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    • 1 hour, 56 minutes ago
      Ahh Life likes your comment at
      How often does diabetes disrupt your sleep?
      Lows wake me up. The CGM alarm system kicks in if my body doesn’t. I will shut the alarm system off after I’ve treated the low because gastroparesis slows absorption and that alarm can continue needlessly for another hour until the is sufficiently corrected.
    • 1 hour, 56 minutes ago
      Ahh Life likes your comment at
      How often does diabetes disrupt your sleep?
      Diabetes doesn't necessarily interrupt my sleep per se. Its always the darn dexcom G7 losing signal at random waking me up.
    • 1 hour, 57 minutes ago
      Ahh Life likes your comment at
      How often does diabetes disrupt your sleep?
      Occasionally from lows - the biggest disruption is the every 3 day reminder to change my pump that goes off at 2am
    • 7 hours, 23 minutes ago
      Lawrence S. likes your comment at
      How often does diabetes disrupt your sleep?
      Lows wake me up. The CGM alarm system kicks in if my body doesn’t. I will shut the alarm system off after I’ve treated the low because gastroparesis slows absorption and that alarm can continue needlessly for another hour until the is sufficiently corrected.
    • 7 hours, 28 minutes ago
      Lawrence S. likes your comment at
      How often does diabetes disrupt your sleep?
      Occasionally from lows - the biggest disruption is the every 3 day reminder to change my pump that goes off at 2am
    • 7 hours, 28 minutes ago
      Lawrence S. likes your comment at
      How often does diabetes disrupt your sleep?
      Almost every night, my sleep is interrupted, at least 9 times out of 10 nights. My BG drops and the T:slim pumps insulin on the down slide until I get to 70 before it stops. It is, in my opinion, a flaw in the algorithm. I don't understand why the algorithm can see the continuous drop in BG. I have numerous screen captures of this situation. I have gotten into the habit of checking my BG right at bed time. Even taking some carbs at bedtime doesn't prohibit lows at night. It is literally exhausting.
    • 9 hours, 33 minutes ago
      Marty likes your comment at
      How often does diabetes disrupt your sleep?
      Diabetes doesn't necessarily interrupt my sleep per se. Its always the darn dexcom G7 losing signal at random waking me up.
    • 10 hours, 16 minutes ago
      D-connect likes your comment at
      How often does diabetes disrupt your sleep?
      Almost every night, my sleep is interrupted, at least 9 times out of 10 nights. My BG drops and the T:slim pumps insulin on the down slide until I get to 70 before it stops. It is, in my opinion, a flaw in the algorithm. I don't understand why the algorithm can see the continuous drop in BG. I have numerous screen captures of this situation. I have gotten into the habit of checking my BG right at bed time. Even taking some carbs at bedtime doesn't prohibit lows at night. It is literally exhausting.
    • 11 hours, 28 minutes ago
      atr likes your comment at
      How often does diabetes disrupt your sleep?
      Almost every night, my sleep is interrupted, at least 9 times out of 10 nights. My BG drops and the T:slim pumps insulin on the down slide until I get to 70 before it stops. It is, in my opinion, a flaw in the algorithm. I don't understand why the algorithm can see the continuous drop in BG. I have numerous screen captures of this situation. I have gotten into the habit of checking my BG right at bed time. Even taking some carbs at bedtime doesn't prohibit lows at night. It is literally exhausting.
    • 1 day, 6 hours ago
      KarenM6 likes your comment at
      Since starting on a CGM, has your healthcare provider’s frequency of ordering A1C testing changed?
      T1D comes with more than its fair share of dystopian grace notes. However, the indefatigable frequency of A1c testing seems to go on forever. I started with the Medtronic CGM dubbed "The Harpoon" in 2006. Tests and frequencies have not changed an inch in 20 years. (¬////¬)
    • 1 day, 10 hours ago
      Natalie Daley likes your comment at
      Since starting on a CGM, has your healthcare provider’s frequency of ordering A1C testing changed?
