Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 20 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.
    • 20 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
    • 21 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!
    • 1 hour, 3 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.
    • 2 hours, 26 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.
    • 4 hours, 24 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
    • 19 hours, 46 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.
    • 19 hours, 49 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.
    • 19 hours, 50 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.
    • 19 hours, 50 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
    • 19 hours, 58 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 ´ )⎠⎞
    • 21 hours, 51 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.
    • 21 hours, 51 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.
    • 21 hours, 54 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 ´ )⎠⎞
    • 1 day, 1 hour 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, 3 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, 4 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, 5 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, 5 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".
    • 1 day, 5 hours 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, 5 hours 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, 5 hours 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, 5 hours 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, 5 hours 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, 5 hours 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 ´ )⎠⎞
    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

    How often do you get bruises at injection sites or device sites?

    Home > LC Polls > How often do you get bruises at injection sites or device sites?
    Previous

    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?

    Next

    Do you currently use an insulin pump?

    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  

    26 Comments

    1. Molly Jones

      It has been a long time since I have bruised. I currently use a 6mm cannula and have not bruised since starting this nor did I bruise often/sometimes previous to this. It was rarely while using a syringe quite a long time ago.

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

      Never is my answer.

      3 years ago Log in to Reply
    3. karolinamalecki7@gmail.com

      I answered “sometimes” but it really depends on the site for me. My arms / back basically never bruise, my thighs sometimes, and my belly basically always. I avoid my belly bc it basically always hurts and bruises. This was true for both mdi & now omnipod.

      3 years ago Log in to Reply
    4. Annie Wall

      Often. Except for a two year vacation in 2019-2020, I’ve been on a pump for 25 years and infusion set sites have caused scarring. Though I had two years of no pumping, I’m back on the pump, using TruSteel instead of cannulas but I still bruise, though they’re mostly yellow. Still hunting for new places for infusion set sites. Frustrating.

      3 years ago Log in to Reply
      1. Bob Durstenfeld

        Try your hips and lower back. They add a few more sires to rotate and more time to heal.

        3 years ago Log in to Reply
    5. Joan Benedetto

      Only a few times in almost nine years. Never on Cgm sites, only pump sites, and most were from Medtronic Quickserter. My son has had only one or two bruises since we switched to steel insets six months after going on a pump.

      3 years ago Log in to Reply
    6. Jeff Balbirnie

      Device sites 100% every single time 🤬

      Injection sites very very rarely, only when I hit a capillary/get hit-nudged during the injection itself… ouch

      3 years ago Log in to Reply
    7. pru barry

      With tru-steel and Dexcom G6, almost never. Doesn’t make a lot of sense, because I’m usually covered in black and blue spots from just bumping into things. Think it must be old age…

      4
      3 years ago Log in to Reply
      1. Ahh Life

        I bump into things all the time. Including my wife. I am somewhat dangerous. And the blood thinners don’t help with the proliferation of bruises. Sigh!

        Injection & device cites? Machts nichts.

        1
        3 years ago Log in to Reply
    8. Bob Durstenfeld

      The only time I get bruises is when I leave a site in too long [my normal is 5 days].

      3 years ago Log in to Reply
    9. E24murph@gmail.com

      I have a pump and I do not inject any more. When I did inject I did bruise often.

      3 years ago Log in to Reply
    10. David & Kaleo of Team Nani

      I rotate w/ a bib/site marker that has 35 pump infusion spots and 10 cgm sensor/transmitter spots, so I am not using any sites more than 8 times a year, yet still I sometimes have a site that causes bleeding or is not effective (likely b/c workout causes disturbance or I leave infusion in for more than 3 days.
      Still, it’s always annoying when a site causes pain, bleeding or an irritated bump

      3 years ago Log in to Reply
      1. Lynn Smith

        I would like to know more about the bib/site markers that you use to mark injection sites. Could you please tell me more about that?

        1
        3 years ago Log in to Reply
    11. Karen Mason

      Often get bruises at the sites. But I am 79 years old so I get bruises from everything.

      2
      3 years ago Log in to Reply
    12. Ernie Richmann

      Bruises are the least of my worries. I am proud of all my bruises and scars – a roadmap of my active and sometimes risky lifestyle.

      1
      3 years ago Log in to Reply
    13. Janis Senungetuk

      Sometimes bruised and/or irritated sites on my abdomen from the cannula. I have limited reach because of arthritis in both shoulders and decades of using my thighs for MDI caused scarring. After 67 years of T1 I’m running out of useable sites.

      3 years ago Log in to Reply
    14. cynthia jaworski

      needles for my insulin pens are so sharp and so thin these days! As for my libre cgm, the inserted wire is almost invisible. A long time ago my answer would have been different.

      3 years ago Log in to Reply
      1. sweet charlie

        It sure was!!

        3 years ago Log in to Reply
    15. Lori Lehnen

      I bruise with Dexcom. I used to bruise with a 31 g 5 mm pen needle so I asked my endo for her recommendation to get rid of the bruises. She wrote a script for a 4 mm 32 g pen needle. I called my DME supplier and explained the bruises and she found one that was specifically designed for easier insertion (you can read this as, more expensive, but still 100% covered by insurance). I’m incredibly happy with the new needles. No bruises and it just slides right in.

      3 years ago Log in to Reply
    16. BARRY HUNSINGER

      I use a pump, I don’t get bruising, I get bleeding. Sometimes {alot} I hit a vein or capillary and when I change the quickset I get a gusher of blood.

      1
      3 years ago Log in to Reply
    17. Thomas Cline

      Never from the Dexcom CGM (though I can get temporary bleeding) but mostly on occasion from MDI injections through my shirt (no big deal though), perhaps because I jab with more force when I do that (and yes I know dr.s say not to, but I’ve had no trouble in 20 years of doing it — and it allows one to be discrete in public).

      3 years ago Log in to Reply
    18. Ms Cris

      I used to get bruised a lot from omnipod and tandem 90deg angle cannulas.

      But now I use the Varisoft manual insertion infusion sets – SO much better. I still hate how long the introducer needle is, but the results are worth it.

      3 years ago Log in to Reply
    19. KarenM6

      I bruise all the time but not every time.
      I once got such a spectacular bruise that I took a picture of it. Then there are “the gushers” that bruise after whichever device is removed.

      3 years ago Log in to Reply
    20. Andrea Hultman

      I suspect I have hypermobile Ehlers-Danlos Syndrome (hEDS); I bruise very easily.

      We suspect hEDS runs in our family — the side that has autoimmune diseases and cancers. My sister’s geneticist told us that connective tissue disorders (CTDs), autoimmune conditions, and cancers often are comorbid in family lines.

      3 years ago Log in to Reply
    21. persevereT1D52

      Sometimes I bruise from pump sites but always have pink swollen painful infusion sites. It is internal not adhesive caused. I use Tru-steel and change everyday due to this issue. 52 years with 30+ of pumping so I have many site issues. No one has ever narrowed it down to any specific reason other than long term pump use. No issues with CGM

      3 years ago Log in to Reply
    22. Cheryl Seibert

      Once in a rare while, I get irritation and redness but have not had bruising.

      3 years ago Log in to Reply

    How often do you get bruises at injection sites or device sites? 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"]