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    • 1 hour, 39 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.
    • 1 hour, 40 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.
    • 1 hour, 42 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 ´ )⎠⎞
    • 5 hours, 42 minutes 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
    • 7 hours, 45 minutes 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".
    • 8 hours, 26 minutes ago
      Anita Stokar likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 8 hours, 30 minutes 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 ´ )⎠⎞
    • 8 hours, 54 minutes 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.
    • 8 hours, 54 minutes 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".
    • 8 hours, 55 minutes 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.
    • 8 hours, 56 minutes 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.
    • 8 hours, 56 minutes 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.
    • 8 hours, 59 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 9 hours, 1 minute 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 ´ )⎠⎞
    • 9 hours, 3 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 9 hours, 4 minutes 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.
    • 9 hours, 16 minutes 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 ´ )⎠⎞
    • 9 hours, 29 minutes ago
      ConnieT1D62 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 ´ )⎠⎞
    • 9 hours, 45 minutes ago
      eherban1 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 ´ )⎠⎞
    • 21 hours, 41 minutes ago
      NANCY NECIA 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
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day ago
      Anita Stokar 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
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
    • 1 day, 1 hour ago
      ConnieT1D62 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I get the 'you can't eat that, can you?' comments when friends see me eat a lot of carbs or have a nice dessert. I remind them that as long as I have insulin, I can eat whatever I want.
    • 1 day, 1 hour ago
      ConnieT1D62 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.
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    If you have used a diabetes pump in the past, have you ever switched from pumping back to MDI (Multiple Daily Injections)?

    Home > LC Polls > If you have used a diabetes pump in the past, have you ever switched from pumping back to MDI (Multiple Daily Injections)?
    Previous

    As an adult with T1D, have you ever followed an intermittent fasting routine? What is your primary reason for starting, stopping, or never starting? Share your experiences in the comments!

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    Do you currently use any of the following insulin pumps?

    Ray Burgett

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    30 Comments

    1. Annie Wall

      I’ve mostly been pumping since 1995, took a pump “vacation” two years ago because I had so much scarring from nearly 25 years of infusion sets. I used the InPen for two years and now I’m back to pumping on the Tandem t:slim with Control IQ, using TruSteel. Much happier using fast acting insulin for basal than one shot of long acting.

      2
      4 years ago Log in to Reply
    2. Gary Taylor

      The email I received was yesterday’s question. It brought me to the site where I could answer today’s question.

      5
      4 years ago Log in to Reply
      1. AnitaS

        same here

        4 years ago Log in to Reply
    3. Sahran Holiday

      Only inject when I’ve left my Omnipod remote home or a few times in the past when multiple pods failed and blood glucose went dangerously high.

      4 years ago Log in to Reply
    4. connie ker

      Do MDI with correction doses if needed. Lantus and Humalog are the insulins. Why change what works at the senior age of 73. I do have an Abbott Freestyle Libre and scan many times a day and night. My fingers thank me each and every day, even as I type this message!

      4 years ago Log in to Reply
    5. Dave Barden

      The comment box worked for me this with my iPhone SE. But not same as Gary, received yesterday’s email and was taken to a different question, presumably today’s. New gripe: why is column for comments so narrow? It’s not even 10 characters requiring an excessive amount of scrolling and there’s all that empty space right and left😾

      4 years ago Log in to Reply
    6. Dave Barden

      Typo in my reply re. Gary’s; I meant “NOTED same…” but typed “not”. I regret the error🙀

      4 years ago Log in to Reply
    7. Lawrence Stearns

      NO WAY! The insulin pump was an extreme improvement in the quality of my life. I would never voluntarily return to multiple daily injections. My life was out of control on injections. I immediately felt and behaved 1000 percent better with the pump. And, the CGM was another significant improvement.

      3
      4 years ago Log in to Reply
    8. Sharon Lillibridge

      never have and never will

      4 years ago Log in to Reply
    9. Conniekaycox

      Been doing this for 16 months now am a novice lol love my omnipod dash but do take a break sometimes. It is uncomfortable minorly. Awesome to ditch both devices short term and shower and sleep comfortably.

      4 years ago Log in to Reply
    10. Andrea Rueff

      I received my Insulin Pump and have been on it sence December 1997. I have had the pump removed from Aug. 2013 and I had gotten a Traumatic Brain Injury August 24, 2013 and restarted in 2015. I love the pump. I have certain times that I don’t like the pump because of items that I have had to change but those item’s that I had changed are not good. All the issues that I have with my Insulin Pump, I will never give up on it. I absolutely love my pump and giving shots I don’t like tjat at all and do not want to use them.

      4 years ago Log in to Reply
    11. Janis Senungetuk

      Used MDI for 60 yrs. before getting a pump. Now 6 years later I won’t willingly go back.

      4 years ago Log in to Reply
    12. Becky Hertz

      Wish there was an “other” choice. I switched from pump to MDI for about 2 years because I was having absorption issues most likely related to scar tissue. That was years ago before one handed insertion devices and I’m back on the pump with using many more varied sites.

      1
      4 years ago Log in to Reply
    13. Amanda Barras

      It was due to loss of insurance entirely, not just because they didn’t cover my “preferred” pump.

