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    • 13 hours, 6 minutes ago
      Greg Felton likes your comment at
      If you have T1D, have you ever dated or married someone who also has T1D?
      I fell in love with an insulin-dependent Type 2 20 years ago. There’s something terribly romantic about taking Lantus together at the end of the day.
    • 13 hours, 38 minutes ago
      ConnieT1D62 likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      One time I was explaining that a new pump would be too expensive at the time because my deductible had just started over.. and she asked if I had insurance and I said yes….. then she said “then it should be free with insurance.” 🤦‍♀️ She may know a little about the challenges of living with diabetes, but she knows nothing about how insurance works or how costly T1D supplies are.
    • 13 hours, 56 minutes ago
      Steve Rumble likes your comment at
      If you have T1D, have you ever dated or married someone who also has T1D?
      I fell in love with an insulin-dependent Type 2 20 years ago. There’s something terribly romantic about taking Lantus together at the end of the day.
    • 14 hours, 27 minutes ago
      Lawrence S. likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      I am an RN. Been going to same doctor for about ten years. Took me six years to train him. I am very well read when it comes to my LADA. He trusts my judgement and gives me excellent parameters to make decisions. Recently had a bad case of Covid. Insulin needs changed dramatically. Getting back to normal but he made sure I had scripts to cover my ups and downs with insulin needs.
    • 14 hours, 28 minutes ago
      Lawrence S. likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      Mine acknowledges the struggles and challenges that go along with managing T1D in my daily life. She gives suggestions as to what may or may not help and has often asked me I how I handle situations so she can give suggestions to other T1D patient's.
    • 14 hours, 29 minutes ago
      Lawrence S. likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      None of my endocrinologists or NPs have had T1D but I always discuss my challenges and they are incredibly helpful. What I always find astonishing is they are constantly amazed at how well I’m doing even when i don’t think I’m doing that well because most of their patients have nowhere near the A1c’s I’m able to achieve. And just hovers in the 6’s!
    • 14 hours, 54 minutes ago
      Jubin Veera likes your comment at
      Have you developed lipohypertrophy due to repeated injections/infusions of insulin? Lipohypertrophy is a term to describe hardened lumps of body fat just under the skin that resulted from repeated insulin injections/infusion sites. If so, share how you’ve handled lipohypertrophy in the comments!
      The hard spots are fairly frequent with the pump infusion sets. Especially if I go past 3 days which I try to avoid! I don’t think I ever got one from injections. I try heat and massaging to treat them and they normally go away after a day or so. Once I had a large area that I had to treat with antibiotics.
    • 14 hours, 56 minutes ago
      Magnus Hiis likes your comment at
      Have you experienced any symptoms of physical sexual dysfunction as a result of having diabetes, or having diabetes-related complications?
      I’m 79. My last orgasm was springtime about 3 or 4 years ago. When I complained of ED, my PCP Rxd 3 to 5 (60-100 mg) sildenafil tablets by mouth about one hour prior to sexual activity. This alone hasn’t worked to bring me up to former sexual capacity that I had 10 years years ago. I’m still considering consulting finding a doctor who’ll prescribe a safe but effective way of administering testosterone or an anabolic steroid in a dose low enough to avoid causing cardiovascular problems but high enough to restore normal ability that I had up to my sixties. My present doctors say it can’t be done, but there are doctors who advertise otherwise. Analogs of the hormone insulin can be delivered in small safe doses, why not testosterone?
    • 1 day, 6 hours ago
      Becky Hertz likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      We are all so very different, and trying to say that all of us with T1 understand what it's like for another who has the same hill to climb is unproductive. Having a health care provider with T1 may often be helpful just because there's apt to be more knowledge about the specifics. How we respond to the disease is such a personal matter, that I really don't think there are any guaranteed benefits beyond the grasp of the factual. Finding a doc with the same general attitude about the disease does feel good, and sometimes that's all I hope for after working hard to make peace with the disease for 70 years. Asking my doc to "get it" used to be almost my mantra, but I've come to realize that the ones who don't just see us as unruly childrenchildren
    • 1 day, 6 hours ago
      Becky Hertz likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      Both my endocrinologist and my nurse practitioner are great. They compliment me on the way I take care of my life and health and make aure I get all the supplies I need managing all the paperwork Medicare and insurance requires. My nurse practitioner who works with me on managing the pump has her own opinion about the pump settings based on her technical knowledge which is different than what I do with my settings based on living with them. She has thru the years learned to respect what I do and is surprised with how my settings work. So we are now at peace. Both very supportive.
    • 1 day, 9 hours ago
      pru barry likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      Yes. However, for those of you who assert, "It takes one to know one," the same might be said of age. Geriatrics is a marvelous array of marvels.
    • 1 day, 9 hours ago
      mojoseje likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      I said yes but that refers to my nurse practitioner who sees me every other visit, if not more often. The doctor may know how hard I try but perhaps takes my efforts for granted.
    • 1 day, 12 hours ago
      Anneyun likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      How can someone without the disease really understand what it is to live with it? I have never had a doctor with T1D in 60 years.
    • 1 day, 12 hours ago
      Bruce Schnitzler likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      Yes. However, for those of you who assert, "It takes one to know one," the same might be said of age. Geriatrics is a marvelous array of marvels.
    • 1 day, 13 hours ago
      Kristine Warmecke likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      My endo is young, very empathetic, thorough, always asks for my input, and does research. I am blessed too. have him, and the one before for over 25 yrs.
    • 1 day, 13 hours ago
      Kristine Warmecke likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      Yes. However, for those of you who assert, "It takes one to know one," the same might be said of age. Geriatrics is a marvelous array of marvels.
