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    • 20 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, 8 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, 50 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, 17 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, 17 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, 17 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, 30 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, 30 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, 31 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, 13 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, 36 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, 33 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, 13 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, 13 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, 15 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, 15 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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    Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?

    Home > LC Polls > Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
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    If you have T1D, have you ever dated or married someone who also has T1D?

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    Have you developed lipohypertrophy due to repeated injections/infusions of insulin? Lipohypertrophy is a term to describe hardened lumps of body fat just under the skin that resulted from repeated insulin injections/infusion sites. If so, share how you’ve handled lipohypertrophy in the comments!

    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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    38 Comments

    1. Becky Hertz

      My provider does not have T1. Only someone with it can truly understand the various daily challenges and worth it takes to manage this.

      4
      3 years ago Log in to Reply
    2. Gerald Oefelein

      My diabetologist is a type 1 diabetic himself, using the s:slim x2 and G6 as I do.

      3 years ago Log in to Reply
    3. Patricia Kilwein

      My endocrinologist is also T1D.

      3 years ago Log in to Reply
    4. Kathleen Juzenas

      I said yes but that refers to my nurse practitioner who sees me every other visit, if not more often. The doctor may know how hard I try but perhaps takes my efforts for granted.

      1
      3 years ago Log in to Reply
    5. Ernie Richmann

      I have no clue what my T1D health care provider understands about my daily challenges and I don’t know about his daily challenges either. Not sure why I should care as long as I have access to information how to best take care of myself.

      1
      3 years ago Log in to Reply
    6. TEH

      My Endo and PA definitely understand. My GP not so much.

      3 years ago Log in to Reply
    7. James Phelps

      Yes my NP definitely understands what living with diabetes is like because she also lives with t1 diabetes so she understands all the ups and downs living with this disease so when I had a bad day and going over numbers she is like I know I have them too.

      3 years ago Log in to Reply
      1. Mig Vascos

        Both my endocrinologist and my nurse practitioner are great. They compliment me on the way I take care of my life and health and make aure I get all the supplies I need managing all the paperwork Medicare and insurance requires.
        My nurse practitioner who works with me on managing the pump has her own opinion about the pump settings based on her technical knowledge which is different than what I do with my settings based on living with them. She has thru the years learned to respect what I do and is surprised with how my settings work. So we are now at peace.
        Both very supportive.

        1
        3 years ago Log in to Reply
    8. Lawrence S.

      I answered “Other.” You are asking about my feelings about my healthcare provider’s understanding of my daily challenges? I have no feelings about what my healthcare provider understands. I cannot know what she understands about my daily challenges.

      My opinion is that my provider is very knowledgeable in the field of Endocrinology. She provides me the information I need to continue dealing with my disease. She occasionally provides information about new technologies and treatment, as I also provide her with information that I have found . She has no awareness of my “daily challenges,” or the thousands of other patients she sees. And, I am unaware of her daily challenges.

      I hope this is an appropriate response to your question.

      1
      3 years ago Log in to Reply
    9. Lisa Moir

      The last two providers I’ve had, that have spanned over 25 years, have both also had T1D. They didn’t share much personal stuff beyond the fact that they had diabetes and what technology they used, but it was comforting to know they were experiencing the same challenges as me.

      3 years ago Log in to Reply
    10. Jeanne McMillan-Olson

      My endo also has T1D. He is a full professor and does lots of research on T1D. I’m very fortunate to have had him as my doctor since 1993.

      3 years ago Log in to Reply
    11. Georgina Sokol

      How can someone without the disease really understand what it is to live with it? I have never had a doctor with T1D in 60 years.

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

      None of my endocrinologists or NPs have had T1D but I always discuss my challenges and they are incredibly helpful. What I always find astonishing is they are constantly amazed at how well I’m doing even when i don’t think I’m doing that well because most of their patients have nowhere near the A1c’s I’m able to achieve. And just hovers in the 6’s!

      2
      3 years ago Log in to Reply
    13. Jian

      My endo is young, very empathetic, thorough, always asks for my input, and does research. I am blessed too. have him, and the one before for over 25 yrs.

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

      Yes. However, for those of you who assert, “It takes one to know one,” the same might be said of age. Geriatrics is a marvelous array of marvels.

      3
      3 years ago Log in to Reply
    15. Kristine Warmecke

      Mine acknowledges the struggles and challenges that go along with managing T1D in my daily life. She gives suggestions as to what may or may not help and has often asked me I how I handle situations so she can give suggestions to other T1D patient’s.

      1
      3 years ago Log in to Reply
    16. Greg Felton

      My endo has T1D

      3 years ago Log in to Reply
    17. Jane Cerullo

      I am an RN. Been going to same doctor for about ten years. Took me six years to train him. I am very well read when it comes to my LADA. He trusts my judgement and gives me excellent parameters to make decisions. Recently had a bad case of Covid. Insulin needs changed dramatically. Getting back to normal but he made sure I had scripts to cover my ups and downs with insulin needs.

      1
      3 years ago Log in to Reply
    18. NANCY NECIA

      Very much so! He is T1D since 15 years of age!

      3 years ago Log in to Reply
    19. Lynn Smith

      Yes, as well as anyone without T1D can understand.

      3 years ago Log in to Reply
    20. terrih57@msn.com

      My current endo is very understanding and seems to get all the struggles. I have had some in the past that thought they were but…actions speak louder

      3 years ago Log in to Reply
    21. Tracy Jean

      My nurse practitioner understands so much! I really appreciate her.

