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    • 6 hours, 43 minutes ago
      ConnieT1D62 likes your comment at
      Do you currently take metformin?
      In the late 2010s, I began to become insulin resistant and started packing on a lot of weight. I believe using a pump facilitated this because of the abundance of insulin readily available. My doctor put me on metformin, then Jardiance, then Victoza. As a result, my insulin use went from 120-140 units per day to a minimum of 24, up to 40 depending on carb loads. I also lost 102 lbs. It may not be for everyone, but if you're starting to notice insulin resistance, it can be a good weapon to have.
    • 9 hours, 14 minutes ago
      Kristi Warmecke likes your comment at
      Do you currently take metformin?
      Wow!
    • 9 hours, 15 minutes ago
      Kristi Warmecke likes your comment at
      Do you currently take metformin?
      I've had T1D for 50 years. I started taking Metformin 9 months ago. I take full dose at bedtime to manage my morning glucose rise. It keeps the liver from releasing glucose. It has helped.
    • 12 hours, 16 minutes ago
      Lawrence S. likes your comment at
      Do you currently take metformin?
      In the late 2010s, I began to become insulin resistant and started packing on a lot of weight. I believe using a pump facilitated this because of the abundance of insulin readily available. My doctor put me on metformin, then Jardiance, then Victoza. As a result, my insulin use went from 120-140 units per day to a minimum of 24, up to 40 depending on carb loads. I also lost 102 lbs. It may not be for everyone, but if you're starting to notice insulin resistance, it can be a good weapon to have.
    • 12 hours, 17 minutes ago
      Lawrence S. likes your comment at
      Do you currently take metformin?
      I took it for four years when I was diagnosed with T2. After four years of not being able to control my bs I asked my endocrinologist if I could go on insulin and he said yes and the T2 drugs stopped.
    • 12 hours, 19 minutes ago
      Gerald Oefelein likes your comment at
      Do you currently take metformin?
      Other I took Metformim for 3 months when I was first incorrectly diagnosed with T2. I am very sensitive to insulin and don’t need it yet.
    • 12 hours, 19 minutes ago
      Gerald Oefelein likes your comment at
      Do you currently take metformin?
      I took it for four years when I was diagnosed with T2. After four years of not being able to control my bs I asked my endocrinologist if I could go on insulin and he said yes and the T2 drugs stopped.
    • 12 hours, 19 minutes ago
      Gerald Oefelein likes your comment at
      Do you currently take metformin?
      In the late 2010s, I began to become insulin resistant and started packing on a lot of weight. I believe using a pump facilitated this because of the abundance of insulin readily available. My doctor put me on metformin, then Jardiance, then Victoza. As a result, my insulin use went from 120-140 units per day to a minimum of 24, up to 40 depending on carb loads. I also lost 102 lbs. It may not be for everyone, but if you're starting to notice insulin resistance, it can be a good weapon to have.
    • 21 hours, 37 minutes ago
      René Wagner likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      I hate formulary changes mid year. They should not be allowed!
    • 21 hours, 38 minutes ago
      René Wagner likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      I will be possibly switching from Humalog to Novalog next year. There is NO Medicare Part D plan in my county that now covers Humalog. Complicated by the fact that I use a Humalog specific Smart Pen, it will be one more hassle in T1 world. My endo will submit a formulary exception request next year. My hoarded supply of cartridges will carry me through while waiting for the response 🤞🏻I cannot believe that this is the broken system that we have to settle for in the richest country in the world.
    • 1 day, 6 hours ago
      NANCY NECIA likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      My doctor switched me without telling me from Humalog to novolog and told me it was due to insurance. I’m on Medicare and I never saw anything that said that was necessary. They call me periodically to see how I’m doing and I told them I didn’t appreciate being switched without being told. I thought initially it was a mistake when I picked it up at the pharmacy but they said that’s what the doctor ordered. Then the next visit, he told me all my issues with insulin switching and preauthorization holdups was my fault basically because he says “I have the wrong insurance”. Like I’m going to NOT use Medicare. My opinion? I think I have the wrong doctor, but it’s a hassle to switch.
    • 1 day, 6 hours ago
      NANCY NECIA likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      Not this year, but in 2026, I need to switch from Humalog to Novolog.
    • 1 day, 9 hours ago
