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    • 11 hours, 24 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.
    • 13 hours, 21 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.
    • 13 hours, 23 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.
    • 16 hours, 14 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.
    • 16 hours, 30 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.
    • 17 hours, 27 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.
    • 17 hours, 48 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, 12 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, 17 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, 17 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, 17 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, 14 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, 14 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, 14 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, 17 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, 14 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, 15 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, 15 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, 16 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, 17 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, 18 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, 5 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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    On average, how many test strips do you currently use in a day?

    Home > LC Polls > On average, how many test strips do you currently use in a day?
    Previous

    If you wear any T1D devices, how do you get rid of the adhesive residue left behind on your skin after removing your CGM or pump site? Share your tips in the comments!

    Next

    If you wear an insulin pump, how often do you carry a backup method of insulin delivery when you leave your home? (I.e. supplies for a pump site change, an insulin pen, syringes, etc.)

    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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    25 Comments

    1. Sasha Wooldridge

      3-4 with Medtronic CGM because of the stupid calibration cycle. Would use more if I could get the script for it since the CGM isn’t always all that accurate.

      1
      2 years ago Log in to Reply
    2. connie ker

      39% are saying they are wearing a CGM, and I am one of them. I only test when I think the CGM is not accurate towards the end of the 14 day cycle. Often the sensor just wears out and is inaccurate before 14 days or blood appears on the sensor and it doesn’t read properly.

      2 years ago Log in to Reply
    3. gary rind

      my Libre 14 day can be inaccurate overnight and first thing in the morning. using more strips to double check lately than I ever thought I would.

      2 years ago Log in to Reply
    4. Nevin Bowman

      Depends on the day. I wear a Dexcom but always verify morning and before bedtime. If I’m sick etc or BSs are unstable, I test more frequently.

      2 years ago Log in to Reply
    5. Jennifer H

      Use a Dexcom 6. Rarely if ever have to do a finger stick as my readings are always in line with my symptoms.

      2 years ago Log in to Reply
    6. MARIE PEELER

      Don’t use any some days, but may go through a lot with a new sensor or an 8 day + sensor.

      2 years ago Log in to Reply
    7. kristina blake

      Since the Dexcom G6 us okay for dosing, I answered 1-2. I was a 15-20x a day person prior to being able to dose from my CGM. An expensive habit indeed – can’t use the meter covered by my health plan shown to read higher than actual for people who are anemic – meaning I was correcting high bg’s I was experiencing and ignoring lows or pending lows when I was alerted). If my symptoms don’t seem to match, I will do a fingerstick with the Contour Next (paid for out of pocket – but considered the most accurate).

      2 years ago Log in to Reply
    8. Kristine Warmecke

      I use 0 to 1 a day with my G6. Love it and so do my finger tips!

      1
      2 years ago Log in to Reply
    9. George Lovelace

      Dex 6, sometimes 1 in 10 days, sometimes 0

      1
      2 years ago Log in to Reply
    10. LizB

      I chose 5. I have a Medtronic pump/CGM and I’m forced to calibrate a minimum of 2x a day for most days, more on the first. Because the timing of 2x daily might mean I’d have to wake up early one morning if I don’t want to I generally calibrate 3x daily. On the first day I can test (but not calibrate every time) up to 12 times because of how bad the sensor can be in the beginning. Then there are the random times it demands a BG/calibration for no reason. I chose 5-6 because over the course of a month that’s probably close.

      2 years ago Log in to Reply
    11. Sherolyn Newell

      Also a Dexcom G6 user, so unless I look at it and think it can’t be right, I don’t test. I will test on the first reading of a new one to make sure it’s on track sometimes. I bought a CVS meter for backup. The test strips are relatively cheap and seem to be accurate, based on the G6.

      1
      2 years ago Log in to Reply
    12. HMW

      3 to 4. One per meal plus before bed. Usually before snacks too. I have the Medtronic 670G system so I don’t have to test more than every 12 hours or so, but even if I had a Dexcom cgm I would still test before boluses/meals or if I have high or low alarms.

      1
      2 years ago Log in to Reply
    13. Janis Senungetuk

      I chose 1 to 2 as an average, but using the Dex G6 I can go many days without needing to check. If I doubt a low alarm I’ll test with my Contour One meter. Most of the time the results confirm the CGM reading and I haven’t felt any symptoms. I have found that as the CGM transmitter nears replacement the reading aren’t as accurate and will verify with a test before taking a correction bolus.

