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    • 14 hours, 41 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.
    • 14 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 have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 14 hours, 44 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.
    • 14 hours, 45 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
    • 14 hours, 53 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 ´ )⎠⎞
    • 16 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 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.
    • 16 hours, 46 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.
    • 16 hours, 48 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 ´ )⎠⎞
    • 20 hours, 49 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
    • 22 hours, 51 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".
    • 23 hours, 36 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 ´ )⎠⎞
    • 1 day 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 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 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 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 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 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 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 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 ´ )⎠⎞
    • 1 day 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 ´ )⎠⎞
    • 1 day 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 ´ )⎠⎞
    • 1 day, 12 hours 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, 15 hours 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, 15 hours 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, 15 hours 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?"
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    Did you add, remove, or change T1D devices in 2021? Select all that apply.

    Home > LC Polls > Did you add, remove, or change T1D devices in 2021? Select all that apply.
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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. Louise Jesserer

      Added a Dexcom and Tandem t-slim with IQ control! Both great devices…

      4 years ago Log in to Reply
    2. Lisa Sierra

      I would switch to a pump and cgm that are compatible, but can’t and since they had to switch out my recalled medtronic pump, they didn’t upgrade, just sent me a refurbished crappy pump and added more time since it had been replaced. No upgrade.

      1
      4 years ago Log in to Reply
      1. Lisa Sierra

        Now I can’t upgrade and get compatible devices. I only need to change one device, but no.

        4 years ago Log in to Reply
    3. Antsy

      I’ve been waiting for the newest Medtronic pump to be released (rumor was it would come out by the end of the year, hoping my “expired” 670G doesn’t fail completely. If it is a big enough improvement over the current system, I’ll stick with Medtronic, otherwise I’m jumping ship to the Dexcom/Tandem combo.

      4 years ago Log in to Reply
      1. Joan Fray

        Tandem with Control IQ changed my life. Sometimes I even sleep through the night! Exercise is now possible for me too.

        3
        4 years ago Log in to Reply
      2. Steven Gill

        I got the 770G system this past fall, 100% the same as the previous with the exception of the app get can utilize a cell phone to reach contacts it there are concerns.

        While I read the complaints and concerns with the MEDTRONIC system it does well. Especially since my insurance has no trouble with coverage.

        In answer to the poll: I stopped using the Guardian3 sensor three years ago because of the cost. Inherited an old dog with congestive heart failure, the option was to forego her meds ($250 a month) or the sensor. She passed away a happy deaf, half blind, old lady at 16 this past spring. Waiting for the upgrades MEDTRONIC’s rep contacted me, and thankfully I’m now on their patient assistance program cutting my “after insurance” costs. BUT Motorola phones don’t work the app, so no idea on that yet.

        1
        4 years ago Log in to Reply
      3. Antsy

        Steven, I’m sorry about your dog, good for you for you for taking such good care of her. As for the 770g, seeing my numbers on my phone is not something I need. Now if my BG could pop up on my dashboard screen when I’m driving and my pump starts buzzing, I’d stick with Medtronic for another 4+ years.

        4 years ago Log in to Reply
    4. George Lovelace

      I will Never give up my Tandem X2 and hope the Dexcom G6 will upgrade to the G7 but the G6 works just Great now

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

      I Kept the same Tandem X2 pump and Dexcom G6 CGM. However, I did buy a new telephone, Samsung A1 G5 because it was supposed to receive the Dexcom G6 sensor signal. I downloaded the G6 app and used it for about 2 month. It did not work correctly, and ended up messing up my transmitters, sensors, and had continuously and repeatedly losing the CGM signals. The phone was a waste of money.

      1
      4 years ago Log in to Reply
    6. Andrew Stewart

      I changed from the Omnipod to Tandem tslim with Control-IQ. My only complaint is the tubes but I’m getting used to it.

