At the end of the day – it is our responsibility to stay up to date on diabetes management tools and tricks. There is a LOT of information available and I don’t know about you, but I’ve learned more from the diabetes community than in any medical setting.
Farhaneh Ahmadi is the Founder and CEO of eddii, a virtual in-app character designed to engage people living with diabetes. Her vision is to make every eddii user feel motivated to achieve long-lasting health outcomes, and enjoy doing so! In this episode we discuss her personal Type 1 diabetes journey, the inception and benefits of eddii, gamification, and why the app operations are based in Oklahoma.
Harold Hamm is world renowned for his entrepreneurial spirit and successful career in the oil and natural gas industry, but there is SO much more to this story. In this episode we discuss how a Type 2 diabetes diagnosis was a personal game changer, the Giving Pledge, the International Biomedical Research in Diabetes Award, and his commitment to solving many of humanity’s greatest challenges including diabetes, energy poverty, literacy and education.
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.
Katie Bone had the diabetes community in awe of her drive and competitive spirit as she dominated the third ever American Ninja Warrior Women’s Championship. In this episode we discuss a T1D family history, incremental boluses, teenage hormones, when to compete in wet shoes, and her motivation to continue a strict workout regimen.
It’s been awhile since I interviewed a T1D parent, but Sara Spencer-Kinoti stands out. Her LinkedIn profile reads unapologetic, ridiculously excited diabetes advocate, ally and part-time pancreas. In this episode we discuss her college side hustle taking care of insulin dependent cats, her family history of Type 2 and how she uses her unique platform as a healthcare provider to not only influence and educate those living with diabetes, but also members of their care team.
I had the pleasure of finally connecting with my dear friend Katie – a busy mother of two active boys, business professional, and person who dedicates time to so many causes. We don’t get to see each other often so I cherish when we can and I was thrilled to have her youngest son Vail (aka BEEF) join us for a stroll around town. I’ve known Vail since birth and he has always been interested in my life with diabetes. He asks the hard hitting questions – some that are honestly hard for me to answer and the very reason why I’m writing this post.
May is mental health awareness month and is the perfect time to release this episode with Allison Nimlos, a licensed marriage and family therapist and co-founder of the Diabetes + Mental Health Virtual Conference who specializes in behavior change psychology for diabetes. In this episode we discuss the importance of addressing mental health for those living with a chronic disease.
I’ve known Marwin Begaye for years and stumbled across one of his pieces that stopped me dead in my tracks titled, Super Size Angels. In this episode we discuss he and his families journey to prevent a diabetes diagnosis, holistic medicine, the growing numbers of diabetes within the American Indian communities, and the controversial body of work he created around this topic.
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.
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.
