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    • 7 hours, 37 minutes ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 8 hours, 28 minutes ago
      Mick Martin likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 9 hours, 23 minutes ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 10 hours, 6 minutes ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 10 hours, 26 minutes ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 10 hours, 57 minutes ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 11 hours, 2 minutes ago
      KCR likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 11 hours, 56 minutes ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 11 hours, 58 minutes ago
      Chrisanda likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 12 hours, 27 minutes ago
      Gary Rind likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 12 hours, 35 minutes ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 12 hours, 40 minutes ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 23 hours, 56 minutes ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 23 hours, 56 minutes ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 23 hours, 56 minutes ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 1 day, 4 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 1 day, 4 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 1 day, 21 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 1 day, 21 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 2 days, 4 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    • 2 days, 5 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Hmmm... I'd almost welcome it, another challenge to enjoy?
    • 2 days, 5 hours ago
      KarenM6 likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I am rough on insulin pumps and cracked 2 minimed pump cases. I found the bare T:slim pump too slippery. I use the MEDmax silicone case. I put that in a AGOZ case with a belp clip. But I don't like the clip. It's too sharp and too stif. Looking for a belt for night time use.
    • 2 days, 5 hours ago
      KarenM6 likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I use the Tandem provided case and added a gorilla glass screen protector. I wear it on my belt in an pouch.
    • 2 days, 7 hours ago
      lis be likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 2 days, 8 hours ago
      Karen Tay likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      No. I hate the clip on the case that came with my Tandem pump. I bought a couple of other cases, including Type 1 Tactical, and hate the bulk and the awful clips. I just stick the pump in my pocket and it's fine. At night I do use one of the other cases, from Type 1 Secura, because I can keep it clipped to my undies and easily slide the pump in/out if I have to look at it during the night.
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    If you use an insulin pump, how long have you this brand/model of pump?

    Home > LC Polls > If you use an insulin pump, how long have you this brand/model of pump?
    Previous

    Have you ever used a smart insulin pen?

    Next

    How often do you typically change your insulin dosage settings outside of T1D-related appointments (e.g. basal rates, insulin-to-carb ratios, etc.)?

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    26 Comments

    1. Molly Jones

      I have used a t:slim X2 pump since Dec 2018 and been happy enough with it.

      2 years ago Log in to Reply
    2. Ahh Life

      I know not what kind of balefire the benfactors of brand loyalty perceive. But as a devoted brand loyalists myself, I can swear by the Medtronic pumps of 1996-2015 and the Tandem tSlim X2’s of 2016-2022.

      Oh, and I can also swear at them too. I think it’s called a love-hate relationship.

      8
      2 years ago Log in to Reply
    3. GLORIA MILLER

      I used Medtronic from the early 1990s until 2010 and I really loved it. Then I switched to Omnipod and I am quite happy with it as well. I can hardly wait for the Omnipod 5 to be released for the public so I can switch to that with the Dexcom (but I will miss my Libre).

      2 years ago Log in to Reply
      1. Michelle Saunders

        I loved my Libre, but love my dexcom even more.

        1
        2 years ago Log in to Reply
    4. Sharon Lillibridge

      and .NEVER..will

      2 years ago Log in to Reply
    5. Retired and glad

      I started with Medtronic (Minimed) pumps in 1993, and have upgraded many times but always stayed with Medtronic. After trying their CGM capability for a while, however, I abandoned it in favor of Dexcom. The Medtronic sensors were too picky and inaccurate and kept me awake all night demanding to be calibrated. As far as pumps go, as I get closer to the end of warranty on my current one I will definitely look into alternatives that are more compatible with Dexcom.

      3
      2 years ago Log in to Reply
      1. Julie Nalibov

        I was on Medtronic pumps for nearly 10 years but changed to the Tandem IQ with Dexcom CGM. I love the capacity to actually set basal rate while still having the semi-closed loop of insulin delivery. Also, the NOT having to calibrate constantly has vastly improved my sleep. Additionally, I feel like the algorithms or whatever it is in the Tandem IQ work FAR better than Medtronic G6. It also allows you to give extra bolus without leaving automode. Dexcom sensors more comfortable and last considerably longer.

        2
        2 years ago Log in to Reply
    6. Jane Cerullo

      I am off pumps after 20 years (Medtronic and Omnipod depending on insurance). It’s been 2 months and I love the freedom. Will be traveling and looking forward to not having to bring so many supplies.

      2 years ago Log in to Reply
      1. Linda Murphy

        Sounds thrilling to be “unplugged”.. perhaps someday. Meantime I’m finding TSlim (5 mos.) helps keep in range (unless I over/under estimate carbs); I hear Omnipod coming out w/ ability to add/slow down insulin depending on trend picked up from Dexcom CGM, which is the feature I like about the TSlim, minus the tubing..looking forward to trying that when it comes out

        1
        2 years ago Log in to Reply
    7. Ken Raiche

      Animas Vibe for almost 5 years which is now defunct, accompanied with Dexcom G4 and G5. So I switched to my current Tandem X2 / dexcom G6 and looking forward a potential switch over to whatever is the next best pump in 3 years. From the looks of things that will most probably be the Omnipod with probably a G7, G8 or G9. Time will tell

      2 years ago Log in to Reply
    8. Becky Cain

      I used Animas and Dexcom from 2011-2018. Got the Tandem x2 in 2018 when Animas closed down. Love Dexcom and now with upgrades to x2, things have certainly come a long way since 2011.

