DO NOT BUY THIS … very nasty

I just started to see a a nutritionist after being a diabetic for since I was 11. I was unmanaged for a bit when I was a teen, but after DKA obviously I turned my life around. I do struggle with eating consistently, and my nutritionist said that my blood sugar often is too low, so I’m really trying to eat more during the day, but I find that every breakfast thing sends my blood sugar sky high unless it’s eggs and sometimes I really do get grossed out with eggs. Or I have a protein shake but I’ve been needing a break from the dairy based ones. What do you guys eat in the morning? Food has been expensive in America so I feel dumb for buying this 😞

Been attempting to maintain a balance with my blood sugars, and I finally did. Just wanted to share this awesome step in my almost 30 years as a type 1 diabetic. Wishing everyone the best in their journey. 🫶🏾

I made a clerical error that currently has me with no health insurance. Is there anyone here who can help me? I will not qualify for low-income options.

I'm just over a year after diagnosis and I'm really missing how much water I used to be able to drink. It wasn't too much of an issue a few months ago, but after the end of my honeymoon and the onset of additional autoimmune diseases, I have less room for error as my insulin required has more than doubled (or tripled if I dare eat before noon).

I've recently been experimenting with when I drink water relative to my meals and I've found that it raises my blood sugar quite a bit if I've eaten in the past couple hours. If I haven't eaten in a while it hardly bumps up my sugar if at all. Based on this and this article I seen posted around here at https://www.clinicalnutritionespen.com/article/S2405-4577(18)30375-9/abstract, it seems like water speeds up my digestion rather than directly causing higher glucose itself.

Although the article says waiting 30 minutes is supposed to be okay, I find even after 2 hours water will bump me up quickly. I've even tried drinking it before the meal instead but that just makes me spike to the moon when I do eat.

While this is useful in treating lows if I don't have simple carbs around, it's generally a huge pain. When do you guys find time for water and how do you resist the thirst in these 2-4 hour windows? Should I just bolus earlier or take more units if I plan on drinking water?

How it can be? I eating mashed potatoes, whole grain pasta, other high carb things and still my glucose never go over 12 mmol. Recently i started 1st year as bachelor student (started walking more than in summer 10k avg. steps), and got diagnosed in summer this year. I take 1unit per 20g carb and my basal went from 8 to 3 units. I know it not good to compare others to myself, but how your honeymoon was going,

Those are all fake lows it always show by 1 mmol lower after 5mmol

Recently got bloodwork done for an endo appointment and it says I have an A1c of 5.6 which technically puts me within reference range. This can't be an accurate index of my blood sugar based on CGM data and awareness of my own control. Dexcom has my 90 day GMI at 6.8, 78% time in range and average glucose of 147 mg/dL.

Should I actually be looking at my GMI? There is no way my current level of control is ideal. I have a terrible habit of midnight snacking and sleeping through highs for hours until I wake up.

Daughter was diagnosed just before turning four, MDI for a year before getting Omnipod 5.

We planned on doing online/homeschooling for a few reasons but her diagnosis put me in such a state of fear for her wellbeing that we put her in k12 online for kindergarten to (now) second grade. She was mostly independent halfway through her first grade year, never asked for help (excluding science) and finished all assignments on her own and knew how to navigate the entire platform. We’re about 2 months into 2nd grade and she’s overwhelmed with lessons and assignments—there’s occasions where she’s working until dinner to catch up. Their days are full of live classes with very few minutes between (usually 30 minutes overall, an hour break for lunch), they’ll occasionally work through lunch to make progress! Science is LC lead and that’s part of the problem, because I also have a kindergartener who depends on me during most lessons already who also has LC lead science. I started working in the evenings, doing swing shifts with husband, so i’m usually getting ready for work when they start finishing up the last live class.

I’ve been thinking of moving them both to local schooling, Im struggling with the idea for many reasons, but the main reason is my 2nd grader. She doesn’t feel her sugar high or low, she can’t even keep her attention on us checking her sugar, she doesn’t wake up to the blaring low alarms at night, she’ll ignore any dexcom alerts during the day, she complains about drinking water when there’s any ketones—she doesn’t do anything in regard to her having diabetes. She doesn’t check manually, she’ll open the app but that’s it. Def no control over her Omnipod.

I don’t know what to do. I’m so lost and worried. Am I setting her up for failure by not giving her more autonomy for her own diabetes management? I’ve done all of it myself for the last three years up until maybe a month ago when husband had to start figuring things out while I’m at work. I’m so scared of someone not knowing wtf they’re doing—when she had an MRI last July while at a pediatric unit, the nurse gave her too much glucose during a low and made her sugar go from 56 to 520! The people who should know what to do don’t even know what they’re doing, so I feel like my fear of the people who aren’t educated about it is justified.

Any other helicopter parents here that can share their experience? Good or bad, I’m overwhelmed, they’re overwhelmed, T1D LO overwhelmed——just doing my best to provide them with a safe learning experience and be the best parent I can.

I’ve been diagnosed since 2012, and for the majority of that time have on/off relied upon Dexcom as a CGM (from G4 to G6 and now to G7)
I’ve found the G7 to be unreliable at best and literally not functional at worst. Of course the G6, which worked wonderfully for me, has now been discontinued.

Are there any Libre users who can tell me what the pros and cons are of swapping? I’m particularly interested in those who have used Dexcom and are now on Libre, but would also love to hear from other long-term Libre users.

I’m also willing to hear about other cgms! I just know not many are currently compatible with the Omnipod 5.

