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    • 2 minutes ago
      Deborah Wright likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      N/A was the best answer I had. I have been tested for celiac disease in multiple ways all negative.
    • 1 hour, 6 minutes ago
      atr likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      Yes. I was diagnosed in 2008 or 2009. I don't know how to explain how difficult it is living with celiac disease. It affects everything I eat. Eating at restaurants or other peoples houses, pot-luck dinners are high risk. There are many foods, or food supplements that have hidden gluten ingredients, such as soy sauce, caramel, licorice, and many more. I avoid eating food that other people cook. There is no such thing as a gluten free restaurant, unless the restaurant is completely gluten free (cross contamination of foods). Any food that may contain wheat, rye and barley cannot be eaten. Also, oats are a risk because of cross contamination with wheat, rye or barley. I bake my own bread from gluten free flour. There are lots of books and articles on the subject, but it is mostly learn as you go.
    • 1 hour, 54 minutes ago
      Kristi Warmecke likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      N/A was the best answer I had. I have been tested for celiac disease in multiple ways all negative.
    • 1 hour, 54 minutes ago
      Kristi Warmecke likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      Also tested negative. That should have been an option.
    • 3 hours, 6 minutes ago
      Sarah Berry likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      Tested. No celiac
    • 3 hours, 6 minutes ago
      Sarah Berry likes your comment at
      Have you been tested for and diagnosed with celiac disease?
      N/A was the best answer I had. I have been tested for celiac disease in multiple ways all negative.
    • 4 hours, 24 minutes ago
      Derek West likes your comment at
      Have you noticed a difference in how hot versus cold caffeinated drinks affect your glucose levels?
      I do not drink cold caffeinated drinks!
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      Lawrence S. likes your comment at
      Have you noticed a difference in how hot versus cold caffeinated drinks affect your glucose levels?
      I don’t drink caffeinated drinks.
    • 1 day, 23 hours ago
      Ahh Life likes your comment at
      Have any of your T1D devices ever been recalled? Share in the comments on what steps you took after learning about the recall.
      No recalls, but there should be one right now for Tandem infusion sets. The new sets are impossible to remove when trying to separate in order to take a shower. Even my health care provider tried her luck with mine and failed. The times when I would just have to rip the whole thing off for a shower and then put a new one back on afterwards are accumulating. I have started to keep a record of how much insulin is being wasted and how many times it occurs. Called Tamden twice and so far got not much more than a "call us back if it continues".
    • 2 days, 2 hours ago
      Mike S likes your comment at
      Have any of your T1D devices ever been recalled? Share in the comments on what steps you took after learning about the recall.
      I use Omnipod 5 pods and there have been recalls of these pods, however i did not have any of therecalled batches!
    • 2 days, 21 hours ago
      Kathy Hanavan likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      Only can take Zepbound if insurance is willing to cover it because I don’t have a T2 dx required for Monujaro, etc. Zepbound is cost prohibitive and Monujaro is much more affordable, even tho they are the exact same product in different packaging. Before the Zepbound price Increase and/or insurance not covering it at all, I was very successful on it but was only able to take it for 9 months. They need to open these medications for severely insulin resistant T1s like myself.
    • 2 days, 22 hours ago
      Hadley likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      It’s extremely easy if you’re a multi-millionaire and can afford $1000+ per month. Normal people, not so much. Medicare won’t cover it. Man insurance plans have stopped covering it. Another scam by BIG pharma to get rich ( check the prices in other countries!).
    • 3 days ago
      Amanda Barras likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      It was not hard if one is paying out of pocket, but that's the rub. Medicare won't cover unless your doc goes through a lot of hoops and can document that you also have insulin resistance/Type 2 in addition to Type 1.
    • 3 days ago
      Amanda Barras likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      It’s extremely easy if you’re a multi-millionaire and can afford $1000+ per month. Normal people, not so much. Medicare won’t cover it. Man insurance plans have stopped covering it. Another scam by BIG pharma to get rich ( check the prices in other countries!).
    • 3 days, 2 hours ago
      Lawrence S. likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      It’s extremely easy if you’re a multi-millionaire and can afford $1000+ per month. Normal people, not so much. Medicare won’t cover it. Man insurance plans have stopped covering it. Another scam by BIG pharma to get rich ( check the prices in other countries!).
    • 3 days, 3 hours ago
      TEH likes your comment at
      If you’re using a GLP-1 medication, how easy was it to obtain access?
      It’s extremely easy if you’re a multi-millionaire and can afford $1000+ per month. Normal people, not so much. Medicare won’t cover it. Man insurance plans have stopped covering it. Another scam by BIG pharma to get rich ( check the prices in other countries!).
    • 4 days, 1 hour ago
      Lawrence S. likes your comment at
      Have you ever tried CBD or marijuana while living with T1D? Share more about your experience and tips.
      NEVER HAVE AND NEVER WILL. PERIOD.
    • 4 days, 1 hour ago
      Lawrence S. likes your comment at
      If you’re taking a GLP-1 medication, what side effects have you experienced? Select all that apply.
      I have been taking very low dose tirzepetide for about 6 months. Initially, I had some nausea which resolved after about a week. It is an amazing drug for us T1d's. My insulin dose is about 30% less with an increase in TIR and it is just easier to manage. I do not need to lose weight, but my doc who prescribes it a lot said I would not lose much and that is so. I lost about 7 lbs initially, but regained about 4 once the side effects wore off. Food noise is down which I didn't even realize was a particular issue. Paying out of pocket is onerous, but with low dose and a vial, it is not too bad.
    • 4 days, 20 hours ago
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      Have you ever tried CBD or marijuana while living with T1D? Share more about your experience and tips.
      I use a CBD/THC balm for joint and muscle pain.
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      Have you ever tried CBD or marijuana while living with T1D? Share more about your experience and tips.
      I use a CBD/THC balm for joint and muscle pain.
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      lis be likes your comment at
      What is the best advice you would have for someone who is newly diagnosed with type 1?
      Take a deep breath. It is a marathon not a sprint. Get a good healthcare team including an endocrinologist, diabetes care and education specialist, and mental health professionals. Do your own research but use well respected sources.
    • 4 days, 23 hours ago
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      What is the best advice you would have for someone who is newly diagnosed with type 1?
      The curve-balls that life throws at you may seem like the cosmic unfairness of a brain-cancer diagnosis. But T1D is not like that. It's a condition, not a disease so much. But as such the condition will require attention, awareness, tight-rope walking, and the help of others if you fall off the high wire. And, man oh man, is it ever an exciting high-wire act. --〜⁠(⁠꒪⁠꒳⁠꒪⁠)⁠〜--
    • 4 days, 23 hours ago
      lis be likes your comment at
      What is the best advice you would have for someone who is newly diagnosed with type 1?
      Educate yourself on this condition from many perspectives. From the professional level, the patients, and many different books of those living with it. Try and keep up to date with changing hypotheses of treatment. Get to know your body and digestion so you can choose the best insulin rates. Keep a daily diet along with activity and stresses to correlate to your blood glucose.
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      What is the best advice you would have for someone who is newly diagnosed with type 1?
      Keep glucose under control in order to avoid long-term complications. As soon as practical, obtain CGM and insulin pump.
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      What is the best advice you would have for someone who is newly diagnosed with type 1?
      Do your best to control your blood sugar but don't aim for perfection. That will never happen.
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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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