Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 14 hours, 52 minutes 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.
    • 14 hours, 54 minutes 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.
    • 14 hours, 55 minutes 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.
    • 14 hours, 56 minutes 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
    • 15 hours, 4 minutes 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 ´ )⎠⎞
    • 16 hours, 56 minutes 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.
    • 16 hours, 57 minutes 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.
    • 16 hours, 59 minutes 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 ´ )⎠⎞
    • 21 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
    • 23 hours, 2 minutes 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".
    • 23 hours, 47 minutes 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 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 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".
    • 1 day ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 1 day ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 1 day ago
      Lawrence S. 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 ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day ago
      Gary R. 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 ago
      ConnieT1D62 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, 1 hour ago
      eherban1 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, 12 hours ago
      NANCY NECIA 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, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day, 15 hours ago
      Anita Stokar 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, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
    Clear All
Pages
    • T1D Exchange T1D Exchange T1D Exchange
    • Articles
    • Community
      • About
      • Insights
      • T1D Screening
        • T1D Screening How-To
        • T1D Screening Results
        • T1D Screening Resources
      • Donate
      • Join the Community
    • Quality Improvement
      • About
      • Collaborative
        • Leadership
        • Committees
      • Centers
      • Meet the Experts
      • Learning Sessions
      • Resources
        • Change Packages
        • Sick Day Guide
        • FOH Screener
      • Portal
      • Health Equity
        • Heal Advisors
    • Registry
      • About
      • Recruit for the Registry
    • Research
      • About
      • Publications
      • COVID-19 Research
      • Our Initiatives
    • Partnerships
      • About
      • Previous Work
      • Academic Partnerships
      • Industry Partnerships
    • About
      • Team
      • Board of Directors
      • Culture & Careers
      • Annual Report
    • Join / Login
    • Search
    • Donate

    For insulin pump users: On average, how often do you take insulin using a different method other than through your pump? (E.g., giving an injection, using inhaled insulin, etc.)

    Home > LC Polls > For insulin pump users: On average, how often do you take insulin using a different method other than through your pump? (E.g., giving an injection, using inhaled insulin, etc.)
    Previous

    Do you have celiac disease in addition to T1D?

    Next

    If you use a CGM, at what blood glucose level is your “high” alert set? If you use multiple alert schedules, select the number that is your “high” alert at 3 p.m. in your time zone.

    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.

    Related Stories

    Advocacy

    Blue Circle Health: A Free Virtual Program Expanding Support for Adults Living with Type 1 Diabetes 

    Michael Howerton, 3 days ago 4 min read  
    News

    Thyroid Eye Disease (TED): What You Need to Know 

    Jewels Doskicz, 5 days ago 4 min read  
    News

    Immunosuppressants in T1D Research: Expert Opinions from Diabetes Pharmacist Diana Isaacs 

    Jewels Doskicz, 1 week ago 5 min read  
    2025 Learning Session

    The 2025 T1DX-QI Learning Session: Driving Better Diabetes Care 

    Sarah Howard, 2 weeks ago 7 min read  
    Lifestyle

    Barriers to Care in Aging: Voices from the T1D Community 

    Jewels Doskicz, 3 weeks ago 7 min read  
    Lifestyle

    When T1D Becomes a Calling: Stories From our Team 

    Jewels Doskicz, 4 weeks ago 11 min read  

    29 Comments

    1. Mary Ann Sayers

      ONLY when I haven’t gotten my CGM!!! (Because my pre-approval was delayed 10 days!!!) I tested bgs 12times daily to make up partially from the loss of not having a CGM!!!)

      2
      2 years ago Log in to Reply
    2. AimmcG

      I was in Ireland many years ago and pump broke. The cap that holds the insulin in place broke when I was replacing the cartridge. It was near the end of my trip and they wouldn’t be able to get me a new pump before I left 3 days later. I only had the quick acting insulin and a few needs. I was like a pin cushion for those days. I was anxious and ate very little. It was pre CGM too so my fingers hurt. A new one was at my home when I arrived

      5
      2 years ago Log in to Reply
    3. Lawrence S.