      T1D comes with more than its fair share of dystopian grace notes. However, the indefatigable frequency of A1c testing seems to go on forever. I started with the Medtronic CGM dubbed "The Harpoon" in 2006. Tests and frequencies have not changed an inch in 20 years. (¬////¬)
    • 1 day, 11 hours ago
      Lawrence S. likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      Often? Try Always! I only see my doc 1x a year to legally fill Rx. Otherwise I manage 100% on my own and make all my own dosing adjustments.
    • 1 day, 11 hours ago
      Lawrence S. likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      My pump and I use the data to make adjustments at every meal, and even during the day, e.g. corrections. But I also use the data to track longer term trends and usage so that I can make adjustments to my pump regimen, bolus rates, correction rates, basal rates etc.
    • 2 days, 7 hours ago
      Amanda Barras likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      My pump and I use the data to make adjustments at every meal, and even during the day, e.g. corrections. But I also use the data to track longer term trends and usage so that I can make adjustments to my pump regimen, bolus rates, correction rates, basal rates etc.
    • 2 days, 10 hours ago
      kristina blake likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      As noted by Lawrence, isn’t that what CGM’s are for? I’m on MDI’s and a SmartPen. Data is what determines my doses.
    • 2 days, 10 hours ago
      Marty likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      My pump and I use the data to make adjustments at every meal, and even during the day, e.g. corrections. But I also use the data to track longer term trends and usage so that I can make adjustments to my pump regimen, bolus rates, correction rates, basal rates etc.
    • 2 days, 11 hours ago
      Mike S likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      This is one of those times when I want to ask T1DExchange “what is the motivation behind this question”? What are you trying to learn from it?
    • 2 days, 11 hours ago
      Mike S likes your comment at
      Do you use your CGM data to help make adjustments in your diabetes management plan?
      As noted by Lawrence, isn’t that what CGM’s are for? I’m on MDI’s and a SmartPen. Data is what determines my doses.
    • 2 days, 23 hours ago
      Bekki Weston likes your comment at
      If you use a CGM, is it accurate on day 1?
      It takes a few hours to get close.
    • 2 days, 23 hours ago
      Bekki Weston likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      Usually when it's about to expire.
    • 3 days, 7 hours ago
      lis be likes your comment at
      How often do you adjust a planned physical activity because of how your glucose is trending?
      If I am above 150mg/dl don't need to carb up. If I am around 100mg/dl I definitely need to carb up. Aren't we always evaluating where we are and anticipating where we might land. That is part of active management.
    • 3 days, 10 hours ago
      Phyllis Biederman likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      For me it's compression lows - and that's it. I see that most complaints are about connection to phones. I don't (won't) use my phone. I have to have a work phone with me at least 60 hours a week, and I'm not interested in carrying (or wearing) two phones. I rarely lose connection between my Tandem X2 pump and the sensor/transmitter. Sometimes I will walk away while it's charging and take myself out of range, but that's on me.
    • 3 days, 12 hours ago
      Derek West likes your comment at
      What is the best spot for CGM accuracy
      Dexcom is ok with other locations if approved by your doctor.
    • 3 days, 12 hours ago
      Lawrence S. likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      1 and 2 days before its about to expire. It goes out of range several times those days. They should prescribe a 10 day CGM for every 8 days because on average, that is the use it seems we get.. and if you call to report it, you lose an hour on the phone!
    • 3 days, 12 hours ago
      Lawrence S. likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      It's a G7...one feature they added to the new version was random signal loss.
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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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    47 Comments

