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    • 7 hours, 4 minutes ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 9 hours ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 9 hours, 2 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 11 hours, 53 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 12 hours, 9 minutes ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 13 hours, 6 minutes ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 13 hours, 27 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 8 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 2 days, 9 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 2 days, 9 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 2 days, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 2 days, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 13 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 8 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 10 hours ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 11 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 11 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 11 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 12 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 13 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 3 days, 13 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 4 days ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
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    If you were to go on a 7-day trip away from home, which of the following supplies would you bring, in addition to what you would normally use in 7 days? Select all that apply to you.

    Home > LC Polls > If you were to go on a 7-day trip away from home, which of the following supplies would you bring, in addition to what you would normally use in 7 days? Select all that apply to you.
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    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    40 Comments

    1. LizB

      I have older pumps I would use in an emergency. The hassle of getting a loaner pump and then having to return it isn’t worth it for me. Even though my old Medtronic pump uses different supplies than Tandem, I do still have a bunch of them.
      I also pack SkinTac and adhesive remover when I go away.

      4 months ago Log in to Reply
    2. Jennifer Bounds

      Over lays for both my pod and sensor. Skin Tac adhesive wipes.

      4 months ago Log in to Reply
    3. Lawrence S.

      Having been a Boy Scout when I was young taught me to be prepared for anything. I tend to over pack for everything. So, I pack just about everything listed. However, I never considered taking one of my old insulin pumps. I’ll consider it. But for a 7 day trip, I’m not sure. I guess it depend upon where I’m going.

      3
      4 months ago Log in to Reply
    4. Jewels Doskicz

      Glucagon, CGM overpatches

      3
      4 months ago Log in to Reply
    5. Kristen Clifford

      AA batteries, which is what my pump takes

      4 months ago Log in to Reply
    6. Janice Bohn

      I bring backups of my supplies then xtra basal and bolus insulin, meter and test strips Incase I need to go old school.

      2
      4 months ago Log in to Reply
    7. Marty

      I was in Boston in 2013 when we were all confined to our hotels while they searched for the marathon bomber. I also remember 9/11 when planes were grounded. I never assume I can easily restock supplies and always take at least double the amount I’ll need of everything including my backup pump. Fingers crossed that I never need it. I hope I could be one of the ones who share live saving stuff with anyone who gets caught without it.

      9
      4 months ago Log in to Reply
    8. Jeremy Hanson

      Ughhh the extra CGM sensor is the worst. It takes up an unnecessarily large amount of space.

      4
      4 months ago Log in to Reply
    9. MARIE

      I’m really surprised at the low percentages of people that take extra supplies. We don’t carry an extra pump and haven’t used one long enough to have old extras. But even though we are, in general, very light packers, we always make sure we have extra D-supplies, in case a sensor fails or is ripped off, a bottle of insulin gets damaged, etc.

      But it also depends on WHERE we are going. On an overseas trip of any length we’d always take an extra transmitter. But we’d be unlikely to take one on a domestic trip unless we were going for several weeks. We always take pens even on an overnight trip ever since my husband flew to NYC on a day trip with some buddies, his pump failed, he had not brought pens for back-up and his BG soared!

      I see the burden of carrying extra supplies as the price to pay for insurance that nothing will actually fail.

      4
      4 months ago Log in to Reply
      1. Lori Lehnen

        I agree that it depends on where the trip is. My decision point is how long would it take to get replacement supplies and what are the effects of a delay. I’m MDI Tresiba which lasts >24 hours, which significantly reduces the urgency to replace background insulin.

        For NYC, I brought nothing extra.

        For my trip to a third world country- I brought one, and only one, extra of each supply including a CGM receiver. Dexcom wasn’t available where I went and I worried if something happened to my phone, I wouldn’t be able to download the software if I bought a replacement phone.

        1
        4 months ago Log in to Reply
    10. Henry Renn

      Skin prep pads.

      1
      4 months ago Log in to Reply
    11. KCR

      Glucose tabs and snacks.

      5
      4 months ago Log in to Reply
    12. GLORIA MILLER

      I take twice as much pods, CGM supplies as I know I will need. It is a pain to carry all that junk but necessary. We never know when a pod or sensor will fail. I also take syringes just in case my pump fails which it never has in the almost three decades I have used one. I also carry a few Baqsimi just in case I have a severe low. I carry more insulin than I know I will need since I broke a bottle once when overseas and almost ran out on another foreign trip.

