Julian The Diabadass

Julian The Diabadass T1Dia-badass 💉Living Dr. Bernstein’s Low Carb Life 💪🏼💙

Call it overkill if you want, but I just bought a baby monitor for my 8-year-old. 😆Julian recently started sleeping upst...
05/29/2026

Call it overkill if you want, but I just bought a baby monitor for my 8-year-old. 😆

Julian recently started sleeping upstairs in his own bed again after it being off and on for quite a while. As a type 1 diabetes parent, old habits die hard. I sleep better knowing I can see him and hear him if I need to.

If you've ever stayed awake watching blood sugars, you probably understand.

New glasses. What do yall think? Julian thinks he looks like Harry Potter 🧙🏻
05/26/2026

New glasses. What do yall think?

Julian thinks he looks like Harry Potter 🧙🏻

Nothing like still being awake at 3:30 am because I’ve been up all night watching Julian’s blood sugar slowly creep to 2...
05/26/2026

Nothing like still being awake at 3:30 am because I’ve been up all night watching Julian’s blood sugar slowly creep to 200 and micro dosing, hoping it’s not him getting sick… only to realize it was a pump site fail. 😵‍💫

Finally changed the site, dosed, and now I’m finally getting into bed. Luckily, Julian stayed asleep through it all. T1D parenting keeps you humble and exhausted.😴

05/25/2026

I see every puncture my baby has endured since he was 10 months old - he’s six now.

Every Dexcom insertion.
Every insulin injection.
Every lancet finger or toe poke.
Every insulin cannula pushed into his skin to keep him alive.

This pod came off after 3 days.
Three days of insulin flowing through a tiny tube inserted directly into my six-year-old’s body.

And then we do it all over again.
Again.
Again.
Again.

Since he started on an insulin pump at 16 months old, we’ve changed sites every 3 days - sometimes sooner when they fail. Before that, it was multiple insulin shots every single day.

I honestly can’t wrap my mind around how many times type 1 diabetes has required us to puncture this sweet boy’s body just to keep him here.

What gets me the most is that he still offers us his little leg. Or his little arm.
Still holds still.
Still trusts us.
Sadly his norm.

And somehow, he smiles through most of it.

Type 1 diabetes asks so much from such tiny bodies. Most would never realize or understand - but I will never ever forget.

🦊
05/25/2026

🦊

05/21/2026

Watching Julian stand up and speak at his move up ceremony to third grade was such an emotional moment for us. ❤️

When he first started at Montessori, he was so unsure of himself, and seeing the confidence he showed yesterday felt like night and day. We are beyond proud of how far he has come and so grateful for the teachers and community who have helped him grow into the amazing little boy he is becoming.❤️

This is such a heartbreaking and powerful reminder of how quickly Type 1 Diabetes can turn into a life-threatening emerg...
05/19/2026

This is such a heartbreaking and powerful reminder of how quickly Type 1 Diabetes can turn into a life-threatening emergency. Knowing of this family makes this hit even harder. We live with this same fear every single day with our son, Julian.

As I read her words, I am sitting here in tears because every parent of a child with Type 1 knows this nightmare is always in the back of our minds. No matter how experienced you are, no matter how careful and vigilant you are, diabetes can still do something terrifying without warning. It is relentless and unpredictable.

What happened to London was not because her parents did anything wrong. In fact, they did everything exactly right. They heard the alarm, treated the low, recognized the seizure, administered glucagon immediately, and saved their daughter’s life. Their quick thinking and preparedness are the reason London is here today asking if the firemen were cute.

Stories like this are a sobering reminder to all of us in the Type 1 community: always carry glucagon and know how to use it. Having to use it is not a sign of failure. It is a sign that you were prepared for one of the scariest realities of this disease.

My heart goes out to this incredible family. I am so grateful London is okay, and I am holding my own children a little tighter today. Type 1 Diabetes is exhausting, relentless, and sometimes terrifying, but sharing these real and raw experiences helps all of us feel less alone.

