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    • 4 hours, 6 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 4 hours, 7 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 4 hours, 8 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 1 day ago
      Wanacure 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 answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 1 day ago
      Wanacure 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 have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 1 day, 1 hour ago
      Wanacure 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 have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 1 day, 1 hour ago
      Wanacure 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
    • 1 day, 4 hours ago
      Samantha Walsh 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.
    • 1 day, 23 hours 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
    • 2 days, 1 hour 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
    • 2 days, 1 hour 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
    • 2 days, 2 hours 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.
    • 2 days, 2 hours 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
    • 2 days, 3 hours 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
    • 2 days, 4 hours 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!
    • 2 days, 4 hours 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
    • 2 days, 15 hours 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.
    • 2 days, 15 hours 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.
    • 2 days, 15 hours 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!
    • 2 days, 20 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.......
    • 2 days, 20 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....
    • 3 days, 13 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.
    • 3 days, 13 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.
    • 3 days, 20 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.
    • 3 days, 20 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?
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    If you use a CGM, how did your A1c change in the first 6 months of use?

    Home > LC Polls > If you use a CGM, how did your A1c change in the first 6 months of use?
    Previous

    How many people do you know in person (not online) who have T1D?

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    Do you currently have any smartphone apps that you use to look up the carbohydrates in various foods? Share your favorites in the comments!

    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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    31 Comments

    1. Britni

      I don’t remember what happened to my A1c in the first 6 months, but it probably went up as I was having frequent low blood sugars (45 low glucose events in 30 days) when I first started wearing my CGM.

      1
      2 years ago Log in to Reply
    2. Janice B

      My A1C did not change but I spent more time in range

      1
      2 years ago Log in to Reply
    3. Ahh Life

      A1c did not change. Standard deviation dropped from 90 to 45. All this in 2006 with the Minimed Harpoon, aptly named for the size of the insertion needle.

      2 years ago Log in to Reply
      1. AnitaS

        Hahahaha………
        I like your sense of humor.

        1
        2 years ago Log in to Reply
    4. Carolann Hunt

      Looping brought it down even more

      1
      2 years ago Log in to Reply
    5. paulinams28

      I feel that something that compromises the CGM’s blood glucose reading accuracy is the insertion step. Not sure if its the design or what, but in my experience I have lost many sensor tapes (guardian sensor 3/medtronic) because of puncturing capillaries. And at times I have to calibrate up to 4-5 times a day, which makes you think if the sensor is actually doing its job.

      1
      2 years ago Log in to Reply
    6. Mary Dexter

      My A1C did not change; it has been below 7 since I was correctly diagnosed and given insulin. The biggest change was that my husband was able to sleep at night.

      2
      2 years ago Log in to Reply
    7. Kristine Warmecke

      When I was made to get my first CGM, in July 2007, I wasn’t given a chose on which one I wanted, it was just Medtronic’s. It was a pain and inaccurate, so much that I stopped wearing it because of all the issues with it.

      2
      2 years ago Log in to Reply
    8. Bonatay

      I thought I would never be in the 8s. After CGM use I made it into the 7s.

      2
      2 years ago Log in to Reply
      1. Wanacure

        Hey, Bonatay, you can get into normal range with a CGM. Exercise, go to low carb diet. IF I CAN DO IT, YOU CAN DO IT. Eat veggies like spinach and Brussels sprouts at every meal. Eat nuts and seeds every meal. Include non-sugared peanut butter, almond butter. Get protein from sardines and wild-caught canned or smoked salmon. Add avocados and olive oil to your diet. Eggs, cheese, unsweetened yoghurt or kefir are good for you. Two ounces sweet potatoes, “yams” or canned pumpkin taste good, add fiber. Two tablespoons flax meal per day. I Tb wheat germ & 1 Tb yeast at breakfast and again at dinner. Don’t forget 4 Tb tomato sauce every day. For polyphenols have at least 1 cup Green Tea (decaf available). Save your kidneys by carrying a water bottle in your backpack. Yeah, it’s hard to kick carb addiction.

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

      I don’t recall my A1c’s changing when I first started on a CGM system. I usually ran between 5.5 and 6.0. However, since I’ve been on the Control IQ system with Dexcom G6 and Tandem, may A1c has consistently run at 6.1

      1
      2 years ago Log in to Reply
    10. George Lovelace

      In 2009 I started on the Dexcom System 7+ and don’t remember much change in A1c but it did bring down the anxiety over Hypo events. Now the G6 with Tandem CIQ I have eliminated almost All Hypos

      2
      2 years ago Log in to Reply
    11. Amanda Barras

      Pre-pump on 8 shots a day I was at 7.2 with hard work. Adding a pump dropped to 6.8, adding CGM dropped to 6.3.