      2 years ago Log in to Reply
      1. Sherrie Johnson

        Come along way since 1961 for me

        2 years ago Log in to Reply
    9. Michelle Saunders

      I had a Medtronic minimed for 10 years and then switched to the tSlim and dexcom g6 for the closed loop system at the recommendation of my CDE who is also a type 1 who had been on a minimed. I’m glad I made the switch I have better control now with the closed loop system.

      4
      2 years ago Log in to Reply
    10. Carol Meares

      I have had this Tandem model for almost 4 years, Medtronic for 4 before that, and MDI for 20. The Tandem has been replaced twice and very promptly. Both times because of breakage. TY Tandem. I will be looking to try tubeless for a bit to see if I can do better with that but love Tandem. I do wish though with the algorithms that we could set a lower target of 100, but I think that may be an FDA problem.

      1
      2 years ago Log in to Reply
    11. Mig Vascos

      I’ve been on Tandem t:slim 2x for 5 years. I’m due for a new one on April and will replace it with the same brand. It does have some annoying alarms but it also has some features not found in any of the other pumps in the market. I found the combination of this pump and the Dexcom g6 pretty amazing.
      Before that I had a Medtronic pump, but was much bulkier and worked with the Medtronic sensors which were very inaccurate and drove me insane.

      2
      2 years ago Log in to Reply
    12. pru barry

      I’ve been using the Tandem, Dexcom combo for years, after starting out with Medtronic. At 82, with 68 years of “experience” with diabetes, I no longer get up every morning hoping for a cure. My insulin dependent labradoodle and I get up in the morning, reckon with pumps and glucometers and syringes, and feel glad that we can still face our Maine winters :*) !

      6
      2 years ago Log in to Reply
      1. Tracy Jean

        Hi, Pru!

        2 years ago Log in to Reply
    13. Liz Avery

      I have been a Medtronic pump and sensor user since 2006. I really hated the Medtronic sensors until my husband started installing the weekly sensor for me. He does a great job and aside from the occasional “blood at site” issue, we are both much happier with the results.

      2 years ago Log in to Reply
    14. Patricia Maddix

      I have been on a Medtronic pump since 1997. When I got my most recent pump in 2015 Medicare was not yet allowing us to get the one with the automated system so have just been using Dexcom and the pump manually the same as I did in 1997. Tomorrow I meet with the Tandem trainer to start my new tandem T slim X2 and I am very excited to finally have a hybrid closed loop system. Time will tell but in following people’s comments about this pump over the last few years it should be great. pump

      2 years ago Log in to Reply
    15. Patricia Dalrymple

      Switching to a Medtronic 770G on Tuesday from a 630. Haven’t used a CGM but after I retire in a couple of years will have the time to figure all that out and get trained etc.

      2 years ago Log in to Reply
    16. LizB

      I have had my current Medtronic 770g for around 8 months but I did the upgrade from the 670. I have only ever used Medtronic, since 2005. I started using their sensors as soon as they integrated with a pump (Sof-Sensors and the 522/722 pumps). They worked great, but the Enlite sensors did not. I went without a CGM for a number of years, unwilling to carry another device with me(Dexcom receiver). When I got the 670g in 2018 I did so only because they said there were new sensors & transmitters. The Guardian sensors have worked great for me. Not sure if I want to switch to Tandem when my warranty is up later this year.

      2 years ago Log in to Reply
    17. ConnieT1D62

      I have been on a Tandem pump with various incarnations of Dexcom since 2014. Prior to that I used a Medtronic system, which was okay at the time until I had a chance to wear a 10 day saline trial with both a Tandem pump and an Omnipod along with Dexcom G4 in 2013 – all the while wearing the Medtronic pump & sensor. What a difference! I impatiently waited patiently for my Medtronic warranty to be over so I could upgrade to a new system and I chose Tandem with Dexcom. It felt like I was reborn!!!

      1
      2 years ago Log in to Reply
    18. Glenda Schuessler

      6 months with Tandem along with Dexcom. I starting pumping in 1997 with Disetronic pumps and stayed with that and various updates to Accumulate-Chek Combo until it was a few years out of warranty and difficult to get supplies in the U.S.

      2 years ago Log in to Reply
    19. mbulzomi@optonline.net

      Started used my Tandem X2 15 months ago. However, been on a Pump for over 39 years. Starting with a Baxter/Travanol pump then to a Baxter pump, on to Medtronic.

      2 years ago Log in to Reply
    20. Chris Deutsch

      Although I’ve used Tandem brand pumps since at least 2016 (= 6 years), my move to Control-IQ wasn’t possible until March, 2020 (not quite 2 years ago).

      2 years ago Log in to Reply
    21. Savanna Vance

      I have using tandem for less than a year but I’ve used an insulin pump since 2007.

      2 years ago Log in to Reply

    If you use an insulin pump, how long have you this brand/model of pump? Cancel reply

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