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  • Activity
    • 10 hours, 30 minutes ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 12 hours, 26 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 12 hours, 28 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 15 hours, 20 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 15 hours, 36 minutes ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 16 hours, 33 minutes ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 16 hours, 54 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 11 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 16 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 12 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 13 hours ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 14 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 14 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 15 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 16 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 17 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 3 days, 17 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 4 days, 4 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
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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.

    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.
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    In the past 7 days, have you stayed up later than you planned to make sure your blood glucose levels were stable before going to sleep?

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    37 Comments

    1. AnitaS

      I have it for an emergency but luckily have not had to use it. I definitely could have had it used on me a few times before getting a cgm

      1 year ago Log in to Reply
    2. Steve Rumble

      I misread the question. I have used nasal glucagon on myself and have explained to others how to use it to help me, but so far others have not used it to help me.

      1 year ago Log in to Reply
    3. persevereT1D52

      I used it myself. It was a horrible experience. It worked great on my BG and raised it quickly and the prefect amount BUT IT WAS LIKE POURING ACID INTO MY NASAL PASSAGES. My eyes, face, nose, ear and to the back of my head burned for hours. I will never use it again.

      1
      1 year ago Log in to Reply
    4. ConnieT1D62

      Yes I have used Baqsimi on myself when my BG is approaching 40 and plummeting with two downward arrows. I must say that Baqsimi is a lifesaver. Once you get past the initial sting as you press the plunger to release the glucagon into the nasal passage it is not so unpleasant or uncomfortable at all.

      I value it because it brings me out of a severe low really fast and I don’t experience a rollercoaster rebound afterward. Plus I don’t get that after effect feeling of nausea like I do when I have had to swallow a packet or two of glucose gel, apple juice, or a handful of glucose gummies. It works VERY fast and is the best remedy for rapidly plummeting lows.

      2
      1 year ago Log in to Reply
    5. Carolann Hunt

      We have it, but my daughter the T1, has sinus issues so not sure I would use it. Would probably use the prefilled syringe

      1 year ago Log in to Reply
    6. Lizzi Skywalker

      It works pretty fast but it burns like the dickens.

      1
      1 year ago Log in to Reply
    7. mojoseje

      I’ve never heard of it.

      1
      1 year ago Log in to Reply
    8. GLORIA MILLER

      I keep Baqsimi at all times. I have not used it on myself but my husband has once used it on me. It burned/stung badly but I will tolerate that when it is needed. It certainly beats eating or drinking a lot of glucose that will take an hour to work for me and then the rebound effect afterwards for overtreating.

      1 year ago Log in to Reply
    9. Brent Perris

      I got the nasal glucagon very recently but thankfully havent needed to use it yet

      1 year ago Log in to Reply
    10. Sonya Onyx

      I bought it but never had to use it.

      1 year ago Log in to Reply
      1. Hark87

        Ohmygoodness- I thought I was the only one! At my last endo visit, I told her I had to use it and felt like the Baqsimi went straight to my eyeball and brain. So much coming out of my nose for hours. I was definitely not a fan of the burning in my nose. Literally nothing I could do to make the pain go away. I am thankful that it worked quickly and like others have said, zero rollercoaster effect. However, I would prefer to never have to use it again. I ended up sleeping the whole day because of how bad my head felt. Kind of like a hangover. Terrible headache along with all the other feels. I’d be first in line for a super glucose tab or inhaler.

        1 year ago Log in to Reply
    11. Lizzi Skywalker

      If anyone tells you that this stuff doesn’t burn, they’re lying. Your eye feels like it was going to explode out of my head. It works great on BG. What you would want to do is place the tip at a slant so that it’s pressing against the side of your nostril. If you put the tip straight in, the burn 🔥 will be 100x worse.

      3
      1 year ago Log in to Reply
    12. jeredb

      I recently got a couple of these to have for emergencies but haven’t had to use them yet. Since I got my CGM, I am able to get something to eat quickly enough that these haven’t been necessary. But I have them just in case! After reading these comments, I will be in no hurry to use it but still a great tool for my wife to use if necessary instead of having to give me an injection.

      1 year ago Log in to Reply
    13. Tina Roberts

      No. Not yet. It was just prescribed to me recently.

      1 year ago Log in to Reply
    14. kflying1@yahoo.com

      In my continuing education, I have never heard anything about nasal glucagon. There is so much to learn.

      1 year ago Log in to Reply
    15. Randi Niemer

      I just used it yesterday for the first time! It worked quickly and raised my blood sugar as expected. However, it gave me an awful headache that lasted for hours. I’d never needed to use the injectable glucagon before or the Basquimi prior to yesterday in my 34 years of having Type 1. I hope to never have to use it again. I never want to feel that way again.

