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    • 1 hour, 30 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 5 hours, 10 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 5 hours, 11 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 5 hours, 11 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 5 hours, 54 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 17 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 9 hours, 14 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 1 day ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 1 day ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 6 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 8 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 9 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 9 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 9 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 9 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 9 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
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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.?
    Previous

    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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