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    • 8 hours, 14 minutes ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 10 hours, 1 minute ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 10 hours, 2 minutes ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 10 hours, 2 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 11 hours ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 11 hours, 1 minute ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 11 hours, 2 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 11 hours, 5 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 11 hours, 7 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 11 hours, 21 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 13 hours, 55 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 14 hours, 27 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 14 hours, 45 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 14 hours, 46 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 14 hours, 46 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 16 hours, 13 minutes ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 23 hours, 13 minutes ago
      Sandy Norman likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 6 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 6 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 6 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 8 hours ago
      Kristi Warmecke likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 11 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 13 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 1 day, 14 hours ago
      John Barbuto likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      I have been using a insulin smart pen for the last 2 years; I find that it meets my current needs to ensure good management and results
    • 1 day, 15 hours ago
      Lawrence S. likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
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    If you had T1D while you were in school, were your blood sugars typically impacted when you had tests or exams?

    Home > LC Polls > If you had T1D while you were in school, were your blood sugars typically impacted when you had tests or exams?
    Previous

    Do you usually suggest to your doctor what T1D devices/medications you want to use, or does your doctor tend to suggest to you which T1D devices/medications you should use?

    Next

    What was your most recent A1c?

    Sarah Howard

    Sarah Howard has worked in the diabetes research field ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Marketing Manager at T1D Exchange.

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    23 Comments

    1. Larry Martin

      There were no CGMs back in the 60s so I had no clue.

      1
      5 years ago Log in to Reply
    2. Tod Herman

      Similar to Larry’s comment, when I was in highschool and college I had no way to monitor my blood sugars regularly.

      5 years ago Log in to Reply
    3. Jana Foley

      I went back to school at age 62 to get my associates degree and did not notice that tests had any affects on my blood sugar either way, high or low.

      5 years ago Log in to Reply
    4. Kristine Warmecke

      Mine would be high as I waited to take the test, but they could bottom out during test, especially finials. Wish I could have had a pump back then, instead of just my R and N regimen.

      5 years ago Log in to Reply
    5. Bill Williams

      I finished grad school in 1977. I got my first glucometer in about 1985. Any questions?

      5 years ago Log in to Reply
    6. Philip Vachon

      I did not have a glucometer in high school or college. Based on my current results, I would say most likely yes.

      5 years ago Log in to Reply
    7. Gary Taylor

      I answered “other”. Like many commenters, I was diagnosed before the availability of glucometer, much less sensors. I had no way of knowing what happened during tests.

      1
      5 years ago Log in to Reply
    8. Abigail Elias

      I’m joining the other old timers. My last exam was the bar exam in 1976 when we still were limited to urine dip strips – so could not track highs and lows very well my senior year in high school, in college or in law school. I overslept my last law school exam my first year either because I’d been studying until 2:30am or – in hindsight – because I slipped into a pre-dawn low and didn’t hear my alarm. (Jumped into my cleanest dirty jeans and ran to the exam without breakfast, insulin or a shower … )

      1
      5 years ago Log in to Reply
    9. Janice Bianchi-Lurati

      I was diagnosed in 1960 and graduated high school in 1967. I had no idea what my blood sugars were in real time, as meters did not exist until 10 plus years into the future.

      5 years ago Log in to Reply
    10. Sarah Berry

      I was diagnosed in 1972. No blood sugar testing or A1C back then.

      5 years ago Log in to Reply
    11. George Hamilton

      I had T1D when I was in school, but that was long before we had any way to check BG personally. I had to get BG tests at a lab. I never considered whether my BG might be high or low during a school exam unless it was extremely high or low (hypoglycemia etc.).

      5 years ago Log in to Reply
    12. Becky Hertz

      Old timer here too. Nuff said.

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

      I could answer both high and low from exam stress. As others have commented personal glucose meters were still a dream when I was in high school, ’60 – ’64 and undergrad studies ’65-’70. Later in graduate school, ’76-’80, still without personal meters, I had a low while taking my Masters written exam. Fortunately, I completed enough of the essay questions to pass. The oral defense of my Master of Fine Arts thesis was very stressful. I ‘m sure both my glucose and blood pressure levels were high.

      5 years ago Log in to Reply
    14. Amy Nance

      In the 80s and first few years of the 1990s, wasn’t able to test before or after an exam, so I’m sure my blood sugars were all over the place…

      5 years ago Log in to Reply
    15. Keira Thurheimer

      This tech wasn’t available when I was in school, but I rarely felt stressed in school so I doubt it would have had any effect on my blood sugars.

      5 years ago Log in to Reply
    16. Mary Ann Sayers

      When I was in school I didn’t have a glucose meter!!! It hadn’t been invented yet!!!

      2
      5 years ago Log in to Reply
    17. Ken Raiche

      Back in those days I really didn’t do much monitoring it was all done through the urine which wasn’t exactly accurate.

      5 years ago Log in to Reply
    18. ConnieT1D62

      As a child, adolescent, and in early college years – IDK. There were no meters or cgms back then – only urine tests and my pee was usually mucky olive green or mucky bright orange.
      During first phase of nursing school in the 1980s I would get stressed during exam time and BGs would run higher. Was on MDI and a BG meter in those days.
      Later on in graduate school as an older middle aged adult I did get stressed while writing term papers and researching material for Masters in Nursing Science thesis. My BGs could/would run higher but it may have also been from lack of sleep. I was working full-time AND going to school online, plus doing hands-on diabetes care and education in clinical settings with an academic advisor.

      5 years ago Log in to Reply
    19. Sally Numrich

      No blood testing when I was in school, so who knows.

      5 years ago Log in to Reply
    20. Christina Trudo

      Other: during my school and college years the only available glucose testing was for urine. It was notoriously unreliable, so i don’t know the answer to this.

      5 years ago Log in to Reply
    21. Germaine Sarda

      My answer is the same as many here, no way to check blood sugars back then. I think if I had a CGM and pump my studies would have been better. I liked school but depression became a part of my life around 10. I suspect it was from the roller coaster we were all on in those days.

      1
      5 years ago Log in to Reply
    22. Jeff Perzan

      When I was in HS, urine tests were ‘state of the art’ for T1D. No ability to know what was going on prior (or during) tests.

      2
      5 years ago Log in to Reply
    23. Robby Doyle

      My comment is very similar to many others. I was diagnosed in the early 70’s. Urine testing was the norm.

      5 years ago Log in to Reply

    If you had T1D while you were in school, were your blood sugars typically impacted when you had tests or exams? Cancel reply

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