      1
      1 year ago Log in to Reply
    16. Tom Caesar

      Yes it does irate nasal passages initially but is so much easier and simpler than old glucagon mixing and injecting, much more user friendly. And it doesn’t have the hangover effects of old. Everyone needs this just in case!

      3
      1 year ago Log in to Reply
    17. Linda Zottoli

      Since it often takes a long time to raise my bg, and my nearest and dearest have always shied away from injected glucagon, my doctor did prescribe the nasal one. But the pharmacist warned me what my copay would be, and I decided it wasn’t worth paying that for something I was really unlikely to use, since we have managed all these years without it. Since pumping, and now with CIQ in addition to cgm, it’s been at least 25 years since the issue even came up, and then my husband put gel in my cheek.

      1 year ago Log in to Reply
    18. Maureen Helinski

      I have Basquimi, which my doctor prescribed but have not needed to use it yet.

      1 year ago Log in to Reply
    19. pru barry

      Guess there’s a time and a place for everything…

      1
      1 year ago Log in to Reply
    20. Ken Raiche

      After reading the comments above I’m not going to try this product. Thank goodness they have created a means to monitor and control T1D with CGM and fairly smart pumps.

      1 year ago Log in to Reply
      1. AnitaS

        If you are unconscious, I bet you would want someone to use it on you. Thankfully I haven’t needed mine and probably never will as my cgm keeps me aware of blood sugar levels.

        1
        1 year ago Log in to Reply
    21. Jim Cobbe

      I have it on my bedside table, but I also have a Dexcom and I have never needed it — I also have a bottle of glucose tablets there and they have always been enough (and I note that oddly, 95% of the time I wake up before the Dexcom alarm sounds!)

      1
      1 year ago Log in to Reply
    22. LizB

      I have never used any kind of glucagon. I had the old school kit when I was first diagnosed and it sat in the fridge for 20 years, forgotten, until my mother moved and threw it away.

      1 year ago Log in to Reply
    23. Bob Durstenfeld

      In fact, with 65 years of T1D I have never used Glucagon.

      1
      1 year ago Log in to Reply
    24. Marcia Pulleyblank

      I actually used some expired nasal glucagon to bring my diabetic cat round.

      2
      1 year ago Log in to Reply
    25. TomH

      I have a prescription and filled it, but haven’t had to use it on myself or have others use it for me. I’ve used an expired one to show folks how it works.

      1
      1 year ago Log in to Reply
      1. AnitaS

        Good thinking about using the expired one to show others. I still wouldn’t have used it in my nose in case it was still potent and you probably didn’t either.

        1 year ago Log in to Reply
    26. Glenda Schuessler

      I have it, thankfully have not needed to use it. I also have Gvoke which has not been needed. Before that I carried Glucagon, also not used.

      1 year ago Log in to Reply
    27. KarenM6

      I used Baqsimi in the early morning hours when I was having surgery that morning (and, so, couldn’t eat or drink anything). My BS was in the 40s and I was barely conscious. I had trouble coordinating limbs and such. (I had clearly not dropped my basal enough!)
      I did get a headache and some burning, but not the day long and generally awful experiences others have had. (I am so sorry for those who experienced such side effects!!!)
      I was able to get my surgery that morning, so it worked a charm and I was super glad to have it on hand!

      1
      1 year ago Log in to Reply
    28. Kim Murphy

      I have it and I have shown the video on how to use it to my husband. He forgets I have it and calls 911.

      1 year ago Log in to Reply
    29. Hieromonk Alexis

      I don’t believe it’s covered by Medicare and Medicaid, and I rely on both.

      1 year ago Log in to Reply
    30. Joan Fray

      I have it by the kitchen phone but have never used it. For a bad low, rare with cgm, I like a slug of maple syrup straight from the bottle. Yum ! Never have pancakes, bottle is a couple of years old. In 60 years with T1d, lowest I’ve gone was 25, and I was alert enough to get to the fridge. That was years ago, way before cgm. I have never passed out, or had to have help. Lucky me. My sympathies to all who plummet. My dad was like that. He had some bad experiences—one involved fighting with the Highway Patrol and getting thrown in the drunk tank for an hour! Scary stuff!

      1 year ago Log in to Reply
    31. Sue Herflicker

      I do have it though I have never had to use it. Let’s keep it that way!!!

      1 year ago Log in to Reply
    32. mbulzomi@optonline.net

      No. I have a Gvoke HypoPen set available if needed.

      1 year ago Log in to Reply
    33. Mike Plante

      I have a nasal in case I ever require glucagon, but in 19 years of t1d I have yet to use any glucagon. I chose nasal because I felt it would be easier for my partner to administer since they have an aversion to needles.

      1
      1 year ago Log in to Reply
    34. vbaum1956

      I have some nasal glucagon but have not used it yet.

      1 year 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. Cancel reply

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