      mojoseje likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      NEVER accerptable or appropriate. Nobody's healthcare should ever be determined by a third party's profit margin(s) to determine what we are forced to take.
    • 1 day, 11 hours ago
      Phyllis Biederman likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      My doctor switched me without telling me from Humalog to novolog and told me it was due to insurance. I’m on Medicare and I never saw anything that said that was necessary. They call me periodically to see how I’m doing and I told them I didn’t appreciate being switched without being told. I thought initially it was a mistake when I picked it up at the pharmacy but they said that’s what the doctor ordered. Then the next visit, he told me all my issues with insulin switching and preauthorization holdups was my fault basically because he says “I have the wrong insurance”. Like I’m going to NOT use Medicare. My opinion? I think I have the wrong doctor, but it’s a hassle to switch.
    • 1 day, 11 hours ago
      Lawrence S. likes your comment at
      Do you have Glucagon on hand that is not expired? If not, please share why in the comments.
      Insurance won't cover and it was several hundred dollars.
    • 1 day, 11 hours ago
      Marty likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      Had to, no. But Medicare is adding coverage for FIASP in '26 so it will be "bye, bye, bye, bye, bye" to Lyumjev!
    • 1 day, 12 hours ago
      Gerald Oefelein likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      Had to, no. But Medicare is adding coverage for FIASP in '26 so it will be "bye, bye, bye, bye, bye" to Lyumjev!
    • 1 day, 12 hours ago
      Scott Rudolph likes your comment at
      Have you had to switch diabetes medications in the past year due to health insurance changes?
      Had to, no. But Medicare is adding coverage for FIASP in '26 so it will be "bye, bye, bye, bye, bye" to Lyumjev!
    • 2 days, 9 hours ago
      eherban1 likes your comment at
      Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below!
      I use InPen and it's great. Except they aren't keeping up with iOS so you now have to unlock your phone and open the app to check IOB instead of simply looking at the home screen. You can tell when app developers aren't users, otherwise they'd know how much of a pain this is when you check 50 times a day
    • 2 days, 10 hours ago
      Trish Bowers likes your comment at
      Do you have Glucagon on hand that is not expired? If not, please share why in the comments.
      Insurance won't cover and it was several hundred dollars.
    • 2 days, 10 hours ago
      Trish Bowers likes your comment at
      Do you have Glucagon on hand that is not expired? If not, please share why in the comments.
      Glucagon is $425 for me on Medicare. It is cheaper to get an ambulance! I have an expired one that will work if I ever need it, but I won't.
    • 2 days, 10 hours ago
      Trish Bowers likes your comment at
      Do you have Glucagon on hand that is not expired? If not, please share why in the comments.
      No. During the past century I threw out many glucagon doses about 5 years after each had expired - having never used a single glucagon dose.. This century, two dose kits were disposed of and never used. At this point, in my opinion, with modern tools for accurately monitoring one's body glucose levels, AND common awareness of how one is feeling, severe low BGL can be easily avoided thus not needing "emergency' glucagon. NOTE WELL!!! what I wrote in the last sentence, does NOT apply to the very young, and some newly diagnosed who have not yet mastered insulin dosing and who have not yet been accustomed to recognizing low or quickly dropping BGL.
    • 2 days, 10 hours ago
      Trish Bowers likes your comment at
      Do you have Glucagon on hand that is not expired? If not, please share why in the comments.
      I do because it Costc me over $300 to replace it. Too expensive.
    • 2 days, 11 hours ago
      John Barbuto likes your comment at
      Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below!
      Medicare has added FIASP for 2026! Besides the great news of being able to use this once again, it is one of the few fast acting insulins that works with the inPen. I am considering doing that in the new year
    • 2 days, 11 hours ago
      John Barbuto likes your comment at
      Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below!
      Been using fiasp for 2 years (in the UK) and it's significantly better than novorapid. Would highly recommend to everyone, especially if you find your insulin a bit slow to act.
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    For insulin pump users: If you were to spend 4 hours away from home but still in your local area (e.g., an afternoon of running errands around town, or going out for dinner and a movie), would you bring a backup insulin delivery method, such as supplies for a pump site change, an insulin pen, syringes, etc.?

