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    • 17 minutes ago
      Steve Rumble likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 3 hours, 5 minutes ago
      Donna Owens likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 13 hours, 48 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 15 hours, 14 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 15 hours, 14 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 15 hours, 15 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 17 hours, 27 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 17 hours, 28 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 17 hours, 29 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 18 hours, 11 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 19 hours, 34 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 21 hours, 31 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 1 day, 12 hours ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 day, 12 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 1 day, 12 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 day, 12 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 1 day, 13 hours ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 14 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 1 day, 14 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 1 day, 15 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 19 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 21 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 21 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 22 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 22 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
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    Recent advancements in insulin pens have led to the availability of “smart” insulin pens, pen caps, and other attachments with higher tech features compared to standard insulin pens. Do you currently use any of the following smart insulin pens/caps, or smart attachments?

    Home > LC Polls > Recent advancements in insulin pens have led to the availability of “smart” insulin pens, pen caps, and other attachments with higher tech features compared to standard insulin pens. Do you currently use any of the following smart insulin pens/caps, or smart attachments?
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    What type of health insurance do you have?

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    If you are an adult with T1D, does someone you live with know how to give you emergency glucagon? (This might include any type of glucagon that you’re prescribed).

    Sarah Howard

    Sarah Howard has worked in the diabetes research field 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 Marketing Manager at T1D Exchange.

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    18 Comments

    1. RegMunro

      My smart pen cap records when last I removed the cap.
      Great when memory fails to record whether or not I’ve injected. At 80 I previously often forgot and either under or double injected
      Don’t know trade name. Have to rediscover when stops working

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

        I put the needle caps into a French yogurt jar and write the dose in my paper logbook. To determine whether I took the dose, I count the caps.

        2
        3 years ago Log in to Reply
    2. Mary Dexter

      The battery in my Novopen Echo is dead, so it’s not smart anymore. Still works better than the Medtronic InPen

      3 years ago Log in to Reply
    3. Jane Cerullo

      Ditched the pump a year and half ago. Omni pod too expensive on Medicare and tired of tubing. InPen covered under part D. Not sure why not under part B as it lasts a year. So I pay a copay. Phone app shows all the info that a pump does. Also have an Iport which I change every three days. Can give my insulin doses through this device to eliminate poking skin multiple times.

      1
      3 years ago Log in to Reply
      1. Annie Wall

        Interesting to read about the port. that was not available when I was using the InPen. If I need another pump vacation (from scarring), I would go with the InPen.

        3 years ago Log in to Reply
    4. Annie Wall

      I am not using it now, I took a “pump vacation” for two years and used the InPen (before it was bought my Medtronic.) I liked using the InPen and appreciated the software that let me track so much and that worked with Dexcom. For that brief period of time, I enjoyed the freedom of not having the pump attached to me. I used the pen until I learned about Tandem and control IQ so I am now tethered to a pump again but doing very well.

      3 years ago Log in to Reply
    5. james zellerhoff

      I use a Companion In Pen
      Not aware of any “advanced features”
      Jim Z

      3 years ago Log in to Reply
    6. cynthia jaworski

      I would love to augment my insulin pen. Haven’t looked into it properly.

      1
      3 years ago Log in to Reply
    7. Trina Blake

      I haven’t used a pen in about 15+ years. But I have heard of the smart pens and am intrigued – especially if I need to take a pump vacation. Am I correct that they not only track your latest bolus and IOB?

      1
      3 years ago Log in to Reply
      1. Sue Martin

        Yes, they track your bolus and IOB, which I find very helpful. The app also will give you recommendations for injections depending on your i/c ratio. My doctor like to view this report along with my DexCom report.

        3 years ago Log in to Reply
    8. Kris Sykes-David

      I love my InPen! Admittedly, I didn’t realize there were other choices for MDI. I recently went on Medicare and kept our BC/BS Federal, we’ll see how things come out in the wash! It is very frustrating trying to figure out the best way to order supplies.

      1
      3 years ago Log in to Reply
    9. Natalie Daley

      I never heard of any of these, and I doubt that my insurance would pay for them, especially after the $35 insulin law.

      3 years ago Log in to Reply
    10. TomH

      I tried the Malaya during a T1_Dexi exercise study; it may have been me as new user, but didn’t accept a couple of readings and didn’t fit particularly well on my pens. I contacted the study and advised I didn’t want to continue its use . Also tried the Novo Echo, because it allowed for 1/2 unit dosing, it wasn’t as “smart” as I had hoped and I moved on to use Omnipod Dash pumps with DIY Loop. I haven’t looked back, but realize some people can’t afford, insurance doesn’t cover, their jobs/part of the world doesn’t have, or they just don’t want a pump.

      3 years ago Log in to Reply
    11. Bill Williams

      Is anyone aware of a comparison study that looks at these devices?

      2
      3 years ago Log in to Reply
    12. Cristina Jorge Schwarz

      I used the NovoPen Echo early in my diagnosis, when I was still MDI. The half unit increments were crucial because I am so sensitive. I keep it for my emergency backup should my pump fail, and for muscular injections. I love it.

      3 years ago Log in to Reply
    13. qachemist

      Not only to I not use “smart” devices but I deeply resent the assumption on the part of my physician and device providers that I would want to. I do not stay tethered to my phone 24/7 and given the prevalence of hacking, I have real security concerns.

      1
      3 years ago Log in to Reply
    14. mbulzomi@optonline.net

      Been on and Insulin pump since 1983 and using a CGMS,
      for over 11 years.

      3 years ago Log in to Reply
    15. Wanacure

      I’m ignorant of these options. Maybe my diabetes tech team will alert me.

      3 years ago Log in to Reply

    Recent advancements in insulin pens have led to the availability of “smart” insulin pens, pen caps, and other attachments with higher tech features compared to standard insulin pens. Do you currently use any of the following smart insulin pens/caps, or smart attachments? Cancel reply

    You must be logged in to post a comment.




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