have to do it alone.
The Power of Community Support
Depression often thrives in isolation—but connection can be one of the most powerful antidotes. For individuals living with herpes, finding a community of peers who understand the emotional and social complexities of the condition can be a lifeline. It offers not just comfort, but also a pathway to healing.
The Strength of Shared Experience
Connecting with others who have walked a similar path can ease the burden of feeling different or alone. Peer support brings more than just empathy—it fosters understanding, breaks down stigma, and reminds people they aren’t navigating this alone. These relationships can create a sense of solidarity that is often missing from clinical care alone.
People who engage in peer communities frequently report feeling more hopeful and less ashamed. Talking with someone who “gets it” helps normalize the emotional challenges of herpes, from managing disclosure anxiety to coping with recurring symptoms. Over time, these connections build resilience and help individuals rediscover a sense of agency in their lives.
Peer Support as a Path to Healing
Studies show that peer support can be just as effective as professional therapy in improving quality of life and reducing depressive symptoms. Through mutual storytelling, emotional validation, and shared tools for coping, individuals often find a renewed sense of purpose and confidence. It’s not just about talking—it’s about being seen and accepted without judgment.
Structured programs, both online and offline, offer even more targeted support. Peer-led groups, mutual aid circles, and community-based initiatives can create consistent, stigma-sensitive spaces for reflection and growth. Whether through formal peer mentorship or informal conversations, these platforms help reframe illness as part of a shared human experience—not a personal failing.
Finding the Right Community
There’s no one-size-fits-all approach to support. Some may prefer in-person groups where body language and presence deepen connection, while others may find safety and flexibility in online spaces. Certified programs and trained peer leaders can also provide guidance grounded in both personal experience and evidence-based practice.
What matters most is finding a space where openness is met with empathy. When individuals feel safe to share, they’re more likely to process their emotions honestly, challenge internalized shame, and take steps toward recovery.
Engaging in Healing Together
Healing doesn’t always happen alone—and it doesn’t need to. Participating in community support is a reminder that emotional pain is not a personal defect, but a shared part of being human. Through peer connection, many rediscover a sense of belonging, trust, and even joy. It’s a space where growth is nurtured not in spite of struggle, but because of the courage it takes to face it—together.
Preventing Depression: Proactive Strategies
Depression doesn’t always arrive suddenly. For many, it builds gradually—fed by stress, isolation, or unspoken fears. The good news is that it’s possible to take steps before emotional distress deepens. Preventing depression, especially for individuals living with herpes, means staying attentive to your mental health, finding ways to manage stress, and creating an environment where support can flourish.
Staying Connected Through Open Communication
When you’re dealing with the emotional complexity of a herpes diagnosis, it can be tempting to shut down or withdraw. But staying connected—especially through honest, open conversations—can be one of the most protective things you do for your mental health.
Talking about what you’re feeling with trusted partners or friends not only relieves emotional pressure but also invites meaningful support. These conversations don’t have to be dramatic or overly structured. Even small check-ins, when shared with empathy and vulnerability, help reduce feelings of isolation and encourage mutual understanding.
This kind of openness also extends to your relationships with healthcare professionals. When you’re transparent about your emotional needs, providers are better equipped to guide you toward appropriate resources and care. Whether it’s a therapist, doctor, or nurse, establishing a dialogue that includes mental health is a step toward treating the whole person—not just the diagnosis.
Managing Stress Around Herpes Triggers
Stress doesn’t just affect your mood—it can also play a direct role in triggering herpes outbreaks. That overlap makes stress management a particularly important part of both physical and emotional care. But not all stress-reduction techniques are one-size-fits-all. Tailoring your approach to your specific triggers—such as anxiety about disclosure, social rejection, or medical uncertainty—can help you stay more balanced in the face of challenges.
Mind-body practices like meditation, progressive relaxation, and moderate physical activity can all help calm the stress response and support mood regulation. Over time, these habits help quiet the nervous system, reducing the kind of chronic tension that wears down resilience.
Therapeutic strategies like cognitive-behavioral therapy can also be adapted for prevention, helping to interrupt unhelpful thinking patterns before they spiral into depression. When these approaches are personalized—based on your unique experiences and emotional risks—they become even more powerful tools for long-term mental wellness.
Prioritizing Mental Health Daily
Taking care of your emotional wellbeing doesn’t have to mean making huge changes overnight. It often begins with consistent, everyday choices: checking in with yourself regularly, reaching out when things feel heavy, and practicing self-compassion instead of self-judgment. By staying emotionally proactive, you give yourself the best chance of protecting your mental health—before distress becomes depression.
This is not about perfection. It’s about learning to notice your needs early, and honoring them with care.
When and How to Seek Immediate Help
Depression can become overwhelming, especially when combined with the emotional challenges of living with a stigmatized condition like herpes. While many people experience manageable lows, some begin to slip into more dangerous territory without realizing just how serious their symptoms have become. Recognizing when to seek immediate help is not just important—it can be lifesaving.
Understanding the Warning Signs
Severe depression often doesn’t announce itself all at once. It may start with persistent sadness or a sense of hopelessness that doesn’t lift, even with rest, support, or time. Over time, these feelings can intensify into thoughts of worthlessness or, in more urgent cases, thoughts of death or suicide.
