PodcastDX

PodcastDX

PodcastDX is an interview based weekly series. Guests share experience based medical insight for our global audience. We have found that many people are looking for a platform, a way to share their voice and the story that their health journey has created. Each one is unique since even with the same diagnosis, symptoms and the way each person will react to a diagnosis, is different. Sharing what they have experienced and overcome is a powerful way our guests can teach others with similar ailments. Many of our guests are engaging in self-advocacy while navigating a health condition, many are complex and without a road-map to guide them along their journey they have developed their own. Sharing stories may help others avoid delays in diagnosis or treatment or just give hope to others that are listening. Sharing is empowering and has a healing quality of its own. Our podcast provides tips, hints, and support for common healthcare conditions. Our guests and our listeners are just like you- navigating the complex medical world. We hope to ease some tension we all face when confronted with a new diagnosis. We encourage anyone wanting to share their story with our listeners to email us at info@PodcastDX.com ​

  1. 1d ago

    Diary of An Epileptic

    In this episode of PodcastDX, we speak with Allany Muniz, founder of Diary of an Epileptic, about the realities of living with epilepsy beyond what most people see. Allany shares how her diagnosis changed her life and led her to create a platform built on honest storytelling, awareness, and connection. Together, we explore the many ways epilepsy can affect memory, confidence, relationships, mental health, daily routines, and a person's sense of identity—not only seizures. ​ This thoughtful conversation also addresses misinformation and stigma, the value of tracking symptoms and triggers, and the importance of informed, compassionate support from family, friends, and healthcare providers. Allany offers an encouraging message for people who are newly diagnosed: life may look different, but it can still be full, meaningful, and connected. ​ For more information and support: Visit the CDC's epilepsy resources, the Epilepsy Foundation's seizure-first-aid materials, and the National Association of Epilepsy Centers' patient resources. You can also follow our guest, Allany Muniz, and Diary of an Epileptic on Instagram and TikTok at @DiaryofanEpileptic, and on YouTube at Diary of an Epileptic. ​ ​Bio: Hey, my name is Allany Muniz, a woman who happens to have epilepsy. In my 14 going on 15 years of having epilepsy, I have experienced PTSD, healing, mental health issues, paranoia, finding my confidence/voice, and isolation. I got diagnosed in August of 2011. That particular day was typical, except for feeling excited to start my freshman year. I was ready to get rid of the nightmares I endured in middle school and saw high school as my fresh start. Honestly, I can't even tell you what he said; all I heard was seizures and epilepsy. A few days later, I had a seizure, which confirmed my epilepsy diagnosis. Of course, in my life, I've been the center of embarrassment and humiliation, so when I had 3 seizures at school, I became known as the "seizure girl."  Throughout the years, I received opportunities to speak about my story and spread awareness. The idea of Diary of an Epileptic started in 2019 when I would have these creative... self-talk moments (now known as vivid visions/dreams). In November 2020, I fractured my ankle and thought, " Might as well, since I had nothing else to do. It was weird at first because I forgot I was still loopy from the anesthesia, but it felt... right like I was on the right path.

  2. Aug 4

    Ebola

    In this PodcastDX episode, Lita and Jean Marie unpack Ebola as a severe but not casually spread viral disease, explaining that infection requires direct contact with blood or other body fluids or contaminated materials, not simple proximity or everyday social contact. They outline key facts about animal reservoirs (likely bats), how spillover into humans occurs, and why understanding zoonotic origins helps shape outbreak prevention in affected regions. The conversation walks listeners through typical Ebola symptoms, the incubation period, and why early recognition and intensive supportive care—fluids, electrolytes, careful monitoring—can be lifesaving despite the virus's high average case‑fatality rate. The hosts discuss recent outbreaks in Central Africa, how tools like surveillance, contact tracing, safe burials, isolation, infection‑control practices, and targeted vaccination work together, and they debunk common myths about airborne spread or presymptomatic transmission. Lita and Jean Marie also explain that available vaccines and monoclonal antibody treatments apply mainly to the Zaire species, making strain identification crucial, and highlight why survivors need long‑term medical and emotional support. Throughout the episode they emphasize community education, stigma reduction, and practical prevention—especially for families, healthcare workers, and travelers—showing that while Ebola is dangerous, accurate information and coordinated public health action can contain outbreaks and replace fear with wise, compassionate response.

  3. Jul 21

    Vagus Nerve Reset

    In this solo PodcastDX episode, Lita introduces the concept of the vagus nerve and explains why it has become such a focus in wellness, neurology, psychiatry, and online health spaces. She describes the vagus nerve's path from brainstem through neck, chest, and abdomen, highlighting its role in heart rate, breathing patterns, digestion, and the body's stress response, and explains that most people using the term "reset" are really talking about wanting to feel less stuck in a chronic high‑alert or fight‑or‑flight state. ​Lita then breaks down the different things people may mean by "vagus nerve stimulation," from implanted medical devices to non‑invasive transcutaneous stimulation, and to everyday practices like breathing exercises, humming, singing, cold exposure, movement, and meditation. She emphasizes that these are not equivalent, that each has different levels of evidence and risk, and that implanted vagus nerve stimulation has established—but carefully defined—roles in difficult‑to‑control epilepsy, treatment‑resistant depression, and selected cases of rheumatoid arthritis, along with potential side effects such as voice changes, cough, throat discomfort, and surgical risks. ​The episode spends time on transcutaneous vagus nerve stimulation (tVNS), explaining that early research is promising but not definitive for conditions like anxiety, depression, insomnia, migraine, pain, autonomic dysfunction, and inflammatory conditions. Lita cautions against blanket claims about "frequencies" that reset the nervous system, noting that real neuromodulation protocols are highly specific to device parameters, placement, clinical context, and individual variability, and that the autonomic nervous system itself is a dynamic network influenced by sleep, trauma, hormones, pain, illness, medications, and environment. ​Throughout, she offers a practical framework for listeners who are eager for relief but wary of marketing promises, encouraging them to ask concrete questions about device type, studied condition, trial design, sample size, meaningfulness of benefits, side effects, and whether a product is truly a medical treatment or a wellness gadget borrowing medical language. The episode closes by affirming the genuine promise of bioelectronic medicine and vagus‑focused therapies, while reminding listeners that "vagus nerve reset" is a catchy phrase for a complex field—not a diagnosis, not a cure‑all, and never a substitute for careful, shared decision‑making with qualified healthcare professionals.

4.9
out of 5
29 Ratings

About

PodcastDX is an interview based weekly series. Guests share experience based medical insight for our global audience. We have found that many people are looking for a platform, a way to share their voice and the story that their health journey has created. Each one is unique since even with the same diagnosis, symptoms and the way each person will react to a diagnosis, is different. Sharing what they have experienced and overcome is a powerful way our guests can teach others with similar ailments. Many of our guests are engaging in self-advocacy while navigating a health condition, many are complex and without a road-map to guide them along their journey they have developed their own. Sharing stories may help others avoid delays in diagnosis or treatment or just give hope to others that are listening. Sharing is empowering and has a healing quality of its own. Our podcast provides tips, hints, and support for common healthcare conditions. Our guests and our listeners are just like you- navigating the complex medical world. We hope to ease some tension we all face when confronted with a new diagnosis. We encourage anyone wanting to share their story with our listeners to email us at info@PodcastDX.com ​