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    • 14 hours, 6 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.
    • 16 hours, 2 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.
    • 16 hours, 4 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.
    • 18 hours, 55 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.
    • 19 hours, 11 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.
    • 20 hours, 8 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.
    • 20 hours, 29 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, 15 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, 20 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, 20 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, 20 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, 16 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, 17 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, 17 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, 17 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, 20 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, 15 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, 17 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, 18 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, 18 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, 19 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, 19 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, 20 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, 20 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, 7 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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    In which room(s) of your home do you keep your diabetes supplies? Select all that apply.

    Home > LC Polls > In which room(s) of your home do you keep your diabetes supplies? Select all that apply.
    Previous

    If you wear a CGM and share your data with people (ex. Dexcom Follow or Medtronic’s Carelink Connect), with whom have you shared your CGM info? Select all that apply.

    Next

    When your pump or CGM sites feel irritated or uncomfortable on your skin, do you change your site or wait for the session to be over?

    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. Carol Meares

      I wait for CGM to expire because insurance won’t allow me to get additional CGMs. For infusion sites I use a Tru Steel for TSlim. The trusteel I can take out and prepare another location to insert the same one. I only go 2-3 days with it, so it works just fine. The worst part with either CGM or infusion site is whether it is a bleeder or I get it too close to a rib or other bone, or something like hitting a nerve. A bleeder, dexcom will replace. Most bleeders I have found to work after a couple days but have to calibrate a lot during that time from pump requests. I take baby aspirin daily. I get annoyed with the new Dexcom insertion that wakes me up with wild numbers that make no sense either high or low, and invalidated with finger pricks. But overall, Dexcom is the very best and I look forward to the G7 and easier access and smaller. I have had very few replacements in the overall scheme of things, I think. Perhaps 2-3/year. I don’t know. Is that high? A little less than 10%. Hmmm

      3 years ago Log in to Reply
    2. Carol Meares

      The comment above was supposed to go to a different question. Don’t know how that happened, sorry

      3 years ago Log in to Reply
    3. Pat Reynolds

      Don’t worry, Carol. Something at t1d exchange has broken – emails no longer link to the correct questions!

      3 years ago Log in to Reply
    4. Ahh Life

      Other. Closet next to secondary bathroom. Why or why are closets not listed? Also in there are towels, pillow cases, other medicines, old Christmas wrapping paper, USB rechargers, spare eye glasses, pill boxes, appliance instructions, cough drops and other absolutely delightful curiosity items. Some closet, that one. (>‿◠)✌

      3 years ago Log in to Reply
    5. Anthony Harder

      Other – I keep insulin I’m not currently using in the basement fridge.

      3 years ago Log in to Reply
    6. Britni Steingard

      Kitchen: insulin, sharps container, snacks Bedroom: mores snacks plus syringes, strips, lancets, spare meters, spare inject-eases, extra glucagon kits, glucose tablets, simpatches… all the spare stuff, basically Living room: test kit (logbook, calculator, and inject-ease plus syringes, lancets, and strips for the day) and CGM sensor (at least while I’m home and not I’m not out and about)

      3 years ago Log in to Reply
    7. Shannon Barnaby

      Other than insulin, I keep other supplies in a hall closet.

      3 years ago Log in to Reply
    8. Mick Martin

      I keep insulin and glucagon kits in the refrigerator in the kitchen. The rest of my supplies, such as sharps container, blood glucose test strips, Beta-ketone test strips, lancets, glucose tablets, insulin set changes, CGM supplies, log books, batteries, USB chargers, etc. are kept in my bedroom.

      3 years ago Log in to Reply
    9. connie ker

      I keep a stash of supplies in an upstairs bathroom, and bring them downstairs by packages as needed. I keep all cgm supplies in a downstairs closet, and all insulin is kept in the refrigerator, even the vials in use. This is kind of a personal question, you just do what works for you with your floorplan and living arrangements. If you want something to pray about today, think of the type 1 diabetics living in Texas this week without power, heat, water, food and security. The pictures are horrifying and I can’t help but think of the insulin dependent diabetics.

      3 years ago Log in to Reply
    10. MARIE PEELER

      First floor hall closet, near kitchen.

