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Reverend Mireya Martinez was a panelist on the Crushing: The Burden of Diabetes on Patients session during SXSW in Austin, Texas where she dominated the conversation in my opinion. In this episode we discuss her life as an insulin dependent person living with Type 2 diabetes, healthcare disparities and how she is writing her own story.
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Sarah Petti is back on the show and her life has drastically changed since her last appearance three years ago. In this episode we discuss T1D pregnancy, body image and what’s new in her very active life with a guest appearance from Angus.
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Rachael Dyer and Scott Alexander Ruderman are the directors of Pay or Die, a feature documentary that provides an inside look at how the soaring price of insulin in America is threatening, if not deadly.
We’ve heard WAY too many stories about people rationing their insulin and this film documents what life is like with this disease and the impact it has on our pocket books.
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Serena Valentine, was misdiagnosed with Type 1 diabetes in her twenties. This misdiagnosis is one of the many reasons she is a passionate advocate for health equity, eye health and diabetes education. In this episode we discuss Serena’s misdiagnosis, diabetes complications, healthcare disparities, food deserts and her advocacy efforts.
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Thapi Semenya is in her final year of law school, is an IDF Young Leader in Diabetes Trainee, a Dedoc voice, a professional advisor for the Luna Project UK and a strong diabetes advocate. We connected on LinkedIn after I read her mindful post about lowering her A1c and what steps it took to get there.
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Lauren Cox, the first ever WNBA player living with Type 1 diabetes, did not let a T1D diagnosis at an early age keep her from reaching personal and professional goals. In this episode we discuss her diabetes management tools on the road, and on the court.
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It’s time to celebrate! On January 28th, I’ll roll into my 40th year living with Type 1 diabetes. Each year as this milestone approaches I reflect on how I’ve managed my diabetes over the decades. I’ve created a few ideas on how you can join me in celebrating another eventful year living with this disease.
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Jessica Landon, like many T1D parents, is doing her best to put a positive spin on the new “normal” life she and her family are living. In this episode we discuss how and why her family celebrate Lindsey’s diagnosis date, a Facebook post and the flood of comments from the online community – both good and bad.
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Watch on YoutubeIt’s always nice to connect with someone equally as passionate as I am about serving our community. Rob Howe is a fellow podcast host and serial entrepreneur making a difference in the diabetes space. In this episode we discuss Rob’s latest project and how we can work together to reach the underserved – one Regional Food Bank at a time.
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If you can name it, you can tame it! In this episode, Qiana Drew clears up some misconceptions and shares how, when it came to her diabetes, she would often do things to try and keep up with her thin peers. Eventually, she realized this mindset was not a healthy way to live and decided to share her journey with Type 1 diabetes and diabulimia to help others live their best life.