    1. Mary Dexter

      Their heads are stuck firmly in the sand, believing none of this exists and could never come into their lives.

      1
      3 years ago Log in to Reply
    2. Mary Ann Sayers

      My two daughters have no interest in being screened. But I recently learned that my brother was diagnosed with type 2—
      at age 77! I was dx with T1D at 7!

      1
      3 years ago Log in to Reply
    3. Kristen Clifford

      There should be another option for my answer, which is no one in my family has been screened, and I’m not sure if they’re interested.

      6
      3 years ago Log in to Reply
      1. KCR

        I agree and am in the same situation.

        2
        3 years ago Log in to Reply
    4. Patricia Dalrymple

      My family is aware I have it and probably any time blood work is done when there is something wrong with them, that is something the doctors look at anyway. I was unaware that my grandfather had T2 until I was diagnosed wit T1. My father was hypoglycemic but not diabetic. One thing I will ask them, though, is do they report when asked that there is someone in the family with it. But, they would not want to know ahead of time probably. I think there probably has to be a trigger. I had the gene but it was during a very stressful time at work that I got very rundown and I knew I had it before the diagnosis.

      1
      3 years ago Log in to Reply
      1. Louise Robinson

        I, too, developed Type 1 during a stressful period in my life. I was in my late 20’s in 1976 when diagnosed. My Dad had been dx’d in 1953 but back then, there was no differentiation made about the different Types of diabetes. To my knowledge, Dad and I are the only ones in my very large extended family who were dx’d with diabetes.

        1
        3 years ago Log in to Reply
    5. Louise Robinson

      I am estranged from my only living sibling. To my knowledge, I am the only Type 1 in my currently living extended family. My father developed diabetes in the early 1950’s while he was in his early 60’s. That was before distinctions were made about type of diabetes. He used U-40 Protomine Zinc insulin as I believe no other diabetes treatment was available back then. I’m not certain whether my cousins (mostly maternal side of the family) would be interested in testing for T1D antibodies. I do genealogy and have found diabetes listed as a cause of death for several distant relatives on my father’s side of the family leading me to believe that any genetic predisposition to diabetes emanates from my Dad’s lineage. (Mom lived til she was 98. Neither she nor any of her 14 siblings nor their offspring nor her parents had/have diabetes.)

      2
      3 years ago Log in to Reply
    6. Robert Wilson

      I did not know this was an option. None of my healthcare team ever mentioned this.

      1
      3 years ago Log in to Reply
    7. Katrina Mundinger

      I’m another one with family members who’ve not been screened. We’ve never discussed them getting screened, so I have no idea whether they’d be interested.

      1
      3 years ago Log in to Reply
    8. dholl62@gmail.com

      Daughter was tested 30 yrs ago not sure if that was this test , showed she was prone to diabetes , fortunately no Diabetes. Going to suggest to her to get children tested .

      3 years ago Log in to Reply
    9. pru barry

      My three children were tested decades ago. Don’t think my parents, brother, or any other relatives ever were tested. Thankfully, there’s a lot more testing being done now.

      3 years ago Log in to Reply
    10. Kathleen Juzenas

      I don’t remember hearing the term before. I’ve had a C-peptide test. After 40 yrs of living with T1d, Medicare required a C-peptide test to prove that I had T1d!

      1
      3 years ago Log in to Reply
      1. Patricia Dalrymple

        I’ve never been given one either and go into Medicare next year. I’m grateful for it but am anxious.

        3 years ago Log in to Reply
    11. cynthia jaworski

      How useful is the knowledge that one has a positive screening test? I have always been alert for signs/symptoms of T1 in family members, especially my son, and I even noticed and advised a co-worker prior to his official diagnosis. But how effective and available are prevention protocols? I do not know the answer.

      1
      3 years ago Log in to Reply
      1. Ms Cris

        With low level antibodies, they can now provide some therapies that can delay full onset several years.

        1
        3 years ago Log in to Reply
      2. cynthia jaworski

        Ms Cris: I assumed there must be some kind of action to be taken, but WHAT IS IT? Broad spectrum immune suppression? Back to the idea of administering small amounts of insulin to the not-quite-yet T1d? I haven’t seen anything in the news recently……I was hoping someone here might know.

        3 years ago Log in to Reply
    12. Lawrence S.

      Honestly, I was not aware of T1D autoantibodies screening. I’m not sure that I have been tested. If so, I am unaware. Most of my siblings are in their 60’s and 70’s, and if they have had it done, I am not aware. If not, I doubt they would be inclined at their ages. My daughter is in her 40’s, and I have no awareness of her medical procedures.