People experiencing suicidal ideation might talk about feeling like a burden, express that they’re in unbearable emotional pain, or say they feel trapped with no way out. These are not simply emotional “phases”—they’re red flags that should never be ignored.
If you’re living with a chronic condition like herpes, you may already be dealing with added emotional strain. Studies have shown that individuals managing both physical and social burdens are at higher risk for depressive symptoms and suicidality. Regular mental health check-ins, whether self-directed or with a professional, are crucial to catching these signs early.
Where to Turn in a Crisis
If you or someone you know is in immediate danger or thinking about suicide, professional help is available right now:
- 988 Suicide & Crisis Lifeline offers 24/7 support across the U.S. You can call or text 988 to connect with trained counselors who understand mental health crises and are ready to help.
- Crisis Text Line allows you to text HOME to 741741 to speak with a trained crisis counselor via text—ideal for those who may find talking out loud difficult.
- Emergency Services are available at any time. If the risk is imminent, call 911 or go to the nearest emergency room. Hospitals have mental health professionals on staff who can assess your safety and provide immediate care.
You don’t have to navigate this alone. If your mind is telling you there’s no way forward, let someone else help you find the next step. Your life matters, and there is always support—quiet, nonjudgmental, and ready when you need it.
You’re Not Alone in This
Living with herpes can sometimes feel like navigating two challenges at once—the physical realities of a viral condition and the emotional toll of stigma, secrecy, and misunderstanding. Depression, when it shows up in this context, is not a personal failure. It’s a valid, human response to complex stress. And most importantly, it’s something that can be faced with support, care, and hope.
If you’ve recognized parts of yourself in these pages—whether in the quiet sadness, the fear of disclosure, or the slow drift from joy—know that help is not out of reach. You deserve to feel whole again. That healing might come from talking with a trusted friend, joining a peer support group, finding the right therapist, or simply reminding yourself, every day, that your worth isn’t diminished by a diagnosis.
Mental health is just as vital as physical health, and tending to it is an act of strength, not weakness. There is no shame in needing support—and there is so much strength in seeking it.
If you’ve found this article helpful, we invite you to join our mailing list. You’ll get thoughtful updates, new articles, and practical resources delivered with care—because no one should have to navigate this journey alone.
Asking for help doesn’t mean you’re broken. It means you’re brave enough to keep going.
References
American Psychiatric Association. (2022). Diagnostic and Statistical Manual of Mental Disorders (5th ed., text rev.).
Barnack-Tavlaris, J. L., Reddy, D. M., & Ports, K. (2011). Psychological adjustment among women living with genital herpes. Journal of health psychology, 16(1), 12–21.
Barney, L. J., Griffiths, K. M., Jorm, A. F., & Christensen, H. (2006). Stigma about depression and its impact on help-seeking intentions. Australian & New Zealand Journal of Psychiatry, 40(1), 51–54.
Bickford, J., Barton, S. E., & Mandalia, S. (2007). Chronic genital herpes and disclosure…. The influence of stigma. International journal of STD & AIDS, 18(9), 589–592.
Bobrow, M. (2016). Full Disclosure: Herpes Stigma and Communication Practices among HSV+ Individuals.
Campbell, D. G., Bonner, L. M., Bolkan, C. R., Lanto, A. B., Zivin, K., Waltz, T. J., Klap, R., Rubenstein, L. V., & Chaney, E. F. (2016). Stigma Predicts Treatment Preferences and Care Engagement Among Veterans Affairs Primary Care Patients with Depression. Annals of behavioral medicine : a publication of the Society of Behavioral Medicine, 50(4), 533–544.
Campos, F., Sousa, A.R., Rodrigues, V., Marques, A.J., Dores, A.R., & Queirós, C.M. (2014). Peer support for people with mental illness. Revista De Psiquiatria Clinica, 41, 49-55.
Catallozzi, M., Ebel, S. C., Chávez, N., Shearer, L., Mindel, A., & Rosenthal, S. (2013). Disclosing Genital Herpes: Perceptions of Motivation, Logistics and Timing. Sexually Transmitted Infections, 89(Suppl 1), A332–A333.
Centers for Disease Control and Prevention. (2023). How Right Now: Mental Health and Coping.
Centers for Disease Control and Prevention. (2023). Suicide Prevention.
Davidson, L., Chinman, M.J., Sells, D., & Rowe, M. (2005). Peer support among adults with serious mental illness: a report from the field. Schizophrenia bulletin, 32 3, 443-50 .
Dibble, S.L., & Swanson, J.M. (2000). Gender differences for the predictors of depression in young adults with genital herpes. Public health nursing, 17 3, 187-94 .
Drob, S.L. (1985). Psychotherapy with Patients Suffering from Genital Herpes. Psychotherapy in private practice, 3, 129-137.
Forchuk, C., Solomon, M., & Viran, T. (2016). Peer Support. Healthcare quarterly, 18 Spec No, 32-6 .
Franczak, M., & Dye, C. (2016). Peer Support Services. In Springer.
