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    • 1 hour, 4 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.
    • 1 hour, 5 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
    • 1 hour, 6 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!
    • 1 hour, 48 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.
    • 3 hours, 11 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.
    • 5 hours, 8 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
    • 20 hours, 31 minutes 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.
    • 20 hours, 33 minutes 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.
    • 20 hours, 34 minutes 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.
    • 20 hours, 35 minutes 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
    • 20 hours, 43 minutes 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 ´ )⎠⎞
    • 22 hours, 35 minutes 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.
    • 22 hours, 36 minutes 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.
    • 22 hours, 38 minutes 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, 2 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, 4 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, 5 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, 5 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, 5 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, 5 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, 5 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.
    • 1 day, 5 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 1 day, 5 hours ago
      Lawrence S. 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
      KCR 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, 6 hours ago
      Gary R. 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 ´ )⎠⎞
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    Do you currently have an unexpired glucagon kit? If so, what kind?

    Home > LC Polls > Do you currently have an unexpired glucagon kit? If so, what kind?
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    Have you ever used inhaled insulin? Share your experience in the comments!

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    If you use a CGM, on a scale of 1-5, how satisfied are you with the accuracy of your CGM? (1 = least satisfied, 5 = most satisfied)

    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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    25 Comments

    1. Wanacure

      I’m a little confused. People use nasal glucose and nasal insulin. But my pulmonologist warned me the respiratory system was “not designed” for medical marijuana; it’s all hype. Maybe I should have asked her about cooling and filtering marijuana smoke thru a water pipe, a bong?

      For low bg, I’m trying to think like a pancreas and just use 1 or 2 sugar cubes (4-8 grams sugar) and waiting 15’ to test bg again. I try to catch rising bg with just 1 unit of injected lispro if above 130. This helps me avoid having to take an extra 2 or 3 units later.

      4 years ago Log in to Reply
    2. Lawrence S.

      I answered “no”. But, I recently threw out my old expired glucagon when I got a new prescription of Gvoke hypo-pen.

      4 years ago Log in to Reply
    3. Gary Taylor

      I answered “no” but I do have an expired (2019) glucagon kit, the powder/liquid mix kind. Would it still work if I had to use it? What is the real purpose of “expiration dates”?

      4 years ago Log in to Reply
      1. Stang777

        The only time one was used on me, it was the kind you described and had been expired for over 4 years, may have been 5 years, and it worked great.

        4 years ago Log in to Reply
    4. Kristen Clifford

      I had a glucagon kit a long time ago, which included a syringe filled with liquid and a vial of powder. You had to inject the liquid into the powder, shake it, and then draw it out again. It was given to me in 2008 when I was first diagnosed. I kept it for about three or four years, but I eventually threw it out because I was afraid it was no longer effective.

      4 years ago Log in to Reply
    5. Sherolyn Newell

      I’ve never had a glucagon kit. I’ve had two different Endo’s and neither one ever prescribed one or said I should get one. I’ve always wondered why not, but never think to ask.

      4 years ago Log in to Reply
      1. AnitaS

        If you actually want one, keep a list of concerns the next time you go see your doctor to prevent you from forgetting to ask about any medical concerns.

        4 years ago Log in to Reply
    6. Francisco Varea

      I have two that expired ages ago. I have never used one.

      1
      4 years ago Log in to Reply
    7. Anna Kiff

      I think the last time a glucagon kit was in “my” possession was in the 1970’s as a teenager. Leaving home at 16, I never thought to buy one and even now, here at least in Canada where I currently live .. I’ve so far never had such a bad low that I cannot manage it on my own. Plus you’re looking at an average cost of $150.

      1
      4 years ago Log in to Reply
    8. Ken Raiche

      I’ve had a couple of these over the years and have never used them which becomes a unnecessary expensive. Without a doubt it’s a potentially helpful preventative but with the CGM and pump situation that I’m living with I have opted out.

      1
      4 years ago Log in to Reply
    9. Joan Fray

      Yes! First time in all my years as T1d. My new endo prescribed and Kaiser paid for it. Never gone low enough not to treat it myself though .

      1
      4 years ago Log in to Reply
    10. Louise Robinson

      The Lilly Glugacon pen we have expired in Nov 2018. I haven’t needed glucagon since I began using a pump in 2011. I learned the hard way in 2010 that using an expired glucagon pen will not work as well as one that is not expired. While on vacation in Idaho (I live in Florida), my husband couldn’t wake me on our first morning in Pocatello. He injected me with glucagon (which had worked well in the past) and, although I became conscious and ambulatroy, I was confused and incoherent. He drove me to the nearby hospital. I was admitted because they feared I might have suffered a stroke. After multiple tests, I was discharged the next day after the determination that I had suffered severe hypoglycemia. Luckily, there were no long-lasting effects but we cancelled our vacation. I should toss the expired glucagon pen we have.

      1
      4 years ago Log in to Reply
    11. LizB

      No. When I was first diagnosed in 1987 we got one but never had to use it. It said in the fridge for years. When I moved out on my own I never got one because even though I had some severe lows, at those times I would not have been able to administer the glucagon to myself. Now I know they have the nasal kind that you can leave by your bed, but being on a pump & CGM has prevented those super scary lows. Also, my insurance doesn’t cover ANY of the available glucagon types.