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

      My A1c did not change so much but I am guessing that my time in range and standard deviation changed a lot. I had many lows and and highs but my A1c overall was good. Now I have less lows and highs maintaining much more even management of my diabetes. CGM is a glorious addition to my life. I could not live without it.

      4
      2 years ago Log in to Reply
    13. Joan McGinnis

      It was 2008 and I have no idea but under 7 now and I am happy for someone with T1D for 43 yrs

      1
      2 years ago Log in to Reply
    14. TEH

      Going on GGM helped me drop from 7.8 to 7.1. Going on modified close loop with the 770G I have been able to drop A1C further to 6.9.

      2 years ago Log in to Reply
    15. M C

      The only thing that changed when I started using a CGM was the average number of times I check my BG level each day.

      2
      2 years ago Log in to Reply
    16. Natalie Daley

      I check more often, so fewer lows and highs, learning the trends and not being as concerned about lows, especially at night have been great. Libre 2 is a work of art.

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

      I tried the Medtronic version of CGM and it was terrible, ended abandoning it after 2 years(A1c went from 7.6>9>8.7>8.8) when I was able to get insurance that covered Dexcom then Tandem. Constant false alerts with Medtronic with no improvement in A1c. Pre Dexcom CGM, I was struggling with high A1c and trying for tighter control. Ended up having lows that I could t see coming and A1c went up. Post Dexcom CGM, the accuracy and seeing trends that I could trust allowed me to get my A1c went down dramatically from 8.8 to 6.5 in the first few months.

      5
      2 years ago Log in to Reply
    18. Tina Roberts

      Decreased 2.% 10.5 to 8.5.

      2
      2 years ago Log in to Reply
    19. kflying1@yahoo.com

      Not a good question. Since beginning to use a CGM my occurrences of hypoglycemia have dropped to zero. especially during exercise or sleep.

      2
      2 years ago Log in to Reply
    20. LizB

      I don’t think my A1c changed too much because pre-CGM I had so many lows that I wasn’t aware of. I started using Medtronic’s Sof-Sensors when they first integrated with the pump (2007 or 2008) and I can’t remember my numbers from that far back. It definitely helped me to avoid some of the most serious lows and highs.

      1
      2 years ago Log in to Reply
    21. Janis Senungetuk

      My A1c didn’t change in the first 6 months of using the Dexcom G5. The changes came later using the G6 because my endo insisted that I needed to raise my A1c to 6.5 – 7.0 from the 6.0 level it had been at for years.

      2 years ago Log in to Reply
    22. Bill Williams

      Using a CGM was never about “improving” my A1c. I’d fluctuated between 6.5 and 7.5 for years using finger sticks and MDI. Libre and Omnipod are, for me, about ease of use, not reducing A1c or increasing time in range. Those numbers have changed very little.

      2 years ago Log in to Reply
    23. AnitaS

      My A1c really didn’t change but the highs and lows don’t happen as frequently nor are they as dramatic as before.

      1
      2 years ago Log in to Reply
    24. Lenora Ventura

      I can’t remember because I began using Dexcom when they 1st came out back in 2008. Been with them ever since & will never go without!!!

      2 years ago Log in to Reply
    25. Mark Schweim

      I don’t remember any effect on my A1c, but I started using Dexcom CGM in 2008 and that’s already 13, almost 14 years ago.

      2 years ago Log in to Reply
    26. Steve Rumble

      I recently started using a CGM and have not yet used one for 6 months.

      2 years ago Log in to Reply
    27. Carlene Vaitones

      My A1C improved because I’m able to be in the range of 120-95 more often without lows because I can see the low coming on the app. So I snack a little more often and skirt that nice lower “normal” range.

      2 years ago Log in to Reply
    28. David Smith

      I answered “NA” because I have been on a CGM less than 6 months, although the early trend seems to be decreasing A1C.

      2 years ago Log in to Reply
    29. Cheryl Seibert

      My A1C before a CGM was a good 6.9 (the highest I ever had) and with the CGM it dropped to 6.5. While my BGs wildly swing in a wide range, they change quickly, so it balances out. Still not in control (TIR) and StDev that I would like, but maybe the best a brittle diabetic with a big appetite can hope for.

      2 years ago Log in to Reply

    If you use a CGM, how did your A1c change in the first 6 months of use? Cancel reply

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