      3 years ago Log in to Reply
    11. Amanda Barras

      Bathroom and hall linen closet.

      3 years ago Log in to Reply
    12. mwmeganwolff@gmail.com

      I use a shelf in my closet for things I use often (meter, insulin pens in use currently, pen needles) and a drawer below with extra supplies and other items and extra pens in the kitchen fridge.

      3 years ago Log in to Reply
    13. Ceolmhor

      In addition to storing the bulk of my supplies and equipment in the master bathroom, I keep a two-month supply in a downstairs storage room in an emergency evacuation tub prepared for my car. I rotate the supplies through there so nothing goes out of date.

      3 years ago Log in to Reply
    14. Sherolyn Newell

      Insulin in refrigerator in kitchen. Omnipods, G6 sensors in bedroom closet. Alcohol wipes in a candy box on table by sofa, because I usually sit there to change stuff. Lancets and test strips in a decorative box in dining room, only reason is because that’s where the box is.

      3 years ago Log in to Reply
    15. Gene Maggard

      Although I only take one fingerstick test a day on average, I have glucose meters in the kitchen, bedroom, and “one for the road” (travel). My other supplies (pump and CGM) I keep in the bedroom closet. Keeping a set of everything in the basement in case of emergency (like a tornado, we live in the south) is a great idea and one that I’ll implement immediately.

      3 years ago Log in to Reply
    16. Megen Blackburn

      Between my insulin pump, CGM, and related belts, cases, adhesive tapes, and insulin coolers for travel, I keep my supplies in cloth storage cubes in my closet. There are way too many pieces of my diabetic supplies to keep them in my limited bathroom or kitchen cabinets.

      3 years ago Log in to Reply
    17. Carol Meares

      I answered other. It should have been bedroom and bathroom.

      3 years ago Log in to Reply
    18. Molly Jones

      I keep all insulin in the fridge besides the next full cartridge to use which is in a closed bag on the kitchen counter. All other diabetic supplies are in their specific shelf I have in a hall closet with other shelves for other supplies: medications, colostomy supplies, and bath room supplies.

      3 years ago Log in to Reply
    19. Ann Taylor

      My youngest sons’ bedroom (he’s 34 now) has become my “medical room”. I have a cute desk I keep wipes, test strips and other odds and ends. Plus lots of pictures of my grandkids. I remember when I first started using the Dexcom G5 I would watch videos of my grandson. Made it a lot easier. Then I keep my supplies of pods and sensors and used sharps, etc in the closet. That’s a good idea about keeping supplies in the basement. We have tornados here in the Midwest too. I keep my bag on the kitchen table that has my testing supplies in it

      3 years ago Log in to Reply
    20. ConnieT1D62

      Most diabetes supply stuff is kept in a hallway linen closet between the dining room and living room. Spare injectable hormone replacements not currently in use (Novolog, Victoza, Fiasp, Basaglar) are stored in the fridge. Glucagon supplies are kept in the linen closet, as well as an up-to-date grab & go diabetes stuff supply kit. The few oral meds I take everyday are kept on a countertop in the kitchen.

      3 years ago Log in to Reply
    21. Debbie Knowles

      I had an extra Tupperware divided vegetable/dip serving tray. It has 7 compartments. I keep it on my kitchen counter. Separate sections for needles, lancets, alcohol swabs, enzyme pills, blood tester, meter, test strips, etc. Extra insulin in fridge. Extra supplies in my living room, in a drawer and cabinet at one end of my entertainment center.

      3 years ago Log in to Reply
    22. Chris Deutsch

      Both of our cars

      3 years ago Log in to Reply
    23. Leona Hanson

      I live in an rv I keep my supplies in the cabinet over the couch in the living room insulin in the fridge and what is use in the day in my purse

      3 years ago Log in to Reply
    24. Sally Numrich

      I also use the linen cabinets outside my bedroom. Everything is I. There except for the whole shelve I. The refrigerator for all my supplies that need to be refrigerated. My emergency kit is always in this cabinet right outside my door. Easy to grab if I have to run out of the house.

      3 years ago Log in to Reply

    In which room(s) of your home do you keep your diabetes supplies? Select all that apply. Cancel reply

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