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    • 3 hours, 46 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 3 hours, 47 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 3 hours, 48 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 1 day ago
      Wanacure likes your comment at
      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?
      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.
    • 1 day ago
      Wanacure likes your comment at
      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?
      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 day ago
      Wanacure likes your comment at
      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?
      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 day ago
      Wanacure likes your comment at
      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?
      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
    • 1 day, 3 hours ago
      Samantha Walsh likes your comment at
      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?
      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 day, 23 hours ago
      KarenM6 likes your comment at
      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?
      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
    • 2 days ago
      Katie Bennett likes your comment at
      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?
      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
    • 2 days, 1 hour ago
      Kate Kuhn likes your comment at
      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?
      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
    • 2 days, 1 hour ago
      Karen DeVeaux likes your comment at
      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?
      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.
    • 2 days, 2 hours ago
      Kelly-Dayne likes your comment at
      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?
      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
    • 2 days, 3 hours ago
      William Bennett likes your comment at
      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?
      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
    • 2 days, 4 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      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?
      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
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 20 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 2 days, 20 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 3 days, 12 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 3 days, 13 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 3 days, 20 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    • 3 days, 20 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Hmmm... I'd almost welcome it, another challenge to enjoy?
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    When you were diagnosed with diabetes, did you go through a “Honeymoon” phase? If so, for how long did it last?

    Home > LC Polls > When you were diagnosed with diabetes, did you go through a “Honeymoon” phase? If so, for how long did it last?
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    At your last appointment with your diabetes healthcare provider, did they ask about your mental/emotional wellbeing?

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    If you wear a CGM and share your data with people (ex. Dexcom Follow or Medtronic’s Carelink Connect), with whom have you shared your CGM info? Select all that apply.

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    26 Comments

    1. Leona Hanson

      I went through a 2year honeymoon phase it ended when I had emergency surgery and then everything went crazy brittle diabetic fun every day

      3 years ago Log in to Reply
    2. Steven Gill

      I was originally diagnosed TYPE 2 (understandable, I ate and drank anything available), 3 years later after losing 105 lbs the diagnosis was changed to TYPE 1. Had the antibodies, the doc at the medical studies suggested had the test for GAD autoantibodies been done several years earlier I might have extended the “honeymoon” period even longer with only a BASAL dose. For me 3 years although the last several months the “quack” I fired kept saying I was too old to require insulin: kept changing pills and said to lose more weight (eventually 20lbs under weight).

      3 years ago Log in to Reply
    3. HMW

      I was diagnosed at age 7. I went through honeymoon phases (where I would only need 1 shot of nph once a day) off and on. I particularly remember having one at diabetes summer camp at age 9 (over a year after diagnosis) because of how active we were there and how much I could snack vs at home.

      3 years ago Log in to Reply
    4. Anthony Harder

      I was diagnosed with T1D in 1965 when I was 7 years old. My doctors quickly settled on T1D and insulin injections which I have been taking ever since.

      3 years ago Log in to Reply
    5. connie ker

      My diabetes was not diagnosed when I presented with a frozen shoulder, no energy and kept losing weight. My diabetic husband suggested he test me on his meter and it read HIGH. So a call to his endo meant insulin dosages over the telephone and an office appointment forthcoming. Even though I was 49, I could not get off of insulin and my body was frail. That was 23 years ago before the term LADA. Thankful for insulin which is turning 100 years in 2021, marketed in 2022. Happy 100th Birthday Insulin!!

      3 years ago Log in to Reply
    6. Joan Fray

      You think I remember 59 years ago? Ha ha ha, that’s hilarious!

      3 years ago Log in to Reply
    7. Lorri McLuckie

      I’m not sure that “Honeymoon Phase” was known about in 1967 when I was diagnosed. I was only 10 at the time and don’t remember that term being used or any changes to my treatment protocol being implemented to reflect that.

      3 years ago Log in to Reply
    8. Ernie Richmann

      What is a honeymoon phase?

      3 years ago Log in to Reply
    9. Annie Wall

      I had to look up honeymoon phase diabetes. Here’s what I found: “The “honeymoon period” is a phase that some people with type 1 diabetes experience shortly after being diagnosed. During this time, a person with diabetes seems to get better and may only need minimal amounts of insulin. Some people even experience normal or near-normal blood sugar levels without taking insulin.” I definitely never had a honeymoon phase when I was diagnosed T1D at age 32.

      3 years ago Log in to Reply
    10. William Bennett

      Dx’d 1983, age 28. My Dr warned me about the honeymoon phase, but I think what happened was that I retained some endogenous insulin production that never quite completely went away. I seem to still produce some, which makes DKA less likely, though it can make figuring dosage a little unpredictable.

      3 years ago Log in to Reply
    11. Steven Jerdee

      My dad told me I got really sick taking insulin. So they stopped for a week and everything was good. It lasted a week. Then I got sick again and I have been on insulin ever since. That was 1967

      3 years ago Log in to Reply
    12. George Lovelace

      57 years ago I remember times where the NPH would ‘surprise’ me with lows, I assume that was “Honeymoon” but don’t remember when that levelled off. DX was easy because my father had been a LADA Dmer since the early 40’s,, my Dx in 65

      3 years ago Log in to Reply
    13. Amanda Barras

      I was barely 4 when dx so I too young to remember.

      3 years ago Log in to Reply
    14. Sally Numrich

      I said, no idea. Who knows, it was one injection of Lente and urine testing. So really, who knows! I know there was lots of highs and lots of lows.

      3 years ago Log in to Reply
    15. Nicholas Argento

      Like others, I don’t know, but it is not that I could not remember, more that in 1968, you really could not tell because there were no A1c’s, or fingersticks. Evidence from the Diabetes Control and Complications Trial, which was the first prospective randomized large scale trial to prove that tight control improved the chance of avoiding complications, also showed that those newly diagnosed who were well controlled (average A1c 7-7.2) had detectable insulin secretion for twice as long as those who were in standard control (A1c around 9 on average). So high blood sugar hurts remaining beta cells, and tight control helps from day 1 after diagnosis…

      3 years ago Log in to Reply
    16. kristina blake

      My D symptoms came on fast and furious. I may have been my “honeymoon” period prior to Dx and thus not been aware of it. I was a professional ballet dancer in the years leading up to my Dx and that hard physical labor (it is hard labor – we just make it look easy and ethereal). I was Dx’d with T2 cuz I was 30 years old (no risk factors especially the one re: my family tree – no D of any kind back several generations. Family had lots of medical folks – so the records were meticulous). When I first went to see a doctor I had gone from my “working weight” of 110 lbs (I am 5’6′) to 102. By the time was correctly Dx’d – in DKA I was 95 lbs.

      3 years ago Log in to Reply
    17. Abraham Remson

      I guess as they said I controlled too fast and went blind for a couple of weeks. Let me tell you, it was a a lot of fun . I could see some shadow like figures during the day but at night I was totally blind the honeymoon was over real fast if in fact it actually happened

      3 years ago Log in to Reply
    18. Ken Raiche

      Unfortunately I’m not to sure how long mine lasted. That said becoming a diabetic was never ever a big issue for me due to my older having had it for 7 years prior to my sudden onset. Admittedly things seemed to be much easier way back when due to the lack of instruments for testing, single dosing etc. Now days we’ve got all these different tools that are available like CGM’s, pumps, or MDI, Inhaled etc…. Admittedly these things are great, yet at times can be a tad bit hectic and a constant reminder of our disease which for me can encourage depressive state.

      3 years ago Log in to Reply
    19. Carol Meares

      I don’t remember anything significant about honeymoon. Because I was an adult I was not put on insulin for quite some time. I was on metformin for T2. When they accepted metformin wouldn’t help, they put me on insulin about 6-12 months after dx. I was still scrawny but was never extreme to where I ended up in the hospital. I think there are some differences between LADA and Juvenile T1D. Both autoimmune but different in its presentation in my perspective. My young 1St cousins once removed with T1D ended up in the hospital with very quick presentation, my sister and I with LADA had more stretched out presentation in the beginning. I didn’t know of the word “honeymoon” at the time.

      3 years ago Log in to Reply
    20. ConnieT1D62

      I have no idea. I was diagnosed in December 1962 at the age of 8. They weren’t tracking residual beta cell function back in those days, so even if I was in a honeymoon phase it wasn’t on the radar, so no one paid attention to it. I do remember that I had a lot of severe insulin reactions up until age 10 or 11 – often resulting in middle of the night/overnight seizures. Perhaps I was going through a honeymoon phase then?

      3 years ago Log in to Reply
    21. KarenM6

      I did, but I was about 5 when it happened. I remember the doctors telling my Mom to continue to give me a small amount (~1 unit) of insulin so that I didn’t become allergic to it if she stopped giving any insulin.

      3 years ago Log in to Reply
    22. Donna Condi

      I was. 42 when diagnosed T2 and put on pills. Four years later and 60 pounds lighter I asked to go on insulin because I couldn’t keep my bs numbers down with the pills, exercise and eating like a bird.

      3 years ago Log in to Reply
    23. Cub Scout

      I didn’t go through a honeymoon phase til my last pump, 670G & CGM. A1c improved 2 points. Improved control, less worry, and more freedom eating.

      3 years ago Log in to Reply
    24. Anita Galliher

      I was diagnosed at age 14 in 1963. I was in shock and hated every minute of it. Peeing in a cup or on a stick was worthless. My A1C was 12 for a while, and only took one injection a day until I was in my 40s. Finally when I was about 50 I went on the Omnipod and turned things around. I still hate it and struggle every day, but I keep trying. And that’s all I can do until a cure is found.

      3 years ago Log in to Reply
    25. kilupx

      I had a high a1c in a routine blood test when I was 66. Internist told me I had type 2. Metformin made me sick and I told doctor I would follow a strict low carb diet. Then I found an endocrinologist on my own and he immediately diagnosed me with LADA. Probably because of ingesting fewer than 80 grams of carbs a day, I was able to prolong honeymoon phase to 1 1/2 years. Then I started on a couple of units of long-acting insulin a night and didn’t add Humalog until a year after that. Five and a half years from diagnosis, I still take what I’m told are smaller than normal doses of insulin—4 units of Tresiba daily and a total of 7 units of Humalog a day.

      3 years ago Log in to Reply
    26. Cheryl Seibert

      I was diagnosed just over 54 years ago, so don’t recall any ‘honeymoon’ phase. At age 6, I came home just before Christmas and went back to being a kid. I don’t recall any anger, adjustment period or anything like that. Just seems like it was “ok you have to take shots and don’t eat many cookies”. At age 6, I had more bad memories of and trouble adjusting to having tonsillitis every winter. I guess diabetes diagnosis didn’t impact me much at that age.

      3 years ago Log in to Reply

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