    Home > LC Polls > For insulin pump users: If you were to spend 4 hours away from home but still in your local area (e.g., an afternoon of running errands around town, or going out for dinner and a movie), would you bring a backup insulin delivery method, such as supplies for a pump site change, an insulin pen, syringes, etc.?
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    Have you ever used any therapies in addition to insulin delivered under the skin? For example, inhaled insulin, type 2 diabetes drugs, etc. Tell us about your experience in the comments!

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    If you use an insulin pump or CGM, how do you get rid of the adhesive residue left behind on your skin after removing your CGM or pump site? Select all that apply, and share your tips in the comments!

    Sarah Howard

    Sarah Howard has worked in the diabetes research field ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Marketing Manager at T1D Exchange.

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    46 Comments

    1. Ernie Richmann

      I said probably not but I think a spare infusion set is a good idea. I once tore the tubing without realizing it and mg bg went over 300. My bolus for lunch never reached its destination. I was about 1 hour from home working at a camp for diabetic children. Not sure at what point I tore the line.

      1
      3 years ago Log in to Reply
      1. Patricia Dalrymple

        Yes, happened to me too.

        3 years ago Log in to Reply
      2. Lisa Coyne

        i keep one in my work desk and car.

        1
        3 years ago Log in to Reply
    2. Ahh Life

      Hard question. 4 hours, maybe maybe not, but 6 hours or more definitely. ¯\_( ͡❛ ͜ʖ ͡❛)_/¯

      1
      3 years ago Log in to Reply
    3. GLORIA MILLER

      If I stayed in my local area I never bring any backup. I have never needed a backup in all the years I have been on a pump (1990s).

      3
      3 years ago Log in to Reply
    4. Janice Bohn

      I rarely leave the house without back-up supplies. Pod, syringe, meter, test strips, glucose powder. I rarely carry extra insulin for a short trip out as I can pull the insulin out of my pump if it fails.

      2
      3 years ago Log in to Reply
    5. Francisco Varea

      Not unless I am down to my last 20 units

      3 years ago Log in to Reply
    6. Carolann Hunt

      If it’s day three if a pod or more than 30 minutes from home we bring a pod and a pen to fill it with

      3 years ago Log in to Reply
    7. Richard Vaughn

      I am retired for more than 20 years. I plan my activities so they do not interfere with my times for a set or sensor change.

      3
      3 years ago Log in to Reply
    8. mojoseje

      I only bring back up when I am leaving town overnight.

      1
      3 years ago Log in to Reply
    9. Lisa Coyne

      I keep a syringe in my purse and car for emergencies. I pull insulin out of my pump cartridge if needed!

      3
      3 years ago Log in to Reply
    10. Becky Hertz

      I said probably not, but if I know I’m going to need to change my site or if I’m low on insulin and going to eat I’d bring appropriate supplies.

      1
      3 years ago Log in to Reply
    11. Chrisanda

      I always keep an infusion set package in my purse. I never know when it may be accidently pulled out. That way I don’t need to interrupt my shopping or meal out to run home.

      1
      3 years ago Log in to Reply
    12. Mike Plante

      When I was on Medtronic, I would keep a couple infusion sites in my car. Now that I’m on Omnipod, I just keep syringes in my car, which I can use to pull insulin from a pod and inject in case the pod falls off.

      1
      3 years ago Log in to Reply
    13. KCR

      I carry 2 insulin syringes in my meter kit in my purse so if my pump failed I could use the pod reservoir togive myself an injection if needed.

