Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 1 hour, 8 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.
    • 1 hour, 8 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
    • 1 hour, 9 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, 51 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.
    • 3 hours, 14 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.
    • 5 hours, 11 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
    • 20 hours, 34 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.
    • 20 hours, 36 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.
    • 20 hours, 37 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.
    • 20 hours, 38 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
    • 20 hours, 46 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 ´ )⎠⎞
    • 22 hours, 38 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.
    • 22 hours, 39 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.
    • 22 hours, 41 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, 2 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, 4 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, 5 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, 6 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, 6 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, 6 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

    Before making changes to your insulin management, do you check with your healthcare provider?

    Home > LC Polls > Before making changes to your insulin management, do you check with your healthcare provider?
    Previous

    How comfortable do you feel giving injections, testing blood sugars and/or changing infusion/sensor sites in front of strangers (ex: at a restaurant, airport, on public transportation, etc.)?

    Next

    In your experience, what are the biggest barriers to accessing diabetes-related medical care? Select all that apply.

    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  

    22 Comments

    1. Ahh Life

      I pull the pin on the grenade I hold. I pull the strap on the parachute I use. I buckle the seat belt on the cars I drive. Why shouldn’t I put the changes in insulin doses? It’s my body. It’s my life. The experts and professionals have been advising me for 70 years. Sometimes their wisdom rubs off, even on us slow learners. ( ͡°👅 ͡°) ( ͠° ͟ʖ ͡°) ( ͡°👅 ͡°)

      5 years ago Log in to Reply
    2. Molly Jones

      I see my endo my often now and wait to discuss changes with her. I used to make these changes on my own more often.

      5 years ago Log in to Reply
    3. Grey Gray

      Self management… real time decisions… Too many variables to wait for a doctors opinion… sometimes I tell him about it. My body. My pump. If it weren’t for needing scripts I would probably never see the doctor.

      5 years ago Log in to Reply
    4. Janis Senungetuk

      Sometimes, depends on how drastic a change. I’ve only been using the Control IQ app for 5 months, so right now I hesitate to make any big changes without first asking my CDE what she thinks. Before starting with Tandem last June I often altered basil rates on my Animas Vibe on my own.

      5 years ago Log in to Reply
    5. Michelle Tepley

      Never.

      5 years ago Log in to Reply
    6. Patricia Dalrymple

      Agree with everyone: sometimes I do and sometimes I don’t consult with them. This really annoys me: they ask for my pump, make a change based on my numbers, hand it back to me with no comment. That pump is part of me. They wouldn’t touch me without telling me what they were going to do. Don’t grab at my pump. Tell me what you are doing and why. Sometimes they change things and I change them back. Funny part about that is they never seem to notice.

      5 years ago Log in to Reply
    7. HMW

      I make adjustments to my insulin to carb ratios as needed. Sometimes my endocrinologist makes suggestions when I see her. I let her tell me how to adjust my insulin sensitivity factor if needed.

      5 years ago Log in to Reply
    8. Amy Nance

      All on my own, my life and my body. If I contacted my diabetes specialist with every change I make, she would have time for her own life.

      5 years ago Log in to Reply
    9. Gene Maggard

      I do all the changes myself. I meet with my endo four times a year (apparently required by Medicare), and he and I discuss my TIR, my A1C, and he always asks me if I’ve made any changes in my basal and bolus settings. He sometimes makes suggestions based on my answers, but otherwise leaves it to me to make my own decisions.

      5 years ago Log in to Reply
    10. Chip Brookes

      In the legal profession there is a saying: “A person who represents himself has a fool for a client”. Treating diabetes yourself is analogous to the above. I regularly submit my data to my Endo so that he can make changes necessary.

      5 years ago Log in to Reply
    11. connie ker

      It depends on what the changes are before checking or not checking with your Drs. If you want to change insulins, or pumps, or size of syringes or medications – you need a script written by your health care provider. If it is a simple correction, you can do that without making an inquiry. Live and learn but controlling diabetes is a team effort for sure. I always see my Dr. with questions written down before the apt.