      3 years ago Log in to Reply
    13. Patricia Kilwein

      I marked “other” because of the cost. Insurance may not cover it.

      3 years ago Log in to Reply
      1. Patricia Kilwein

        I should add that my Dr explained to me the need to be tested and why. The stickler was if it turned out to be negative my ins would not cover the hundreds of dollars it costs to get tested. If it’s positive there’s no cost, my ins would cover 100% of costs. It was positive. T1D diagnosis went into my chart.

        3 years ago Log in to Reply
      2. Lynn Smith

        Just an FYI, Patricia. You can order an at home T1D antibody screening test online. Go to Enable Biosciences at https://T1D.medi-stats.com/landing to order. The kits are $55 each. I used these to screen my 2 grandkids.

        2
        3 years ago Log in to Reply
    14. Ms Cris

      I’ve asked my kids’ pediatrician to screen them once/year. He won’t, saying they have no symptoms. I try to explain the science…
      Other family, such as my sibling and nieces/nephews believe it’s unhelpful.
      So I’m thinking to go to the Benaroya Institute, where they’ll even do genetic screening as part of their autoimmune research.

      1
      3 years ago Log in to Reply
    15. Kristin Rosner

      My husband and I were too old to participate in the trialnet study when our daughter was first diagnosed 7.5 years ago. We had our son participate. This Spring his annual screening detected the first stages of diabetes. He has progressed to a clinical diagnosis over the summer. If we hadn’t been in the study he would have likely had a traumatic experience at overnight camp. Instead he had a healthy and safe summer. So sign up if you can. It might save you or another family from a traumatic diagnosis experience.

      1
      3 years ago Log in to Reply
    16. Lauren Carey

      No, as my diabetes is not hereditary (I’m the only T1D as far back as anyone can remember) and I do not have nor plan to have any children.

      1
      3 years ago Log in to Reply
    17. Joan Benedetto

      We had only one sibling (half) who qualified for testing via TrialNet while attending an FFL conference. No antibodies present.

      3 years ago Log in to Reply
    18. Kristine Warmecke

      This testing wasn’t available in 1972 when my younger brother was diagnosed, I was just watched closely, then diagnosed in 1982.
      My brother’s oldest daughter was diagnosed at 23 months old in 2004. A cord blood test was done on my middle niece a couple weeks later when she was born and my youngest niece 2 years later. My youngest niece is in the study until she is diagnosed.

      3 years ago Log in to Reply
    19. Maureen Helinski

      I did not get T1D until an adult and they said my family was not part of group they wanted to screen. No one has gotten it, thank goodness, but grandchildren have asthma and food allergies.

      3 years ago Log in to Reply
    20. Janis Senungetuk

      There’s a history of diabetes and auto-immune disease on both sides of my family. I was dx at 8 my maternal grandfather in his late 20’s or 30’s . When I asked my daughter to be screened and have her three kids screened she firmly declined.

      3 years ago Log in to Reply
    21. Drina Nicole Jewell

      I’m the first in the family to have been diagnosed back in 2000. I didn’t actually know about the antibodies testing until 2 yrs ago. By then, my middle son had been diagnosed and my youngest son as well. We discussed it with my oldest and he has no interest. He told us, if it came back positive his anxiety would destroy him always waiting for the proverbial shoe to drop.

      3 years ago Log in to Reply
    22. Diana L.

      I have surgical diabetes due to a distal pancreatectomy neuroendocrine tumor , it is not necessary for my family to test.

      3 years ago Log in to Reply
    23. Donald Cragun

      My parents are no longer with us, I am an only child and I do not have any children. There is no one to test.

      3 years ago Log in to Reply
    24. Becky Hertz

      My sister hasn’t been screened. I’m sure she would in the interest of science, but she ages out for Trial Net.

      3 years ago Log in to Reply
    25. Pauline M Reynolds

      My husband and children and I all have diabetes, except for one. That’s five of us with diabetes. As far as the next generation, it hasn’t popped up and the subject of getting tested has not come up, so I don’t know if they would be for it.