      3 years ago Log in to Reply
    22. Abigail Elias

      I think my endo does, though it’s not usually a focus of our discussion, other than the usual variations in highs and lows with no particular pattern and often no identifiable cause. The last time I had an appointment my pump failed at my endo’s office during the data download, and they heard the end of my discussion with customer support to get a replacement. So we had an unplanned discussion logistics for insulin delivery while I waited for the replacement pump, and they rushed through the visit a bit so I could get home to implement Plan B for insulin delivery. My comment was: “welcome to a day in the life of someone with T1D.” They were empathic, but not so much as to prevent thinking through and discussing options.

      3 years ago Log in to Reply
    23. Chrisanda

      My PA has had T1D since she was 7, so she definitely understands!

      3 years ago Log in to Reply
      1. Donal Conway

        My Diabetes Consultant is new in the post, but she is young and seems to be very up to speed in everything regarding Diabetes, she has a good attitude and is very complimentary towards my good HbA1c results and because I have T1 Diabetes for 53 years now, she says you don’t come with that knowledge and good management process without doing the right things. That compared to the previous Consultant who was older and out of fashion with technologies etc and never complicated the patient when they got things right. Some diabetes care staff including some Doctors still don’t understand how difficult it is for us people with the condition Diabetes to avoid the lows & highs and get the balance right.

        3 years ago Log in to Reply
    24. Sue Martin

      My Edro and their staff are very understanding.

      3 years ago Log in to Reply
    25. pru barry

      We are all so very different, and trying to say that all of us with T1 understand what it’s like for another who has the same hill to climb is unproductive. Having a health care provider with T1 may often be helpful just because there’s apt to be more knowledge
      about the specifics. How we respond to the disease is such a personal matter, that I really don’t think there are any guaranteed benefits beyond the grasp of the factual. Finding a doc with the same general attitude about the disease does feel good, and sometimes that’s all I hope for after working hard to make peace with the disease for 70 years.
      Asking my doc to “get it” used to be almost my mantra, but I’ve come to realize that the ones who don’t just see us as unruly childrenchildren

      1
      3 years ago Log in to Reply
    26. anj1832

      One time I was explaining that a new pump would be too expensive at the time because my deductible had just started over.. and she asked if I had insurance and I said yes….. then she said “then it should be free with insurance.” 🤦‍♀️ She may know a little about the challenges of living with diabetes, but she knows nothing about how insurance works or how costly T1D supplies are.

      1
      3 years ago Log in to Reply
    27. Cheryl Weaver

      They know because of working with us. But they personally haven’t experienced it unless they are also type 1. No one can really understand unless they also have type 1.

      3 years ago Log in to Reply
    28. Steven Gill

      I’ve seen 5 endocrinologists, 3 general practitioners, 2 eye doctors, 3 educators (or at least nurses in the field). Only 3 times did a physician seem to understand the daily concerns. The first doctor at my diagnosis (25 years ago) admitted no knowledge but “we can learn together.” My eye doctor discussed cravings of food, waking up high or low, and “hiding” diabetes. The doctor at those medical trials. All the others looked at lab works, gave generic “textbook” responses.

      Thus I now see a general practitioner now who normally sends all his TYPE 1’s to a clinic, he handles it all.

      3 years ago Log in to Reply
    29. PamK

      My current endo seems to understand at least a little better than my previous doctors. The best endo I ever had definitely understood. He had T1D!

      3 years ago Log in to Reply
    30. ConnieT1D62

      Some do, sometimes.

      One in a while a sensitive and caring HCP will empathize with kind and reassuring words because some are trained to do that. However, IMHO unless they have T1D themselves most really don’t understand and get it. They can go home at the end of a diabetes care work day, or retire after a career in diabetes health care. They don’t live with it 24/7/365 for the rest of their lives.

      3 years ago Log in to Reply
    31. Emily Meister

      My endocrinologist has T1D

      3 years ago Log in to Reply
    32. Nicholas Argento

      I am my own diabetes doc, though I have a PCP. They I need for the rest of my healthcare, not T1D. I think it is impossible for someone who does not either have T1D or live w someone who has T1D to fully grasp the lived experience it entails. But those HCP’s that listen and engage can offer meaningful help and advice.

      3 years ago Log in to Reply
    33. Carlie Trepanier

      My endo not so much – I like him and I feel like he’s the most up to date on the technology compared to other endo’s I’ve had, but I don’t feel like empathy is there. My diabetes educator though is a T1D herself so I really feel like she gets it!

      3 years ago Log in to Reply
    34. Wanacure

      I would not be surprised if my endo or any other doctor treating me felt frustrated with me or other T1Ds. I would not be surprised if they blew off steam by secretly making disparaging or sarcastic comments. There are reckless T1Ds in complete denial of their condition. When an occasional patient comes along who’s well-informed and well controlled, the doctor may be defensive. I noticed this when I brought in an extensive study showing the risks of taking daily baby aspirin outweighed the advantages. But after reading the medical journal article online, the doctor stopped prescribing it for me.

      3 years ago Log in to Reply
    35. Patricia Dalrymple

      Never even gets discussed. I am controlled with A1C 5.7-6.2, no other health issues although I have gone on a statin recently and cholesterol dropped from 226 to 133. Last labs showed hypothyroidism so I expect I’ll get medication for that next week. Since I feel I am under control and am very active in my own health decisions, I don’t feel stressed about it and don’t feel a need to talk to him about it. I am blessed: fairly good genes, weight under control, good job, good health coverage, no money concerns, therefore, worry us at a minimum. I don’t have children. I feel for everyone with many stressors. I’m sure having T1D along with even 1 other issue can be difficult.

      3 years ago Log in to Reply
    36. Jeff Balbirnie

      Nurse Practitioner 100,000%. The doctor, not a freakin clue (on any level).

      3 years ago Log in to Reply

    Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D? Cancel reply

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