    • 1 day, 13 hours ago
      lis be likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      None of my endocrinologists or NPs have had T1D but I always discuss my challenges and they are incredibly helpful. What I always find astonishing is they are constantly amazed at how well I’m doing even when i don’t think I’m doing that well because most of their patients have nowhere near the A1c’s I’m able to achieve. And just hovers in the 6’s!
    • 1 day, 13 hours ago
      Daniel Bestvater likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      My provider does not have T1. Only someone with it can truly understand the various daily challenges and worth it takes to manage this.
    • 1 day, 14 hours ago
      TEH likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      My provider does not have T1. Only someone with it can truly understand the various daily challenges and worth it takes to manage this.
    • 1 day, 14 hours ago
      Lawrence S. likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      I have no clue what my T1D health care provider understands about my daily challenges and I don’t know about his daily challenges either. Not sure why I should care as long as I have access to information how to best take care of myself.
    • 1 day, 14 hours ago
      Jeff Marvel likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      My provider does not have T1. Only someone with it can truly understand the various daily challenges and worth it takes to manage this.
    • 1 day, 14 hours ago
      Richard Wiener likes your comment at
      Do you feel that your T1D healthcare provider understands the daily challenges and work that goes into living with T1D?
      My provider does not have T1. Only someone with it can truly understand the various daily challenges and worth it takes to manage this.
    • 2 days, 6 hours ago
      sweetcharlie likes your comment at
      Have you developed lipohypertrophy due to repeated injections/infusions of insulin? Lipohypertrophy is a term to describe hardened lumps of body fat just under the skin that resulted from repeated insulin injections/infusion sites. If so, share how you’ve handled lipohypertrophy in the comments!
      Hi Connie, I still have my glass syringe and show it off occasionally. We boiled the needle and syringe every morning and sharpened the needle with a file. I was diagnosed at age 6 in 1963. Life is so different now! Then, my diet was extremely limited as was my exercise. Now, I am very active and eat pretty much as I please. I maintain an A1C in the low 6s (6.2 was my last).
    • 2 days, 6 hours ago
      sweetcharlie likes your comment at
      Have you developed lipohypertrophy due to repeated injections/infusions of insulin? Lipohypertrophy is a term to describe hardened lumps of body fat just under the skin that resulted from repeated insulin injections/infusion sites. If so, share how you’ve handled lipohypertrophy in the comments!
      Connie and Beth, I was diagnosed in Nov 1962, age 10. During the early years I developed lumps and indentations on my upper thighs from my injections. In fact, I was able t o spot other t1 kids in my junior high school based upon the lumps in their upper arms.. (I eventually met up with them and learned that I was correct.) By the time I reached my twenties, these indentations had more or less disappeared, but I still have remnants of the lumps. I wish I could say that the layers of tissue now deposited on my legs disguises them, but they don't. I think the changes in insulin have been responsible for this improvement: the isolation and purification of animal insulins were refined, and then the various human clones were game changers in many ways.
    • 2 days, 6 hours ago
      sweetcharlie likes your comment at
      Have you developed lipohypertrophy due to repeated injections/infusions of insulin? Lipohypertrophy is a term to describe hardened lumps of body fat just under the skin that resulted from repeated insulin injections/infusion sites. If so, share how you’ve handled lipohypertrophy in the comments!
      Yes in my upper arms when I was a petite and skinny child in the 1960s with T1D. In those days we used glass syringes with stainless steel 1/2 inch long heavy gauge needles. My mother would jab me in the upper arms, it hurt like the dickens, and I developed several hard nodules. I was diagnosed at age 8 in December 1962 and after the initial two months of her jabbing me in the upper arms, I took over giving my own "shots" and started self injecting via site rotation in my thighs for several years. Eventually the lipohypertrophy in my upper arms resolved and I never injected there again until many years later as an adult on MDI using disposable syringes with very short and fine gauge needle tips. Periodically I would give my tired pin cushion thighs a rest and take a break for a few months or a couple of years and rotate injections in my abdomen or upper arms. Have been using a pump for over 20 years now and rarely use MDI unless I am taking a pump break for a short period of time. Happily, I no longer have lumpy sites.
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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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    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 Marketing Manager 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

      2 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).

      2 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.

      2 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.

      2 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!!

      2 years ago Log in to Reply
    6. Joan Fray

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

      2 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.

      2 years ago Log in to Reply
    8. Ernie Richmann

      What is a honeymoon phase?

      2 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.

      2 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.

      2 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

      2 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

      2 years ago Log in to Reply
    13. Amanda Barras

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

      2 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.

      2 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…

      2 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.

      2 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

      2 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.

      2 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.

      2 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?

      2 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.

      2 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.

      2 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.

      2 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.

      2 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.

      2 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.

      2 years ago Log in to Reply

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