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  • Activity
    • 9 hours, 57 minutes ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 11 hours, 53 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 11 hours, 55 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 14 hours, 46 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 15 hours, 2 minutes ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 15 hours, 59 minutes ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 16 hours, 20 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 11 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.
      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...
    • 1 day, 16 hours 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.
    • 1 day, 16 hours 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.
    • 1 day, 16 hours 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.
    • 2 days, 12 hours 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.
    • 2 days, 12 hours 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.
    • 2 days, 13 hours 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.
    • 2 days, 13 hours 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
    • 2 days, 16 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.
    • 3 days, 11 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
    • 3 days, 13 hours 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
    • 3 days, 14 hours 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
    • 3 days, 14 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.
    • 3 days, 14 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
    • 3 days, 15 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
    • 3 days, 16 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!
    • 3 days, 16 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
    • 4 days, 3 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.
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    When purchasing a new smartphone, do you consider the phone’s compatibility with T1D devices and apps?

    Home > LC Polls > When purchasing a new smartphone, do you consider the phone’s compatibility with T1D devices and apps?
    Previous

    If you were diagnosed with T1D as an adult, on a scale of 1-5, how easy or difficult was it to find an endocrinology clinic near you? (1 = the easiest, 5 = the most difficult)

    Next

    How do you handle unsolicited advice and judgements about T1D from family and friends?

    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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    21 Comments

    1. Wanacure

      Yes, I did AND I REGRET IT.

      1. I had to pay more.

      2. Transmitting your personal medical info (easily hackable) via WiFi or the internet can violate your privacy resulting in higher insurance costs.

      3. I want my doctor to see the good, bad and ugly of my lifestyle and blood glucose levels. With a smartphone, you can” “adjust” your blood glucose readings. This is a very self-defeating choice IMHO.

      If your doctor gives you bad advice on objective readings, FIND ANOTHER DOCTOR. TRYING TO FOOL YOUR DOCTOR IS NOT IN YOUR BEST INTEREST.

      1
      2 years ago Log in to Reply
    2. connie ker

      I know I am certainly in the minority, but I bought my first mobile phone in 2019. Being a senior with T1D, I decided to start simple and purchased a Jitterbug Flip phone for seniors. The larger buttons, ease of use, and a 5Star alert button all seemed good options for me when I am out. When I am home, I use this laptop and landline phones. The contract for the Jitterbug flip is $14.99 plus the tax and surcharges = $22 a month. I can take pics, unlimited texting, and 250 minutes monthly, but no DATA.

      2 years ago Log in to Reply
    3. Clare Fishman

      I am using my phone to Loop so it does a lot more than just be a phone for me. It is command central for all insulin delivery.

      1
      2 years ago Log in to Reply
    4. Larry Martin

      T1D devices should be required to be compatibile with EVERY smartphone. T1D controls enough of our lives. If these companies do not care enough to be universal, screw them! It’s my life. My choice.

      2
      2 years ago Log in to Reply
    5. Jenn Velez

      That’s my first thought when buying a smartphone.

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

      I use my phone to see my CGM readings, count my steps (and stair climbs), and hold other health data. The calendar alerts me to doctor visits and other important appointments. Sometimes it seems that actually using it as a phone is secondary. I also now have an Apple Watch which delivers all that to my wrist, meaning I don’t have to continually pull out my phone. Even better. I believe in embracing the technology, because every new innovation helps me improve my life.

      3
      2 years ago Log in to Reply
    7. Sue Martin

      I brought a phone then returned it since it didn’t allow my DexCom app. I am glad that I did. Same with a smartwatch.

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

      I spent an extra $100+ to buy a Samsung Galaxy A71 5G phone. I downloaded the Dexcom G6 app. I tried it for about 1 1/2 months. During that period, my transmitter signal got lost between 8 and 32 times per day. I worked with Dexcom technical staff and Tandem technical staff. We could not figure the problem. They replaced numerous sensors, two or three transmitters, and finally tried a new Tandem X2 pump exchange. I finally figured out that the Dexcom G6 app was causing the problem. When I turned off the G6 app., all of my problems went away. So now I get my readings from my pump. My Dexcom receiver is not working (went through several of those). They are too expensive to keep replacing. Medicare won’t pay for another one for 5 years. I went through a lot of expense, and stress with no benefit from using the phone app.

      1
      2 years ago Log in to Reply
    9. kristina blake

      I answered no. Two reasons: First my TAndem pump and Dexcom are integrated, I can see my bg on my pump, and take whatever action I need to. It is also easy to upload to my computer on TConnect and the data goes to the Endo’s office. Second, I choose phones for my partner and I that are similar to the ones we are replacing (we are android phone folks) and let’s just say he is a painter and sculptor, well-versed in centuries old technology – moving into the 21st century kicking and screaming. The second reason is that I don’t always want to have to carry the (damned) phone with me. Don’t know if it’s cuz I was on call 24/7 at times while I was working or what, but I have a sense of freedom when the phone is at home and I’m not! The pump is connected to me and my clothing. I don’t have to carry anything else.

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

      I’ve always used an iPhone, so I don’t worry. It seems everything uses iPhone.

      2 years ago Log in to Reply
    11. Kristine Warmecke

      No, but I use iPhones. Mostly because I can take all business info with me, so I’m not tied to being home to run it. I try to use the tConnect app, when it stay’s connected, so I don’t have to worry about uploading to my laptop, and my endocrinologist has access to real time readings.

      2 years ago Log in to Reply
    12. George Lovelace

      iPhone

      2 years ago Log in to Reply
    13. Patricia Kilwein

      I have minimed 770g. The minimed app works great with my Samsung phone. Just bought Samsung s20.

      2 years ago Log in to Reply
    14. Janis Senungetuk

      Yes, that’s the primary reason. I also control my hearing aids with a phone app.

      2 years ago Log in to Reply
    15. Brad Cohen

      This question and it’s answers are a bit misleading. Yes, I consider it but wouldn’t not buy an iPhone because the new omnipod doesn’t have an app for it yet.

      2 years ago Log in to Reply
    16. betsy valian

      for something this important… I use the receiver for the CGM exclusively.

      1
      2 years ago Log in to Reply
    17. Sarah Berry

      I have not in the past but will be with future purchase.

      2 years ago Log in to Reply
    18. Beth F

      Currently use a phone that is not “Dexcom-approved” and found a developer to make it work anyway. Dexcom and phone companies/software shouldn’t be determining this stuff anyway. There’s almost always a work-around. I feel safer with a receiver since there’s only bluetooth to keep the data local to the device.

      2 years ago Log in to Reply
    19. Molly Jones

      I chose yes, as I had only had one inexpensive mobile phone before using Dexcom, but it was necessary to purchase an iphone unless I wanted to carry along another medical device provided by Dexcom. The cost was very shocking. I think they have expanded their compatible phones now.

      2 years ago Log in to Reply
    20. Donna Owens

      This was the first time I considered T1D devices/apps when purchasing a new smartphone; but it wasn’t a primary factor in my decision.

      2 years ago Log in to Reply
    21. PamK

      I always check to see if the phone is compatible with my Dexcom.

      2 years ago Log in to Reply

    When purchasing a new smartphone, do you consider the phone’s compatibility with T1D devices and apps? Cancel reply

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