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    • 4 hours, 57 minutes ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 6 hours, 44 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 6 hours, 45 minutes ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 6 hours, 45 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 7 hours, 43 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 7 hours, 44 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 7 hours, 45 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 7 hours, 48 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 7 hours, 50 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 8 hours, 4 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 10 hours, 38 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 11 hours, 11 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 11 hours, 28 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 11 hours, 29 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 11 hours, 29 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 12 hours, 56 minutes ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 19 hours, 57 minutes ago
      Sandy Norman likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 3 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 3 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 3 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 5 hours ago
      Kristi Warmecke likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 8 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 10 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 1 day, 11 hours ago
      John Barbuto likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      I have been using a insulin smart pen for the last 2 years; I find that it meets my current needs to ensure good management and results
    • 1 day, 12 hours ago
      Lawrence S. likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
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    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?

    Home > LC Polls > 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?
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    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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    33 Comments

    1. Wanacure

      The only close family member is a paternal cousin. She isn’t even interested in getting her DNA tested because “it may reveal some bad disease tendency.” She has children and a grandchild who could be tested. Her older sister and her cousins (me & my brother) all had/have T1D by age 15.

      2 years ago Log in to Reply
    2. Wanacure

      I answered “Other” because I DO wish my cousin & her offspring WOULD get screened for antibodies.

      2 years ago Log in to Reply
    3. Kathleen Begbie

      Several family members have been diagnosed with T1D or T2D

      2 years ago Log in to Reply
    4. Gary Rind

      my siblings & parents are older (like me) and they’ve never expressed any interest in getting tested. my nieces and nephews have never said anything either

      1
      2 years ago Log in to Reply
    5. Lawrence S.

      No. As far as I know, no one in my family has been tested for T1D autoantibodies. I don’t believe any of us has ever thought of it. Also, I don’t know what purpose it would serve. I am 70 years young. My siblings are around my age. My daughter, neices and nephews are all grown and scattered around the USA.

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

        Also, no one else in my family has T1D.

        2 years ago Log in to Reply
      2. Wanacure

        But, Lawrence, how can you or they be sure until they’re tested for antibodies?

        2 years ago Log in to Reply
    6. HMW

      My family (parents and sibling) participated in a study around 30 years ago before screening was something you could request.

      2 years ago Log in to Reply
    7. Kristen Clifford

      First of all, I’ve said it before, and I’ll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of “I have not discussed antibody screenings with my family,” which is the category under which I fall.

      4
      2 years ago Log in to Reply
      1. Samantha Walsh

        Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D.
        We do offer “No, my family members have no been screened” as an option.
        We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions.
        All the best,
        The T1D Exchange team

        6
        2 years ago Log in to Reply
    8. pru barry

      Just my children, all grown and all clear:*)!

      2 years ago Log in to Reply
    9. Chrisanda

      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.

      1
      2 years ago Log in to Reply
    10. William Bennett

      I have a huge extended family–siblings, cousins, kids and grandkids–and afaik no one else has it, with the exception of my first cousin’s daughter. I was told at diagnosis back in 1983 that T1 doesn’t necessarily track in families the way T2 does, and that certainly seems to be true in my case. So it doesn’t really seem necessary.

      2 years ago Log in to Reply
      1. Wanacure

        William, that was then. This is now! Please read Samantha’s reply to Kristen! 😎

        2 years ago Log in to Reply
    11. Richard Vaughn

      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday.
      I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives.
      I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.

      1
      2 years ago Log in to Reply
      1. Wanacure

        Richard, why not suggest they be tested to be sure? Why not let them make the decision? ❤️😎

        2 years ago Log in to Reply
    12. KCR

      My brother and I have never talked about this.

      2 years ago Log in to Reply
    13. Kristine Warmecke

      Only my 2 youngest niece have been screened, middle born about a month after my oldest ones diagnosis. Their Dad & I both have have T1D.

      1
      2 years ago Log in to Reply
    14. Yaffa Steubinger

      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who’s the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.

      1
      2 years ago Log in to Reply
      1. Wanacure

        Aha! So the test was an accurate predictor? Did the doctor (s) suggest any preventive course of action?

        2 years ago Log in to Reply
    15. Karen DeVeaux

      No and no because I got T1D at 47 years old from a virus.

      2 years ago Log in to Reply
    16. Janis Senungetuk

      I’ve previously answered this question. My daughter and my three grandchildren, who are now in their 20’s, have no interest in being screened. I asked them when screening first became available and have repeated my request as my grandchildren grew into their teens. They refuse.

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

      I was genetically screened and found to have monogenic Type 1 Diabetes. Not caused by antibiotics, but a gene defect. So does my eldest of three sons and his eldest of two daughters.

      2 years ago Log in to Reply
      1. Wanacure

        ❤️ Good on you for trying, Janis. So often we humans make decisions based on emotions, like fear, not rationality. I guess Freud was on to something. 😎

        2 years ago Log in to Reply
      2. Wanacure

        I wonder how many of us T1Ds have been tested for monogenic diabetes? Theoretically couldn’t this be treated by CRISPR?

        2 years ago Log in to Reply
    18. Mick Martin

      I have 1 brother that was also Type 1 … sadly, no longer with us; 2 first cousins that are both Type 1, and 2 brothers that are Type 2.

      0
      2 years ago Log in to Reply
    19. Jana Wardian

      I’ve not discussed this with family members.

      2 years ago Log in to Reply
    20. Becky Hertz

      I’m sure my sister would be screened, but she ages (64) out of most past screening requests.

      2 years ago Log in to Reply
    21. Molly Jones

      I chose other as I don’t know what family was defined as (extended or primary) and my desired answer was not available.
      I know my brother, the only primary family remaining, would have little interest, but I am unsure of extended family members.

      2 years ago Log in to Reply
    22. AnitaS

      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin’s 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.

      0
      2 years ago Log in to Reply
    23. Anne Mueller

      In my immediate family, both my son and I are T1D’s. After my son was diagnosed, his older sister was tested for the antibodies, but she didn’t have them. My husband has neve been tested, and neither have my siblings. I have a sister who was diagnosed as Type 2.

      2 years ago Log in to Reply
    24. Joindy23

      As a T1D, if I had children I’d have them screened-but I have none because when I was child-bearing age (20+ years ago), it felt too dangerous. My brother and sister (in their 50s & healthy) don’t seem interested and are presumably safe from T1D at this point.

      2 years ago Log in to Reply
    25. T1D4LongTime

      No, none of my close family has been screened. I have one natural-born son and he has only 1 child. He will not agree to screening (he’s an adult so his decision). My granddaughter is now 18 and can decide for herself if she wants screened. She may be willing.

      2 years ago Log in to Reply

    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? Cancel reply

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