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    • 1 hour, 13 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.
    • 11 hours, 56 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, 22 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, 23 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, 23 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, 35 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, 36 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, 37 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, 19 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, 42 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, 39 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, 19 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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    When you are traveling away from home for a few days, do you typically take glucagon with you?

    Home > LC Polls > When you are traveling away from home for a few days, do you typically take glucagon with you?
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    When purchasing condiments or dressings (i.e. ketchup, BBQ Sauce, Mustard, etc.) do you ever buy the products labeled “sugar-free”?

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    How much do you currently pay out-of-pocket for one month’s supply of insulin?

    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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    29 Comments

    1. Stephen Woodward

      In 51 yrs I’ve never used it. However, with the gvoke auto injector I will be taking that with me on long trips.

      1
      4 years ago Log in to Reply
      1. Kristine Warmecke

        Yes, I agree. Gvoke is a game changer, for me. It’s so easy to use.

        1
        4 years ago Log in to Reply
    2. Beckett Nelson

      It all depends. If I’m going backcountry canoeing, then yes (which I answered). If I’m going to my folks for the weekend, then no.

      1
      4 years ago Log in to Reply
    3. james murphy

      With the dex measuring me and always have some quick sugar, that glucagon is sort of useless. Have never got one in my 35 years

      4 years ago Log in to Reply
    4. Franklin Rios

      I don’t use it.

      4 years ago Log in to Reply
      1. Franklin Rios

        I use another carb.

        4 years ago Log in to Reply
    5. GLORIA MILLER

      I carry Baqsimi instead. I have had T1 for 64 years and I have used glucagon many decades ago.

      4 years ago Log in to Reply
      1. Rose Lentzke

        Congratulations! I only take it along on cycling trips. My CGM helps me stay aware of my carb intake needs while biking. T1D for 65 years.

        4 years ago Log in to Reply
    6. connie ker

      I answered NO because I cannot give it to myself. So with the CGM and candy beside my bed and on my person; this works OK for me.

      1
      4 years ago Log in to Reply
    7. Janice Bianchi-Lurati

      No I have the glucose gel packs or 8 oz bottles of apple juice. I’ve had T1 for 61+ years and this works well for me.

      1
      4 years ago Log in to Reply
    8. Robert Brooks

      I’ve had a glucagon kit, but I have never used it. In 64 years of TM1, I have managed well with oral glucose sources. Since I do not wander far from civilization, I do not carry glucagon with me. Good control and CGM seem to work to keep me from needing intervention for severe hypoglycemia.

      4 years ago Log in to Reply
    9. Annie Wall

      I used to buy glucagon so my husband could inject if I was too far gone to eat or swallow anything but he could never figure it out mainly because the instructions were so tiny! Now that I have Dexcom and Tandem Control IQ, I always manage to keep on top of things, waking or sleeping, so I don’t see that I would never need to have glucagon administered (even if the print instructions were LARGE!)

      1
      4 years ago Log in to Reply
      1. Annie Wall

        I don’t see that I would ‘ever’ need glucagon.

        4 years ago Log in to Reply
    10. Kristine Warmecke

      It depends on where and what I will be doing.

      1
      4 years ago Log in to Reply
    11. Jneticdiabetic

      I haven’t needed a good glucagon injection for about 10 years, but my history with severe hypoglycemia makes me continue to throw it in my overnight bag just in case.

      1
      4 years ago Log in to Reply
    12. Sondra Mangan

      Now that I have Gvoke, it’s easy to have with me.

      1
      4 years ago Log in to Reply
    13. Mark Schweim

      Not only do I not typically take glucagon with me, but my Type 1 diabetes was diagnosed in September 1991, and I have NEVER had any Glucagon either used on me or prescribed for me. When diagnosed, it was left up to me, then when I moved to Alabama, my Doctors said that the only times I’d maybe need glucagon, I wouldn’t be able to give it to myself so since I lived alone there was no sense in me bothering to get any glucagon.

      4 years ago Log in to Reply
    14. Lucia Maya

      I have always kept glucagon in my diabetes travel bag, but not ever needed it. I’m getting Baqsimi to have on hand, but with dexcom and tandem pump CIQ, I rarely get very low anyway.

      4 years ago Log in to Reply
    15. Amanda Barras

      I haven’t used glucagon since 2007. After switching to a insulin pump I no longer have horrible lows from long acting insulin that require an emergency glucagon injection.

      4 years ago Log in to Reply
    16. ConnieT1D62

      Yes. Always. I was at a meditation in nature retreat this past weekend and low and behold, my BG unexpectedly tanked into the nether region of <50 and was sinking rapidly several hours after a long walk in the woods. I used the "emergency" Gvoke I had in my diabetes self-care stuff to quickly recover. And I administered it to myself.

      4 years ago Log in to Reply
    17. Janis Senungetuk

      No, in 66+ years living with T1 I’ve never needed to use glucagon. Buying the kits and then throwing them away after they expired was senseless.

      2
      4 years ago Log in to Reply
    18. Molly Jones

      Even though I refill it yearly as I was told to have it on hand about ten years after diagnosis, but my BG has only ever been as low as 28 (1.6) and I am still capable of eating or drinking. Hopefully I never need it. My husband keeps it in the cabinet in the front room.

      4 years ago Log in to Reply
    19. Hilary Welter

      Answer: Sometimes! When I go on vacation, I throw it in my bag. But if it’s a weekend trip or day trip, I don’t bring it with me. It’s usually at home in the closet… That said, I always keep more than enough glucose tabs, glucose gel, and other snacks on me no matter where I am.

      4 years ago Log in to Reply
    20. Patricia Dalrymple

      Only used it once when I had to have surgery and I went low the morning of and I couldn’t eat or drink anything. I’ve been as low as 19 (only once – learned my lesson after the experience) and stayed on my feet and able to feed myself.

      4 years ago Log in to Reply
    21. LizB

      I live alone and have never had glucagon on hand. When I lived at home we had it and never used it. Prior to being on a pump I had a number of overnight lows where I had seizures, fell out of bed etc. Even if I had glucagon there is no way I would have been able to use it on myself. Even the new nasal stuff would have been useless as I had no control over my limbs during those seizures.

      4 years ago Log in to Reply
    22. KarenM6

      Until recently, the answer would have been no. And, since I’ve had a nasal glucagon, I haven’t travelled.
      But, I will be traveling soon and I will be taking the nasal glucagon. I had a very bad low recently where it really came in handy. Glucose tablets wouldn’t have been enough or usable with my recent situation. So, my answer is, I will do… but I haven’t yet technically done so.

      4 years ago Log in to Reply
    23. Sahran Holiday

      Candy always with me including bedside and reduced fat potato chips. At work and at the dance studio, enough for everyone, big jars of individually wrapped chocolate in my work station, people stop by to get one and know if my CGM starts beeping to see if I’m OK.

      4 years ago Log in to Reply
    24. Janice B

      I always have baqsimi nasal spray glucagon in my purse.

      4 years ago Log in to Reply
    25. Cheryl Seibert

      I’ve never had glucagon, but I do take fast-acting carbs that can be laid in my mouth and dissolve (Welch’s fruit gummies).

      4 years ago Log in to Reply

    When you are traveling away from home for a few days, do you typically take glucagon with you? Cancel reply

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