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    • 6 hours, 49 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
    • 7 hours, 39 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.
    • 8 hours, 35 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
    • 9 hours, 18 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
    • 9 hours, 37 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, 9 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
    • 10 hours, 13 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, 8 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, 9 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.
    • 11 hours, 38 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.
    • 11 hours, 47 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!
    • 11 hours, 52 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, 7 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, 8 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, 8 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, 3 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, 3 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, 20 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, 20 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, 4 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, 4 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, 4 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, 6 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, 7 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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    Do you currently use any of the following CGM systems?

    Home > LC Polls > Do you currently use any of the following CGM systems?
    Previous

    Do you ever change your insulin to carb ratio for different types of foods?

    Next

    If you wear a CGM and share your CGM data with any of your loved ones through an app, for which types of CGM alerts does your network receive notifications? Select all that apply!

    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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    24 Comments

    1. Judy Hampton

      I have used the Freestyle Libre system for 4 years and currently use the Libre 2. I did not realize most people used Dexcom. Just curious if I should change over. Can anyone tell me why Dexcom is better than Libre? I am not opposed the making the change.

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

        I can’t provide your comparison with Freestyle, but will tell you about my experience with Dexcom. I started with Medtronic and then was forced into changing to the Dexcom G5 when I went on Medicare (they didn’t support Medtronic at that time). It was the best upgrade ever, as the Medtronic units were never accurate. Both the G5 and G6 have been amazingly accurate, and their high and low alerts, their interface with my IPhone, and the feedback reports provided by Clarity enable my doctor and I to easily work out any changes in my insulin pump delivery. Obviously I would like to try something that would automate basal and other settings, but giving up my G6 (and soon G7) will be very hard for me.

        3
        2 years ago Log in to Reply
      2. Gerald Oefelein

        The primary advantage of the Dexcom G6 is that in conjunction with a Tandem t:slim x2 it makes a hybrid closed-loop system. The pump adjusts your insulin based on CGM readings with (limited and occasional) user input.

        3
        2 years ago Log in to Reply
      3. Sherolyn Newell

        I don’t know that it’s better, but it was the only one FDA-approved for insulin dosing. That may have changed. I didn’t have one before G6 came out.

        2 years ago Log in to Reply
      4. Jocelyn BROOKS

        Hi Judy. As a T1D who has tried both systems, the Libre does not give as much support. I needed something that would wake me up at night to let me know if I have lows. The Libre has to be engaged by you to update the readings. The Dexcom automatically reads without any intervention from you. It signals/alarms when you go out of the optimal range.

        2
        2 years ago Log in to Reply
      5. casey shane

        No scanning. Automatic BG updates every 5 minutes to an app on your phone. Or if you use a Tandem T-slim X2 pump and Dexcom g6 it’s a closed loop system. (Bg Readings from the Dexcom transmitted via Bluetooth to pump, pump controls basal/bolus based on readings) NO SCANNING

        2
        2 years ago Log in to Reply
    2. Steve Rumble

      Actually, starting use of a G6 tomorrow as part of a study testing virtual coaching as a means to improve T1D management. Six month trial will let me know how I like using a CGM.

      2 years ago Log in to Reply
      1. AnitaS

        I am sure you will realize how beneficial CGMs are after using them. Most people on them hate it when one cannot be used for even a few hours as you love always knowing if you are going too high, and especially if going too low. I believe low blood sugars are the reason most diabetics want to start a CGM. They do have some downfalls (the most common being that they are inaccurate during the first day), but if you wear your sensor for at least 12 to 24 hours before actually starting it, the inaccuracy problem is gone. Good luck. p.s. I believe CGMs are the most helpful things to help diabetics beside insulin.

        2 years ago Log in to Reply
    3. LizB

      I currently use the Medtronic Guardian Link 3 with my 770 pump. While many people have had issues with their sensors they work great for me.

      1
      2 years ago Log in to Reply
    4. Sahran Holiday

      Dexcom G6. Generally works well. When it doesn’t company is responsive, gives excellent support, provides replacements. Just looking towards it communicating with Omnipod since I’m not switching pumps.

      2 years ago Log in to Reply
    5. cynthia jaworski

      I use the libre 2 and am very pleased with it. It is easy to apply and remove. . Jocelyn Brooks, above, is describing the libre 14 day system, which did not have alarms. The current model, ibre 2, will make an audio alert for highs or lows. It is necessary to scan for all other readings (which are in-range.)

      2 years ago Log in to Reply
    6. Jodi Greenfield

      The results really surprised me! So many people on Dexcom. I love my FreeStyle 14-day. My T1D sister had a Dexcom in the past and she had to calibrate it, tweak it and all the alarming drove her crazy. Things must have improved with the system over the years, heh?
      For now, I’m sticking with the less complicated FreeStyle.

