Technology has a life cycle and the ol' iPhone 7+ Google Chromebook combo I've used for the last three years are no more. We took in listener questions including how I contracted herpes, managing herpes outbreaks, pushing away love, and feeling sexy after a herpes diagnosis. Until I get this new process down, I'll do solo episodes with questions. This solo show, I talk about my dad and therapy.

Friends! How many of us have them?Brenda Emily (@BrendaEmily on Instagram) is an HIV survivor who did not contract it sexually as one may assume. We discuss some of her experiences with hookups and rejection as someone navigating the dating world with HIV and cerebral palsy. We touch on HIV criminalization laws, despite the U equals U campaign, being more strict than the criminalization of rape. There's some overlap in herpes and HIV stigma that we address. Overall, we can let others mistake our being empowered for intimidating. Those drawn to us will affirm our being empowered whereas those who find us intimidating well, are just intimidated.

I get excited when I connect with people I see myself in. Prince joins us to talk about his experience battling suicide ideation after his herpes diagnosis. As a member of the polyamorous community, we get his backstory about opening that conversation up with his partner who when he did, she expressed that she didn't think she was monogamous. We talk about some of the stigma prevalence of HSV in the polyamorous community and how a partner may manipulate us by using our status to control us. One major takeaway is that no relationship style is better or worse than another, there's only honest relationships and dishonest ones. Hearing from a man in the polyamorous community living with herpes shows us that our diagnosis just isn't the end for us. Join us for this insightful conversation.

White people are currently asking the question, "What can I do?" In reference to people with conditions, we use people-first language, so applying that here, you are a person with whiteness. Don't question your humanity, your natural instinct to see the human in another human. Question your perpetual use of your whiteness. YOU have to look at HOW and WHERE it is being put to use. When you ask, "What can I do?", that shouldn't even be a question a human has to ask about injustices done to other humans. There shouldn't be questioning at all, only reflection on the use of your inherited whiteness in a time where those without whiteness are suffering because of it.

In this episode of Something Positive for Positive People, we explore the critical role of healthcare providers in shaping patients' emotional responses to their herpes diagnoses. We discuss the importance of equipping providers with consistent, honest resources to empower them in delivering empathetic diagnoses and fostering patient confidence for future disclosures. Featuring tools from the American Sexual Health Association, this episode provides invaluable insights for both patients and providers.

People use the most shameful parts of themselves as a source of power

In this episode, we finally welcome Laureen HD, whose YouTube channel was a pivotal resource for many after a herpes diagnosis. Laureen and Courtney delve into societal discomfort with silence, sharing dating stories, the challenges of rejection, and the power of preferences. They also explore why Laureen started her channel, the importance of informed public disclosure, and maintaining consistency through an obsession with truth.

If you're unsure about publicly disclosing your herpes status online, this episode is for you. Our guest shares her experiences and challenges the assumption that public disclosure always leads to rejection. Discover the three possible responses: "me too," "no thanks," or "tell me how we can be safe moving forward," and learn why liberation isn't always tied to public disclosure.

Our guest shares the empowering decision to publicly disclose her herpes diagnosis, emphasizing the importance of a great support system or self-reflection through journaling. A herpes diagnosis carries an energetic weight, often influenced by how the first person receives our disclosure. Learn how to handle this weight and find strength in yourself, just like our guest.

In this episode, a New York-based healthcare worker with HSV shares her experience testing positive for COVID-19. We delve into the stigma similarities between the two viruses and how the pandemic re-triggered her feelings. We explore the future of virus disclosure and health histories as we navigate this new landscape. Listen to part 1 of this discussion and send in your questions for our guest's return.

In this episode, we explore the dynamic energy of the younger generation diagnosed with HSV, who are actively engaging in advocacy and using their experiences to uplift others. Our guest, who runs the Instagram page @YouMeAndHSV, shares their journey of compassion-driven advocacy. They focus on providing factual information about the virus and supporting others in finding resources and support.

When you publicly disclose, you give permission to those you know to tell people you don’t know.

Brittany Policastro joins the SPFPP podcast to share her 18-year journey with genital herpes, discussing the evolution of information and experiences over time. We delve into silent rejection in partnerships, disclosure in polyamory, and the narratives we tell ourselves. Brittany’s openness challenges us to explore and heal our own stories gently.

Mr. Sting and Mrs. Sting, hosts of the ‘Just Keep Swinging’ podcast, navigate the stigma of swinging and discuss their first STI diagnosis. They share their journey, seeking resources, and the importance of faith-driven core values in their relationship. Their story offers insights for those in the lifestyle and emphasizes that long-term navigation of an incurable STI is possible.

In this episode, I close out my introspective journey, sharing insights from my week off social media and an honest look at my dating life. I reveal a pivotal discovery made through self-reflection and the best advice I’ve ever received: knowing when to shut up. This episode emphasizes the importance of holding intention over expectation in the ongoing healing process.

In this episode, we honor Nadiya Johanna Wortham and explore the intersection of trauma, grief, and mental health stigma with Grief Counselor Christine Frampus. Discussing the profound impact of suicide on survivors, Christine provides insights into supporting each other through grief and healing. This episode underscores the importance of understanding trauma, suicide, and grief in mental health.

Following my newfound understanding of trauma from the previous episode, I realized I had personal healing to do. This episode serves as a guide to what it looks like to "do the work" of healing. It's an uncomfortable and frustrating process, but essential. By reconnecting with myself, I aim to better utilize my experiences to help others navigate their healing journeys.

In this episode, we feature the hosts of the Inner Hoe Uprising Podcast, who share their powerful sexual healthcare experiences. At the STD Engage conference, they discussed issues such as provider discomfort, bias, and lack of proper STI testing protocol. These stories highlight the urgent need for sex-positive, empathetic, and queer-friendly healthcare providers.