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    • 7 hours, 43 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.
    • 9 hours, 39 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.
    • 9 hours, 41 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.
    • 12 hours, 32 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.
    • 12 hours, 48 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.
    • 13 hours, 45 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.
    • 14 hours, 7 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, 8 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, 13 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, 14 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, 14 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, 10 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, 10 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, 10 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, 10 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, 14 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, 9 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, 11 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, 11 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, 12 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, 12 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, 13 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, 14 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, 14 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, 1 hour 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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    If you have experienced severe hypoglycemia that resulted in a loss of consciousness, when was your most recent experience losing consciousness during a low?

    Home > LC Polls > If you have experienced severe hypoglycemia that resulted in a loss of consciousness, when was your most recent experience losing consciousness during a low?
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    Do you have any programmed diabetes-related “reminders” on your phone or other technology? For example, a reminder to take your long-acting insulin every night at 10 p.m., or a reminder to bolus every day at 1 p.m.?

    Next

    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.

    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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    27 Comments

    1. TEH

      I woke up in the hospital 3 times the first 3 years after Dx. Split mix doses MDI flat out dangerous!
      Got better. NEVER sens being on the pump for the last 20 years

      3 weeks ago Log in to Reply
      1. William Bennett

        I used to do that back in the R/NPH days, kind of dr-recommended SOP back then. NPH was the worst bc so unpredictable when it was really going to hit, and combined with R you never really knew where the fade of one was going to cross the onset of the other. Used to call it the Eat Now or DIE regimen. Never actually passed out but came close too many times to number.

        3
        3 weeks ago Log in to Reply
    2. KIMBERELY SMITH

      Since 2012 to Now

      3 weeks ago Log in to Reply
    3. Juha Kankaanpaa

      Once, about 30 years ago, I needed help to get out of a hypo, but I didn’t lose consciousness.

      3 weeks ago Log in to Reply
    4. AimmcG

      I was asleep and couldn’t be awoken until I was given a glucagon shot, I wasn’t conscious and then unconscious exactly.

      3 weeks ago Log in to Reply
    5. Lawrence S.

      I answered, “Within the past year.” But, I don’t know how you define “loss of consciousness.” I could have also answered “never,” depending upon the definition. A few months ago, close to the time I had my first case of Covid 19 (but, may not have been associated with the Covid 19), I had 3 serious low blood glucoses where my wife needed to use the Gvoke pen on me. I was not out, unconscious on the floor. But, I had lost awareness of what I was doing, or what was going on around me. Is that unconsciousness?

      3 weeks ago Log in to Reply
    6. William Bennett

      Never totally lost consciousness but I’ve had the center of my eyesight blank out a few times. Worst was about a year ago, in a restaurant after being up most of the night playing a gig, which often screws my BG up unpredictably. We were ordering breakfast from the menu posted on the wall behind the counter and I suddenly realized I couldn’t read it–couldn’t see words. Hadn’t even felt low, but then suddenly it hit me. Had to sit, friend got me some OJ, that horrible feeling of having your plug pulled. Didn’t quite pass out but losing eyesight is close enough for me.

      3
      3 weeks ago Log in to Reply
    7. Jneticdiabetic

      I’m not sure I ever lost consciousness due to severe hypoglycemia, but many times when I went severely low overnight and couldn’t be woken until a family member gave me glucagon. Also many close calls during the day when I was conscious but not really responsive. Most occured 20+ ago while I was on R/NPH insulin injection combo. Only a couple since starting a pump in 2000 thank goodness.

      1
      3 weeks ago Log in to Reply
    8. Ahh Life

      1984. My internal temperature dropped to 93 degrees F. Felt like an Antarctica iceberg. By biological necessity, the brain gets all the glucose and heat. The rest of the body? Forget about it. Ugh!

      2
      3 weeks ago Log in to Reply
      1. LizB

        The freezing cold after a severe low was the worst. One time at work, after the lovely paramedics got my BG up, I was shivering so bad I could barely talk. One of them looked at the thermostat and said “But it’s 86 degrees in here”. To me it felt like I was outside in the snow with no coat on, soaking wet.

        3 weeks ago Log in to Reply
    9. T1diabetic

      That was when I ordered my first DexCom!

      1
      3 weeks ago Log in to Reply
    10. mlettinga

      Since I’ve been on insulin pump and sensor I haven’t had a sever low in 25 years. Previous to that it was several times a year. Been type 1 for 58 years.

      1
      3 weeks ago Log in to Reply
    11. Lynn Smith

      Only when I was pregnant about 44 years ago. EMS came to visit me twice in my first trimester. I also went through a period of time that when I was seriously low that I would have seizures. In between seizures, I would somehow make it to the kitchen to get some OJ. Usually ended up with a few bruises from falling. It was really scary because I was all alone.

      3 weeks ago Log in to Reply
    12. pru barry

      For the first 15 or so years, I don’t think control was ever good enough to lower my blood sugar enough. Being a new teenager didn’t help either. But after getting married in my late twenties, I began waking up in an emergency room, not having a clue about each of those journeys, except learning from my husband that he’d somehow managed to dress an unconscious and sometimes seizing wife and haul her into our ancient VW beetle and head to the emergency room. I think those all happened when I was pregnant, and there wasn’t all that much information and certainly no google way to find out what was going on. Scary, but I was already so intent on having a couple of successful pregnancies. I’d been convinced by my doctors that it was a pipe dream.
      Now, at age 83 with three (!) wonderful adult healthy children all in their 50’s, I can see how incredibly lucky I’ve been. Don’t know if the fetuses were trying to help us along, but my kids are absolutely amazing, even if I have to remind them occasionally that they don’t have to worry about me.
      The youngest one is now here in Maine for a short stint overseeing my recent release from the hospital after breaking a hip for the second time. I’ll use any excuse to get to see these “kids!” Sorry to be so long-winded, but I love to share that this trip isn’t all a drudge!