      1
      3 years ago Log in to Reply
    14. karolinamalecki7@gmail.com

      I always have an extra pod with me. It’s not very big and would be so much easier to replace than having to go home during a movie or dinner with friends.

      3 years ago Log in to Reply
    15. Jneticdiabetic

      I usually bring my diabetes kit with me when I go out. It contains my BG meter, strips, lancer, a vial of almost empty Humalog insulin (last ~10-20u), syringes and alcohol swabs. This has covered me in cases of accidental infusion site or CGM tear outs.

      2
      3 years ago Log in to Reply
    16. Marty

      I carry a small pouch in my bag with finger stick testing supplies and a spare infusion set. I have occasionally needed both.

      3 years ago Log in to Reply
    17. Patricia Kilwein

      I make sure my pump has enough before leaving my house.

      3 years ago Log in to Reply
    18. RegMunro

      There’s no option for T1D insulin dependents to say they don’t have a pump
      We feel neglected!

      1
      3 years ago Log in to Reply
    19. Sasha Wooldridge

      I’d prep a new cartridge and site before leaving if I knew my current cartridge might run out while I’m away from the house. But it has to be less than 10-15 units left for me to consider this. If I’m eating a big dinner out, I might worry about it with only 20 units left, just in case. Otherwise, I leave the house for extended periods of time constantly and have never been in a situation where I had to do something about a site. Even being away from home overnight (but still local) might not matter to me if I just started a new site. To me, that would be like not sleeping just in case my house caught fire and my smoke alarms stopped working. Could it happen? Sure. Is it likely to happen? Not at all.

      3 years ago Log in to Reply
    20. AimmcG

      If I’m traveling with in 4 hours I have all of my supplies. Day trips I don’t bring a back up. I would just cut it short or run home and return

      3 years ago Log in to Reply
    21. Linda Zottoli

      I answered “probably not”, and usually don’t — unlikely to need it, and likely to be able to go home if something did happen. But can imagine reasons why I might, on occasion.

      3 years ago Log in to Reply
    22. Joan Fray

      I always carry a syringe and extra insulin bottle in a plastic bag in my purse. Never without that.

      3 years ago Log in to Reply
    23. Bob Durstenfeld

      I have only had pumps fail twice and that was decades ago. So, I do not carry backup insulin delivery. However, I do check to make sure I will have enough insulin in my pump, or I refill.

      1
      3 years ago Log in to Reply
    24. Melinda Lipe

      I answered Unsure, because I always keep a prefilled syringe with short acting insulin in my purse.

      3 years ago Log in to Reply
    25. Nicholas Argento

      A syringe is a low tech highly reliable back up to a pump short term (<12 hours). More than that, you need a basal insulin to have reasonable control.

      1
      3 years ago Log in to Reply
    26. Krystal Udey

      Typically I ado not carry extra stuff with me. If I know I need a site change, I do that before I leave. I do however pack supplies when I go boating or know it will be a long day out of the house.

      1
      3 years ago Log in to Reply
    27. dave hedeen

      only pack the insulin spares 4 overnights

      3 years ago Log in to Reply
    28. William Bennett

      Here’s a circumstance: before leaving for work I get a Low Reservoir alert, which for me means 12 hrs basal left. Plenty to get through the day basal-wise and a waste of insulin if I change right away, but not enough to let me bolus for carbs at lunch. This is why I have a script for injectors. If I want to have a sandwich, I can bring one to bolus with.

      3 years ago Log in to Reply
    29. Keira Thurheimer

      I always keep an extra infusion set in my car, just in case.

      3 years ago Log in to Reply
    30. Janis Senungetuk

      I selected “unsure” because it would depend on the circumstances. If I’m using public transportation I’d include an extra alcohol swab and infusion set in my purse. I have had a site tear out as I was getting off a bus for a medical appointment. Not something I want to repeat. If the 4 hr. local trip was our regular pharmacy, pet supply, grocery shopping run I usually don’t include anything extra because we’d just quit and drive back home.