      4 years ago Log in to Reply
    14. George Lovelace

      Spent less than 18 hours on MDI in the past 23 years

      1
      4 years ago Log in to Reply
    15. Kristine Warmecke

      Once I started pumping in Feb. 1997 I didn’t look back. I have no desire to go back to MDI.

      1
      4 years ago Log in to Reply
    16. Christina Trudo

      Like others, I have never looked back….. 30 years and counting. In the early years had one pump failure, replaced within 24 hours.

      1
      4 years ago Log in to Reply
    17. KarenM6

      I have had multiple pump failures requiring replacements and have spent up to about 4 days on MDI while waiting, but I have not intentionally gone back to MDI since starting pump therapy in 1996.

      4 years ago Log in to Reply
      1. Ahh Life

        Identical with my experience. I even started with a Medtronic pump in 1996. Prior to that I had 35 years of MDI, probably 40,000 to 45,000 injections. The new micro-micro-micro pen needles are soooooooo good, however, that those of you doing MDI don’t realize how good you have it.

        4 years ago Log in to Reply
    18. ConnieT1D62

      I have switched to MDI for a month at a time on a few rare occasions as a pump vacation to give my insertion sites a rest – and have only done so since using Dexcom as my CGM. However, it is unlikely that I would ever go back to living life with T1D without a closed loop pump/cgm system. I like not having to do the carb ratio and insulin onboard math all the time. The Tandem X2 with CIQ keeps my TIR between 80 to 92% (~88%) most of the time.

      4 years ago Log in to Reply
    19. Carol Meares

      I put “yes” #1 because I just went to MDI because I had a my tslimx2 go down and had to stop using it until I could get hold of someone at the company so I decided to go MDI for a couple weeks to determine if I wanted to go back to MDI and also further develop and refine my backup plan. I get frustrated with my tslim control iq. I wish I could go back to basal iq on which I did so much better: I am now back on the pump because I rely on the iob algorithm in my daily insulin calculations and also need the ability to give small amounts of insulin to adjust my bg.

      4 years ago Log in to Reply
    20. M C

      The only time I might do an injection will be on one of the days thinks are going wonky with the pump… Otherwise, no. Although I am tired of being attached to the contraption, the amount of control the pump has provided me is the factor that will keep me continuing to use a pump.

      4 years ago Log in to Reply
    21. PamK

      I would switch back to MDI, but my doctor told me not to. She did not believe me when I told her my control was better on MDI. I’ve got a different doctor now, and he understands that sometimes MDI is better. We’re working together to try to get the pump settings to work for me, but if he can’t he will let me go back to MDI. So, time will tell!

      4 years ago Log in to Reply
    22. Britni

      I tried using the Omnipod for 11 months and then went back to MDI. It malfunctioned often enough that I went over 500 more in that one year than in all the rest of my life. My blood sugars were such a mess that my A1c actually came down but my time in range decreased, too. And on top of all that I was often in physical pain from the pod. The insertion sites almost always became inflamed and painful, a couple times so badly that I had to remove the pod early. And if I wore it on my stomach the corners would often jab into me every time I had to bend over or carry something heavy (I work outdoors, constantly moving, bending, twisting, lifting, carrying, etc.). I actually have a new scar from the corner of a pod cutting into my skin. I started using the Omnipod thinking a pump would give me more flexibility and peace of mind while at work, but instead I was in pain and sick all the time. It wasn’t worth it.

      4 years ago Log in to Reply
    23. Mary Dexter

      Bubbles, bubbles caused lots of troubles. Figured if I was going to need to take multiple corrections with a syringe to compensate for the bubbles blocking the tubing, I might as well just take my insulin with a pen.
      Both my CDE and the Medtronic rep observed my technique (which had been working) and couldn’t figure out why the bubbles kept forming. Pump never did alarm. Instead, I would notice I had been sitting in the 300s and it was still rising despite dialing in several corrections. I will never use a pump again.

      4 years ago Log in to Reply
    24. Ken Raiche

      Lacking more options, I tend to alternate between pump and MDI every so often. It’s all a question of how I feel.

      4 years ago Log in to Reply
    25. Phyllis Kaplan

      I went on my first insulin pump 21 years ago and have not switched back. The first pump I had didn’t have many features besides basal and bolus (no bolus wizard!) but it afforded me so much flexiblity even then. Now my pump has more features and does more, and I have no plans to go back to MDI, or even a pump vacation. Though, I do of course realize there have been new insulin’s since 2000 that may offer some of the flexibitly those in 2000 didn’t.

      4 years ago Log in to Reply
    26. NAK Marshall

      I’d LIKE to use a pump (probably the Omnipod) but my skin cannot tolerate more than 1 adhesive, so I choose the CGM.

      4 years ago Log in to Reply
      1. NAK Marshall

        Also I now have the InPen that gives me the same lovely data and does the math that the pumps users get. It’s the best thing for my bolus insulin EVER, and requires much less brain power because it tracks everything! ALL MDI-ers should check it out.!!!

        1
        4 years ago Log in to Reply
    27. Cheryl Seibert

      I would never go back to MDI unless forced. I was on 5 shots a day and my poor, thin body couldn’t stand being touched because I was a pincushion. Love my pump even with the frustrations of tweaking the technology to match my brittle diabetes (T1D 55 years)

      4 years ago Log in to Reply

    If you have used a diabetes pump in the past, have you ever switched from pumping back to MDI (Multiple Daily Injections)? Cancel reply

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