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The goal of my podcast is to have a central place for people afflicted with Scleroderma and a place for their families and friends to be informed by specialists in either Scleroderma or autoimmune topics. I will cover a wide range of topics like nutrition, medications, vitamins, and lifestyles. I will also showcase stories from others affected by Scleroderma and how they have dealt with the disease. For additional information you can visit my website-Mogilsmobcast.com, or follow me on Instagram-mogilsmob and Facebook mogilsmob
116 Episodes
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Today’s topic is one I’ve wanted to discuss for a very long time and one that’s particularly troubling to me: calcinosis. I was absolutely thrilled when Dr. Ariane Herrick agreed to join me for this conversation. She is incredibly knowledgeable on the subject and shared such valuable insight and information about this challenging condition. I’m so grateful for her time and expertise
Today’s guest is Dr. Kathryn Torok, a pediatric rheumatologist at the University of Pittsburgh and UPMC Children’s Hospital of Pittsburgh, where she directs the Pediatric Craniofacial Scleroderma Clinic. Scleroderma in children is rare, about five in 100,000 develop localized disease, and only about one in a million develop systemic disease. It's crucial to treat to target as early as possible. I learned so much from Dr. Torok about how scleroderma affects children and the best approaches to ...
Today’s guest is Dave Hanson, who shares his journey from his first confusing symptoms to finally receiving a diagnosis. It all began in the fall of 2019, when Dave started experiencing unusual symptoms — painful cramps and a vague but unsettling feeling that something wasn’t right. By early 2020, just before the pandemic, he noticed swelling in his hands and went to the ER. With no signs of Raynaud’s, doctors initially diagnosed him with psoriatic arthritis. It would take another year before...
Today’s guest is the incredible Dr. Sara Reardon, a renowned pelvic floor physical therapist, author, and founder of V-Hive, a groundbreaking app for pelvic health. I wanted to have Dr. Reardon on the show because nearly 80% of people living with scleroderma are women, and many face challenges such as urinary issues and fecal incontinence topics we don’t talk about enough. Dr. Reardon offers thoughtful, practical, and empowering ways to address these concerns. Her book, Floored, is full of he...
Today’s guest is Dr. Laura Hummers, a rheumatologist and co-director of the Scleroderma Clinic at the Johns Hopkins Scleroderma Center. In our conversation, we dive into the different phenotypes observable characteristics of scleroderma, as well as the three major antibodies commonly found in patients and how they aid in diagnosis. This episode is packed with valuable insights and information you won’t want to miss.
Today’s guest, Scleroderma Warrior Dr. Joseph Washington, is the definition of resilience and perseverance. His journey began with Raynaud’s symptoms in junior high, but it wasn’t until pharmacy school that he was diagnosed with diffuse systemic sclerosis. So much has happened in just four years since then, and I can’t wait for you to hear his inspiring story.
Today’s guest is another incredible scleroderma warrior, Natalie Puccio. As many of you know, no two scleroderma journeys look exactly alike. Natalie and I discovered we had so much in common—both personally and in our symptoms—which made our conversation especially meaningful. One big difference, though, is that Natalie was diagnosed at just 24 years old and went on to have three children while living with scleroderma. She’s an amazing resource for anyone navigating questions or concerns abo...
Today’s guest is rheumatologist Dr. Jessica Gordon. Together, we explore two topics that every scleroderma patient is familiar with skin and Raynaud’s.Dr. Gordon explains the three stages of skin progression in scleroderma, the challenges patients often face, and the treatments available. We also touch on Raynaud’s our discussion may be shorter, but it’s filled with helpful insights.I truly enjoyed this conversation with Dr. Gordon, and I know you will too.
Today’s guest is another incredible scleroderma warrior. Kristina Hamilton was diagnosed in 2022 at just 32 years old, while raising three young children. Like so many women, she was initially told her symptoms were simply due to stress. Not long after, she found herself hospitalized, her weight dropping from 120 to 68 pounds. Her life changed almost overnight. Yet Christina’s story is one of resilience, rising above her diagnosis to share her journey and inspire others. Join us as we hear ho...
Today’s guest is Dr. Ebru, a dynamic force in the world of skincare. With a background in molecular medicine, immunology, and cosmetic chemistry, she created her skincare line, AveSeena, from the ground up. She was one of the first to connect inflammation, “inflammaging,” the immune system, and the skin microbiome in the development of her products. Beyond her scientific expertise, Dr. Ebru brings an upbeat energy and a wealth of valuable insights that you won’t want to miss.
