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    • 1 hour, 22 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!
    • 1 hour, 22 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.
    • 1 hour, 22 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.
    • 3 hours, 35 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.
    • 3 hours, 36 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
    • 3 hours, 36 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!
    • 4 hours, 18 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.
    • 5 hours, 41 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.
    • 7 hours, 39 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
    • 23 hours, 2 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.
    • 23 hours, 4 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.
    • 23 hours, 5 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.
    • 23 hours, 5 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
    • 23 hours, 14 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 ´ )⎠⎞
    • 1 day, 1 hour 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, 1 hour 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, 1 hour 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, 5 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, 7 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, 7 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, 8 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, 8 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, 8 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, 8 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, 8 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.
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    If you use an insulin pump or CGM, how often do you ration your device supplies because you are concerned about running out of supplies before your next refill?

    Home > LC Polls > If you use an insulin pump or CGM, how often do you ration your device supplies because you are concerned about running out of supplies before your next refill?
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    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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    31 Comments

    1. Nevin Bowman

      Pump supplies – never, because my endo I change sites less frequently than my script. CGM – almost always because it’s down to the day, so if anything goes south I have to extend to make it last until my next prescription is ready.

      1
      2 years ago Log in to Reply
    2. Lawrence S.

      Luckily, I’ve never had to ration my supplies. But, over the many years, there was a time or two when my supplies came late, or I had problems getting a prescription fill. There was a time after a hurricane, where all of my insulin froze in my refrigerator, and I had to get all new insulin. But, I did not have to ration.

      2 years ago Log in to Reply
    3. Jane Cerullo

      Never for CGM. Get at Walmart. So don’t have to wait for someone to mail

      2 years ago Log in to Reply
    4. Jian

      if you are a Medicare patient, as I am, supplies are closely monitored and you never get extra. its down to the wire sometimes. I have bought sensors at an independent place several times because the supply company did. not agree with my usage and I would have had to go without, so I bought a few on my own so that would not happen. It sometimes depends on the person on the phone not understanding exactly what a sensor is or the need to have a constant supply Everyone misses occasionally on having the right amount on Medicare. it requires the prescription to be changed if you go through the doctor. sometimes that is a real time taker and hassle.

      2
      2 years ago Log in to Reply
    5. Diane

      I said never but only because I can afford to buy CGM sensor spares. Medicare has made it a nightmare to get refills. Every 30 days I dread what they are going to require this time to refill the prescription. And the dance that goes on between the doctors, pharmacy, Medicare, and me each time is time consuming and so absolutely unnecessary. Once a T1D, always a T1D … at least for now

      3
      2 years ago Log in to Reply
    6. Eileen Heveron

      Pump supplies – never. CGM supplies -always!!! Very stressful and frustrating. I understand the device manufacturers and Medicare have it all tied up in a tidy algorithm but some months have 31 days and several times a year the sensors arrive late. Since I use Tandem’s Control IQ software it is very difficult to maintain my control from finger pricks and boluses if the CGM piece is not there. To say nothing if when a CGM sensor goes bad or other mishap occurs….

      3
      2 years ago Log in to Reply
      1. William Bennett

        Dexcom is pretty generous about mishaps: insertions that become painful in the middle of a session, accidental pull-outs, erratic results, and the like. I don’t recommend doing anything unethical but being diligent about requesting a replacement when such things happen can help to keep you in supplies.

        2 years ago Log in to Reply
    7. KIMBERELY SMITH

      Monthly

      2 years ago Log in to Reply
    8. cynthia jaworski

      With a libre, there is a set time span for each sensor to run. There is no way to save up, except by skipping a day or two. And why skip a day if you have a replacement on hand.

      2 years ago Log in to Reply
    9. Natalie Daley

      How can you ration CGM supplies? You either install another sensor or you don’t.

      1
      2 years ago Log in to Reply
    10. Natalie Daley

      My insurance company requires less than two weeks of “medication.” Libre 2 sensors last two weeks. Nothing better happen to that last sensor. It better not get knocked off, stop working, or in the last, not work at all. They have no idea what CGMs are snd don’t care. They are immovable on that two weeks.

      2 years ago Log in to Reply
    11. Abigail Elias

      My insurance is strict on timing (thank you Medicare), and because delayed doctor visits or snafus in orders from my supplier sometimes cause delays, I sometimes risk not getting supplies in time – and any delay forces a subsequent delay because the insurance timing requirement is reset. I’m now scheduling doctor visits 9 months out to avoid not having a visit with 3 months of a pump supplies reorder. But I’ve had 2 infusion sets pull out prematurely and Medicare (and probably other insurance) won’t adjust timing requirements.

