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    • 11 hours, 28 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. 😬
    • 13 hours, 15 minutes 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.
    • 13 hours, 16 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.
    • 13 hours, 17 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.
    • 14 hours, 15 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 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.
    • 14 hours, 15 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'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.
    • 14 hours, 16 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.
    • 14 hours, 19 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.
    • 14 hours, 22 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.
    • 14 hours, 35 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.
    • 17 hours, 10 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.
    • 17 hours, 42 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?
    • 17 hours, 59 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.
    • 18 hours 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. 😬
    • 18 hours, 1 minute 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.
    • 19 hours, 28 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
    • 1 day, 2 hours 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, 9 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, 9 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, 9 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, 12 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, 14 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, 16 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, 17 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, 18 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 in school (excluding college), were you ever picked on or bullied because of having T1D? If so, did it bother you?

    Home > LC Polls > If you had T1D while in school (excluding college), were you ever picked on or bullied because of having T1D? If so, did it bother you?
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    Have you ever used expired insulin? If so, tell us in the comments about your experience.

    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. Janis Senungetuk

      I was dx. at the age of 8 in the 3rd grade. This was 1955, time of strict adherence to the Exchange Diet and very little general knowledge about diabetes. From the 3rd grade thru 6th grade I was’t allowed to sit with my classmates when they celebrated their birthdays with special treats. In 3rd grade I had to stay at my desk and was given a single graham cracker segment in place of the cake and ice cream. The lack of trust in my behavior along with comments on my “special” treat was very humiliating. In 5th and 6th grades I was sent to the library when there were treats. Some kids made fun of me, others saying they didn’t want to be around me because they didn’t want to “catch my sickness”. As much as I tried to ignore it, it did hurt.

      5 years ago Log in to Reply
    2. Britni Steingard

      I was 6 years old and terrified of needles when I was diagnosed. I used to insist on have a bandaid for every injection _and_ finger stick. So I got made fun of for coming to school with a bandaid on every finger.

      5 years ago Log in to Reply
    3. Ahh Life

      ≧◠‿●‿◠≦ I was 4. No, but I did have one cousin in my class that was somewhat jealous of me seemingly getting special favors. (ㆆ_ㆆ)

      5 years ago Log in to Reply
    4. Claire Schneider

      Wasn’t really teased for being diabetic, but I reckon that’s because no one knew I had it.

      5 years ago Log in to Reply
    5. Becky Buchanan

      I was diagnosed in 1970. I really didn’t tell other kids about it. By high school my close friends knew. I just took my 1 shot a day back then and there was no BG monitoring. It was an easily hidden and ignored disease sadly.

      5 years ago Log in to Reply
    6. connie ker

      I was diagnosed with LADA at the age of 49, so luckily I was out of school. But 4 years later, our 13 year old son was diagnosed with juvenile T1D. One of the scariest moments was when he took his pump off for gym class and left it on the back of a toliet in the restroom. He didn’t miss it until he went to the nurses station before lunch, ran back to the gym restroom, and by the Grace of God it was still on the back of the toliet. I think this diagnosis bothered him more than his classmates, his security and normalcy was threatened. Plus he felt doomed since both of his parents were T1Ds and gave this gene to him. I felt sadness and the 911 incident had just happened at the same time; 20 years ago.

      5 years ago Log in to Reply
    7. Paul GILLINGHAM

      I was 9 when diagnosed. I was immediately treated as different by the other kids. Nickname was sugarlump. Constant teasing and mickey taking. Not a great time but I got through.

      5 years ago Log in to Reply
    8. Ken Raiche

      I was never ever teased or bullied for being a diabetic. All of my friends knew I had it and fortunately it really didn’t make it’s presents known back in those days. I would take my usual one needle per day in the morning a mixture of NPH and Toronto insulin and go on my way. For some reason it seemed much easier back then I relied on how I was feeling no testing well the odd urine test which was never performed while in school. I found that my life back then with T1D was much simpler and less complicated then today and as mentioned no bullying well maybe from my doctor😉😠

      5 years ago Log in to Reply
    9. George Lovelace

      I was 15 at Dx and teasing was minor and mostly ended when my close friends saw me going through a severe hypo,

      5 years ago Log in to Reply
    10. Kristine Warmecke

      My brother, who was diagnosed at 7 months old in 1972, had more than I did. I wasn’t diagnosed until January 1982 at age 11. It wasn’t until I was in high school that some people in my group of people tried to pick on me. Looking back on this, those people haven’t changed.