      1
      3 years ago Log in to Reply
    31. Carol Meares

      No but I have a syringe and an extra infusion set. In an emergency I could get insulin out of the pump with a needle or install a new infusion set.

      3 years ago Log in to Reply
    32. Dave Akers

      I always carry an extra inhaler with me anywhere I go.

      3 years ago Log in to Reply
    33. Amanda Barras

      My purse always has my meter to replace my Dex and a few syringes and a vial of insulin to replace my pump.

      2
      3 years ago Log in to Reply
    34. Lawrence S.

      I said, “probably not”. Generally, I carry a bag with food and supplies, which includes tubing, a cannula and an alcohol swab. I do not carry insulin unless I am running low, or am going overnight.

      Having said that, there have been a few occasions when I wished I had insulin with me.

      3 years ago Log in to Reply
    35. mbulzomi@optonline.net

      No. Being a person with diabetes for over 56 years. No big deal running high for a short while. However, on a pump for over 39 years, never a carried a back-up when I’m local. Living in the New York metropolitan area, 4 hours from home may be only 10 miles!!!

      1
      3 years ago Log in to Reply
    36. Eve Rabbiner

      Always have test kit, battery, insulin, syringes, alcohol in my purse. Haven’t had a pump problem but I have had some bad sites that required a syringe until I could get home and change the site.

      2
      3 years ago Log in to Reply
    37. Lenora Ventura

      I always carry backup methods, ie glucose meter, lancets, strips and insulin pen/vial/syringes. This includes a prefilled cartridge & extra tubing for my pump. You never know what will happen or where u will be. An ounce of prevention is definitely worth a pound of cure

      3 years ago Log in to Reply
    38. Jim Andrews

      Never have, never will. Been pumping for 15 years, have never had an issue. If I were around town and something happened I would just go home. Diabetes does not complicate my life.

      1
      3 years ago Log in to Reply
    39. Liz Avery

      I answered probably not.
      I aLways carry glucose tabs, juice boxes etc, and usually my meter.

      3 years ago Log in to Reply
    40. Milly Bassett

      I don’t use a pump. I carry an insulin pen with me when it’s just running around town doing errands or visiting friends. If I’m traveling, I carry two full pens, extra dexcom sensors, and the extra supplies of alcohol pads, syringe tops and glucose tablets.

      3 years ago Log in to Reply
    41. Ms Cris

      Yes, because the one time I didn’t…my site got pulled off while in the restroom, in the middle of dinner. Needless to say, I ruined the night out having to get back home.

      3 years ago Log in to Reply
    42. Bea Anderson

      Yes. Always. I hate carrying everything I need, but do. I hate inconveniencing people I’m with. I hate being inconvenienced. I feel more independent being able to take care any unforeseen events. Tube kink, cannula kink, sensor failure(I would just use finger sticks). Travel delays, can’t run home, someone needs help. I don’t want to run home to fix something. If errands turn into a chance to do something else fun or needed, I’m ready without having to draw attention to my T1. I don’t want to cripple myself. Leaving my supplies home would be akin to leaving my shoes behind, knowing there might be glass in the parking lot. Overdramatic, but at my age, this regret can be avoided.

      3 years ago Log in to Reply
    43. TEH

      I always have glucose tablets and a cracker pack with me in the car. I have cut errands short when i had run into delivery problems.

      3 years ago Log in to Reply
    44. Cheryl Seibert

      yes, I always carry extra pump/CGM supplies and syringes. If I’m local to home and in a situation where I can easily go back to the house for insulin, I do not carry insulin. If I’m away for 4 hours and can’t return home, even if local, I carry a vial of rapid-acting insulin with me for site issues or highs that won’t come down.

      3 years ago Log in to Reply

    For insulin pump users: If you were to spend 4 hours away from home but still in your local area (e.g., an afternoon of running errands around town, or going out for dinner and a movie), would you bring a backup insulin delivery method, such as supplies for a pump site change, an insulin pen, syringes, etc.? Cancel reply

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