George, L., O’Hagan, M., Bradstreet, S., & Burge, M. (2017). The Emerging Field of Peer Support within Mental Health Services.
Gordon, S. (2007). Suffering in Silence: Managing the Fear Trajectory of Genital Herpes. International Journal for Human Caring, 11(2), 40–46.
Green, J., Ferrier, S., Kocsis, Á., Shadrick, J., Ukoumunne, O., Murphy, S., & Hetherton, J. (2003). Determinants of disclosure of genital herpes to partners. Sexually Transmitted Infections, 79(1), 42–44.
Han, A., & Kim, T. H. (2023). Effects of self‑compassion interventions on reducing depressive symptoms, anxiety, and stress: A meta‑analysis. Mindfulness, 14(7), 1553–1581.
Hook, A., & Andrews, B. (2005). The relationship of non-disclosure in therapy to shame and depression. The British Journal of Clinical Psychology, 44(Pt 3), 425–438.
Hsu, P., Groer, M., Wang, S., Williams, S., & Kane, B. (2013). Prenatal stress, depression, and herpes viral reactivation. Brain, Behavior, and Immunity, 32, e29–e30.
Jones, J. D., Long, E., Hankin, B., Gallop, R., Davis, M., & Young, J. F. (2023). Personalized depression prevention reduces dependent stressors among adolescents. Journal of Clinical Child & Adolescent Psychology.
Lee, J. D., & Craft, E. A. (2002). Protecting one’s self from a stigmatized disease… once one has it. Deviant Behavior, 23(3), 267–299.
Limandri, B. (1989). Disclosure of stigmatizing conditions: the discloser’s perspective. Archives of Psychiatric Nursing, 3(2), 69–78.
Martinez, L. R., Xu, S., & Hebl, M. (2018). Utilizing education and perspective taking to remediate the stigma of taking antidepressants. Community Mental Health Journal, 54, 450–459.
Mayo Clinic. (2023). Depression (major depressive disorder).
Mayo Clinic. (2023). Suicidal thoughts: Emergency treatment.
Merin, A., & Pachankis, J. E. (2011). The psychological impact of genital herpes stigma. Journal of health psychology, 16(1), 80–90.
Mindel, A. (1996). Psychological and psychosexual implications of herpes simplex virus infections. Scandinavian Journal of Infectious Diseases. Supplementum, 100, 27–32.
Mindel, A., & Marks, C. (2005). Psychological symptoms associated with genital herpes virus infections. CNS Drugs, 19(4), 303–312.
Murphy, R., & Higgins, A. (2018). The complex terrain of peer support in mental health. Journal of Psychiatric and Mental Health Nursing, 25, 441–448.
Nakao, M., Takeuchi, T., He, P., Ishikawa, H., & Kumano, H. (2011). Prevention and Psychological Intervention in Depression and Stress-Related Conditions. Asian Perspectives and Evidence on Health Promotion and Education, 374 – 388.
National Institute of Mental Health. (2022). Depression: Overview.
Nicholson, M., & O’Farrell, N. (2020). Genital herpes: diagnosis, treatments, and disclosure. International Journal of STD & AIDS, 32, 23–29.
Park, J., & Lee, L. (2018). Relationship of Communication Skill, Depression, and Clinical Practice Stress of Nursing Students. The Korea Academia-Industrial Cooperation Society, 19(10), 254–262.
Payne, M. (2017). Peer support in mental health: a narrative Review of its relevance to social work.
Qaseem, A., Barry, M. J., Kansagara, D., et al. (2016). Nonpharmacologic versus pharmacologic treatment of adult patients with major depressive disorder. Annals of Internal Medicine, 164(5), 350–359.
Repper, J., & Watson, E. (2015). Peer support in mental health services.
Roberts, R. E. (1997). Power/knowledge and discredited identities: Media representations of herpes. Sociological Quarterly, 38(2), 265–284.
Roy, A., & Roy, R. (2017). Stress and Major Depression.
Song, H., Chan, J. S., & Ryan, C. (2024). Differences and Similarities in the Use of Nine Emotion Regulation Strategies in Western and East-Asian Cultures: Systematic Review and Meta-Analysis. Journal of Cross-Cultural Psychology, 55(8), 865-885.
Stefancic, A., Bochicchio, L. A., & Tuda, D. (2021). Peer Support for Mental Health. Springer.
Substance Abuse and Mental Health Services Administration. (2023). 988 Suicide & Crisis Lifeline.
Taboulet, F., Halioua, B., & Malkin, J. (1999). Quality of life and use of health care among people with genital herpes in France. Acta Dermato-Venereologica, 79(5), 380–384.
Wang, K., Merin, A., Rendina, H. J., & Pachankis, J. E. (2018). Genital herpes stigma: Toward the Measurement and Validation of a highly prevalent yet hidden public health problem. Stigma and health, 3(1), 27–34.
Wertheimer AI, Balduzzi M, Minghetti P. Reactions of community pharmacists to questions by patients with a stigmatized disease. J Clin Pharm Ther. 1991 Dec;16(6):435-42.
World Health Organization. (2023). Depression.