      3
      3 weeks ago Log in to Reply
    13. Janis Senungetuk

      As Mr. Bennett commented, back in the split R/NPH days far too many times I suddenly found myself sitting alone in the lecture hall after the class had ended and everyone else had left. Or working late in the studio and suddenly finding that I desperately needed help to get my legs to coordinate correctly to move to the hall and get a Coke from the vending machine. The last loss of consciousness was approximately 28 years ago, long before pump/CGM use, when I passed out in our apartment after shoveling my car out of a mountain of snow in the parking lot. My spouse came home from work to find me, still in my parka and boots, flat on the living room carpet with our two cats on top of me. Very fortunately, the honey she put in my mouth brought me back.

      1
      3 weeks ago Log in to Reply
    14. Becky Hertz

      Never in 49 years 3 months 6 days.

      3 weeks ago Log in to Reply
    15. Amanda Barras

      Switching to pump made my catatonic lows stop. I think my body had a major problem with long acting insulin. That was before my son was born 15+ years ago

      2
      3 weeks ago Log in to Reply
      1. Lawrence S.

        Amanda,
        I had significant lows every day for 22 years while I was using NPH.

        3 weeks ago Log in to Reply
      2. LizB

        Almost every one of my severe lows happened while I was using NPH

        1
        3 weeks ago Log in to Reply
    16. KarenM6

      I kinda had one about 3 years ago…
      I was in my prep day for a colonoscopy and not allowed to eat. Even though I had turned my basal down, it was not enough. I was barely able to get to the bathroom, struggled with the cabinet doors, got and dropped ( a few times) the Baqsimi, fell to the ground as I was no longer able to stand, then somehow managed to get some Baqsimi into me. It was a rough night.

      Back in 1996 was my last “full on unconscious” episode, where after 25 years of diabetes, I finally got connected with an endo. I was seizuring at night and my regular doctor did not know why. In 1996 (pre-pump and R/NPH days), my brand new husband could not wake me up from one of these seizures and had to call 911. The seizures were brought on by being on twice as much insulin as my body actually needed.
      There have been a few other (afterwards) very memorable incidents… including one where I started a buffet choosing food, had much trouble, then “woke up” to an empty plate), but the other two are the most recent.

      1
      3 weeks ago Log in to Reply
    17. Sandy Norman

      Twice during my teens 50+ years ago – totally unconscious almost bit my tongue off and once more in my 20’s. Never since then though. All of them were overnight after a strenuous day of activity, luckily there was another person in the bedroom, my sister and then my husband.

      3 weeks ago Log in to Reply
    18. Steven Gill

      Several times, never with a CGM. The curse of attempting tight control is just a skip into the hypo’s range.

      3
      3 weeks ago Log in to Reply
    19. Sherrie Johnson

      Back when I was 25 which was 51 years ago I was getting ready for a new roommate on NPH insulin and I did not eat. I remember falling getting up and falling again broke my foot. I don’t know how I made through that one there was no one around, that was a very scary time that NPH insulin was a killer and the fact we didn’t know what was going on

      1
      3 weeks ago Log in to Reply
      1. Lawrence S.

        Sherrie,
        I understand what you’re saying. I broke my ankle while having a low Blood glucose.

        3 weeks ago Log in to Reply
    20. LizB

      I started pumping in 2005. I have had a couple of bad lows since then and they happened when I didn’t have a CGM. One was at work in 2018 and 911 was called but I don’t think I lost consciousness, I was just not responding. The other was at home and I managed to get food/drink and treat the low.

      Prior to getting a pump I had a number of severe lows, seizures, ambulance rides to the ER. The last one was just a couple of months before getting my first pump 18 years ago.

      3 weeks ago Log in to Reply
    21. ConnieT1D62

      It’s been many moons ago … I used to have full on seizures and loss of consciousness as a kid and adolescent. Last one was over 45 to 50 years ago back in the days when I was on “killer” NPH insulin. Like others have stated, it was way too much for a beta cell deprived body to handle.

      3 weeks ago Log in to Reply
    22. Trina Blake

      ! answered 5 years or so – but I think it has been 7 years ow. I was crashing often (even after pumping with humalog and having a CGM). That was in the days of having to do an obligatory fingerstick when the CGM alerted me to trending or being low. The meter would read anything from 160 – 2550 – time for a correction bolus. Actually, it was the last thing I needed.
      It was a bonafide mircal that I got included in the guest list for ENDO CME. One of the topics was the issue of inaccuracy in home glucose monitors. There isn’t a lot of after-market re-evaluation. Turns out the monitor covered by my health plan (and I was doing 15-20 fingersticks a day) has an issue reading higher than actual for people with chronic anemia. I grabbed hard copies of all the reports (by teh Diabetes Tech SOciety, the AACE among others). Read through them and purchased (out of pocket) the highest rated for accuracy meter. I then did my own study. I purchased a month’s worth of strips and using the same blood sample checked on both the covered meter and the new one. The new meter was withing a few points of the CGM. That’s when I decided that it was safer to dose off my CGM readings than the covered meter. I couldn’t afford to pay retail for strips.
      Adding to my frustration and anger, I called the Endo practice I have to use to get an Rx for the strips to get them via GoodRx. When explaining why I needed the Rx, he remarked that he knew about the anemia issue. Why didn’t he tell me years ago?

      1
      3 weeks ago Log in to Reply

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