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    • 7 hours, 55 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, 51 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, 53 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, 45 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.
    • 13 hours, 1 minute 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, 57 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, 19 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, 9 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, 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?
      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, 11 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, 11 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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    When you are in a situation where people are asked to silence their devices (e.g., in a theater, during an important meeting or ceremony, etc.), do you take any steps to ensure that your T1D devices do not alarm? Select all that apply.

    Home > LC Polls > When you are in a situation where people are asked to silence their devices (e.g., in a theater, during an important meeting or ceremony, etc.), do you take any steps to ensure that your T1D devices do not alarm? Select all that apply.
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    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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    47 Comments

    1. Ginger Vieira

      I’m still using the Libre 14-day because it CANNOT ALARM! All those alarms give me anxiety after two pregnancies. There are certainly times when I wish my CGM could alarm, but I make do. Yes, I scan my Libre a lot, but I enjoy the peace and quiet, too. No alarm fatigue for me.

      1
      4 weeks ago Log in to Reply
      1. Lori Lehnen

        Interesting. Thank you for sharing.

        4 weeks ago Log in to Reply
      2. Mitch Chernoff

        I now use the Libre 2, but with a reader rather than my phone. Unlike the phone app the Libre 2 reader has an option to turn off all alarms.

        3 weeks ago Log in to Reply
    2. Nevin Bowman

      My pump and phone are always on vibrate.

      1
      4 weeks ago Log in to Reply
    3. Kathy Hanavan

      My alarms are already on vibrate, so unless it is an urgent low (unlikely to happen), nobody else knows about my alarms.

      4 weeks ago Log in to Reply
    4. Grey Gray

      I normally keep my alarms on vibrate at all times. Should something stupid happen and my pump actually does put out an audible alarm. Answer it as fast as possible and hope it interrupts things less than the baby crying that someone else should have left at home.

      4
      4 weeks ago Log in to Reply
      1. ELYSSE HELLER

        I LOVED YOUR COMMENT!

        4 weeks ago Log in to Reply
    5. Phyllis Biederman

      All my alarms are already set to vibrate.

      1
      4 weeks ago Log in to Reply
    6. Jane Cerullo

      The only alarm I have on is high alert which never happens. Also if under 60 the alarm will sound. But I have numbers on my applewatch so I keep an eye on numbers.

      4 weeks ago Log in to Reply
    7. Sherolyn Newell

      I haven’t really felt the need to turn off or silence alarms. I keep an eye on the CGM though to try and head them off. There are a couple places I can think of that I would.

      1
      4 weeks ago Log in to Reply
    8. KCR

      I put my phone in silent mode and keep it in my purse to muffle any CGM alarms and rely on my watch (Bluejay GTS) to check BG levels.

      4 weeks ago Log in to Reply
    9. KIMBERELY SMITH

      I keep it on

      1
      4 weeks ago Log in to Reply
    10. Annie Wall

      I chose “do something else”. All my pump alarms are on vibrate except for the Dexcom’s urgent low. I never turn my phone off but always turn off my phone ringer and I put my phone on do not disturb.

      1
      4 weeks ago Log in to Reply
    11. ELYSSE HELLER

      If anybody was to moan about my alarm alerting me that I was heading into a possibly dangerous medical event I would tell them “Oh, I am SO SORRY that my disease is annoying you”.

      2
      4 weeks ago Log in to Reply
    12. mlettinga

      I always have my sounds set to vibrate. I turn my I-watch to theater mode.

      1
      4 weeks ago Log in to Reply
      1. Anneyun

        Me too.

        4 weeks ago Log in to Reply
      2. KarenM6

        There’s a “theater mode” on an I-watch?! =:0 How cool!! I don’t have an I-watch, but maybe they’ll lead the way for other devices. 🙂

        4 weeks ago Log in to Reply
    13. Scott Rudolph

      All my sounds come into my hearing aids, so no one else ever hears them.

      2
      4 weeks ago Log in to Reply
      1. Janis Senungetuk

        Wish I could do that! Do you control sound levels thru a phone app? When purchased 2 yrs ago, told phone would stream calls thru aids, not happening.

        4 weeks ago Log in to Reply
    14. Lawrence S.

