
Emotional – Diabetes Daily Grind | Real Life Diabetes Podcast
Emotional – Diabetes Daily Grind | Real Life Diabetes Podcast
Show overview
Emotional – Diabetes Daily Grind | Real Life Diabetes Podcast has been publishing since 2015, and across the 9 years since has built a catalogue of 35 episodes. That works out to roughly 20 hours of audio in total. Releases follow a roughly quarterly cadence.
Episodes typically run thirty-five to sixty minutes — most land between 48 min and 1h 5m — and the run-time is fairly consistent across the catalogue. None of the episodes are flagged explicit by the publisher. It is catalogued as a EN-US-language Health & Fitness show.
The catalogue appears to be on hiatus or wound down — the most recent episode landed 2.1 years ago, with no new episodes in over a year. The busiest year was 2019, with 11 episodes published. Published by Emotional – Diabetes Daily Grind | Real Life Diabetes Podcast.
From the publisher
Creative Inspiration For The Real Diabetes Life
Latest Episodes
View all 35 episodes#155: Dr. Kevin Pantalone | We Truly Do Care
I’m breaking new ground with a special guest: Dr. Kevin Pantalone, an endocrinologist whose insights offer a fresh perspective on patient care. In a recent poignant reflection, Dr. Pantalone shared the emotional impact of losing one of his patients, a woman living with Type 1 diabetes. His words shed light on a side of healthcare […]
#152: Brooks, Dan & Scott | Dads & Diabetes: Navigating the Sweet (and Spiky) Side of Fatherhood with T1D Daughters
I’ve recently had the opportunity to connect with three fathers who shared their experiences of raising daughters, aged 11 to 16, living with Type 1 diabetes. In this groundbreaking episode, Dan Kendall, Brooks Ratzlaff, and returning guest Scott Kinsel, provide insights into the unique challenges and joys of being a father to a T1D daughter. […]
#151: Molly Schreiber | An A1c of 5.0 was a Badge of Honor
I connected with Molly Schreiber after reading a heartfelt LinkedIn post about her family history of Type 1 diabetes and the tragic loss of her father. Molly is a patient living with multiple health conditions and an active patient advocate within those communities. In this episode we discuss growing up with a T1D dad, her […]
#145: Scott & Poppy Kinsel | Determine Who is the Pilot of this T1D Plane
Scott & Poppy Kinsel popped up on my radar after reading a heartfelt Facebook post about not letting type 1 diabetes slow life down after her recent diagnosis. In this episode we discuss Poppy’s misdiagnosis, navigating competitive sports, parenting, and what an epic adventure to Norway looks like with T1D. BIO:  Scott Kinsel – I […]
#111: Madison Thorn | “Sacrifice the Weak, Re-open Tennessee”
It’s time to get rid of the word ‘weak’ when talking about people navigating chronic illnesses. In reality, we are some of the strong, unique and resilient people in the world, and Madison Thorn is spreading that very message. She was fueled by a nasty protest sign and turned that energy into a thought provoking […]
#108: Kayla Mattingly | We Don’t Need a New PlayStation, We Need a Solution
People living with diabetes don’t just need the latest and greatest tech, they need real solutions to unique problems! Kayla Mattingly always knew she wanted 3-4 kids from the start, but never imagined two of her four sons would be diagnosed with Type 1 diabetes. She rolled with the autoimmune punches, but an insulin allergy has her […]
#100: Scott Johnson & Kerri Sparling | Everything is Worth Giving a Shot
In gearing up for this epic unicorn episode I sincerely reflected on the impact becoming a diabetes advocate has had on my life. Two of the first people I discovered were Kerri Sparling and Scott Johnson. I had found my people! Reading their stories and watching them present at various conferences gave me the courage […]
#96: Janet Hatch & Zandra Soanes | I’m Not a China Doll
Thankfully, many of us living with Type 1 diabetes have a supportive parent(s), but have we really taken time to think about how our diagnosis affected our loved ones. When Janet’s media kit fell on my desk, I knew I wanted to connect. Their story of strength and partnership as they navigated through this disease, […]
#93: Ozzy England | Let’s Be Honest – We’re 21st Century Vampires