My hands are still shaking as I write this and it was the most terrifying night of my entire life. Last night at 1:30 am London had a seizure due to low blood sugar. I heard her low alarm going off and I had treated the low twice and went to sleep once I knew she was safe. A little while later I woke up to her screaming in her sleep. When I checked on her I couldn’t wake her up and she was shaking and screaming and was combative. We grabbed the test kit and tried to give her fast acting sugar but she wasn’t able to swallow. Finger prick showed “lo” on our meter so I grabbed the G-Voke immediately and gave it to her while my husband called 911. I think that was the longest 2 minutes of my life while we waited for the glucagon to save her life. She stopped seizing and started to wake up and then the paramedics arrived. Her blood sugar was up to 74 within 5 minutes but she was still very out of it and confused. After being assessed we decided not to go to the hospital because she was stable enough and we know what to do in this situation.

So how did this happen?! We are not new to T1D after 10 years but this is the first time we have used glucagon and her first seizure due to low blood sugar. I know we did nothing wrong or negligent and yet my this still happened. We are on a work trip/mini vacation and London swam all day at the pool. At dinner she had more carbs and insulin than she usually does and Dexcom randomly had a sensor error. When I tested she was higher than normal so I dosed her and she finished dinner. Dexcom came back on and I tested and it was accurate. There was no mistake, no warning, nothing unusual. Type 1 Diabetes doesn’t play nice or care if you do everything perfect. Maybe it was the prolonged activity from swimming all day combined with the correction and the Dexcom sensor error. The thing is that we did everything right. We are on top of it and I feel guilty and upset that this happened. I know it wasn’t anyone’s fault but it just hit me like a ton of bricks.

London is ok. She’s tired and the glucagon made her feel very nauseous and she threw up. Then she asked if the firemen were cute so I knew she was ok lol.
My husband and I are shaken up. Watching your child have a seizure due to low blood sugar is something that will stick with you. London’s older brother helped us when she was having the seizure too and he definitely felt how serious this was. It was traumatic watching her go through this and feeling so helpless.

Sharing this because it’s real and raw and a great reminder to always always always have your glucagon with you. You never know when you might need it and using glucagon doesn’t mean you did anything wrong. This disease is relentless and terrifying.

💐Happy Mother’s Day to all of the amazing moms out there and especially to our fierce, tireless, incredible   moms.To th...
05/10/2026

💐Happy Mother’s Day to all of the amazing moms out there and especially to our fierce, tireless, incredible moms.

To the moms who wake up multiple times a night to check blood sugars, treat lows/highs, change pump sites and CGM’s, count every carb (or not), and carry the constant mental load that comes with raising a child with Type 1 Diabetes… you are nothing short of superheroes.

You do all of this while still being a source of comfort, strength, love, and stability for your children. You fight battles most people never see, and you do it with courage and grace.

Today we celebrate YOU…. your strength, your resilience, and the extraordinary way you show up for your children every single day.

Happy Mother’s Day to all moms, and especially to our fellow Diabadass moms. You are seen, appreciated, and deeply admired. 🩵💙💐

05/10/2026

Happy Mother’s Day! 💐❤️

Pizza night looked a little different (and a lot more fun) over here 🍕A while back, Fattyhead GF Protein Keto Crust sent...
04/29/2026

Pizza night looked a little different (and a lot more fun) over here 🍕

A while back, Fattyhead GF Protein Keto Crust sent us some specialty crusts, and we finally got around to using them. One was shaped like a “J” for Julian, and the other was a snowman—and they made the cutest little pizzas.

Julian absolutely loved them, which made it even better. Sometimes it’s the simple things… turning dinner into something fun and a little personalized just hits different.

Thank you so much Fattyhead 😘❤️🫶🏻

Eating low carb doesn’t have to be hard. Simple swaps, real food, big results. 🙌🏼

😎 Low Carb Legends: Diabadass Edition

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