      I am rarely, if ever, in situations where I need to silence my devices. I could see myself turning the volume down on my phone. However, I doubt I’d do anything with my pump. I guess it would depend upon the circumstances.

      1
      4 weeks ago Log in to Reply
    15. terrih57@msn.com

      I don’t go to many events where devices need to be silenced but I don’t normally change anything. Always thinking everything is in good control. Lol. Occasionally I have had it beep but I have it set to low volume and just a single beep so it’s never been an issue

      4 weeks ago Log in to Reply
    16. Marty

      I seriously annoyed the person sitting next to me at an opera by glancing too frequently at my lighted watch face to check my BG. When I explained to my brother why I wanted to switch seats with him at the break, he commented (loudly) that the guy might prefer having to step aside for the paramedics when they had to rescue me from passing out from a low BG. It did kind of spoil the event for me, but I’m not sure what else I could of done after a brisk walk up a hill to get to the opera house after eating an unfamiliar meal at an unusual time.

      4
      4 weeks ago Log in to Reply
    17. AnitaS

      I may change my CGM low alert. I usually have it at 85 but I will lower it to 70, or even 60 if I know I have already taken steps to avoid a low if needed

      4 weeks ago Log in to Reply
      1. AnitaS

        I very rarely feel a vibration from the vibrate mode so I don’t typically use that setting.

        1
        4 weeks ago Log in to Reply
    18. Yousif Devlin

      Alarms already reduced to the most important ones like going low. All the ones that rise or high reminders are already off on my pump. Watch and phone are already linked to cgm, so vibrate is all I need.

      0
      4 weeks ago Log in to Reply
    19. Mary Halverson

      I turned off my phone at a funeral I recently attended, and had taken steps to make sure my bg would be good for that hour. At an opera, I would turn it to vibrate.

      2
      4 weeks ago Log in to Reply
    20. Jen Farley

      Sometimes I do notify them that due to a medical condition I am unable to silence my devices. If I get a – then you must leave – I will silence what I can and excuse myself before any noise is made. I have noticed with my most recent Tandem pump replacement you can turn all alerts to vibrate. Not sure if it works like that but I do what I can to fix anything that may sound an alarm.

      2
      4 weeks ago Log in to Reply
    21. Becky Hertz

      I have an iPhone and Apple Watch. I get a vibratory alert from my watch before my Dex or pump goes off so am able to silence any alarms that might happen.

      4 weeks ago Log in to Reply
    22. Jodi Greenfield

      My cgm does not have an alarm feature. My pump has no way to silence or turn off all alarms, so I put my pump control device in my purse and be prepared to respond as fast as I can.

      1
      4 weeks ago Log in to Reply
    23. Amanda Barras

      None/Something else.
      I always have mine silenced because I don’t mind a vibrate, but I hate hearing it scream all the time. So, unless it’s a critical low alarm, I am always set to vibrate for everything.

      1
      4 weeks ago Log in to Reply
    24. cynthia jaworski

      I am glad to turn my phone completely off. However, my cgm only alerts me through its scanner (libre), and that is left on.

      4 weeks ago Log in to Reply
    25. Yaffa Steubinger

      Dexcom G7 has a silence feature that I use. It allows me not to receive any alarms but I’ve got my Apple watch to periodically check to be sure blood sugar is in range.

      1
      4 weeks ago Log in to Reply
    26. Janis Senungetuk

      I’ve only experienced one time when there was a complaint…and it was during a medical appointment. The followup appointment after cataract surgery my CGM (Dexcom) kept warning of a low trend. I ate a couple gummies to avert the low, but by the time I was in the exam room, 40 minutes later than scheduled, I started getting severe low alarms. The staff member who had just started the vision test was extremely annoyed by the sound. He told me to turn it off and take it off. I explained what the alarm was, that I wasn’t going to remove it, and that I needed to very briefly reach my purse, where I had more gummies, to treat the low. He stormed out of the exam room. I sat there for maybe 10 minutes eating my supply of fast acting carbs before another staff person popped their head in the door to ask if I needed any assistance. By then the alarms had stopped and my glucose level was quickly raising from all of the carbs. I let her know that I was OK, that the exam could continue. The guy who had been so annoyed returned, rushed through the vision test and told me to go back to the waiting room. Five minutes later I finished the appointment by speaking with the surgeon. I mentioned to her that a staff member had been very annoyed by my CGM alarm. She was aware of that, no apology. Fortunately, that was the second of my two cataract surgeries and I’ve had no reason to need her services again.