      4 years ago Log in to Reply
    12. Bob Durstenfeld

      I have2 Glucagon dry powder kit, I never used either one. In fact, in 66 years with T1D I have never used Glucagon

      1
      4 years ago Log in to Reply
    13. Marty

      I just got a nasal glucagon kit this week. It cost me more than $500, but I decided it was a good way to spend out my deductible for the year. I haven’t kept glucagon around because I live alone and wouldn’t be able to use the mix-and-inject kind myself. I’ve only had a severe hypo once, decades ago, but I feel that the risk of a severe hypo might be greater if I ever have to use large boluses to bring down high blood sugars associated with an illness like Covid. Hope it never becomes necessary-Knock on wood!!!

      1
      4 years ago Log in to Reply
    14. Andrew Stewart

      I have several Baqsimi nasal spray glucagon kits and keep one in my car, my wife’s car, my softball gear bag and surfing gear bag. It is so easy to use and there were no bad side effects for me the one time I needed to use it. I was fasting for some lab tests and my CGM had me trending low (low 70’s mg/dl) an hour before my lab appointment draw so I used one of my Baqsimi nasal devices to bring me back up to low 100’s mg/dl and the lab was none the wiser and I didn’t violate the fasting order. https://www.baqsimi.com/

      1
      4 years ago Log in to Reply
    15. Jeannie Hickey

      I have expired powder mix, and will use it if needed!

      4 years ago Log in to Reply
    16. Anthony Harder

      I do not use glucagon. All of my contacts don’t like using it. Their choice is to feed me some type of sugar concoction.

      4 years ago Log in to Reply
      1. AnitaS

        If you are unconscious however, feeding a type of sugar isn’t recommended. You can have a different opinion, but inhaled insulin (baqsimi) is so easy to use that I would think your contacts could handle just spraying it up your nose. No need to mix any solutions or need to inject any medicines with a needle

        4 years ago Log in to Reply
    17. Teri Morris

      Price is too prohibitive for this life-saving device which is a real injustice to Type 1s everywhere.

      2
      4 years ago Log in to Reply
    18. George Lovelace

      Have never had nor used Glucagon in 57 years, EMT gave Dextrose.

      4 years ago Log in to Reply
    19. Patricia Dalrymple

      Only time I needed it was at 5:30am an hour before surgery and couldn’t eat or drink. For that reason, I’ve continued to keep an unexpired one around. My Endo asks me if I need one. The alternative was to rush to the hospital and get something intravenously. My husband came up with the idea. I was very proud of him. I needed to be at 140 BG before surgery and hit it exactly on the mark. He gave me the exact amount I needed. Amazing!

      4 years ago Log in to Reply
    20. Sherrie Johnson

      These should be free to Type 1 diabetics lor treated as DME at a reduced rate. It’s outrageous.

      1
      4 years ago Log in to Reply
    21. Cheryl Seibert

      I’ve never used glucagon. May not be the wisest decision, but I was diagnosed long before glucagon was available and I’m still here. Probably a good conversation to revisit with my endo.

      1
      4 years ago Log in to Reply
    22. Stang777

      The first few years of having type 1, I didn’t have one, my endo never mentioned it, and luckily I never needed it. When he retired I went to a new doc who asked right off if I had one and prescribed one for me. It was the Glucagon Kit that needed to be mixed and injected and it sat in the drawer, unneeded so unused for years, but one night while sleeping, I had a seizure and was unconscious so my husband used it on me. It worked great and my husband said it was no big deal to mix it up and inject it. It saved my life and saved valuable time that it would have taken for EMT’s to get here, not to mention saving me the expense of EMTS, as well as the embarrassment and hassle of coming to with EMT’s all around. We had no warning that something like that was going to happen that night, it was totally out of the blue and I am very grateful we had the Glucagon Kit, which we would not have had had I not gone to a new doc, who wasn’t even an endo. I will always be grateful for him.

      The one that was used on me had been expired for about 4 years, but it worked great. I will now keep the expired ones to be used first, but always want an unexpired one on hand just in case the expired one doesn’t work.

      I did get some of the Baqsimi when it first came out, but once I read many reviews since then where it was literally and basically described as having a lit firework shoved up the persons nose, leaving them with a massive headache and burning feeling in their nose that lasted hours, and for some, days, I have gone back to the Glucagon Kit that needs to be mixed. I had no side effects from that, it just worked as intended, and as a plus, it didn’t skyrocket my levels. Because of the experience many others have had, I don’t want Baqsimi to ever be used on me, but until I have a couple Glucagon Kits, I am keeping the ones I have of it, just in case, but once I have a couple of back up Glucagon Kits, those are going into the garbage. Even though a few people have described not having any bad effects from it, there are many more who have had horrible effects from it so I don’t want to find out which group I would be in. Once the premixed ones like Gvoke have been around long enough to have many reviews, if those reviews are good, I will switch to it, but for now, the tried and true Glucagon Kit is what I want to have.

      I hope to never have to have it used on me again, but due to the experience I had, I also hope to never be without one. It was well worth the 35 bucks it cost me, with insurance, and even if one never again gets used, I will spend that 35 bucks every year to have an unexpired one always. I feel it is something I should always have, mostly for when I am sleeping as I do think that is the only time it would ever be needed, but don’t know that, but do know that stuff happens when least expected, so it’s best to be prepared. I view it like insurance, something we hope to never use but something we should all have. It it is better than insurance though, as it is something that can actually save our lives.

      4 years ago Log in to Reply

    Do you currently have an unexpired glucagon kit? If so, what kind? Cancel reply

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