Today we are closing out the podcast after 5 years and an amazing number of episodes.
We share more about the decision to retire the podcast, what we have going on in our lives, and where you can continue to connect and stay in touch.
ALL EPISODES WILL REMAIN AVAILABLE.
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As we wrap up this podcast after five years, Jessie and I share our favorite episodes.
Links to all referenced episodes:
T1D Bad Habits: https://www.thisistype1.com/episode13
Police Officer Guest: https://www.thisistype1.com/episode16
Emergency Backups: https://www.thisistype1.com/episode17
Working in Retail: https://www.thisistype1.com/episode19
Diabetes Goals: https://www.thisistype1.com/episode21
Managing T1D in College: https://www.thisistype1.com/episode53
Educating Your Parents: https://www.thisistype1.com/episode60
Bogus Cures: https://www.thisistype1.com/episode78
How to Read Nutrition Labels: https://www.thisistype1.com/episode86
Mammoth Creameries: https://www.thisistype1.com/episode89
Ken Berry Guest (Keto/Carnivore): https://www.thisistype1.com/episode111
College Drinking Culture: https://www.thisistype1.com/episode130
Solo Road Tripping: https://www.thisistype1.com/episode142
I Hiked 52 Times in 2022: https://www.thisistype1.com/episode176
Adult T1D Camp: https://www.thisistype1.com/episode209
Thoughts on Ozempic: https://www.thisistype1.com/episode210
Bonus with Noah Averbach-Katz: https://www.thisistype1.com/nak/
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September 2024 brought three big milestones for us:
Colleen's had T1D for 29 years, Jessie's had it for 13 years, and the podcast turned 5!
We're sharing our high points, low points, and lessons learned over the years for these big markers.
Listen all the way through for an announcement.
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Jessie's new dog, Nala, has prior seizure alert training.
Because that's a "transferable skill", Jessie is teaching Nala how to recognize her highs and lows!
Self-training an alert dog is hard work, but it's made easier with a dog that actually wants to work.
Find out more about Jessie's training process, and her long-term plans with Nala.
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After years getting supplies directly from Medtronic, Jessie had to navigate a frustrating and lengthy back-and-forth to start getting supplies through a 3rd-party distributor.
In this episode, Jessie breaks down the timeline of what happened, why it happened, and how she rolled with the punches.
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We all know that what we eat affects our blood sugars (which can send us on emotional roller coasters sometimes) but did you know that your food will directly affect your mood?
Sarah and Tamara, certified nutritionists and founders of The Living Kitchen, came on the pod to share how what we eat impacts our entire lives.
Sarah's husband has type 1 diabetes, and watching him deal with it helped Sarah understand the importance of how we choose our food.
Take a listen and find out... is your food supporting your mood (and your BGs)?
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This episode really focuses on the differences of both type 1 and 2 while giving a short lesson on how the pancreas works.
But the main difference is that type 1 is permanent and type 2 is usually reversible. They are also completely different mechanisms, meaning type 1 is an autoimmune condition while type 2 is a metabolic condition.
We explain more about this and talk about what insulin therapy is and what treatment type 2s usually need.
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Author Caitlin Shetterly joins us to talk about her experience being diagnosed in the winter of 2020-2021, and how that impacted her life and her writing.
She is the author of Pete and Alice in Maine, and her diagnosis resulted in 3 months of lost writing... but it also brought healing in an unexpected way.
Graciously, Caitlin is offering to give away two copies of Pete and Alice in Maine!
The FIRST TWO people to DM @thisistype1pod on Instagram with your NAME and SHIPPING ADDRESS will receive a copy of the book directly from Caitlin's publisher.
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Jessie went to Rugby Nationals again this year (2024) and had a wild experience with supplies, blood sugars, and an injury that happened in the LAST 2 MINUTES of the last game.
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What does “embracing discomfort” mean?
As T1Ds, we deal with discomfort every day of our lives. Changing infusion sites, sensors, giving injections, checking blood sugars, waking up in the middle of the night, doing Herculean mental calculations for our meals..
But what if this was all easier if we leaned into embracing discomfort?
Spoiler alert: it is. Listen in to find out why.
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Jessie recently switched from the Medtronic 770G to the new 780G software update.
In this episode she talks about the improvements in the tech and how her management has been affected by the change.
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Singer/songwriter and former pediatric clinical researcher Kieran James joins us to talk about his daughter's diagnosis, the importance of clinical trials, and how music gave him an outlet from the frustrations of T1D.
