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  • Activity
    • 3 hours, 33 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.
    • 3 hours, 34 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.
    • 3 hours, 35 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.
    • 23 hours, 51 minutes 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 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 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, 3 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, 22 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 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, 1 hour 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, 3 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, 3 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, 19 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, 19 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, 12 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, 12 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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    When you see a stranger in public wearing a CGM or insulin pump, do you approach them?

    Home > LC Polls > When you see a stranger in public wearing a CGM or insulin pump, do you approach them?
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    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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    23 Comments

    1. George Lovelace

      I try to High Five and Flash my Pump or CGM

      3
      1 year ago Log in to Reply
      1. Kris Sykes-David

        Whenever I see anyone with a Dexcom or pump I comment, usually. The best time was a new neighbor out walking her dog. We have been good friends ever since!

        1
        1 year ago Log in to Reply
    2. Lawrence S.

      I would probably have answered, “yes, if at all possible.” However, I think I’ve seen another person wearing an insulin pump about 2 times.

      1 year ago Log in to Reply
    3. Amanda Barras

      I say hi and flash my pump or Dex if the opportunity presents. Lately people have spotted me before I have spotted them. Or, they want to start using Dexcom but want to ask me questions about it. I’ve been spotted in the wild 3x in last 2 weeks and I think that’s a new record.

      1
      1 year ago Log in to Reply
    4. Jim Andrews

      I would approach them if I ever saw anyone with a pump.

      1 year ago Log in to Reply
    5. Sherolyn Newell

      I haven’t noticed anyone yet. A mom came up to me once with her little T1D son. He was maybe around 3 or 4. She asked if I would talk to him and I was happy to.

      3
      1 year ago Log in to Reply
    6. AnitaS

      I have stopped one person I believe. She was my waitress. I saw a woman riding her bike on a walking/biking path but she was going quickly past me so I didn’t talk to her. I really didn’t have a reason to stop her just because I saw her CGM.

      1 year ago Log in to Reply
    7. RegMunro

      I would love to share charts with fellow sufferers. Stopping ways to learn when to cheat or anticipate lows would be great

      1 year ago Log in to Reply
    8. Joan Fray

      I’ve o ly seen one person wearing a pump, and it was at a wedding. And yes, I did. It was fun to compare notes. I’ve never met anyone who’s had diabetes as long as I have. I’d like to someday.

      1 year ago Log in to Reply
    9. KCR

      People have sure stopped to ask me! And I am happy to talk with them.

      1 year ago Log in to Reply
    10. rick phillips

      Some of the best convestations occur when I spot diabetes in the wild.

      7
      1 year ago Log in to Reply
    11. M C

      I wouldn’t think to intrude on their privacy. However, a funny thing happened when going through security at an airport in Ireland a few years ago. I was being asked what the white knob on my arm was, and before I could answer, someone in line further behind me shouted out; “It’s a CGM – to monitor blood sugar levels!” Found it very amusing!

      1
      1 year ago Log in to Reply
    12. Sue Herflicker

      I had a great conversation with my waitress about our Dexcoms. I did see a lady at the beach with hers but she was walking by too fast to start up a conversation. I have had people come up to me and ask about it because they are interested in getting one or know someone who has T1D. I was approached at a county fair about my pump, the young man was thinking of switching from mini med to tandem!! I seriously don’t mind talking with people who can relate to our situations. Its fun meeting new people. Oh yeah one last thing, an elderly gent actually touched my dex while we were standing in an elevator. That I did not appreciate!

      1 year ago Log in to Reply
    13. Bea Anderson

      If it is casually possible. Usually have positive response.

      1 year ago Log in to Reply
    14. Patricia Dalrymple

      About 4 times: once a young man came running up to me when he saw me use it saying he had just gotten his. He was so excited. I loved it. Once at a conference, I sat down next to a man. We both heard an alarm and reached for our pumps at the same time. It was his. We had a laugh. Once at a gelato store, a young child. I bumped elbows with her after showing her my pump. And once at a bar but it wasn’t a good time to talk. But I love meeting others.

      1 year ago Log in to Reply
    15. Janis Senungetuk

      If at all possible I’ll attempt to introduce myself and have a conversation.

      1
      1 year ago Log in to Reply
    16. LizB

      I have never seen anyone wearing a pump or CGM in the wild. 5-6 years ago at work there was a new person who used a Dexcom. The only reason I knew was because his brother also worked there and he told me. I asked my co-worker if he also used a pump but he said he didn’t like having two things attached to his body so he gave up the pump when he started using the Dexcom.

      1 year ago Log in to Reply
    17. Marla Peaslee

      I was recently at our local recreation center and my Dexcom G6 alarm sounded. I was immediately surrounded by 3 women, of various ages, asking if I needed help. They were all Dexcom users and one woman had the same pump as I do. I didn’t need help but I was very appreciative of their caring response to my alarm going off and I meet 3 new individuals in the process.

      3
      1 year ago Log in to Reply
    18. ConnieT1D62

      Sometimes – depends on the situation. I have actually made some good heart to heart connections with people wearing a pump and CGM – in airports, on planes, in restaurants, standing in a check-out line, or at the post office. It feels like we are from the same tribe and even though we are meeting for the first time, we feel a camaraderie and totally get each other.

      1
      1 year ago Log in to Reply
    19. dgmarrero

      met a young man at my health club pool where we were both swiming laps. He wore his Dexcom on the back of his arm where I have never tried. Interesting chat!

      1 year ago Log in to Reply
    20. Lucia Maya

      it’s been rare, but I’m always super excited and happy to connect with someone with a pump! just happened on a flight, sitting next to another type one – was fun getting to chat for a bit about it, and she was younger and pregnant, and was happy to hear how long I’ve lived with it, had healthy pregnancies, etc.

      1 year ago Log in to Reply
    21. Cheryl Weaver

      No. But if they look like they are in trouble with low or high blood sugar, I would approach them to help them.

      1 year ago Log in to Reply
    22. mbulzomi@optonline.net

      In my five years as a Docent at the American Airpower Museum, Farmingdale, LI, NY, I have only met two persons waring a pump. We had a very interesting conversation when I told them I have been using a Pump for over 39 years (T1D for over 55 years) and on a CGM for over nine years. What startles them is when asked is telling them my age (77), along with all the traveling I did when I worked all over the Country/World. (FAA). I just changed my Pump time on my very long trips as I passed thru the time zones. This lessens a big insulin infusion/too small insulin infusion.

      1 year ago Log in to Reply

    When you see a stranger in public wearing a CGM or insulin pump, do you approach them? Cancel reply

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