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Regarding the experience of using the Omnipod 5 with the Dexcom G7 15day, the pods have been mostly great, with occasional bad days, while the Dexcom devices seem to fail more often. I usually try to extend the Omnipod usage to get the full 3 days plus 8 hour grace period, so I replace the pod at either 6 AM (it will have truly failed at 5 AM) or 9 PM, approximately. One minor issue I have, being concerned about timing, is placement choices. The Dexcom last 15 days, which means if I use a back of arm, all my pods need to go on that same side of the body. If I use the abdomen, I can alternate the pod to reduce skin damage. But then there is the mismatch between failure times, so choosing a sensor site becomes more important, and sometimes suboptimal.

@Karii0907 - I’m curious how your requests could be denied. Are you calling them or using the online process? Is it just a sense, or something that they told you that they would not replace the sensors? Is it something about how you are using the sensors that is not recommended? Over the past month or two I’ve had three (3) failed Dexcom sensors, reported them online, and each was automatically approved shortly after submitting, and shipped; I did not have to ship back the failed devices. If you are talking with a human, I’d wonder if it is jus ta sense of refusal, rather than an actual.

I found this video interesting. I use both an Omnipod 5 and a Dexcom G7. Although you might know most of this already, Synopsis below linkis. Making Your CGM Work For You Making Your CGM Work For You Gemini Summary This episode of the Voices of T1D podcast is titled Making Your CGM Work For You , hosted by Raquel Baron and presented by the Breakthrough T1D YouTube channel. In this discussion, host Raquel Baron sits down with her own endocrinologist, Dr. David Ahn (Chief of Diabetes Services at Hoag), to explore how continuous glucose monitors (CGMs) work, their benefits and limitations, and practical advice for navigating them without burning out. Key Discussion Points & Insights What CGMs Are and Available Options [ 01:30 ]: Dr. Ahn explains that CGMs measure glucose in interstitial fluid (the fluid between subcutaneous fat cells) rather than direct capillary blood, sampling levels every 1 to 5 minutes. Current sensor models discussed include the Dexcom G7 (10-day and 15-day versions), Abbott Freestyle Libre 3 Plus (15-day), Medtronic/MiniMed options (Simplera and Instinct), and the implantable Eversense 365 (a fully sub-dermal sensor worn with an external transmitter for up to a full year). Trend Visibility vs. Fingersticks [ 03:06 ]: While traditional fingersticks provide only a handful of static snapshots per day (typically 4–12 readings), a CGM provides 300 to 500 data points daily. Dr. Ahn compares this difference to watching a video versus looking at a few still photog

Here it is directly from Dexcom Dexcom Calibration Guidance for Dexcom CGM Systems | Dexcom Learn when and how to calibrate Dexcom ONE, ONE+, G6, and G7 sensors. Understand when calibration is optional, required, or discouraged. It’s also good instrument practice, but the main problem is a finger stick has just as much uncertainty, if not more than a CGM. I might calibrate only if I feel fine and the CGM reads below 60 or I feel low, get a confirmation by finger stick and the CGM reads high. I haven’t calibrated a g7 in a year. They work themselves out for me.

Dorie @wadawabbit , as I recall that information came from DexCpm. Both in the FAQ on DexCom web(advertising) page and in links contained in the email messages informing me that replacement sensor was being shipped.

Hi Dennis! This post is a few years old but I was wondering about your source for the info on over calibrating? I’ve done a bit of googling but have yet to stumble across anything and was just wondering for those who might be interested. Thanks and I hope all is well.

Thank you so much for providing your experience and opinion.

