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    • 11 hours, 3 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 11 hours, 3 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 11 hours, 4 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 16 hours, 51 minutes ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 16 hours, 51 minutes ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 17 hours, 51 minutes ago
      Marthaeg likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 2 minutes ago
      kristina blake likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 18 hours, 10 minutes ago
      Mike S likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 30 minutes ago
      Eve Rabbiner likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 18 hours, 33 minutes ago
      Marty likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 45 minutes ago
      John Barbuto likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      not for those of moderate income.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 1 day, 15 hours ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 15 hours ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 16 hours ago
      Bruce Schnitzler likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 17 hours ago
      Steve Rumble likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 1 day, 17 hours ago
      Natalie Daley likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 17 hours ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 17 hours ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 1 day, 17 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
    • 1 day, 17 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      as long as it doesn't require immunosuppression, I'm interested
    • 1 day, 17 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      I was going to comment that there's always a trade off. Am I trading insulin replacement with some other daily treatment? If so, what's the difference? Is the new daily grind more harmful than the old?
    • 1 day, 17 hours ago
      Kathy Hanavan likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
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    Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you. Please select all that apply to you.

    Home > LC Polls > Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you. Please select all that apply to you.
    Previous

    If you have experienced severe hypoglycemia that resulted in a loss of consciousness, when was your most recent experience losing consciousness during a low?

    Next

    Recent advancements in insulin pens have led to the availability of “smart” insulin pens, pen caps, and other attachments with higher tech features compared to standard insulin pens. Do you currently use any of the following smart insulin pens/caps, or smart attachments?

    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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    30 Comments

    1. Jodi Greenfield

      I have 3 doses in my medicine cupboard, but luckily, I have not had any lows that rendered me unconscious. My hubby knows where I keep it because I keep showing him every couple of months.

      1
      3 years ago Log in to Reply
    2. Mark Schweim

      I have some of the injectible pre-mixed glucagon, but since my T1D was diagnosed in September 1991, I have never had any form of glucagon used on me.

      I’m pretty sure the glucagon I have in the fridge is probably expired by now, but since I’ve never needed any, I’m not planning on getting more of it.

      1
      3 years ago Log in to Reply
    3. Jen Farley

      Had a prescription for it, refilled it, never used it. Next prescription after it had expired my insurance no longer covered it. Always wondered why.

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

      No, never nasal glucagon. I have Gvoke Hypopens on the ready. A few months ago, my system was out-of-wack and I needed 3 Gvoke pens. Before that, I had only used 1 or 2.

      3 years ago Log in to Reply
    5. Jeff Balbirnie

      Inhaled, benign literally for anybody. Inhaled and a small child can “cure” dad, mommy, etc. Mixing substances, a needle THAT size is a recipe for failure. Cannot get insurance to cover the two-step syringe nightmare, guaranteed certain they won’t cover the inhaled…

      3 years ago Log in to Reply
    6. Steve Rumble

      For years I had injectable glucagon at my house, but used it only once when an EMT gave used it on me. More recently my insurance has covered nasal glucagon. I travel frequently, alone, and I have used the nasal glucagon a couple times when my other remedies (primarily glucose tabs) raised my BG too slowly. Very easy to use, even when quite low.

      2
      3 years ago Log in to Reply
    7. KIMBERELY SMITH

      No

      3 years ago Log in to Reply
    8. Marty

      I have it but I’ve never used it. Oddly, last week an anesthesiologist told me to use it if my BG went below target while fasting before surgery. We had just gone over my list of meds so she knew I had it. I’ve heard that it raises BG dramatically and can make people feel ill so I told her that I thought that would be overkill. Then she agreed to my suggestion that I just eat a couple of glucose tabs instead. It seemed like the first time she’d been asked that question. I admit I’m a bit worried about her experience with diabetic patients.

      1
      3 years ago Log in to Reply
      1. AnitaS

        At least she understood what Baqsimi is used for so she is not completely in the dark about blood sugars.

        1
        3 years ago Log in to Reply
    9. GLORIA MILLER

      As soon as Baqsimi became available I got some. I keep some on hand and when I travel. Decades ago I kept the injectable glucagon available. Baqsimi is much easier for anyone to use.

      3 years ago Log in to Reply
    10. Tina Roberts

      I have it, but have not used it yet.

