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    • 1 hour, 22 minutes ago
      Donna Owens likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 12 hours, 5 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.
    • 13 hours, 32 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!
    • 13 hours, 32 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.
    • 13 hours, 32 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.
    • 15 hours, 44 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.
    • 15 hours, 45 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
    • 15 hours, 46 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!
    • 16 hours, 28 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.
    • 17 hours, 51 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.
    • 19 hours, 48 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, 11 hours 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, 11 hours 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, 11 hours 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, 11 hours 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, 11 hours 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, 13 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, 13 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, 13 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, 17 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, 19 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, 20 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, 20 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, 20 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, 20 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.
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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 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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    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.

      3 years ago Log in to Reply
    2. Jennifer Bounds

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

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

      Glucagon, CGM overpatches

      3
      3 years ago Log in to Reply
    5. Kristen Clifford

      AA batteries, which is what my pump takes

      3 years 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
      3 years 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
      3 years 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
      3 years 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
      3 years 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
        3 years ago Log in to Reply
    10. Henry Renn

      Skin prep pads.

      1
      3 years ago Log in to Reply
    11. KCR

      Glucose tabs and snacks.

      5
      3 years 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
      3 years 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
      3 years 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
      3 years 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
      3 years ago Log in to Reply
    16. Becky Hertz

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

      3
      3 years 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
      3 years 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
      3 years 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.

      3 years ago Log in to Reply
    20. Ernie Richmann

      Extra everything that I currently use.

      3 years ago Log in to Reply
    21. Randy Molen

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

      3 years 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.

      3 years ago Log in to Reply
    23. Chris Albright

      Xtra batteries for meter and pump if applicable

      3 years 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👍

      3 years ago Log in to Reply
    25. Leigh French

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

      3 years 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
      3 years 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.

      3 years 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.

      3 years 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.

      3 years ago Log in to Reply
    30. Chris Deutsch

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

      3 years 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
      3 years 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
      3 years ago Log in to Reply
    33. Dave Akers

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

      1
      3 years ago Log in to Reply
    34. Bruce Johnson

      Definitely HYPO resources of all kinds

      1
      3 years 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
      3 years 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

      3 years 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!

      3 years 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.

      3 years ago Log in to Reply
    39. Savanna Vance

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

      3 years 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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