      1
      2 years ago Log in to Reply
    14. Carol Meares

      0-2 is really the answer. I only test when I think Dex 6 might be significantly off. Many/most days it is 0. Day 1 of Dex can still be difficult but not always.

      2 years ago Log in to Reply
    15. ConnieT1D62

      Hardly ever – once in awhile I use a test strip with a Contour Next meter to verify BG during Dexcom G6 warm-up.

      1
      2 years ago Log in to Reply
    16. Ken Raiche

      Only if I’m high which hardly ever happens or extremely low. My Dexcom G6 has proven to be extremely reliable for me. 👍👍

      2 years ago Log in to Reply
    17. Becky Hertz

      “other” needs to be an option. Although I’m in Dexcom, I use steroids when I feel the reading is out of range, when the sensor is wonky (one can tell), during warm-up, whenever my DAD alerts. It can be 0 and up to 8 times a day.

      2 years ago Log in to Reply
    18. Abigail Elias

      Because I use the Dexcom G6 CGM, I do not need to test daily (and Medicare will not cover ANY test strips). However, every 10 days when I change the sensor, I sometimes test 1-2 times with a strip during the sensor warm up period. And every few months I occasionally check if I think the CGM reading feels off. (I think my bg meter has been at odds with the CGM only once over all the years, though I no longer remember when or the reason, but I like the option of being able to check if I feel a check is warranted.)

      1
      2 years ago Log in to Reply
    19. Sally Numrich

      Dexcom G6, so 0. Once in awhile I might test if I want to eat during warmup session, but otherwise I just let it do its thing and it tells the pump what to do. Love it! And I don’t think about my diabetes much. Just when I’m going to eat, exercise or change a pump site. It has been very freeing!

      2 years ago Log in to Reply
    20. Thomas Cline

      I also use a G6 (I was happy with the G5 but forced to switch when they discontinued it). I have found it useful to test at least once a day, and I use at least two strips to be sure the strip reading is accurate. Although the G6 is generally within 10% or so, sometimes it is a bit more off, and sometimes spot on. The big problem is that although the new applicator (which is a HUGE waste of plastic) works nicely and so far has been painless, I’ve found that it has been much more likely to cause bleeding, and that bleeding adversely affects readings (with several drop outs). Maybe this is just a fluke, but I never had such a bleeding problem with the G5 sensor applicator — it has caused me to stop using my arms as a convenient sensor site (which the instructions do not mention — they only mention the front belly).

      2 years ago Log in to Reply
    21. KarenM6

      4 or more a day even though I am also on the G6. I don’t fully trust the G6 readings as they are frequently wildly different than my meter… and I do _everything_ that is recommended to get good readings.
      As an example, this morning, my G6 said my blood was 67. I tested with my meter and it said 214.
      I had this same sort of “bad” data at the beginning of the month.
      So, there’s no way I would trust the G6 to give me accurate data. I always test against it for meals and corrections, and lows, etc.
      These vast differences in data are also frustrating because I have hypoglycemia and hyperglycemia unawareness… so, “picking one” as accurate is basically like throwing dice to make diabetes decisions.

      2 years ago Log in to Reply
    22. Ahh Life

      Zero with G6. However . . . . . . I still buy and purchase with my own money (in spite of excellent insurance!!!) bottles of test strips for down times, equipment failure, being away from home, etc. etc. for ☂☂☂

      2 years ago Log in to Reply
    23. Sahran Holiday

      Continue to test very frequently. G6 is fairly accurate but still wrong a lot. Almost never bolus without finger stick. Omnipod meter can also be very inaccurate. When the two differ by too much I test many times until the readings start to become consistent. Sometimes I have to calibrate the Dexcom.

      1
      2 years ago Log in to Reply
    24. Cheryl Seibert

      I’m using a Tandem TSlim X2 pump and Dexcom G6 CGM. Therefore, I only test with a meter if my symptoms do not match the Sensor or if my Sensor says I’m rising/falling more rapidly than is normal. I choose 1-2 but it is really more like 3 a week if my BGs are up and down. Some weeks I don’t test at all.

      2 years ago Log in to Reply
    25. Bonatay

      Twice a week I calibrate my pump cgm. I use 8 strips a month unless something is going on and I feel the need to te st more often for pump verification.

      2 years ago Log in to Reply

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