      5 years ago Log in to Reply
    11. Elif DeSimone

      I was bullied for other things, but never for my Diabetes

      5 years ago Log in to Reply
    12. Nevin Bowman

      If I anything, I was cool for having something that no one else understood. I got to eat whenever I wanted to, while everyone else had to wait til snack time.

      5 years ago Log in to Reply
    13. Tod Herman

      I was just starting my senior year of high school, and about a month after my 17th birthday. I had to constantly run to the bathroom to take a leak between each class and I was losing a lot of weight (about 35 lbs). I had no idea what was going on (as nobody in my family, including cousins had ever had diabetes). My vision was getting bad (eyes were now dehydrated) and I was always tired. My friends at school said I didn’t look right, I was getting very skinny. Finally, I left school and drove by my mom’s office to tell her I was going home but she called the doctor. After explaining my symptoms he said to go to his office immediately. I never made it home and ended up in the hospital for several days… This was a shock to all of us. Back at school, nobody bothered me about my diabetes (few in my school probably had it). But my life drastically changed after that.

      5 years ago Log in to Reply
    14. Ginger Vieira

      Just once, by a dummy who teased me for wearing a pager when it was actually my insulin pump. I felt more sorry for him than I did for myself!

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

      I was picked on like any other kid– nobody knew anything about diabetes! I WAS THE ONLY KID IN THE ENTIRE SCHOOL THAT HAD DIABETES!!! That was 1954! Today, type 2 is rampant in schools! And covid-19 compounds the seriousness of treatment!

      5 years ago Log in to Reply
    16. Richard Vaughn

      I was diagnosed in 1945, when I was 6. Teachers and students had not heard of diabetes. The students knew I was different. I was not allowed to participate in gym, to avoid insulin reactions. I was ignored, but not teased. I did not make friends in Elementary School.

      5 years ago Log in to Reply
    17. Stephen Woodward

      I was not bullied, however the naive or joking comments that I did encounter were often hurtful.

      5 years ago Log in to Reply
    18. cynthia jaworski

      I would occasionally be teased about my thick sandwiches (2 meat exchanges as opposed to the pb and j eaten by other kids) but it was never mean.

      5 years ago Log in to Reply
    19. Germaine Sarda

      Dx 1974 at age 8. My teacher gave out candy bars to the kids as rewards and she always had something else for me (colorful pencils, stickers, etc.). The other kids were envious and would ask if I’d trade so I really appreciated what she did. I only talked about diabetes with my best friend who was like a sister to me. I don’t ever remember being teased for it, but I also never knew of any other students who had Type 1. It was still unknown to many.

      5 years ago Log in to Reply
    20. Sally Numrich

      Never. Diagnosed in 1970 at the age of 8. Everyone knew because I was in the hospital for almost 2 weeks. I shared everything, everyone knew and nothing really changed except for school parties. My Mom would send some kind of treat, usually some fruit cup with vanilla wafer cookies instead of the cupcakes everyone else got. Oh well, as had as it was, I survived! And vanilla wafer cookies are still to this day one of my favorites!

      5 years ago Log in to Reply
    21. Dennis Dacey

      Never teased, because no one at the school knew I had diabetes. I was diagnosed, and spent two weeks in hospital, during summer break while in high-school. I lived in a suburb and commuted alone to a preparatory school in Boston, so I was able to shield my personal life from my educational experience. My experience remained the same as I matriculated into college.

      5 years ago Log in to Reply
    22. KarenM6

      Like others, I was not teased because no one knew… there were no blood sugar meters… no CGMs… no pumps… nothing to outwardly say, “I am diabetic.” So, the only people who knew were the people I told (and I didn’t tell anyone but the closest of friends). In my entire school career, I only went to the nurse once (because I got to school and remembered I had not taken my shot that morning.) I don’t think even the PE teachers knew. So, basically, hiding in plain sight. ;p

      5 years ago Log in to Reply
    23. Leona Hanson

      In School I was pre diabetic I was only picked on when I would pass out for no reason or and picked on because I was a straight A student

      5 years ago Log in to Reply

    If you had T1D while in school (excluding college), were you ever picked on or bullied because of having T1D? If so, did it bother you? Cancel reply

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