      I’ve been using an insulin pump since 1998. As far as I’m concerned, the pump is best method of insulin delivery that I’ve used. I said, “never.”

      2 years ago Log in to Reply
      1. William Bennett

        You’ve never needed a backup plan in case of a pump failure? I had the notorious “button freeze” with my old Paradigm not long after I started pumping and it took three days for a replacement to arrive. I was very glad I still had Lantus and Novolog injectors in my fridge, and I’ve made sure to get a new set of each every year for contingencies like this.

        1
        2 years ago Log in to Reply
    4. Jian

      Have done it once or twice in years when blood sugar very high and prior to going to the ER for
      some kind of gastritis. I gave some SQ

      2 years ago Log in to Reply
    5. Mick Martin

      I selected “Never”, but that’s not strictly true. It’s just that this was the closest option made available.

      I use an insulin injection whenever I get an unexpected ‘High’ value on my pump. I then look at what might be causing the high and remedy the situation.

      1
      2 years ago Log in to Reply
    6. William Bennett

      I have a script for Lantus and Fiasp injectors to use in case of pump failure. I’ve only rarely needed them for that reason, but I find the Fiasp pens very handy at times. Two uses that crop up a few times a year:
      -To bring down a stubborn high due to some issue yet to be determined.
      -To bolus for a meal when my reservoir is getting low but the timing for changing it is inconvenient

      I know some insurance carriers won’t cover injectors for pump patients, which sucks. Pumps are great, but they have FAR more failure points than MDI, and having a backup is critical.

      4
      2 years ago Log in to Reply
    7. Patricia Kilwein

      Recently had a code after an alarm on my insulin pump. Auto basal delivery stopped. Gave myself injection of insulin to cover, called medtronic helpline and they were able to walk me through getting it working properly again.

      2 years ago Log in to Reply
    8. Joan Benedetto

      My son, age eleven, has been on a pump for 9.5 years. If we have a stubborn BG over 200, we give a syringe correction. It’s just part of our management style, and our son prefers that as he does not like being “high”. We do this 2-3 times per month.

      2 years ago Log in to Reply
    9. ConnieT1D62

      I answered one or twice a year because that was kinda the best answer for my experience …
      Truth be told, it varies because I take injected insulin when pump catheter occludes or when I take a pump vacation, which I often do during the month of July. Right now I went off the pump about a week ago due to scar tissue build-up in my lower abdomen sites and have been using Tresiba and Fiasp pens with Dexcom on my phone. All is going well and I am injecting in my upper arms and thighs that provide “fresh flesh” territory.

      2 years ago Log in to Reply
    10. Lynn Smith

      I wear a pump for my basal. But for all meals, and any highs, I use Afrezza inhaled insulin. Works much better for me.

      2 years ago Log in to Reply
    11. Kathy Hanavan

      I use Humalog in my pump, but if I am high, I will use Lyumjev by injection to come down faster. I tried Lyumjev in the pump, but I developed redness and irritation at all of my sites in about 18 hours. I also have Toujeo for back up in case of pump failure which I have had to use twice now.

      1
      2 years ago Log in to Reply
      1. terrih57@msn.com

        I tried Lyumjev and it also caused a burning and Tandem informed me to only use hu along in the pump.

        2 years ago Log in to Reply
    12. Bob Durstenfeld

      I use Fiasp in a pen when I have a stubborn high. Usually of my own doing.
      Works great.

      1
      2 years ago Log in to Reply
    13. terrih57@msn.com

      I only use a pen or syringe if I think my pump is malfunctioning and I need a ‘quick fix’!

      2 years ago Log in to Reply
    14. Janis Senungetuk

      I’ll use an injection of Novolog to bring down a stubborn high over the 225 level. The Novolog in my pump takes far longer to make the correction.

