#128: Rachael Jacques | Did COVID Kick Her Dormant Diabetes into Action?

The connection between COVID and diabetes has been all over the news, but I hadn’t met anyone who can speak to this until interviewing Racheal Jacques. In this episode we discuss her family history of chronic conditions, including Type 1 diabetes, and how she received her T1D diagnosis shortly after recovering from COVID. 

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#127: Rob Howe | Information is a Great Currency

It’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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#126: Lisa Hepner | The Human Trial

In June 2022, The Human Trial documentary film was released by writer and director, Lisa Hepner who was given unprecedented access to participants in the sixth ever embryonic stem cell trial in the world. Behind every breakthrough are those who risk everything for everybody else. In this episode we get into the hard hitting details as to what this means, moments of personal reflection, and if the cure really is on the horizon. I truly believe Lisa and her team are bridging the much needed gap between the people living with diabetes and the research teams who are working diligently to be the first to “cure” Type 1 diabetes.

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#122: Qiana Drew | You’re Really Only as Strong as Your Foundation

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.

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Podcast #120: Azure Wolfe | Loving the Skin We’re In

Every change that our body experiences as we age is connected to hormones, and should not be neglected. In this episode we discuss the changes our T1D bodies are experiencing in our forties. Azure also speaks passionately about the importance of connecting with others who are living with diabetes to support one another and recommends a community approach to diabetes management.

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Podcast #119: Naomi Kinnamon | Type 1 of a Kind – A Girl Needs Pockets

You might think fashion is the last thing people living with diabetes have on their mind, but in reality, PWDs could benefit a great deal from clothing that is designed with both utility and style in mind. Naomi Kinnamon, who has lived with Type 1 diabetes since age 11, brings us those solutions that accommodate insulin pumps and injection sites.

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Podcast #118: Noah Averbach-Katz | Searching for a Cache of Insulin Before It’s Too Late

Noah Averbach-Katz blew the doors off a recent Kickstarter campaign for a film that just began production. I believe his experience with live theater AND as a professional actor gave him the upper hand on creating TYPE 1, a short film chosen as one of Kickstarter “projects we love” after it was fully funded in under 8 hours. Stay tuned for more information on the release date and screening opportunities.

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I Kind of Gave Up Caring for Myself Until Technology Changed my Life | Michael Spencer

I have lived with Type 1 diabetes for 30 years. During this time I’ve had to face the horrors of an indifferent insurance industry which branded me “unworthy” due to my “pre existing condition.” I’ve endured injecting myself 4x a day, sometimes more. My fingers have callouses from being pricked for blood glucose measurements, also 4x a day. To be honest, I kind of gave up on caring for myself for a while until technology changed my life.
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#117: Kalex Williams | You Look Fine, Come Back on Monday

Isn’t it time to start injecting some much-needed diabetes humor to cut through the doom and gloom we face? Kalex Williams is a master at extracting positivity and he has to be one of the coolest people I’ve met! In this episode, you will get a taste of Kalex’s resilience in the face of his diagnosis and how he didn’t sit on his pity party, but makes light of it and connects to attendees from across the globe.

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