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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I Had Forgotten What It Was Like To Be Weightless | Madison Thorn

I recently came across a very powerful Facebook post by past Real Life Diabetes Podcast guest, Madison Thorn and had to share. This is real life diabetes and what it can do to the psyche.

I just had the most absolute mind fuck of an experience…
I was out of coffee at home so I walked to the breakfast joint at the end of my block to grab a cup to go. When I walked in, the food smelled amazing and I asked the hostess if, instead of the coffee to-go, I could sit and have breakfast.

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#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 project highlighting other high risk humans like ourselves, a story that needs to be told.

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#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 family and medical team scrambling for solutions. Type IV Hypersensitivity to insulin is rare, but she has found a handful of other parents who are looking for answers. 

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#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 to “really” find my voice. The podcast and blog posts have lifted a huge weight, one I didn’t realize was there. I am truly blessed. 

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Happy Birthday to Me – Real Life Diabetes Virtual Happy Hour

Today, January 7th, 2021 I celebrate my 29th year on this beautiful planet and considering the current shit storm of world events and quarantine I would normally be sad, BUT connecting with my diapeeps every Thursday during the Real Life Diabetes Happy Hour has literally saved my life. I would love for you to join me tonight or any Thursday you are free to pop in between 5 – 6:15pm CST. Please be sure to register – CLICK HERE.

This birthday pic was taken three weeks before I was diagnosed with T1D and celebrating with other people who “get it” is a reminder – I am not alone and you don’t have to be either.



#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, both highs and lows, is a reminder – we are not alone.  (more…)



A T1D Perspective on the Día de los Muertos Celebration

I’m new to San Antonio, Texas and have thoroughly enjoyed soaking up the culture. On November 1st and 2nd they celebrate Día de los Muertos (Day of the Dead) which also kicks off Diabetes Awareness Month. As I researched and witnessed firsthand this beautiful ceremony a few emotions surfaced. My Type 1 diabetes diagnosis almost 38 years ago was literally a death sentence. For most of my life I’ve worn this weight alone, but my mindset has shifted with the current pandemic and political state of affairs/nightmares. (more…)



#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 T1D diagnosis. In a matter of weeks, she went from living a relatively normal life (albeit with Celiac disease) to being put on insulin therapy. Her fiery personality and unapologetic curiosity about life with diabetes made her the perfect guest.

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#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 connections for men dealing with diabetes. Both diagnosed at later ages, they know first hand how diabetes can get in the way of your goals and plans. Now they are on a passionate mission to help those grinding through this disease. Let’s jump right into their stories and start talking about some hard truths and good advice.

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