Connect with Kieran:
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So you've been diagnosed with T1D... Now what? For the newly diagnosed people with diabetes, use this episode as a reference for what you might encounter in the first day, first week, first month, and first year of diagnosis.
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Check out this cross-posted episode from Type 1 in Midlife, with Melissa Slemp from Abundant Health with Melissa.
We talk about self-sabotage, self-compassion, grace, and how to handle yourself in burnout—and why burnout even happens sometimes.
While intended for Melissa's audience of midlife T1Ds, this conversation is chock-full of nuggets beneficial to everyone with T1D.
Abundant Health with Melissa
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Peter Friedfeld was diagnosed with T1D on Valentine's Day at age 55.
In the years since his unexpected thrust into life with type 1 diabetes, he's developed deep self-compassion through yoga, mindfulness, and meditation.
Join us this episode to hear more about his late-adulthood diagnosis, his work with DiabetesSangha and the Diabetes Research Institute, and how to bring more mindfulness into your relationship with T1D.
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Like it or not, some "authority figures" in the medical space get diabetes, especially type 1 diabetes, wrong.
Whether it's a doctor, nurse, nutritionist, dietitian, professor, or someone in your family, it's important to know not only how to recognize when they're wrong, but also how to stand up for the truth when they do.
Just because someone has a degree doesn't mean they have all the answers.
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What's the history of type 1 diabetes since insulin was discovered in 1921?
We have come a long way from animal-sourced insulin and needles that had to be sharpened after multiple uses.
Sometimes it's mind-boggling to think that T1D was a straight-up death sentence just over a hundred years ago.
With that in mind, Jessie walks us through diabetes research and milestones decade by decade, including our own diagnoses.
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Taralyn Jamieson was diagnosed at 8 years old and spent most of her 28 years with T1D trying to ignore her blood sugars.
It wasn't until she settled down in her personal life that it became a priority to get her health under control, but by then it was too late to avoid complications.
Taralyn shares why we need to talk about the reality of diabetes complications that are difficult to hear about, but harder to deal with if you actually have them.
Connect with Taralyn on Instagram: @taralynjamieson
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Have you ever wondered what exactly we mean when we say "support system"?
In this episode, we break down what T1D support systems are, why they're important, and what ours look like.
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Dr. Maureen Michele, an MD and parent to a T1D kiddo who also had pediatric neuroblastoma, joins us to shed light on why it's so important for parents to understand and embrace resilience.
As scary as it is to see your child diagnosed with T1D, it's also scary to navigate it while dealing with fear, overwhelm, and grief from it.
Dr. Maureen shares practical tips for parents of kids with chronic illness to calm the overwhelming thoughts and be an advocate both for their kids and themselves.
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With the changing of the years comes a new set of annual goals, and this year is no different.
Join us in this episode as we review what happened for us in 2023, both on the T1D front as well as the rest of our busy lives, and as we talk about our plans for 2024.
Listen to the end for an important announcement!
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The honeymoon period happens right at diagnosis, if it happens at all.
In this episode, Jessie and I talk about what the honeymoon period is, how long it lasts, who gets it, and why it only happens once.
This is an MVP episode from our very first year of podcasting.
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The last two months of the year can feel like a whirlwind of "let's just throw out all our routines" because Halloween kicks off the season of candy, food, get togethers, more food, family drama, even more food... you get the point.
By the time we land in the week between Christmas and New Year's (AKA what I call "black hole week") it feels like all is lost because we just spent the last two months ignoring good habits and indulging in the season.
So today (in real time, the day after Christmas) we're coming to you with some tips on getting back into routine after the holidays, sort of purposefully timed with everyone's favorite: New Year's Resolutions.
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Diagnosed at age 6, Richard Vaughn has lived with it for over 75 years now. Richard joined us on the podcast to talk about his experience with so many years of T1D.
The most surprising thing I learned? Richard did not know his blood sugar for 40 years.
Now, age 81, he has very few complications or health problems related to T1D. Richard is a wealth of information for any T1D and their families.
He’s one of the most positive voices I see in the diabetes Facebook groups. He regularly posts long-form posts about his life with type 1, the lessons he’s learned, with pictures to go along with it!
This episode was originally aired on August 31st, 2021.
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Who do you talk to about partying safely?
Intimate relationships?
How weed and alcohol affect your BGs?
The Diabetes Link has "answers to even your most cringe questions, shared by people with diabetes (and reviewed by medical experts)."
As they say, it's overwhelming to look for resources on topics you probably won't feel comfortable asking your care team, so The Diabetes Link did it for you and collected it all in the Resource Hub.
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