      3 years ago Log in to Reply
    26. ELYSSE HELLER

      I am adopted but do have a son. He has recently diagnosed with type 2 and am urging him to get screened. He does nothing but junk food though. I will keep persisting that he get screened.

      3 years ago Log in to Reply
    27. Mark Schweim

      If anybody else in my family has been tested or considered getting tested, I don’t know about it so am completely clueless when it comes to being able to give an honest answer to this question.

      3 years ago Log in to Reply
    28. M C

      My children are adopted, so not necessary for them to be tested. My sibling and his children (now adults also) have absolutely no interest in being tested.

      3 years ago Log in to Reply
    29. Yaffa Steubinger

      I have T1 so when one of my grandkids became a T1, the other 3 got screened. The brother of the one with T1 showed a likelihood of getting T1. Unfortunately, that test was accurate. Now my son has two T1 sons.

      3 years ago Log in to Reply
    30. Ben Weyhing

      My childfen snd grandchildren

      3 years ago Log in to Reply
    31. AnitaS

      My parents are in their 80’s so I doubt they would get screened. My sister and brother are in their 40-50s and I am sure they wouldn’t want to get screened. If type 1 symptoms arose, I would let them know to be tested for diabetes. I have tested my sister’s sugar before because she felt like she had low blood sugar. Her sugar level was in the mid 70’s. If my brother started showing symptoms, his wife and sister-in-law who are both in the medical field, would make him get tested for diabetes.

      3 years ago Log in to Reply
    32. ConnieT1D62

      No, none of my family members were ever screened for T1D autoantibodies. I was diagnosed in 1962, and my father, his younger sister and a 1st cousin on my maternal side were all diagnosed as adults in the mid-1960s with T1 LADA. Later my father and his sister died of Huntington’s disease in their early 50s. A maternal 1st cousin was diagnosed with T1 in her late 20s after having two children. Tragically she died at age 62 from a silent heart attack and severe hypoglycemia while she was swimming in a family pool.

      In my case, I am the last remaining member of my immediate family as I do not have children, nor grandchildren, nor nieces and nephews. I have several paternal cousins and second cousins who have died from, or currently have Huntington’s disease – two of whom have T2 diabetes. On my maternal side, three Baby Boomer second cousins have obesity driven insulin resistance or full blown T2D. None have expressed any interest in being screened for T1D autoantibodies for themselves or their extended family members.

      3 years ago Log in to Reply
    33. Milly Bassett

      I’m the first in my family to have T1. We went back as far as my great grandparents and no one had it. My father had 12 brothers and sisters, none had it. I don’t know about their children. My mother had 3 brothers and none had it. I don’t know about their children either. My grandparents on both sides, none had it. And my mom told me that her grandmother did not. My brother does not. My children do not and my grandchildren do not.

      3 years ago Log in to Reply
    34. Molly Jones

      I don’t think my immediate or extended family has been screened for T1D autoantibodies. I only have one sibling left in my immediate family. The maternal side of my family has variable autoimmune conditions and might be willing.

      3 years ago Log in to Reply
    35. Carolann Hunt

      Parents can’t be tested over age 45 😳

      3 years ago Log in to Reply
    36. Kim Murphy

      No one in my family has been screened and I don’t know if this screening is available where we live or if my grown children would want their kids screened.

      3 years ago Log in to Reply
    37. Wanacure

      Given that many T1D people here previously have answered that they were misdiagnosed, I wonder how many of our ancestors were unaware of their diabetes? I wonder how many of my distant relatives know that they are at risk? Someone’s cause of death might have been (or even today might be) listed as “heart attack” or “stroke” while the actual underlying cause was undetected diabetes.

      3 years ago Log in to Reply
    38. PamK

      Only my children have been screened (2 total). I don’t think any of my siblings have been.

      3 years ago Log in to Reply
    39. Andrea Hultman

      Only my sister qualified to be screened, and she has been.

      3 years ago Log in to Reply
    40. Cheryl Seibert

      No and likely not willing. 1 out of 2 of my immediate living family members is a minor so would need parent’s permission.

      3 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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