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    • 1 hour, 13 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 1 hour, 14 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 1 hour, 14 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 1 hour, 57 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 3 hours, 20 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 5 hours, 17 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 20 hours, 40 minutes ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 20 hours, 42 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 20 hours, 43 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 20 hours, 43 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 20 hours, 52 minutes ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 22 hours, 44 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 22 hours, 45 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 22 hours, 47 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 2 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 4 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 5 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 5 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 5 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 6 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 6 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 1 day, 6 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 1 day, 6 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 6 hours ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 6 hours ago
      Gary R. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
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    If you wear a pump or CGM, do you usually change your site or sensor around the same time of day?

    Home > LC Polls > If you wear a pump or CGM, do you usually change your site or sensor around the same time of day?
    Previous

    If you wear a pump or CGM, when in your daily routine do you prefer to change your sites/sensors?

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    Do you keep glucagon in your home? If so, what kind?

    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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    25 Comments

    1. Bob Durstenfeld

      That would be nice, it usually change them when they run out.

      5 years ago Log in to Reply
    2. Clare Fishman

      Since pods are on for 80 hours the time I change them is different every time.

      5 years ago Log in to Reply
    3. Mick Martin

      No. I change sites when I get an ‘alarm’ from my pump informing me that it needs doing.

      5 years ago Log in to Reply
    4. Donna Condi

      No. I change my site when it runs out and that is always different times. And my Dexcom gets changed around the same time unless it dies early.

      5 years ago Log in to Reply
    5. Annie Wall

      It’s pretty much yes for me because Dexcom turns the sensor off 10 days later at the same time the sensor session started. However, if you suddenly have to change out a bum sensor, that can easily change your time of day. My preference is morning.

      5 years ago Log in to Reply
    6. Gene Maggard

      Although I don’t have a specific routine, I try and change my infusion set at a time during the day where I can catch any anomalies (such as highs due to a bad site location). As far as the CGM goes, I change it at a time where I can count on my glucose level being relatively stable for two hours while it warms up. After meals is not a good time for me because then I’m constantly doing a finger stick to see where I am.

      5 years ago Log in to Reply
    7. connie ker

      I change the Freestyle Libre when it times out. However, sometimes it quits a few days earlier, and sometimes the sensor comes loose on the arm. I change when it is necessary to do so.

      5 years ago Log in to Reply
    8. Kristine Warmecke

      I change my pump site when I’m alerted to less than 20 units. With my G6 it’s usually around the same time every 10 days. If I have t have a MIR/MRA, I try to schedule it for day 10 or toward the end of the 10 days as possible.

      5 years ago Log in to Reply
    9. Lynn Green

      This is a yes for CGM which is very regular every 10 days. And a no for pump since I change every 2 days but change at different times due to how much insulin is still available in my pump.

      5 years ago Log in to Reply
    10. Ken Raiche

      The only one out of the two that would possibly be changed at the same time of day would be the CGM. As for the pump that becomes much more difficult due to the never ending changes potential rollercoaster of sugar levels. So yes on CGM if everything goes well no sensor or transmitter issues and no of the infusion sites. That is why I answered this question with other.

      5 years ago Log in to Reply
    11. George Hamilton

      Like many others above, I change the pump cartridge and infusion set when the insulin runs low, and I change the sensor when it quits after 10 days. Time of day varies.

      5 years ago Log in to Reply
    12. Megan L

      Pretty much the same as everybody else here. The time for the pump site changes, but it’s the same time for the sensor.

      5 years ago Log in to Reply
    13. Amanda Barras

      My insulin running out and my sensor expiring rarely correlate.

      5 years ago Log in to Reply
    14. Conniekaycox

      Don’t you hate it when your pump needs changing at 330 am or runs out if insulin While your working. The alarm is so loud.! Lol am trying to learn to find humor. Been in this situation for 10 months. You all give e me hope that survival is possible.

      5 years ago Log in to Reply
    15. Thomas Hatton

      I try to change my CGM sensor in the morning of the last day. That way I can get the “warm up” and 2 calibrations in before I go to bed. If I knock a sensor out I will start a new one right away and get back to my morning cycle as close to the end of the last day that works. I have gotten better wit tape and am more careful not to rub my transmitter against things as I an working.

      5 years ago Log in to Reply
    16. Ceolmhor

      I’m surprised that so many answered “No” to this question. In my case, at least (Medtronic 670G and CGM), it takes many hours for the new sensor to stabilize, and I try to get it as stable as possible before bedtime. So I do sensor replacement in the morning. And if I can’t do the change fairly early in the day (say, by mid-afternoon), I’ll run in manual mode until the next morning, in order to avoid the high level of sleep disruption that would otherwise occur.

      5 years ago Log in to Reply
    17. Christina Trudo

      I did not understand this question to mean change them both at the same time of day, though I like ot do that if it occurs naturally. Instead I understood it to mean either or, and the answer is more like “occasionally” than “usually”. I tend to do that in the evening if that works, but I’m retired with little scheduled, so I’ll do it whenever. I tend to know when it’s coming soon and choose a convenient time.

      5 years ago Log in to Reply
    18. Grey Gray

      Change my CGM in the morning of day it is due. I try to do it on Sundays so it can stabilize before I work on Monday. I have learned to live with auto mode… Sundays can be rough very different basal patterns

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

      No. My CGM is changed every 10 days on schedule. My pump’s warranty expired, so I’m using it with insulin shots to maintain bg levels. I change each of them as needed.

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

      PS. I am making a request for a closed-loop system pump!!!

      5 years ago Log in to Reply
    21. Janis Senungetuk

      No, it’s never exactly the same time. I change my pump set when I’m almost out of insulin and my CGM at different times every 10 days.

      5 years ago Log in to Reply
    22. Ann Taylor

      I change my cgm every 10 days whatever the time of day it was the last time. If i won’t be home at that time I would change it earlier. But that doesn’t happen much nowadays 🙁 My pump I change whenever I get low on insulin. Or if the pump is leaking!

      5 years ago Log in to Reply
    23. Derek West

      I change my CGM around the same time every Sunday morning, a slow day, but my pump I change out when it’s empty.

      5 years ago Log in to Reply
    24. Donald Cragun

      I change my CGM at the same time every 10 days unless a sensor fails. I change pump infusion sets every 3 days at about the same time of day. I change pump cartridges when the current cartridge is empty.

      5 years ago Log in to Reply
    25. Becky Hertz

      I don’t have any set times. I try not to cane my insertion site right before bed, cause, you know.

      5 years ago Log in to Reply

    If you wear a pump or CGM, do you usually change your site or sensor around the same time of day? Cancel reply

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