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    • 1 hour, 31 minutes ago
      Amy Schneider 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.
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 2 hours, 58 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 5 hours, 10 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.
    • 5 hours, 11 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
    • 5 hours, 11 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!
    • 5 hours, 54 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.
    • 7 hours, 17 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.
    • 9 hours, 14 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
    • 1 day 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.
    • 1 day 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.
    • 1 day 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.
    • 1 day 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
    • 1 day 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 ´ )⎠⎞
    • 1 day, 2 hours 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.
    • 1 day, 2 hours 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.
    • 1 day, 2 hours 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, 6 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, 8 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, 9 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, 9 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, 9 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, 9 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, 9 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.
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    If you use an insulin pump, which of these options best describes when you most often change your pump site?

    Home > LC Polls > If you use an insulin pump, which of these options best describes when you most often change your pump site?
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    How do you stay up to date about T1D advancements and community news? Select all that apply!

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    At your current job (or most recent, if you are not currently working), do your coworkers know that you have T1D?

    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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    22 Comments

    1. Larry Martin

      After my shower.

      1
      4 years ago Log in to Reply
    2. Sherolyn Newell

      I try to keep it around 5:30pm. Don’t want to take the time before work or wait until I am getting tired after supper.

      4 years ago Log in to Reply
    3. Marty

      After my post-workout shower-usually late morning.

      4 years ago Log in to Reply
    4. Mary Ann Sayers

      Whenever it’s convenient to respond to the warning! I’m almost 75 and not working, so I change the cartridge when the time is good for me.

      1
      4 years ago Log in to Reply
    5. Glenda Schuessler

      I change my infusion site the day it is due, I try to pick a time when my BG is stable. I try to avoid just before a meal bolus or just after a meal bolus.

      2
      4 years ago Log in to Reply
    6. Mike S

      I tried mornings, but while failures are relatively rare, they do happen and ended up making me stressed/late for work or worse discovering an occlusion while at work meaning I had to re-do the set with an emergency pod. I stick to evenings now. But when I retire, I plan to move back to mornings – prefer them.

      4 years ago Log in to Reply
    7. kristina blake

      I do stick to every 3 days, but the timing varies. I see a rise in bg’s towards the end of day 3, so I do try to be prompt.

      4 years ago Log in to Reply
    8. Christine Zinn

      Twice a week, Monday morning and late Thursday afternoon (every 3 1/2 days) for a consistent routine.

      1
      4 years ago Log in to Reply
      1. Ahh Life

        I like this approach, regularity and consistent predictability. Thanks for suggesting it.👍

        4 years ago Log in to Reply
      2. Bonnie Lundblom

        I love this and also send thanks for this great consistent regimen for pump site changes!

        4 years ago Log in to Reply
    9. Carol Meares

      Sometimes I change because of pain at the site or I notice it not working well

      1
      4 years ago Log in to Reply
    10. Becky Hertz

      No specific time but I try not to change it right before bed.

      4 years ago Log in to Reply
    11. KSannie

      I do it 2 hours before a meal, usually supper. I can then use the food and a lower insulin dose for my supper (or sometimes lunch) to prevent the severe low sugars I get 2-4 hours after changing sets.

      4 years ago Log in to Reply
    12. Patricia Dalrymple

      I try early morning. I work remotely so I don’t have that worry. I always go low the first day even when I lower my basal rate so never close to bed time.

      4 years ago Log in to Reply
    13. John Zipper

      I try to pick a time that will be relatively convenient three days down the line. For example, if I know I will be busy Weds evening I will change out my pod either Sunday afternoon or late Sunday night.

      4 years ago Log in to Reply
    14. Mick Martin

      Although I selected ‘No specific routine – whenever the site expires or the reservoir is too low’, I also change my infusion site if my blood glucose level has been high for several hours and ‘correction boluses’ aren’t bringing down my blood glucose level. I’m fully aware that my body’s own ‘defence [defense] system’ sees the cannula as a ‘foreign object’ so tries to combat it by surrounding it with all sorts of white blood cells called phagocytes and lymphocytes, which produces a gungy-looking surrounding that makes it difficult for the insulin to ‘escape’ the cannula.

      1
      4 years ago Log in to Reply
    15. LizB

      I do it in the morning. The first half day of a new site is not usually good for me and I run higher. I don’t eat breakfast so I like to get the set in early and hope the site is getting saturated by lunchtime.

      4 years ago Log in to Reply
    16. Chris Albright

      I like to change early enough to determine if the site is providing acceptable insulin sensitivity

      4 years ago Log in to Reply
    17. Stephen Woodward

      In all of my 27 years pumping I’ve changed sites every 3-3.5 days and always fill the cartridges full up and change cartridge when needed when it’s low. The medical myth about needing to change cartridges with sites has no science base, it just sells more cartridges.

      4 years ago Log in to Reply
    18. Lawrence S.

      I probably should have answered no specific routine, because I change for many different reasons, other than routine. When I wear the cannula on my leg, it tears off, even with lots of tape. Occasionally, it clogs up. But, mostly, when my pump reminds me to change my site, which I usually notice in the early or late afternoon.

      4 years ago Log in to Reply
    19. Kathleen Begbie

      Every 3 days

      4 years ago Log in to Reply
    20. Kim Murphy

      I change it 8 hours after notified it is expiring because it starts continious alarming. I use Omnipod and always get the extra eight hours because the pods are so expensive using for the extra eight hours gives me an extra day after three changes. It means that sometimes I am getting up in the middle of the night to change it.

      4 years ago Log in to Reply

    If you use an insulin pump, which of these options best describes when you most often change your pump site? Cancel reply

    You must be logged in to post a comment.




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