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    • 1 hour, 58 minutes ago
      Lenora Ventura likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 1 hour, 58 minutes ago
      Lenora Ventura 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 hour, 59 minutes ago
      Lenora Ventura 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?"
    • 3 hours, 11 minutes ago
      kristina blake likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 3 hours, 35 minutes ago
      Mary Coleman 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.
    • 3 hours, 37 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 3 hours, 48 minutes ago
      John Barbuto 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
    • 3 hours, 48 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 3 hours, 48 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 4 hours, 5 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 4 hours, 6 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 4 hours, 7 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 5 hours, 17 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 5 hours, 18 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 6 hours, 42 minutes ago
      mojoseje likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 18 hours, 38 minutes ago
      Neha Shah 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.
    • 20 hours, 38 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      My grandma told me u could never have kid. I had two successful pregnancies.
    • 20 hours, 39 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Oh my goodness… yes! As a child I was often reminded of my limitations because of diabetes. I’m hopeful that those misconceptions about T1D have changed over the decades.
    • 20 hours, 40 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Me too! 2kids and now soon to be 6 grandchildren. We just persevere, don’t we.
    • 20 hours, 40 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      I was diagnosed with t1 41 years ago. I was told to NOT have children. But I did not listen and had two healthy children.
    • 21 hours, 30 minutes ago
      Sarah Berry 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 ago
      René Wagner likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Oh my goodness… yes! As a child I was often reminded of my limitations because of diabetes. I’m hopeful that those misconceptions about T1D have changed over the decades.
    • 1 day ago
      René Wagner 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, 2 hours ago
      Bonnie Lundblom 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.
      Is there a formula for how much more insulin to take when getting a steroid shot?
    • 1 day, 2 hours ago
      Bonnie Lundblom 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.
      Dealing with wild bg swings.
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    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.

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    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

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