      2 years ago Log in to Reply
    15. Marty

      I have a backup pen but I’ve never used it. I tend to drink a lot of water and exercise to bring down highs faster. I like the idea of using Afrezza but I’ve never seriously tried to follow through with my endo. I think she would encourage me to leave well enough alone 🙂

      2 years ago Log in to Reply
    16. Sarah Austin

      I will take an injection of Lyumjev to get a stubborn high down quickly. It works so fast while the Humalog in my pump takes forever to kick in

      1
      2 years ago Log in to Reply
    17. Stephen Woodward

      Afrezza works great.

      2 years ago Log in to Reply
    18. TEH

      In 20+ years of pumping I think I used a syringe to inject insulin only two times. The first time was when my 5 series Minimed stopped working and the Minimed overnighted me a new pump. The second time was when I did not have sufficent supplies when I switched from a Minimed 770G to my new T:slim X2 back in Febuary.

      2 years ago Log in to Reply
    19. KIMBERELY SMITH

      I use Dexcom ge

      2 years ago Log in to Reply
    20. Jneticdiabetic

      I’m in pump but inject a few times per month when I suspect site occlusion, have a stubborn high, or reservoir is running low and I don’t have time to change immediately.

      2 years ago Log in to Reply
    21. Mig Vascos

      the answer “occasional” was missing from the choices which would have been my answer.

      2 years ago Log in to Reply
    22. Molly Jones

      On average, I never take insulin with other methods besides my pump. I have a pen for Lantus and syringes in case of pump failure, which came in handy once before, some twelve years ago, but this is not an average occurrence.

      2 years ago Log in to Reply
    23. Amanda Barras

      If my pump is low but I am eating a meal and don’t want to hassle with a refill or if my blood sugar is high and won’t come down with boluses.

      2 years ago Log in to Reply
    24. George Lovelace

      1 Time in 5 years since I’ve been on the Tandem.

      2 years ago Log in to Reply
    25. Cristina Jorge Schwarz

      If I’m spiking due to a bad site, or food nutrition value was not advertised properly, I’ll give an intramuscular injection to quickly come down. I need to avoid migraines!

      2 years ago Log in to Reply
    26. Cheryl Weaver

      Several times a week, because I have absorption issues. I’m 78 now, and I’ve been Type 1 since I was 14 years old.

      2 years ago Log in to Reply
    27. T1D4LongTime

      My method is injected rapid insulin (Lyumjev). I chose multiple times per month, but this week it was multiple times per week. There seemed to be an issue with pump insulin delivery after it was at 60u or less in the cartridge. So weeks, I inject a lot and others not at all. Depends a lot on stress. Once BG goes high, many times even an injection won’t bring it down. Ugh!

      2 years ago Log in to Reply

    For insulin pump users: On average, how often do you take insulin using a different method other than through your pump? (E.g., giving an injection, using inhaled insulin, etc.) Cancel reply

    You must be logged in to post a comment.




    101 Federal Street, Suite 440
    Boston, MA 02110
    Phone: 617-892-6100
    Email: admin@t1dexchange.org

    Privacy Policy

    Terms of Use

    Follow Us

    • facebook
    • twitter
    • linkedin
    • instagram

    © 2024 T1D Exchange.
    All Rights Reserved.

    © 2023 T1D Exchange. All Rights Reserved.
    • Login
    • Register

    Forgot Password

    Registration confirmation will be emailed to you.

    Skip Next Finish

    Account successfully created.

    Please check your inbox and verify your email in the next 24 hours.

    Your Account Type

    Please select all that apply.

    I have type 1 diabetes

    I'm a parent/guardian of a person with type 1 diabetes

    I'm interested in the diabetes community or industry

    Select Topics

    We will customize your stories feed based on what you select here.

    [userselectcat]

    We're preparing your personalized page.

    This will only take a second...

    Search and filter

    [searchandfilter slug="sort-filter-post"]