I was diagnosed at 17, and have had T1 for over 48 years, and I assume my suggestions wouldn’t naturally fit your needs, so I went for AI (Gemini): Next Steps After Medical Diagnosis Once the diagnosis is confirmed and immediate medical stabilization has begun, focus on establishing the daily routine: Connect with a Pediatric Diabetes Team: Work directly with a pediatric endocrinologist, a Certified Diabetes Care and Education Specialist (CDCES), and a pediatric registered dietitian. Learn the Four Daily Fundamentals: Blood glucose monitoring: Learn to use a standard glucometer and discuss getting a Continuous Glucose Monitor (CGM) like Dexcom or Freestyle Libre. Insulin administration: Master both long-acting (basal) and rapid-acting (bolus for meals/corrections) insulin delivery via pens or syringes. If they are on a pump, understand the software, bolusing strategies, and changing the pump Carbohydrate counting: Learn how to read nutrition labels and calculate insulin-to-carb ratios. Treating hypoglycemia (low blood sugar): Keep fast-acting carbohydrates (glucose tabs, juice boxes) on hand at all times and ensure a glucagon emergency kit (e.g., nasal powder or auto-injector) is prescribed and understood. Setting Up School & Support Systems Notify the school: Contact the school nurse and administration to establish a Section 504 Plan and a Diabetes Medical Management Plan (DMMP) covering blood checks, snack access, insulin administration, and gym accommodations. Establish a

@mschmidt825 Welcome Mandy, to Breakthrough T1D Community Forum! I am guessing right now that diabetes being so new to you that you don’t know where to begin, so, take your time and don’t be afraid to ask any question - nothing is too trivial when it comes to diabetes. Chris and Dorie have offered some very good and useful thoughts and links, and I’ll just add to those is a suggestion not to be afraid to click the “ Resources ” link at the top right to access a wonderful Diabetes Library - unfortunately the “ Find a Chapter ” link isn’t operating correctly today. I’ll also suggest that both you, your son, and extended family and friends try [not always easy] to maintain a positive attitude and avoid the “I / you can’t *** because of diabetes”. There isn’t anything he will not be able to accomplish just because of his diabetes; I’ve been using insulin to keep me living for 70 years and accomplished and been productive the whole time. Mandy, be his guide and don’t fear letting [within reason] him run free and enjoy life.

Hi Mandy and welcome to the Forum! I’ve been on insulin for over 60 years and am doing just fine - well, any issues I’m having at this point are due to age rather than diabetes (arthritis, blood pressure - which is under control) and the like. A few suggestions I would make: When searching for an endocrinologist be sure to specify one who knows how to handheld Type1 specifically. Many if not most work with Type2 so it’s important to make the distinction. You’ll hear a lot about pumps and they’re great but take your time to decide. I’ve been using one for about 30 years now and love it but not everybody wants one. On the other hand there are people who can’t handle lows without. It will take a little time for things to “settle” with your son but hopefully like most of us using one is an option to consider. Don’t feel pressured if a doctor starts to push one. I highly recommend you check out the book Think Like a Pancreas by Gary Scheiner. He has Type1 diabetes and works in the field so has a unique personal perspective that is particularly helpful. Sugar Surfing is another popular one. There’s a high learning curve but hopefully you will find these a good supplement to what you will be learning from your care team. There are a number of apps you can use for tracking: SugarMate, MySugr, Glooko and MyNetDiary are all freev to make just a few. Try them out to see which you like the best. Sometimes I see people post here or elsewhere online in the middle of the night with an emerg

Hi Mandy. Hugs to you and your family. So many hugs. Was the doc able to diagnose your child before an ER visit for DKA happened? Request Care Packs - Breakthrough T1D Find the local BT1D Chapter near you and check for meetups Local Type 1 Diabetes Support - Breakthrough T1D Are you within a few hours of the San Francisco bay area? This Saturday 2026 Community Summit in San Ramon | Breakthrough T1D Northern California A parent wrote the blog https://www.worstgameever.org/ comparing diabetes to a video game. The entries are super short and fun. He made a diabetes education game for kids https://www.playlevelone.com/ Diabetes is expensive. Next time health insurance open enrollment happens check for better plans. Check the next drug plan formulary every year. Feel free to make as many posts about whatever you need to talk about on the forum. The forum search is really good. If you see something from another parent you want to talk to just make a post and put an @ in front of their username, like this @mschmidt825 , and the forum will send them an email.