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

        That employee was WAY out of line. That is NOT patient care. He should have been fired for his extremely rude behavior. I’m glad it didn’t happen to me. I don’t think I would have been so diplomatic. I hope you find a different Ophthalmologist.

        2
        3 weeks ago Log in to Reply
    27. PatC

      I put my phone into Airplane Mode and leave my pump alone. If it sounds off, I step out and take care of myself.

      4 weeks ago Log in to Reply
    28. KarenM6

      My old system, I would do anything and everything possible to avoid a low and turned all high alarms off. The plays I go see are in a small-ish venue and it would disturb the whole theatre if anything beeped or blurped or vibrated.
      I have no idea (yet) how to turn things off on my new system… and being the complicated device that it is, there’s likely something I would miss. So, I haven’t been to a play recently.
      I did not do anything when I had jury duty. I figured that it was better that I beep aloud there so that any trials could stop for me. But, I didn’t even make it into a courtroom, let alone on a jury panel.

      In the past, I would also change my CGM (if necessary) and pump early to make sure there were no “you’re almost done with X” beeps.

      Like others, I have alarm fatigue!

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

        Yes, KarenM6, I too have alarm fatigue.
        I was deleted from being called to jury duty many years ago because I am a T1D. I have not heard from a jury duty call since the 1980’s.

        1
        3 weeks ago Log in to Reply
    29. Donna Condi

      I will eat a glucotab to avoid a low.

      4 weeks ago Log in to Reply
    30. Laura G

      I’m a professional orchestra musician, and loud alarms are absolutely not acceptable. I’ve done all of these strategies to avoid alarms, I’ve been successful so far, but it feels unnecessarily stressful and risky. I can always find a way to cope with or work around a low BG discreetly, but I could get fired from a job I really love for a single loud alarm. I keep hoping that pump manufacturers will let users sign a form to release them from liability and be given opt-in access to an “All-Silent-Mode” setting for work that would override every alarm. I understand this isn’t for everyone, but I’m probably not the only PWD with professional obligations who would be very grateful for this option.

      4
      4 weeks ago Log in to Reply
    31. PamK

      I chose “None” because I normally have my alerts/alarms set to vibrate, so no change is needed. I only set my phone to “airplane mode” when in this type of situation.

      4 weeks ago Log in to Reply
    32. Cristina Jorge Schwarz

      I notify the theatre at least a week in advance of my situation – including the pump screen occasionally being on. Under the ADA, they have to allow me some reasonable accommodation. They’ve always been understanding.

      3 weeks ago Log in to Reply
    33. Melinda Lipe

      I keep all alarms on vibrate due to my job as a nurse, so I do not have to silence anything.

      3 weeks ago Log in to Reply
    34. Jeff Balbirnie

      Summoned to local jury duty, I am literally unable to silence the CGM re lows. Called the courts ADA (American Disabilities Act) clerk what the judge required for diabetes tech? She had no idea what it was, why I could not turn off the alarm, entirely clueless. Sigh…. Contempt of Court for Severe Hypoglycemia Unawareness has a nice ring to it don’t you think???

      3 weeks ago Log in to Reply
      1. Marty

        I was once dismissed from jury duty when I explained about having jelly beans with me to treat possible lows because “No food is allowed in court”.

        3 weeks ago Log in to Reply
    35. mbulzomi@optonline.net

      As checked off, I turnoff my phone, however I always keep my “T” Slim pump alerts on. Thats tough “Do Do” if my beep bothers them!!!

      3 weeks ago Log in to Reply
    36. ChrisW

      On my phone I quit the dexcom app when I need to silence alerts.

      3 weeks ago Log in to Reply
    37. Kim Murphy

      I turn my blue tooth off because there is no way to silence some of the Dexcom and Omnipod 5 alerts. I just have to hope I don’t have any lows below 40 while my Bluetooth is off.

      3 weeks ago Log in to Reply

    When you are in a situation where people are asked to silence their devices (e.g., in a theater, during an important meeting or ceremony, etc.), do you take any steps to ensure that your T1D devices do not alarm? Select all that apply. Cancel reply

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