      5 years ago Log in to Reply
    12. Patty Harris

      I’ve only just started adjusting my basal rates up and down as they just don’t seem right since my stomach is emptying slower than it use it. I NEVER take insulin before a meal anymore as it seems to result in very low blood glucose up to an hour after eating. My endo just doesn’t seem to understand why.

      5 years ago Log in to Reply
    13. Britni Steingard

      Depends on the severity of the change. Changing my doses by 10-20%? I’ll do that on my own. Switching from MDI to pump or vice versa? I check with my doctor first.

      5 years ago Log in to Reply
    14. Jose Almodovar

      My Endo and I are on very good terms. Yes, I can make changes to my Basal rates without conferring but there are limits we have agreed upon.

      5 years ago Log in to Reply
    15. Becky Hertz

      I make small changes based on guidelines I’ve been given from my endo. I live with this 24/7 so should have some idea of what to do.

      5 years ago Log in to Reply
    16. Pat Reynolds

      I spend a _lot_ of my life in diabetes management. I have a PhD, so I know research … And the time involved … So I know that my doctor has both the skills and time to do the leading edge research (or at least follow it) which requires a knowledge and access to.paywalled resources that I don’t have. So I use him for that. The diabetes community is great for real.life experience of new tech, particular situations, etc.

      5 years ago Log in to Reply
    17. Stang777

      From day one of having this I have made my own adjustments as I have had to. If I had not made the changes on my own from the beginning is there is no way I would still be here as they started me off on way too much insulin and never had me call them with my levels or anything else. I learned to figure out what I need and just tell the doc at my appointment how much insulin I need the script written for. I have done well with it so only need to see my doc once a year to get scripts. I have gone in once or twice a year between visits for an A1c test but otherwise, only need the doc to write the scripts, which is all my appointments with them is for. In order to have good control, changes need to be made at the time the shots are being done, not continuing to do what doesn’t work well until one can have an appointment with a doc who is just guessing at how much one should do and setting a set amount to be done with no consideration for all the other factors that can go into making the determination of how much insulin one needs at various times due to various factors that are present at the time. In my opinion, when it come to diabetes management, docs are only needed for writing scripts.

      5 years ago Log in to Reply
    18. Sasha Wooldridge

      Just like many others have mentioned, I only use my doctor for prescriptions, authorizations, and tests. I had a good endo that would look at my information and discuss my BGs just to see if I needed any guidance, but he retired last year. Still on the hunt for a new endo that will write the prescriptions I need rather than what they decide I need.

      5 years ago Log in to Reply
    19. Daniel Bestvater

      I make all of my own insulin type and adjustments decisions. Things change day to day so it is important to be able to quickly adapt with basal and bolus changes for optimum control.

      5 years ago Log in to Reply
    20. Sherolyn Newell

      I only make changes occasionally and only after a couple of days of the same unexpected results. For instance, if the regular bolus leaves me high or low for a couple days in a row, I will adjust. Usually, I might have one bad day, but the next I go back to normal with no adjustments.

      5 years ago Log in to Reply
    21. Cheryl Seibert

      I usually don’t mess with basal patterns unless I review it with my endo. However, he is very open to my self-management. I will tweak carb ratios and frequently use the extended bolus for tighter control. Much of the spikes result from miscounting carbs and/or hidden carbs in home-prepared foods (I take care of an elderly relative and her food served is often made at home or by others). It can be a guessing game! LOL!

      5 years ago Log in to Reply
    22. Carlene Vaitones

      I do inform my doctor when I make a change, with a data sheet of BGs and notes to explain why I made a small change. I would consider it irresponsible to wait for a doctor to make a “hit or miss, trial and error” suggestion instead of taking care of myself.

      5 years ago Log in to Reply

    Before making changes to your insulin management, do you check with your healthcare provider? 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"]