      3 years ago Log in to Reply
    11. Julie Blehm

      It worked very well and did not make me nauseated as subq glucagon does. It is ridiculously expensive though and insurance often does not cover it

      3 years ago Log in to Reply
    12. Pauline M Reynolds

      “Other” because I have never used it, but have it onhand.

      3 years ago Log in to Reply
    13. Edward Geary

      No, however, it’s good to have just in case; and, my wife is much more comfortable with the responsibility of administering a nasal does versus mixing and injecting the powdered product. I’m interested in learning whether first responders I.e. police, fire and EMTs are equipped with the spray. Responses are appreciated and I will report in kind in the event I learn anything. This would be an excellent grant opportunity or state legislative initiative. Massachusetts had mandated all cities and towns to provide and collect sharps/needle receptacles is an example of how we can impact best practices at the local level.

      2
      3 years ago Log in to Reply
      1. AnitaS

        I think that would be a great idea for paramedics to use that or even the new injector brands that don’t have to be pre-mixed instead of using the intravenous glucagon which paramedics have used on me in the past.

        3 years ago Log in to Reply
    14. mlettinga

      I have it with me after years of having the syringe type which people have given me in the past but as I recently have it now it has not been used. I know my friends are excited about not using the syringe.

      3 years ago Log in to Reply
    15. Tom Caesar

      I have it in the fridge just in case but haven’t needed to use it, for several years now. Even with insurance it’s terribly expensive though.

      3 years ago Log in to Reply
      1. ConnieT1D62

        Baqsimi does not need to be kept in the fridge – neither does injectable glucagon.

        3 years ago Log in to Reply
    16. Amanda Barras

      No, and had no clue it existed until now. But, I haven’t used glucogon shots since switching to the pump in 2007 either.

      3 years ago Log in to Reply
    17. kim bullock

      I accidentally took 2 much insulin and used it myself. I had to use it on a dear friend who sugar went low while sleeping.

      1
      3 years ago Log in to Reply
    18. Maureen Helinski

      I have it and read the instructions. It seems easy to use. I have not needed it since I got it. Possibly expired already.

      3 years ago Log in to Reply
    19. AnitaS

      I have it but have never needed it since getting my CGM. Before that, my family could have used it on me (I have had paramedics come to my rescue about 3 times in my life before getting a CGM) before calling 911.

      3 years ago Log in to Reply
    20. john36m

      I have some, but I have nev3er used it yet.

      3 years ago Log in to Reply
    21. Jan Masty

      I have basquini ( think that’s how it’s spelled) but have not needed to use it.

      3 years ago Log in to Reply
    22. ConnieT1D62

      I have used self-administered Baqsimi on several occasions over the past three years when BGs have plummeted dangerously low. So much easier to use than an injectable and works really fast. It has a “sting” sensation to it when the plunger is pushed in the nostril, but it only lasts a second or two. It is expensive even with a pre-auth but it is worth it to save the expense of an ambulance and EMT assistance.

      1
      3 years ago Log in to Reply
      1. KarenM6

        Hi ConnieT1D62 –
        My last order of Baqsimi came in an insulated box with ice packs (like they do with insulin). Do you think this was simply because it was hot and Baqsimi has a temperature range to keep within?
        I’ve been keeping it in my fridge, but it’s constantly in the way!
        Thank you.

        3 years ago Log in to Reply
    23. KarenM6

      One colonoscopy and both hand surgeries required me to use Baqsimi on myself.
      My basal rates are getting better and I hope for the next colonoscopy (which I think is due next year), I will not require Baqsimi to stay in a good BS range!

      3 years ago Log in to Reply
    24. Bonnie Lundblom

      It was used on me once and it skyrocketed my blood sugar for many hours.
      To KarenM6 the nasal glucagon was shipped that way to you was due to incredibly hot temperatures we’ve experienced during the summer months would be my assumption. My nursing drug book states injectable glucagon “Prior to reconstitution store at controlled room temperature (69F to 77F)” so if this information also applies to the nasal version that you received that would make sense that it was sent that way to avoid the high temperatures.

      3 years ago Log in to Reply
    25. vbaum1956

      I have some on hand but have not used it so far.

      3 years ago Log in to Reply
    26. Cristina Jorge Schwarz

      I had nasal glucagon on hand for 18months, but all my glucagon expires, I’ve never needed it. It was so portable I lived the peace of mind.

      Now my insurance covers only gvoke, which isn’t as portable.

      3 years ago Log in to Reply

    Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you. Please select all that apply to you. Cancel reply

    You must be logged in to post a comment.




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