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    • 14 hours, 58 minutes ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 15 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 15 hours, 1 minute ago
      KarenM6 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, 1 minute ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 15 hours, 10 minutes ago
      KarenM6 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 ´ )⎠⎞
    • 17 hours, 2 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 17 hours, 3 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 17 hours, 5 minutes ago
      lis be 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 ´ )⎠⎞
    • 21 hours, 5 minutes ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 23 hours, 7 minutes ago
      Phyllis Biederman 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".
    • 23 hours, 53 minutes ago
      Bill Williams 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 ´ )⎠⎞
    • 1 day 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.
    • 1 day 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".
    • 1 day 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.
    • 1 day 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.
    • 1 day 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.
    • 1 day 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 ´ )⎠⎞
    • 1 day 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.
    • 1 day 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 ´ )⎠⎞
    • 1 day 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 ´ )⎠⎞
    • 1 day, 1 hour 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 ´ )⎠⎞
    • 1 day, 13 hours 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.
    • 1 day, 15 hours 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".
    • 1 day, 15 hours 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.
    • 1 day, 15 hours 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?"
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    If you use an insulin pump, did you try out any pumps before you committed to using one?

    Home > LC Polls > If you use an insulin pump, did you try out any pumps before you committed to using one?
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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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    43 Comments

    1. Theresa Hastings

      I’ve used multiple insulin pumps, but not through samples. I would switch after my warranty had ended if I wasn’t satisfied with my current pump.

      2
      3 years ago Log in to Reply
      1. Tere North

        Me too, Theresa. I was started with Minimed, went through several iterations of that, tried Omnipod, was looking at other options and was ready to go to Asante Snap right when they folded, and now with Tandem. Really liked the idea of using the glass prefilled cartridge with the Snap, but am happy with Tandem.

        1
        3 years ago Log in to Reply
    2. Lawrence S.

      Trying out an insulin pump was not an option offered to me. I used Medtronic/Mini Med the first pump because it was the one my doctor mentioned. I switched to Tandem years later, again without a trial period.

      1
      3 years ago Log in to Reply
    3. Britni

      I was nervous about how my skin would react to the adhesives, so my CDE gave me a deactivated Omnipod to wear.

      3 years ago Log in to Reply
    4. Barbara Bubar

      Back in 2000, Medtronic had 85% of the market share and that was the only pump suggested to me by my endocrinologist at the time.

      2
      3 years ago Log in to Reply
    5. John McHenery

      My local health authority organised a session where companies could present their pumps and answer questions. No one was offering free trials though omnipod offered non-working models to try.

      3 years ago Log in to Reply
    6. Debra Nance

      I decide on my own which pump to use. I started out in 2001 on a Medtronic. Used it a short time and stared on a Desitronic until they stopped making pumps. Went to Animas until they went same as Disetronic. Went on Medtronic. Switched to Omnipod a couple years ago. Now I am on my Medtronic 770g and it’s CGM. Love it!!!

      2
      3 years ago Log in to Reply
    7. Mary Dexter

      I no longer wear a pump, haven’t for 10 years. But up until recently, the endocrinologists and CDEs would only consider Medtronic. Same for CGM: one CDE who was wearing a Dexcom, said I would never be able to get one, only Medtronic. After I quit pumping, I was finally able to get a Dexcom.

      3 years ago Log in to Reply
    8. Cristina Jorge Schwarz

      The trial periods are a joke. I was just off MDI and learning a pump, adjusting settings, etc takes much longer than 10 days to sort out. At the 1 month mark, I knew the pump system would not work for me, and I was stuck for 4 years.

      I suffered with it a full year, then learned of a better health insurance and enrolled. They said they’d cover a new pump for me, and I switched after carefully “playing” with all the ins and outs the first several days. What an improvement.

      2
      3 years ago Log in to Reply
      1. Sue Martin

        What pump did you finally choose?

        1
        3 years ago Log in to Reply
      2. Cristina Jorge Schwarz

        My first was the Omnipod, that was 5 years ago. I then went to Tandem, almost at my 4 year mark with it.

        3 years ago Log in to Reply
    9. KCR

      I went to a TCOYD conference and was able to see all the pump options then available.

      1
      3 years ago Log in to Reply
      1. Kris Sykes-David

        I just found out the ONE conference is on for August in San Diego!

        2
        3 years ago Log in to Reply
    10. Melinda Lipe

      I’ve never been offered a chance to try alternatives before deciding. I just compared the features of each pump online.

      2
      3 years ago Log in to Reply
    11. Marty

      My first endo had a Minimed loaner pump that I was able to try before I got my own. I knew I wanted a pump as soon as I learned they existed, but my endo wanted to make sure it was going to work for me before we embarked on surmounting the insurance barriers.

      1
      3 years ago Log in to Reply
    12. Kevin McCue

      The yes option would be I tried other pumps but no trial or sample.

      3 years ago Log in to Reply
    13. Sherolyn Newell

      My endo said the Medtronic was probably the best when I got a pump, but I knew tubes were not going to be a good option for me. It was Omnipod or MDI. Omnipod gave me a couple of pods to try for “feel”. They did not have any insulin in them.

      1
      3 years ago Log in to Reply
    14. Greg Felton

      I originally chose Minimed/Medtronic because it was the only pump my insurance covered decades ago. When I began looking at new pumps 2 years ago, I wanted to test out the Omnipod through their free trial offer, but a prescription was required for the sample, and that would lock me in to using Omnipod, according to insurance. I got to try out a tandem at my doctor’s office for a day (no insulin delivered) before I opted to use Tandem. I think the trial offer from Omnipod is a scam, so I hope to hear that others were able to do it successfully.

      3
      3 years ago Log in to Reply
      1. Cristina Jorge Schwarz

        I got that too. Then, they said once I got a real one with the Rx, I had 10 days to change my mind. Took more than 10 days to get the settings anywhere near close to working for me…I lost track of time and missed the deadline.

        3 years ago Log in to Reply
    15. kim bullock

      I was on a medtronic pump b4 I switched to tandem. I did get a sample cgm from dexcom b4 I totally switched to dexcom/tandem

      3 years ago Log in to Reply
    16. