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    • 3 hours, 24 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.
    • 3 hours, 29 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
    • 3 hours, 29 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.
    • 5 hours, 34 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.
    • 6 hours, 17 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.
    • 7 hours, 29 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, 2 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, 6 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, 7 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, 7 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, 3 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, 6 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, 6 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, 7 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, 7 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, 19 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, 19 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, 3 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, 6 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, 8 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, 8 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, 8 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.
    • 3 days, 8 hours ago
      Meerkat likes your comment at
      Over the past week, what percent of the time have you been within your glucose target range?
      Around 95%
    • 4 days, 4 hours ago
      lis be likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      It’s usually at the end of my sensor session. Day 8 or 9
    • 4 days, 4 hours ago
      lis be likes your comment at
      When I have a temporary signal loss with my CGM, it’s usually when I’m:
      I tried to answer all of them but it wouldn’t let me. Or maybe my answer should be-for no apparent reason. It happens any time from day five on with no particular reason.
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    If you have T1D and have a child under the age of 18 who has not been diagnosed with T1D, at what age would you start screening your child for T1D autoantibodies?

    Home > LC Polls > If you have T1D and have a child under the age of 18 who has not been diagnosed with T1D, at what age would you start screening your child for T1D autoantibodies?
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    If you or your child had T1D while in school, were your blood glucose (BG) levels typically impacted during tests or exams?

    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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    19 Comments

    1. Lenora Ventura

      Both of my boys are now over 18 but I had them tested when they were 7. They tested negative for the antibodies which gives me tremendous peace after what I went through when diagnosed. Thankful they have been able to test for this.

      4 years ago Log in to Reply
    2. Jneticdiabetic

      I was able to screen both my boys through the TrialNet study at our local JDRF walks, rich read super convenient. Both negative.

      4 years ago Log in to Reply
      1. Jneticdiabetic

        *which was

        4 years ago Log in to Reply
    3. Mick Martin

      I selected “N/A – I do not have T1D and a child under age 18 who does not have T1D” but I did fingerprick tests, especially on my eldest son as he was growing up.

      This was so long ago that antibodies and antiautobodies wasn’t spoken of.

      4 years ago Log in to Reply
      1. Mick Martin

        Oops! I’ve just noticed my error there. It should, of course, have stipulated autoantibodies and NOT antiautobodies.

        More fool me for getting it wrong. Sorry.

        4 years ago Log in to Reply
    4. Amy Jo

      I selected “I would not….” but honestly didn’t know this was an option. Is it only happening in the context of clinical trials? Or are physician offices performing these tests upon request?

      4 years ago Log in to Reply
    5. Vivian Moon

      I have had T1D for 50 years.
      I have 2 children and neither are T1D.
      There was no such test when they were young and I never even thought of their becoming T1D.
      I was diagnosed after having mononucleosis.

      4 years ago Log in to Reply
    6. Lyn McQuaid

      I have a 19 year old and a 15 year old and have just kept a sharp eye on them for symptoms over the years and so far, so good. Not sure I’d want to know about the antibodies, which I suppose may be an ignorant choice but it is the one I’ve made.

      2
      4 years ago Log in to Reply
    7. Karen Newe

      T1D can occur at any age. I was diagnosed at age 51. None of my 1st or 2nd degree relatives meet protocol for TrialNet testing. Since we have autoimmune diseases in my family I encourage my relatives to get tested. https://www.jdrf.org/t1d-resources/t1detect/

      1
      4 years ago Log in to Reply
    8. Cheryl Seibert

      I DO have T1D, but my child is now 40 years old. When he was under 10, I was told that giving small amounts of insulin may prevent a future T1D diagnosis. I refused that option. He is still healthy and does not have diabetes.

      4 years ago Log in to Reply
    9. Chris Albright

      While I chose 1-3 (toddler), I would still perform a test with a glucometer earlier just for the peace of mind.

      1
      4 years ago Log in to Reply
    10. Greg Felton

      I participated in a research study and had both kids screened at birth. Both screened negative, and I still have the letter from the clinic telling us our kids could not participate; it was the best rejection letter I have ever received! Both kids were later screened as toddlers and again tested negative. Lucky so far.

      4 years ago Log in to Reply
    11. Drina Nicole Jewell

      I was diagnosed at 18. My middle son diagnosed at 2, now 17. My youngest diagnosed at 9, now 12. I didn’t know about the screening so neither had them done, nor did my oldest who is now 18. Now it’s his choice and he is aware and chooses not to. Had I known, I’d have started in the beginning of their toddler years 💯

      4 years ago Log in to Reply
    12. PamK

      I wish there was a choice for “Other” on this question, because that is what I would have chosen. I have T1D and I have children who have not been diagnosed with T1D. Both were tested for autoantibodies when they were younger, but they are now adults. So, the question doesn’t really fit our family, which is why I chose “N/A.”

      4 years ago Log in to Reply
    13. Lynn Smith

      I had my son screened in his teenage years. That was 27 years ago and the test was negative.

      4 years ago Log in to Reply
    14. dave hedeen

      I’m 69 and both my daughters were screened at ages 1-3

      4 years ago Log in to Reply
    15. Amanda Barras

      My son is 13, I just ordered a test kit. Just gotta talk him into taking it. He hates needles so I’m grateful he’s been healthy this far.

      4 years ago Log in to Reply
    16. ConnieT1D62

      I have T1D and do not have children. However, if I did have children I would have them screened for autoantibodies at age 3 to 5 years and then again every few years. Type 1 runs in my paternal lineage, but others have not been diagnosed with it until their young adult or middle adult years. You never know when a dormant gene for T1D will surface. I am the only one who was diagnosed as a child at age 8.

      4 years ago Log in to Reply
    17. Coy Kouba

      My 18-yo daughter has T1d and we also have a 14yo son and a 20yo daughter, but we have not had the other 2 screened. Question – what would you do if the result came back showing they’re likely to also get it? There really isn’t anything that can be done to keep them from becoming T1d right? Is there any treatment that can delay or prevent T1d onset??

      4 years ago Log in to Reply

    If you have T1D and have a child under the age of 18 who has not been diagnosed with T1D, at what age would you start screening your child for T1D autoantibodies? Cancel reply

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