      5
      4 months ago Log in to Reply
    13. William Bennett

      A while back I went to the UK for a choir tour. I had just acquired a CGM, a G4 Platinum, specifically as a safety measure for the trip. I don’t bring second meter any more, but this was before the Dexcom was trusted for bolusing, so I was still meter-dependent and felt I needed an extra just in case. As it turned out I DID need it, but not for myself. There was another, newly dx’d, T1 on the trip and she lost her meter when she left her bag on the bus or some such. So I was able to come to the rescue. It was possible to buy a replacement of course but European/Brit ones are calibrated in moles rather than mL so that was still a glitch–she used mine for the remainder of the trip.

      4
      4 months ago Log in to Reply
    14. Amanda Barras

      Just did this and brought almost all of these things. Didn’t think to pack an extra transmitter tho. But, did have 3 ways of administering insulin, plus CGM and regular meter. So, I knew I was good. I choose “loaner pump” too but really it’s an old pump that still works. I actually had to use it the week before my trip for a pump failure emergency, so glad I have it.

      3
      4 months ago Log in to Reply
    15. Jim Cobbe

      Additional (i.e. beyond what I usually carry with me) glucose tablets and a dose of Baqsimi.

      1
      4 months ago Log in to Reply
    16. Becky Hertz

      I usually take 2-3 times what I think I’ll need.

      3
      4 months ago Log in to Reply
    17. Kelly Wilhelm

      Depends where I’m going. If it is a populated area with easy access to pharmacies then I don’t usually bring extra insulin. The more rural the area, the more I carry.

      1
      4 months ago Log in to Reply
    18. Bob Durstenfeld

      It is WAY TOO MUCH stuff to be prepared away from home. Generally, half my suitcase. And even more stuff if it is a two-week trip. You missed snacks and glucose tabs.

      2
      4 months ago Log in to Reply
    19. Jane Cerullo

      On MDI so have an InPen and bring back up cartridges and an extra pen. Alway bring another G7 sensor so don’t need transmitter. Bring back up glucose meter and strips. Also bring syringes in case pens malfunction I can extract insulin to use. Never use it all but I like to feel prepared. Especially if going out of the country.

      4 months ago Log in to Reply
    20. Ernie Richmann

      Extra everything that I currently use.

      4 months ago Log in to Reply
    21. Randy Molen

      I also bring my backup plan supplies, pens of lantus and syringes.

      4 months ago Log in to Reply
    22. Jeff Balbirnie

      International I would take 2x the mandatory supplies. National I would take far less, assuming the location was not wilderness. Wilderness a different creature entirely, and would require vast amounts of food stuff not medication per se.

      4 months ago Log in to Reply
    23. Chris Albright

      Xtra batteries for meter and pump if applicable

      4 months ago Log in to Reply
    24. Annie Simon

      From experience travelling for a week or more I also make sure I have Dex4 tabs and various packaged snacks and bars if needed for any lows. My favourite are Pure Protein bars, Welch’s Fruit Snacks and Sunkist Fruit Snacks👍

      4 months ago Log in to Reply
    25. Leigh French

      recharger for my Tandemx2IQ pump and all the other stuff people have mentioned

      4 months ago Log in to Reply
    26. Jneticdiabetic

      I always bring extra infusion sets and CGM sensors in case of accidental tear out.
      With Tandem pump, a charger is also essential. I forgot mine in my last weekend away.
      I use a Dexcom G6, so don’t need to finger stick, but always bring my meter & strips just in case, and extra lancets as sometimes my non-diabetic family members like me to check their BG.
      I always take a vial and syringes in case of pump failure.
      For overnight trips also bring juice boxes/ glucose tabs and glucagon in case for lows.
      Hard to travel light as a T1D, especially with those GIANT Dexcom sensor inserters! 🧳🧳🧳

      1
      4 months ago Log in to Reply
    27. KarenM6

      I didn’t choose extra meter, but I should have.
      I also take tons of glucose tabs _and_ glucagon/Baqsimi, alcohol wipes, overtapes, batteries and chargers, syringes (one or two filled and then a bunch of empty ones – I don’t have any pens), plus there’s probably one or two things I’m forgetting.

