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    • 1 hour, 13 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.
    • 11 hours, 55 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.
    • 13 hours, 22 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!
    • 13 hours, 22 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.
    • 13 hours, 22 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.
    • 15 hours, 35 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.
    • 15 hours, 36 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
    • 15 hours, 36 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!
    • 16 hours, 18 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.
    • 17 hours, 41 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.
    • 19 hours, 39 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, 11 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, 11 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, 11 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, 11 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, 11 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, 13 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, 13 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, 13 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, 17 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, 19 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, 19 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, 20 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, 20 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, 20 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.
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    Does proximity to your T1D health care provider impact where you choose to live?

    Home > LC Polls > Does proximity to your T1D health care provider impact where you choose to live?
    Previous

    If you have ever gone through the process of getting a prescription for a GLP-1 agonist (e.g., semaglutide, exenatide, dulaglutide, liraglutide, lixisenatide, etc.), how easy or difficult was the process of getting a prescription and obtaining the medication?

    Next

    Do you currently use any of the following insulin pumps?

    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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    24 Comments

    1. ChrisW

      No but that was due to ignorance. I assumed living 30 minutes outside of a city of 220K people would provide adequate healthcare options. I was wrong. Next time I move I will absolutely be checking for endos accepting new patients.

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

      NO was my answer. Living in a large Metropolitan area, many Endos to pick from. Actually, my Endo is in walking distance.

      1
      2 years ago Log in to Reply
    3. Jane Cerullo

      My T1D is under control. If I had to change Endo it would not be difficult

      2 years ago Log in to Reply
    4. Lawrence S.

      I answered “No”. But, really, “Yes.” Where I lived most of my life was a five hours, each way, drive to my Endocrinologist. Location to employment, housing, family and healthcare all play a part. As the saying go, it’s location, location, location.

      1
      2 years ago Log in to Reply
    5. Lori Lehnen

      With telemedicine, there’s a lot more options for finding an endocrinologist that’s a good fit.

      1
      2 years ago Log in to Reply
    6. beth nelson

      Yes, I wouldn’t move to a small town if there wasn’t a great endo I could easily relate to nearby. And with the amazing endo team I have now, I’d prefer to stay close to them. If I was to look for a new house, it would be within a 20 minute drive to my team!

      1
      2 years ago Log in to Reply
    7. Jen Farley

      My husband and I had conversations of when we retired moving to a Caribbean island. After looking at pharmacies and doctors we decided that would not be an option. A diabetic has to have healthcare nearby or it maybe a challenge.

      1
      2 years ago Log in to Reply
    8. Henry Renn

      I answered “no” bc we live in portion of PA where medical services are highly competitive. Availability of medical services for Type 1’s would be a consideration in the unlikely event that we would move.

      2 years ago Log in to Reply
    9. Trina Blake

      I’m a big city girl (an urban rat I guess) have been all my life. As has been said above – lots of Endo’s to choose from. Of course knowing who the good Endo’s are (and who the Endorks are) is important. When I’ve moved it’s been an arduous search. I’m doing well with my T1D mgt (great A1C – in the normal range, and high TIR, so telehealth works very well for me. If we didn’t need Rx’s for insulin and the prior authroization for just about everything, distance wouldn’t be the issue it is for many of us with T1D.

      0
      2 years ago Log in to Reply
    10. Marthaeg

      I said no because I moved from CT to Dallas a year ago. Unfortunately, I still haven’t found an endo in Dallas. Anyone have any recommendations? My endo back east is wonderful and I’ve been traveling back to see her quarterly but I really need to find someone in the Dallas area.

      2 years ago Log in to Reply
    11. Eva

      With zoom, it doesn’t as much. However, I do travel to see my endo. I just don’t trust anyone else. And, after 30 years, I know no one cares as much as his office about maintain and improving my health.

      1
      2 years ago Log in to Reply
    12. Becky Hertz

      It hasn’t in the past, but I’ve always lived in the suburbs close to abundant healthcare.

      0
      2 years ago Log in to Reply
    13. terrih57@msn.com

      I would not move to be close to my endo. I live in a rural area so it was years before I found one close. So I only saw my primary and my diabetes educator nurse until I found my current endo. I still have to drive a bit but it’s worth it and happy to have one in the ‘area’!

      1
      2 years ago Log in to Reply
    14. KIMBERELY SMITH

      She make sure Dietetic is on track

      2 years ago Log in to Reply
    15. Sue Martin

      We were considering moving from the Puget Sound to a warmer state. Proximity to health care was in the top three items of consideration. We decided not to move yet. I have excellent care at the University of Washington Medical Center and its clinics and would need that world-class care anywhere I might move to later. Besides T1D, I have had a kidney transplant, and have had a brain tumor removed. I would need care for all those aspects of my health.

      1
      2 years ago Log in to Reply
    16. Bob Durstenfeld

      I live 20 miles from my endo’s office. If I moved, I would want equivalent access to my doctor and other specialists.

      2 years ago Log in to Reply
      1. Stuart Pelcyger

        I am considering moving over 2 hours away from my Endo. Will travel to keep seeing her.

        1
        2 years ago Log in to Reply
    17. Sheri Marcus

      I have to drive an hour there and an hour back every three months because there is not one available in my area, Seneca, SC.

      2 years ago Log in to Reply
    18. NANCY NECIA

      My biggest consideration in deciding to move from a large urban area to a small city/rural area is availability of diabetes care. We have a second home two plus hours from my diabetes clinic. There is no diabetes clinics nor endos closer. Gives me pause to think of moving here full time.

      2 years ago Log in to Reply
    19. T1diabetic

      I have lived in rural areas most of the 51 years I have been T1D.
      I have never had optimal diabetes care due to there being no such thing as an endocrinologist or none close enough or none taking new patients.
      So I just do the best I can with my Primary Care Physician and my own research.

      1
      2 years ago Log in to Reply
    20. Janis Senungetuk

      I chose “no” because it hasn’t in the past…but, the times are changing. As my spouse and I age our dependence on healthcare has definitely increased. We live in an urban environment that includes several large medical/research centers with clinics. Even with the number of endos, finding one accepting new patients is now very difficult. If I had to rely on my GP, I’d be basically on my own with any pump/glucose management questions. So…it will be a consideration with our next move.

      2 years ago Log in to Reply
    21. Kristine Warmecke

      They somewhat do. While working as a travel nurse, I couldn’t find an endocrinologist who worked with insulin pumps in the good size city I was in. So I drove back to St. Louis, MO to see mine. After that I made sure that there would be one who worked with pumps before accepting an out of state assignment. This was 2015, so there should have been.

      2 years ago Log in to Reply
    22. AnitaS

      The opposite is true for me. I choose an endo who is relatively close to where I live. Will this be the case in the future? I really don’t know.

      1
      2 years ago Log in to Reply
    23. T1D4LongTime

      I answered “Other”. I was blessed that when I moved away from home after college, I married and moved to a city that had one of the top endocrinologists in the region. I’ve lived the same place for over 40 years. Proximity to a new healthcare provider would be a factor in choosing a retirement location.

      2 years ago Log in to Reply

    Does proximity to your T1D health care provider impact where you choose to live? Cancel reply

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