      4 years ago Log in to Reply
    7. Meghan Larson

      I took a pump break and started using the InPen (which I did not see listed as an option to select!).

      4 years ago Log in to Reply
      1. AnitaS

        I think your option would have been “stopped using a pump ?

        4 years ago Log in to Reply
    8. Tom Caesar

      Anxiously waiting until Jan 10 when I can apply for a Tandem to replace my five year old Medtronic. Hoping my numbers and piece of mind level out with the change.

      4 years ago Log in to Reply
    9. Tabatha Rush

      Diagnosed in 2021

      4 years ago Log in to Reply
    10. Annie Wall

      After 25 years pumping, I took a 2 year vacation and was MDI using the InPen. This last spring I ended my “vacation” and started using a Tandem pump with Control IQ, a game changer for sure!

      4 years ago Log in to Reply
      1. Tina Roberts

        How did you like the impen?

        4 years ago Log in to Reply
      2. JoAnn Pinkowitz

        I would also like your impression of using the InPen please.

        4 years ago Log in to Reply
    11. Jneticdiabetic

      Switched from the Medtronic 670G pump/CGM to the Tandem Tslim pump and Dexcom G6 CGM in Nov. I was 98% within range yesterday (despite some residual holiday eating). A new all time best for me!

      3
      4 years ago Log in to Reply
      1. AnitaS

        Good for you!

        2
        4 years ago Log in to Reply
    12. Nicholas Argento

      Stayed with Dexcom G6 and T-slim control IQ- which I love. I sleep better, with higher time in range, than ever before.

      1
      4 years ago Log in to Reply
    13. Karen DeVeaux

      I said I added a new CGM but it was actually a FreeStyle Libre.

      4 years ago Log in to Reply
    14. Jane Cerullo

      Change from Medtronic to Omnipod. Because of insurance had to change from Dexcom to freestyle libre. Omnipod too expensive under Medicare so January first will switch back to MDI using insulin pens. Need a pump break.

      4 years ago Log in to Reply
    15. Janis Senungetuk

      This year I continued using the Tandem t-slim X2 pump with Control-IQ app/Dexcom G6 CGM.

      4 years ago Log in to Reply
    16. Tina Roberts

      I kept the same pump and cgm only because it’s still in warranty and my insurance won’t pay for a new one yet.

      2
      4 years ago Log in to Reply
    17. Rick Martin

      Switched from Tandem t-slim with IQ control to Afrezza (inhaled insulin). Much more time in range than on the pump!

      4 years ago Log in to Reply
    18. Vickie Baumgartner

      Actually changed insulin pump and CGM models that Medtronic sent to me unannounced.

      4 years ago Log in to Reply
      1. Dave Akers

        Typical Medtronic’s! Pushers is why they are!

        1
        4 years ago Log in to Reply
    19. Dave Akers

      AND Completely left the meal time injectable marketplace. Thank you Inhaled Insulin!!! Would love to see a question here one day about inhaled insulin… it’s a thing now!

      4 years ago Log in to Reply
    20. LizB

      I chose that I stayed with the same pump/CGM but realized I did pay for the Pathway upgrade from the Minimed 670g to 770g. But it is pretty much the same exact pump except now I can see the CGM readings on my phone. I’m still under warranty for another 10 months and am thinking of Tandem/Dexcom next year but cost will be a huge factor.

      1
      4 years ago Log in to Reply
    21. Bonnie Lundblom

      I remain on the Tslim pump and Dexcom CGM6. Does anyone know how long Medicare makes you wait to change CGM’s? I’m hoping the Dexcom CGM7 with the shorter cannula will be more accurate.

      4 years ago Log in to Reply
    22. PamK

      I did a trial of a different brand pump, but ended up staying with the one I’ve been on for the past few years.

      4 years ago Log in to Reply

    Did you add, remove, or change T1D devices in 2021? Select all that apply. Cancel reply

    You must be logged in to post a comment.




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