      I have had so many problems while traveling.
      As one “for instance”, I went to the UK and took 3 large bottles of glucose tabs thinking I might only need one. I used all 3 bottles and still had about a week of trip to go. I had turned down my basal, but mid-third bottle, got super serious and turned it down by maybe 70%… sometimes off all the way for an hour or two.
      Then there was the time I went through 3 defective sensors (mechanically, they wouldn’t release the needle), but that incident was while I was at home. However, I always _think_ of it when traveling… “what if 3 of these sensors are defective?… better take more.”… and the time my transmitter failed… and twice having all of my insulin get frozen in defective hotel refrigerators… dead batteries, dead meters… I’ve experienced nearly all of the inconvenient problems with DStuff.

      4 months ago Log in to Reply
    28. ConnieT1D62

      In addition to extra insulin, pump supplies, an extra CGM, a BG meter and testing supplies, insulin pens and needle tips, alcohol wipes, I would bring charger cords and batteries for pump and other gear that needs a cord or batteries, Baqsimi, and plenty of glucose gel, gummies, juice packs, and peanut butter cracker snacks. I keep extra insulin and backup pens in a Frio pack. and I carry all the extra diabetes self-care equipment and supplies in a carry-all bag organized into in zip lock bags and clear plastic zippered cases. Also bring a travel size hard plastic container for sharps disposal.

      4 months ago Log in to Reply
    29. jamesmpii

      I take glucagon along with the other things listed for an MDI pen user. I also take Smarties.

      4 months ago Log in to Reply
    30. Chris Deutsch

      I bring along a copy of my pump settings, & Baqsimi.

      4 months ago Log in to Reply
    31. Sasha Wooldridge

      Extra of anything I might need, plus all the implements for any pieces of equipment like chargers. I recently stopped taking a whole vial of insulin and started prefilling cartridges instead, but I still take twice as many as I think I’ll need and calculate based on the minimum number of days it could last. I don’t like surprises in day-to-day life, I definitely wouldn’t like any surprises while traveling.

      1
      4 months ago Log in to Reply
    32. Kim Davis

      Safe disposal box for infusion set & needle, strips, CGM old sensors. Also backup to keep my vials of insulin @ proper temperature. I wish they adapted device for vials like Tempra-Med( it is only for insulin pens). A letter from MD if flying for TSA

      1
      4 months ago Log in to Reply
    33. Dave Akers

      Extra sealed foil pack of 8u and 4u inhaled insulin. Cartridges.
      Extra inhalers

      1
      4 months ago Log in to Reply
    34. Bruce Johnson

      Definitely HYPO resources of all kinds

      1
      4 months ago Log in to Reply
    35. JuJuB

      I request a backup insulin pump when I travel internationally. I have had so few issues with my Tandem pump, I rarely give it a second thought. But I do pack extra pump supplies, CGM supplies, insulin, and a syringe or two.

      1
      4 months ago Log in to Reply
    36. T1D4LongTime

      Extra everything (supplies and insulin for 14 days). I always double it. I used just take extra BG strips but now I pack an extra meter. If my transmitter has several weeks, I do not take an extra. But if it is on its last 30 days, then I take an extra. The “Something Else” is roll of medical tape to hold the infusion set tubing at 90 degrees, extra overtapes. LOTS of quick snacks for lows, band-aids for bleeders, and a very fast acting insulin like Lyumjev for highs that don’t respond to pump bolusing. In addition, to an extra vial of pump insulin

      4 months ago Log in to Reply
    37. PamK

      I would also bring extra glucose tabs/hypo treatments! I don’t normally carry extra insulin, because one vial lasts me an entire month. If my vial was getting low, I would either bring a second vial or would just open a new one to bring and leave the old one at home. It’s only a week!

      4 months ago Log in to Reply
    38. Wanacure

      I’d always carry extra food that doesn’t require refrigeration, like Luna bars. And if I were going camping or hiking I might carry extra insulin vials well-insulated.

      4 months ago Log in to Reply
    39. Savanna Vance

      In addition to the marked items, I also bring a glucagon and extra low snacks.

      4 months ago Log in to Reply

    If you were to go on a 7-day trip away from home, which of the following supplies would you bring, in addition to what you would normally use in 7 days? Select all that apply to you. Cancel reply

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