You never know when you’ll run into someone who shares a similar life philosophy, but after a chance meeting in college, Mark Carter resurfaces on Okie soil. He’s real and doesn’t hold back about his love of Equal and Chik-Fil-A. In this episode, our longest one yet, he shares his journey of being an ambassador for people with diabetes who don’t have a voice. If you’re brave enough to listen to the whole thing, we hope you’ll leave with the thought – is diabetes a blessing or a curse?
- How many people are alone? He’s an incredible advocate to making sure that folks know that the diabetes community is so important.
- Two kinds of people:
- The ones who won’t eat it.
- I bet I could take a decent guess.
- The burden the parents of T1Ds is real.
- Check out Podcast 31 with T1D parent, Clayton McCook. He does a killer job of sharing his families story.
- Charleston is a BIG part of the Carter’s life, but he didn’t make the diabetes alert dog cut.
- The motto in the medical community when diagnosed is you can’t eat X items. The message is a negative one and could be changed to something like – People with diabetes can eat whatever they choose and do their best to determine how and what foods fluctuate their blood sugar.
- An empowered choice!
- Words are powerful, especially when treating the community.
- In 2010, Mark had a turning point when he met Dr. Moss because he took the time to hear his story.
- Dr. Moss take aways:
- The head, the heart, and the hands.
- Diabetes is a memory disease, it remembers what you do.
- Diabetes doesn’t have to dictate his life.
- PDM (personal diabetes manager)
- Low BGs vs. Panic Attack
- Check out a post Amber wrote, Low BG vs. Hallucinating, Is There Really A Difference?
- Mark has to consider whether or not to use Trialnet.com, which is using knowledge gained through clinical research, TrialNet’s mission is to prevent type 1 diabetes and stop disease progression by preserving insulin production before and after diagnosis.
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