Today’s guest is Shubhda Chaube. Shubhda is a scleroderma warrior who was diagnosed just a year ago on her 47th birthday, no less. Despite being early in her journey, she’s jumped in with both feet: attending multiple support groups, including one based in India, and starting a thoughtful blog called Calm Core Cozy Layer. She’s also working on a powerful project called From Patient to Pattern Seeker. Let’s learn more about her journey and the projects she is working on. Shubhda's blog, Calm,...
Today’s guest is Rashmi Bhasin, a true scleroderma warrior. Like many women seeking a proper diagnosis, she was repeatedly told her symptoms were due to hormones or stress. As a result, it took four years to finally get the correct diagnosis. But rather than letting that struggle define her, she turned it into a force for good. Today, she leads Scleroderma India, advocating for others facing similar challenges. Tune in to hear her inspiring journey firsthand!
Today’s guest is scleroderma warrior Emily Radican. Over the years, Emily has been diagnosed with a range of autoimmune diseases, and five years ago, Limited Scleroderma became part of her journey. Many of her health challenges have revolved around her gut, which inspired her to pursue a degree in nutrition. Now, she’s working toward her Ph.D. in Nutritional Science and Food Chemistry. Join us as we dive into her story, her autoimmune journey, and her exciting plans for the future after gradu...
Get ready for a fascinating deep dive into one of my favorite topics—sleep! In today’s episode, we’re joined by Dr. Sabra Abbott, an expert in all things sleep-related. Together, we explore the three critical stages of sleep, the unique challenges scleroderma patients face when it comes to getting quality rest, and practical strategies to improve your sleep. By the end of our conversation, you’ll feel informed, inspired, and maybe even a little more well-rested!
Today, we have an incredible guest joining us—rheumatologist Dr. David Collier. With 28 years as a Professor of Medicine at the University of Colorado Medical School and 25 years leading the scleroderma clinic, Dr. Collier is a true expert in the field. Currently, he’s consulting with Kyverna Therapeutics, working on groundbreaking (CAR) T-cell therapy. We’ve all been hearing the buzz about this innovative treatment for scleroderma, and today, we’re diving in to learn what it’s all about. Get...
Today, I’m thrilled to introduce Dr. Cristina Padilla, a remarkable physician I had the pleasure of meeting at a recent conference. In this episode, we delve into the work being done at the Pittsburgh Scleroderma Center, where Dr. Padilla focuses on translational research into interstitial lung disease. Through our conversation, you’ll not only learn about her invaluable contributions to the field but also hear her deep passion for advancing scleroderma research and improving patient care. Le...
Today’s guest is Melissa Marquis, who shares her incredible journey of perseverance and advocacy. It took 10 years for Melissa to receive a diagnosis of undifferentiated connective tissue disease—a condition where the immune system attacks connective tissues, but the symptoms and lab results don’t fully align with any specific connective tissue disease. Three years later, she was diagnosed with limited cutaneous systemic sclerosis. After years of uncertainty and navigating frustrating symptom...
In today’s episode, I’m joined by Danielle Rice, a clinical and health psychologist whose PhD research zeroed in on a unique perspective: how to support caregivers of scleroderma patients. Believe it or not, before Danielle’s work, there had only been one small study on this crucial topic! We often overlook how scleroderma affects not only the patients but also their loved ones. Danielle has done incredible work to bring much-needed support to caregivers, and today, she shares insights on the...
Today, I’m thrilled to chat with Dr. Deanna Baker Frost—whom I had the privilege of meeting at the National Scleroderma Conference. When I asked her to join me on the podcast, she agreed enthusiastically, requesting a topic that would be impactful for patients. I suggested osteoporosis, given that 80% of scleroderma patients are women, and 80% of the estimated 10 million Americans with osteoporosis are women, too. In this episode, we dive into everything osteoporosis. Buckle up—there’s a lot ...
Today, I talk with Dr. Sean Fortier, a specialist in pulmonary medicine. Since more than 40% of scleroderma patients show evidence of interstitial lung disease, I thought it was important to discuss pulmonary fibrosis and pulmonary hypertension. Dr. Fortier and I also discuss his research, which I found very encouraging—and I believe you will, too.
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