      1
      2 years ago Log in to Reply
      1. Charles Barnard

        Not to my knowledge, I still need to calibrate it at least once a day, preferably two as mine bounces around up or down by up to 20 points. But this is my first CGM.

        The interface sucks, the analytics are poor (it does an awful job of predicting the direction, frequently telling me it is stable when it is in fact rising or falling rapidly.

        They seem to spend far more money on trying to keep people from using the sensors for more than 10 days than on improving the device. In fact, the programming is styled like the 1980’s so I suspect it was written by the scientists who developed the device without help from professional programmers or testing with real people to see how well the interface performed.

        What I think is that they have managed to get their marketing out to more people, using claims which the FDA supports but which actual use suggests are inflated.

        2 years ago Log in to Reply
      2. KSannie

        I have calibrated my Dexcom 6 twice in 19 months of use. And I am only disturbed by urgent alarms if my sugar goes below 75 at night, which is the point of having the warnings. For highs, I use vibration, which I will only hear if I am awake. The reason I do not want a Libre is because it seems to require use of a phone app, and cell phones often die. Plus apps use up the battery on a cell phone too much. I get alarms on my pump for the Dexcom.

        2 years ago Log in to Reply
    7. Natalie Daley

      I was given a Freestyle Libre 2 by my endocrinologist, who had a free sample. My insurance supports it. My doctor said the latest one has adjustable alarms for highs and lows, which was the important point. I’ve frequently cross checked the accuracy with my meter and strips. It’s accurate, easy to use, and my fingers have healed. I always know what my blood sugar and how it’s trending.

      1
      2 years ago Log in to Reply
      1. Brett Jorgensen

        Me, too. I am very happy with it.

        2 years ago Log in to Reply
    8. lis be

      I have Libre 2. I like it for the low sugar alarms, but it does often get code errors (the staff is super friendly and supportive). It also doesn’t link to tidepool yet (I LOVE tidepool, it combines blood readings, insulin etc.. so its easy to troubleshoot trends)

      2 years ago Log in to Reply
    9. Brandon Denson

      This is always an interesting question. Has anyone ever tried the Eversense CGM by Senseonics?

      2 years ago Log in to Reply
    10. George Lovelace

      I’ve been with Dexcom since System 7Plus in 2009. It’s been so consistent and reliable while hearing the horror stories about MM/Medtronics Once I got past Edgypark’s threats to Sue me I’ve had no issue that wasn’t resolved by an understanding phone call. Ya hear that, Edgypark?

      2 years ago Log in to Reply
      1. Sandra Rosborough

        I switched to Libre2 mostly because of Edgepark. Libre2 is also cheaper too.

        2 years ago Log in to Reply
    11. TEH

      I am now on Medicare. MM/Medtronic offered me boxes of Guardian 3 sensors for $60 each. That is juat a little more than I was paying for them with private health insurance. If they discontinue that offer, or don’t get picked up by Medicare, I will be moving to Dex 6 & Tslim.

      2 years ago Log in to Reply
    12. Judy Hampton

      Thanks everyone for the responses to my question regarding Libre vs. Dexcom. My Libre 2 does have the alerts/alarms. Abbott, the developer, has released the Libre 2 app for iPhone and is working to release the Android app. I did use the phone app with my Libre 14 day system and it was great, but Libre 14 had no alarms. Anyway, I was puzzled why Dexcom received such a high percentage. My Libre is usually accurate and is much cheaper. Medicare supports Libre products. Thanks, again.

      2 years ago Log in to Reply
    13. William Schaffer

      Libre 14 has never been accurate. Used both arms and abdomen. Sensors last about 10 days.
      It always reads low – almost consistently low – finger sticks are usually about 50% higher.

      2 years ago Log in to Reply
    14. Thomas Cline

      The person writing the question clearly didn’t understand that DEXCOM specifically prevented people from continuing to use the G5. I particularly liked the G5 receiver, far superior over the G6 for those that don’t want to use their cell phone for readings. I was very happy with the G5 and would have continued with it if allowed to since I could routinely get two weeks out of it, rather than the 10 days maximum that G6 allows. Moreover, in contrast to others, I have found that I do generally need to calibrate the G6 once or twice during each 10 day sensor session since I don’t like being 10+% off from my finger stick readings. I have found the G6 sensor to be quite erratic during the first day or two of use. Just about the time it settles down and is reliable, it’s time for a new sensor! I will bet that the G6 sensor has the potential to go far beyond 10 days, since DEXCOM has to design it to work with folks who have a higher average blood sugar than I. Still, DEXCOM is a good CGM and a major improvement over pre-CGM life.

      2 years ago Log in to Reply

    Do you currently use any of the following CGM systems? Cancel reply

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