Can you imagine being diagnosed with T1D and five years later stating you’re in the best health of your life? In this episode, we’ll be learning more about my new friend from the land down unda’, Astra-Lia ‘Ozzy’ England. Several years ago, Ozzy would receive news from the doctor that would shake her world; a […]
#92: Matt Tarro & Brandon Denson | The Truth Will Set You Free
You don’t have to hide, let’s have the tough talks. In this episode you’ll learn why this is so important with guests Matt Tarro & Brandon Denson the Founders of Bolus Maximus. Matt and Brandon have created this community with a focus on filling a major void in the male community, the need for vulnerable […]
#91: Diabuddies App Founders | The Importance of Connectivity
The battle against diabetes doesn’t have to be done alone, we need community. That is the mindset of today’s guests (yes plural!) the Diabuddies App Founders, Amy, Sarah and Charlene. As we dive in, you’ll learn how these ladies’ experience with diabetes led them to create something ALL people living with diabetes can support. BIO: […]
S37 Ep 83#83: Tracey D. Brown | A Positive Poster Child for the Type 2 Diabetes Community
For newly diagnosed T2D, it might be overwhelming and many fall into diabetes denial. In an effort to change this mentality, Tracey shares an authentic story of how a question from her daughter was the “aha” moment to take things seriously. In this episode, Tracey unapologetically shares her story because there is no shame in […]
#77: Monica Storozyszyn | Knowing the Difference Between a Constant and a Pest
I am wrapping up this decade with one last long episode, but I promise, it is worth listening to the very end and entertaining if nothing else. The theme of this episode is knowing the difference between being a constant, and being a pest. Monica backs this motto by providing actionable items and tips to […]
#76: Chris & Candace Clement | The Importance of a Supportive Partner
Chris and his wife Candace are honest, vulnerable and a little sappy at times, but are the perfect reminder there are still good ones out there. You know, the ones who support you and your diabetes through the good, the bad and a serious hypo while educating their three kiddos along the way. Together, they […]
#75: Amy Lacey, Cali’flour Foods Founder | A Message Out of the Mess
After reading the Cali’flour Kitchen cookbook from cover to cover, I knew Amy Lacey would be the perfect guest to wrap up diabetes awareness month. Her desire to bring back dietary normalcy, especially her family’s pizza nights, after her auto immune diagnosis was the driving force behind Cali’flour Foods – the first cauliflower pizza crust. […]
#74: The Future of Diabetes Management | DiabetesMine Innovation Summit Mini Pods
I was honored to be chosen as one of ten Patient Voice Contest winners for the DiabetesMine Innovation Summit. During the two day event, I was surrounded by industry leaders, tech gurus, genius creators of diabetes apps, and many fellow advocates. This Summit coalesced the mother lode of advancements in diabetes management, and a few […]
#71: Dr. Jody Stanislaw | From Diagnosis Day to a Naturopathic Medicine Career
This globetrotting T1D just embarked on a 12-month remote year journey with a focus to reach one million people living with diabetes. Her candid approach, charismatic attitude, and ability to touch on hot topics will transform lives and prevent diabetes burnout. With 39 1/2 years of experience and a handful of degrees, Dr. Jody is […]
#69: Rebecca Wilber | Turning a Life Altering Experience into a Philanthropic Dream
It was just by chance our paths would cross at a T1D kiddo and parent support group. I rarely attend and Rebecca and her husband James were guests that evening. When we split off into another room, Rebecca shared her heartfelt story to the parents and there was not a dry eye in the room. […]
#68: Anne Imber | The Power of Connectivity within the T1D Community
Last December, Anne came to the rescue, offering help during my insulin crisis while in San Antonio, Texas. She, like many people in the DOC (diabetes online community) stayed in contact with me while I resolved the problem. She is a leader in the diabetes community and her wealth of knowledge has helped so many […]
#66: Bonnie & Jennifer Allen-Barron | A Gathering of Oklahoma T1D Dinosaurs
Recently, Mayor David Holt declared a pride week in my home town of Oklahoma City. It made me think – do I know any LGBTQ T1Ds? Yep, and not only is she my friend, she is one of the only people I know that has had diabetes as long as I have – hence the […]