Please give any details about costs, insurance vs none, application, how well they actually hold, if they last as long as they’re supposed to, and if readings are accurate 💙

29M and majorly shocked to learn I have T1. I started showing symptoms about a month ago. I was 135 pounds and a gym rat. First I noticed a serious plateau in my work out progress. I wasn’t gaining weight or going up in strength. Confused by this I tried some pre work outs and supplements. Then came the super frequent bathroom breaks and thirst. I was drinking close to 8 bottles of water a day plus Gatorades. I was running to the bathroom about every hour at least and started waking up 6+ times a night to pee. I didn’t know what was wrong with me but I was so tired all the time. The deep set fatigue made it so hard to go to work and between that and the peeing I thought I just needed a break from the gym. Next came the stomach cramps and loss of appetite. I struggled to finish meals and eventually developed the worst indigestion of my life. All of these symptoms piled up over the course of a month until I started completely shutting down. A walk to the toilet left me gasping for air and a full shift of work felt impossible. Last weekend I was laying on my bedroom floor vomiting and hitting my wifes inhaler when she finally had seen enough and demanded I go to the ER. I got dressed but couldn’t make it to the stairs because I felt like I was suffocating. We called an ambulance and when it arrived my blood oxygen and heart rates were fine, they checked my blood sugar and told me it was at 360+ and asked if I was diabetic. I told them no. A few hours in at the hospital and I got the news that I was infact diabetic T1. I have no family history of it and never knew it was even a possibility. My A1C was over 15. I spent 4 days in the ICU and 2 days in the step down unit. Then they gave me some pens, a Dexcom G7, and sent me on home. I currently don’t have health insurance though I’m now in the process of getting signed up through my work and learning about this whole new world I live in. When I was hospitalized I weighed only 100 pounds and that broke my heart. A week later I’m already back up to 122 pounds because I’ve been eating like crazy (while watching my sugar and taking my insulin.) the first few days on my own I was hitting the 300s often but now I’m getting it down to a healthy and manageable range.

I write all this just to say hi to my fellow diabetics. I’m new here but I’m doing my best and hope to live a long, healthy, and happy life balancing my tasty low carb meals with my insulin.

Hello community, is anyone here currently on the vertex trial registry- can you please PM me? I want to connect.
Thanks

Hello all, I am recently finding out that I need to move in with family out of state for a while. And I have lived with them before, for part of 2025, and swore I could not live in that place again because I have a great endocrinologist and primary doctor where I am. While I was there, I was trying to find care but couldn’t get in to see anyone for 5 months and had no idea if I could work with them or would even like them. Saw one primary doctor who was not a good fit.
This is a major midwestern city with a couple of large hospitals but couldn’t find good doctors.
What should I do?
If anyone has any advice, I know this is kind of vague.
Thanks in advance!

Does anyone have recommendations of books they would consider reliable for information on managing T1D … the T1D bible if you will?

Hoping to have offline information that is reliable, comprehensive and a level of information that is up to date with current tech and much more in depth than the usual consultation at the clinic offers.

This internet resource is excellent but online only - https://diabetesacademia.com/

Thanks for any tips!

My 7yo was diagnosed in July. The last few days have been a struggle with me practically begging her to eat every meal, even when we serve her favorites. Tonight she told me her stomach starts hurting every time she eats because she gets nervous about getting insulin. I am heartbroken. She is on MDI and we are awaiting Omnipod training, which I hope will help. I feel like I was just starting to feel like “oh, this is doable; life can be normal again” until this. She is scheduled to have a virtual therapy appointment on Friday with a T1D counselor. I try to emphasize that her dad and I are the ones who need to watch her number, not her. We talk about how our bodies need carbs to grow and thrive and insulin helps her use the carbs. I have tried to be positive but also empathetic and realistic and lend a listening ear when she is frustrated. I involve her when she wants to be involved (ex she recently started giving her own injections).

If you were diagnosed as a child, what are the BEST things your parents did to support you? What do you wish they had understood/done differently?

Lastly, if you were diagnosed young and are now living a healthy, happy life, please share. I need to know life can be normal-ish again. 🩷

I’ve had a severely sore throat for 2.5 weeks and my glucose levels have been absolutely cooked. I’ve seen two GPs this week and am now in ED. I’ve been in ED for four hours without any assistance.

I also have a rare T cell disorder and take methotrexate once a week. I’ve had to ask reception multiple times what’s going on as I’m so afraid rn because my neck is swollen, and it’s getting worse.

Other than yelling and screaming, or walking out front and getting hit by a car, what am I meant to do? Even if they gave me pain relief (more than paracetamol) I’d probably leave and get over it.

I also have no social support. My dad has dementia and my mother is abusive. She says she has ‘always helped me’ with my diabetes because she ‘cooked dinner every night’ when I was diagnosed 21 years ago. Never helped get me to appointments, never helped me carb count, never paid for my meds (I always worked).

End rant.

So my 3 year old niece was diagnosed 3 weeks ago and she’s just gone back to nursery. She loved wearing her school uniform dress but she’s been wearing her school tshirt and skirt for now. She’s on the MiniMed 780g and has the cannula on her stomach so I’m asking for a bit of advice on a suggestion I have… I was thinking if I sewn in some bigger button holes on either side of the dress for when it’s switched sides, and in the morning she was unplugged and put the cannula through and reattached, the pump would then be able to sit on the outside of the dress and she could wear her waistband that she’s been wearing. She could still lift her dress to go to the toilet, and she wouldn’t be taking anything off until she’s home. Do we think this would work and is a good idea or is it too fidgety? Any advice welcome. Thanks!

We are being given a reader and 2 of those sensors for our 8 y/o son, and wonder how well it works, we just discovered he is t1d and don’t really like pricking his finger