      1
      2 years ago Log in to Reply
      1. mojoseje

        If you have an accident, call the supplier, they will send replacements…at least Medtronic does.

        2 years ago Log in to Reply
      2. Kristine Warmecke

        I have my endocrinologist appointments scheduled until 2025, for this reason. It’s a pain at times but at least I know I did my part. Plus I’ve found that if her schedule changes those who’ve been on it the longest get first choice of new appointment time.

        2 years ago Log in to Reply
    12. Kevin McCue

      Insurance restricts doctor ordered supplies and refill frequency causing shortages every time, to offset this I frequently go over on recommendations to change Zippo I have enough to last until resupply arrives

      1
      2 years ago Log in to Reply
      1. Kevin McCue

        Zippo? Gotta love the swipe texting and the weird things it throws unexpectedly

        2 years ago Log in to Reply
    13. Karen DeVeaux

      I have a Dexcom G6 CGM and I use a hack I found on YouTube to reuse a sensor a second time so I won’t run out.

      3
      2 years ago Log in to Reply
      1. JOAN ULMER

        Can you share?

        2 years ago Log in to Reply
      2. Kristine Warmecke

        I’ve tried all the hacks I’ve seen to reuse my G6 and have never had any luck getting it to restart. I’m happy you have.

        1
        2 years ago Log in to Reply
      3. Sue Martin

        Here’s a video that shows a couple of different ways. https://www.youtube.com/watch?v=tx-kTsrkNUM&t=164s

        I’ve read of some people restarting their sensors three to four times.

        2 years ago Log in to Reply
    14. JOAN ULMER

      Always supply issues with G6. Medicare makes it very difficult to have just one on hand in case of sensor failure.

      1
      2 years ago Log in to Reply
      1. Kate Kuhn

        Joan, I too would like to have at least one Sensor on hand. Anything could happen–the current sensor could get knocked off, fail, supply chain held up, etc. I have become VERY dependent on my G6!

        I would like to share that Dexcom is great when issues arise. One sensor happened to hit a blood vessel when I inserted it. I called Dexom, told them what had happened, and they sent a replacement that arrived the next day!

        2 years ago Log in to Reply
    15. Kristine Warmecke

      I should have rationed my G6 sensors this time because I didn’t realize I needed a new prescription for them and my endocrinologist was out of town for 2 weeks. So I went without one for a little over a week.
      I have to say since switching from Edgepark to ADS over a year ago, this is the first time this has happened; and it beyond any ones control, unlike what I was dealing with.

      2 years ago Log in to Reply
    16. Sherolyn Newell

      Not my pods, but I always have a finger-stick day between G7s. That way if there’s a delay, I don’t have to have as many finger-stick days in a row.

      2 years ago Log in to Reply
    17. Janis Senungetuk

      Up until two months ago, rarely. Two month ago I unexpectedly, suddenly lost primary insurance coverage. I had just received a 90 day pump supply but was low on Dex sensors and in need of an extra transmitter. I asked an online group if anyone had extras and two people had just switched to the G7 Dex. They both shipped what remained of their G6 supplies. I grateful paid their shipping costs. Hopefully, before I run out my new insurance coverage will resupply.

      2 years ago Log in to Reply
    18. Russell Buckbee

      I have Medicare so they should be fully covered, but the process can get so complicated that
      just in time” delivery is quite in time.

      2 years ago Log in to Reply
      1. Russell Buckbee

        That’s NOT quite in time.

        1
        2 years ago Log in to Reply
    19. Juha Kankaanpaa

      I haven’t had a need to ration any supplies. In worst case I should be able to get more within 24 hours.

      2 years ago Log in to Reply
    20. Becky Hertz

      Hoarder of diabetes supplies.

      2 years ago Log in to Reply
    21. Pat Sims

      I always want to have at least 3 months of supplies extras. I use the xgm and the infusion set longer than recommended.

      2 years ago Log in to Reply
    22. T1D4LongTime

      Rarely. I proactively reorder. Automated refills are nice, but I prefer to plan when the costs occur. The only time I would ration is if I have difficulties getting the doctor to respond to the DME supplier’s request or they are out of stock.

      2 years ago Log in to Reply

    If you use an insulin pump or CGM, how often do you ration your device supplies because you are concerned about running out of supplies before your next refill? Cancel reply

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