Pancreayinz

Pancreayinz Yinzer Dad to a T1D Champ πŸ–€ πŸ’›
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05/14/2026

As always the source of truth....He tolerates them very well now. Biggest things I've found that help with a fingerstick are: (1) letting the alcohol dry, (2) "bring up" the blood, a little bit of compression at the finger site and appropriate depth help so it's only one poke (3) always asking for consent - every shot and poke is a "are you ready". We're big fans of the Contour NextOne glucometer - it's been very useful and has done us well in terms of accuracy and has an easy to navigate display. And it helps to have a champ of a kiddo!

It's been a busy few weeks for us! B finally got his pump after nearly a year of us being on multiple daily injections (...
05/11/2026

It's been a busy few weeks for us! B finally got his pump after nearly a year of us being on multiple daily injections (MDI). We'll be at the one year mark in 11 days which is wild to think about. The below is from one of our last readings of him solely being on MDI.

The goal is for his blood sugar levels to be between 70-180 mg/dl 70% each day and we measure it by time in range. Blood sugar levels ebb and flow tremendously with T1D, as you've got ~42 factors affecting it daily, and an extra 100+ decisions we've got to make to help him thrive.

This number really is a testament to our dedication and to his hard work as someone learning to manage his condition. It has been a very long road of figuring out what foods are best for him, when and how to time injections, and even how to administer injections when we're at sleepaway camp on the top bunk at 1am...To suffice, the pump has been a massive gamechanger.

When we were first starting out, we used to get wrapped up on how the day went and the decisions we'd made, and how they'd affect Bruce in the short term. Shifting to looking at the TIR really did help our mental health, and move that perspective to the good we're doing for him. This is a very difficult thing to achieve and many people have questioned if it can be done effectively, and we're proud of how hard we've worked to care for him. Love him very much and can't believe how strong he is and how much he's accomplished over the past year.

When we were first starting out managing the diagnosis, we had to wait for the CGM to be approved via insurance which to...
04/18/2026

When we were first starting out managing the diagnosis, we had to wait for the CGM to be approved via insurance which took roughly two arduous weeks. In the meantime, we had to be checking every 3 hrs what his levels were, which included 12am, 3am, and 6am. When sleeping in shifts, we used this wristwatch that vibrates to avoid waking each other up and to ensure we weren't sleeping through checks. Ran for ~$20 on Amazon ( https://a.co/d/0jgWNpkk ) and excellent piece of mind, despite the exhaustion of waking up ~3 hrs. Just used it again when we were moving to starting our first night of his pump and still a worthwhile purchase!

One day I'll come up with a name for this rule.. but the best protection against a high is logging that you made the wro...
02/10/2026

One day I'll come up with a name for this rule.. but the best protection against a high is logging that you made the wrong call.

We've been using Gluroo since nearly Day 1 and it's made a world of a difference for logging, finding patterns, and communicating about how our T1D day is going.

I was inspired to start this page by seeing other parents post about their journey with T1D.   I'll post a variety of th...
02/07/2026

I was inspired to start this page by seeing other parents post about their journey with T1D. I'll post a variety of things here ranging from the foods we try, struggles we've faced, our background, and research we come across. My goal is to learn, grown, and become a better Dad.

B was diagnosed with Type 1 Diabetes over Memorial Day weekend in 2025. I remember feeling like a crazy parent getting a UTI test and glucometer to check him out after he had several nights of using the restroom, drinking a ton of water, and acting out-of-character mad. We rushed to our local children's hospital where he was admitted with a BGC of 514 mg/dL. My wife and I spent the next 72 hours at the hospital immersed in this new world, trying to get our arms around this enormous change. It hurt my heart incredibly to hold my son and give injections as he persisted that he wanted it to be over and go back to normal.

We've come along way since last year and learned a lot. It's made us all a stronger family and we're continuing to find new ways to help him manage his condition and live a wonderful life with T1D.

I'm hopeful for our future as more research and interest in T1D grows, and grateful for all the support we've received so far. Here's to the next steps and where this page goes.

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Pittsburgh, PA

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