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    • 7 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 8 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 8 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 9 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 9 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 13 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 14 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 16 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 17 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 30 minutes ago
      Gary R. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 43 minutes ago
      ConnieT1D62 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 59 minutes ago
      eherban1 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 12 hours, 55 minutes ago
      NANCY NECIA likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 15 hours, 13 minutes ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 15 hours, 15 minutes ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 15 hours, 16 minutes ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
    • 16 hours, 19 minutes ago
      ConnieT1D62 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I get the 'you can't eat that, can you?' comments when friends see me eat a lot of carbs or have a nice dessert. I remind them that as long as I have insulin, I can eat whatever I want.
    • 16 hours, 20 minutes ago
      ConnieT1D62 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 16 hours, 22 minutes ago
      ConnieT1D62 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 19 hours, 48 minutes ago
      Lenora Ventura likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 19 hours, 48 minutes ago
      Lenora Ventura likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 19 hours, 49 minutes ago
      Lenora Ventura likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
    • 21 hours, 1 minute ago
      kristina blake likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 21 hours, 25 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 21 hours, 27 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
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    If you have ever gone through the process of getting a prescription for a GLP-1 agonist (e.g., semaglutide, exenatide, dulaglutide, liraglutide, lixisenatide, etc.), how easy or difficult was the process of getting a prescription and obtaining the medication?

    Home > LC Polls > If you have ever gone through the process of getting a prescription for a GLP-1 agonist (e.g., semaglutide, exenatide, dulaglutide, liraglutide, lixisenatide, etc.), how easy or difficult was the process of getting a prescription and obtaining the medication?
    Previous

    How many days in the past week have you had at least one blood glucose reading below 70 mg/dl (3.9 mmol/l)?

    Next

    Does proximity to your T1D health care provider impact where you choose to live?

    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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    15 Comments

    1. mojoseje

      I was able to get the prescription but because these are not approved for T1 diabetics, my insurance won’t cove4them, hence why I’m not on one.

      1
      2 years ago Log in to Reply
    2. lis be

      I haven’t tried to get a prescription for GLP’s,, but considering how heavily these drugs are being marketed- I almost expect to be approached with a free sample at my endo’s to increase sales.

      2 years ago Log in to Reply
    3. cynthia jaworski

      Slowing gastric emptying is one of the properties of this class of drugs. I don’t need any more uncertainty with gastric emptying.

      3
      2 years ago Log in to Reply
    4. Carrolyn Barloco

      I have taken Trulicity for a few years. My pharmacy used to provide 3 months’ supply. Now they say due to limited supply, I only get enough for 1 month. Also, I can’t see the benefits of taking this medicine!!

      2 years ago Log in to Reply
    5. Trina Blake

      I have tried and tried to get an Rx for these meds due to having developed insulin resistance – together with being scolded at the Endo practice for the 15 extra lbs I am carrying. Having to increase both meal and correction boluses only makes getting rid of the weight harder (yeah, I know insulin doesn’t “cause” weight gain – but having to “OD” on it makes things worse). I only eat when I am at target (around 80 bg) so it isn’t my eating habits that are at fault. The Endo is always talking about the side effect of DKA, but with ketone monitoring, I think I can handle/avoid it. Very frustrating.

      1
      2 years ago Log in to Reply
    6. Tracy Jean

      Victozia was easy for me to get but I couldn’t continue with it due to the price.

      2 years ago Log in to Reply
    7. Becky Hertz

      While my HMO MDs will not prescribe GLP-1 nor SGLT-2, they are covered without hassle if prescribed by an outside provider, in my case an Endo.

      2 years ago Log in to Reply
    8. Tina Roberts

      NA- I have no clue what any of that is. What are the brand names for them?

      2 years ago Log in to Reply
    9. Hadley Horton

      As a Type 1, my provider was very willing to prescribe me a GLP-1 to try, however, because I am not overweight, she told me it would be too difficult to have it covered by insurance.

      2 years ago Log in to Reply
    10. Lenora Ventura

      When first prescribed in March ‘22, it was seamless. Successfully obtained and took for 9 months. Health ins changed 1.1.23 and it was no longer covered because I’m not T2D 🤬. My Dr. tried appeal with no avail. All the benefits I gained have gone down the toilet.

      2 years ago Log in to Reply
    11. KIMBERELY SMITH

      It’s easy

      2 years ago Log in to Reply
    12. ConnieT1D62

      I started out on daily Amylin injections about 12 years ago, which worked very well as an appetite suppressant for stress eating tendencies, plus BG lowering. However I experienced too many unpredictable hypoglycemia episodes.

      My endo provider started me on a trial of Victoza with sample pens … the standard tapered dose was way too much for me and caused GI distress symptoms and side effects. So she had me start on a very low amount … basically one click of the pen at a time until after three months I reached tolerance at 10 clicks of the pen (0.6mg) which is the usual starting dose for most people. I have remained on that dose for several years now and it is a successful part of my overall control.

      It requires prior auth submitted by my endo provider. She is a warrior provider for her patients and steps up to bat for us to get what we need in spite of insurance coverage denials. I am very lucky to have excellent endocrine providers throughout my adult life with T1D.

      2 years ago Log in to Reply
      1. ConnieT1D62

        BTW – amylin is the other beta cell hormone our bodies don’t make. So not only are we insulin deficient, we are also amylin deficient.

        2 years ago Log in to Reply
      2. ConnieT1D62

        The amylin hormone replacement med is called Symlin.

        2 years ago Log in to Reply
    13. Brad Larson

      Only had to ask for it. It is “0ff-label,” so some out of pocket costs.

      2 years ago Log in to Reply

    If you have ever gone through the process of getting a prescription for a GLP-1 agonist (e.g., semaglutide, exenatide, dulaglutide, liraglutide, lixisenatide, etc.), how easy or difficult was the process of getting a prescription and obtaining the medication? Cancel reply

    You must be logged in to post a comment.




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