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    • 14 hours, 43 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, 39 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, 41 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.
    • 19 hours, 33 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, 49 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, 45 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.
    • 21 hours, 7 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, 21 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, 21 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, 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 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, 21 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, 16 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, 18 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, 19 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, 20 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, 21 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, 21 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, 8 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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    If you have ever had extra supplies from a device you no longer use, what did you do with those extra supplies?

    Home > LC Polls > If you have ever had extra supplies from a device you no longer use, what did you do with those extra supplies?
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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. Molly Jones

      I keep a few on hand in case they are needed, an older pump, basal insulin, syringes, …. The rest including other pumps and supplies have been donated to the hospital of my endocrinologist.

      3 years ago Log in to Reply
    2. kilupx

      I would love to donate them but when I have asked endocrinologist and diabetic educators to give insulin and sensors to a patient who really can’t afford them, the professionals tell me they are not allowed to suggest drugs and supplies that came from storage that could not be verified. I also tried to do this with my rheumatologist for rheumatoid arthritis medication and was given the same no answer. Such a shame.

      3 years ago Log in to Reply
    3. Ahh Life

      Current laws will dictate the shape of this graphic representation. If it’s acceptable, fine, so be it. If it’s not, then change your current political representation, not your individual behavior. I suspect, in this instance, that individual behavior matters little, even though I would individually give my eye teeth for a $750 bottle of insulin.

      3 years ago Log in to Reply
    4. Larry Martin

      I have all the leftover parts now from my 670G and I have called Endocrinologist, JDRF, Charities. No one wants them. It is sad we throw so much away in this country but there are people in need. I am sure big pharma has mandated it.

      3 years ago Log in to Reply
    5. Ernie Richmann

      I have given devices to a friend in a support group I attend. Opened or expired stuff I throw away. I gave a few pens of insulin to a relative using the same insulin. I have some unopened stuff I will donate to a diabetic camp if the camp accepts.

      3 years ago Log in to Reply
    6. Mick Martin

      I have given supplies, if they are still within their use by date, to my local Diabetes Centre, who ensure that they are redistributed to other patients that need them.

      3 years ago Log in to Reply
    7. Kathy Hanavan

      Insulin for Life will take supplies for those in need.

      3 years ago Log in to Reply
    8. connie ker

      I always give extra supplies to my endo practice to give to patients who could use them. For example, I don’t use a log book anymore, but some senior patients still prefer paper and pen to record readings. So my endo said “I am so glad to get these because I have requests all of the time for these books. I also donate diabetic magazines but you cannot give any RX in your name. Test strips do not have your name on the box, so those are OK for donation too.

      3 years ago Log in to Reply
    9. William Bennett

      Kept ’em. Because the Zombie Apocalypse could strike at any time, and you can’t be sure you’re not gonna need all that stuff. Including that ca. 1996 OneTouch.

      3 years ago Log in to Reply
    10. Tod Herman

      I gave my old G4 Dexcom sensors (2 boxes) to a friend’s dad who was still using the G4. In the past, the Nurse Practitioner at my primary care physician’s office was also a pumper and I gave her my old pump supplies. I still have some extras, but she no longer works there anymore. Some of these responses are giving me some ideas as to where to send them.

      3 years ago Log in to Reply
    11. Kristine Warmecke

      I’ve given them to T1D friends who used the device still, asked the group leader of the Diabetic Divas, support group of T1D women, to ask if anyone can use them, if still no home I ask my CDE if she can find home for them. I’ve also given extra’s to the local doctor’s group that goes to Honduras several times a year, they now have a permeant building with a year round clinic.

      3 years ago Log in to Reply
    12. Emily Meister

      I have supplies for the Animas pump but have been unable to find anyone that wants them.

      3 years ago Log in to Reply
    13. Jennifer Wilson

      Kept a few as backup. Donated extra to my endocrinologist to distribute to patients in need. Listed on community forum as free for anyone in need.

      3 years ago Log in to Reply
    14. Kathleen Begbie

      I asked my Endocrinologist who told me to toss them

      3 years ago Log in to Reply
    15. Mig Vascos

      I’ve saved some for “just in case” but could donate some other things. My endocrinologist office would not take them. I’ll try the divas that someone mentioned. It’s sad to throw supplies away that someone else needs when they are so expensive and hard to get sometimes.

      3 years ago Log in to Reply
    16. Marie Cardinell-Daldry

      The first time I had extra supplies was before the pandemic. I was able to give them to a charitable organization. When I recently had more insulin because my prescription changed I went to the same organization they refused the insulin because of the pandemic. The vials were completely sealed with excellent expiration dates. My daughter had a friend who was having trouble with the expense of insulin so he was quite happy to get the insulin.

      3 years ago Log in to Reply
    17. Becca Gae Leppanen

      I kept my Cozmo along with a month supply of disposables, I have a BNIB MM630g and 2 months of supplies but when I stopped using the MM I donated the 29 months or so of extra supplies I had left squirreled away. When I switched over from the OmniPod Eros to the Dash, I kept them for 5 months then gave them ALL away, kept none. I am soon to be giving away all the Medtronic supplies as well (pump included which is brand new in a sealed box.. DO NOT ASK ME FOR IT!! I will tell you no)..

      3 years ago Log in to Reply
    18. ConnieT1D62

      The diabetes education center where I used to work as a CDE accepted donated supplies unopened and in their original sealed packaging with an unexpired expiration date to pass on to Doctors Without Borders or given directly to patients in need. For awhile old Medtronic Revel pumps were being sought after by patients seeking older model pump parts to make their own loop system with a Riley link. We kept a current list of folks requesting supplies and notified those on the list if, and when, we had such a donation.

      3 years ago Log in to Reply
    19. Janis Senungetuk

      In the past I’ve donated insulin , meters and strips to Insulin for Life. Before the pandemic I donated meters and strips to a community senior center and Animas pump and G5 Dexcom supplies to people I’ve met through online groups.

      3 years ago Log in to Reply
    20. Cheryl Seibert

      Is there an organization that takes them? I’ve given a couple of individual sealed infusion sets and insert devices to my CDE but would love it if T1D would post organizations to take unused products to give to others who can’t afford them

      3 years ago Log in to Reply
    21. Jan Masty

      I tried to give away 3 BOXES of dexcom 5 sensors. Only got 1 response from someone who sounded a bit fishy. Wish there was a good place to donate them!

      3 years ago Log in to Reply
    22. Marie Seymour-Green

      I gave an extra glucose meter and strips to a friend whose cat had been diagnosed with diabetes. Their ears are used for getting the blood sample and she said that it didn’t bother him at all. 😉

      3 years ago Log in to Reply
    23. Leona Hanson

      I share with a friend when I get a new meter I give him my old one with strips and lancet device and lancets he can’t afford insurance so it helps him out and when the doctor changed his insulin he gave me that it was the same I used so it didn’t go to the trash

      3 years ago Log in to Reply

    If you have ever had extra supplies from a device you no longer use, what did you do with those extra supplies? Cancel reply

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