The diabetes community is fortunate to have so many one of a kind warriors and Thom Solo is top of the list in my opinion. His advocacy efforts at an early age + pursuit of art as a career = my dream guest. In this episode we discuss Thom’s artistic journey, runway lows, diabetes and dating, his fashion family, the LGTBQ+ community, and speaking things into existence. (more…)
It took me months to nail down an interview with Elizabeth Vesely after seeing her Facebook post about taking the polar plunge and it was well worth the wait. In this episode we discuss her misdiagnosis, addressing diabetes denial, and what living life to the fullest while you still can looks like for this T1D world traveler. (more…)
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. (more…)
I tested positive for COVID after living in a bubble for literally four years. I’ve been such a hermit, wore my mask when no one else did, avoided crowds and felt serious social anxiety most of the time, but it finally got me. My COVID free bubble has popped. (more…)
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. (more…)
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. (more…)
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. (more…)
I set out to run a few errands and when I returned home I had a weird feeling in my gut that came out of nowhere. I started sweating and had the chills at the same time. I immediately thought COVID, but before I could administer a home test, I began projectile vomiting.
Rewind a few steps – before I left the house my blood sugar was low so I ate lunch without shooting up (aka bolusing). (more…)
As we roll into the New Year, I’m reminded how living with Type 1 diabetes can make things a little challenging at times. In this episode, Justin shares how he wasn’t going to let his new diagnosis keep him from having the time of his life at Burning Man, an annual event in Nevada’s Black Rock Desert, where people gather for around nine days to celebrate artistic self-expression. Good times. (more…)
I’ve joked, and/or compared my diabetes management to OCD (obsessive compulsive disorder), but hadn’t met anyone living with both conditions until interviewing Brett Ryan Stewart. Brett is a Nashville based producer who shared – “ultimately what OCD kind of comes down to is this inability to accept what you can’t control and then obsessing about a way to control the uncontrollable.” I’m sure many of you living with T1D can relate to this mentality and Brett’s ability to give us a look into his daily life was eye opening to say the least.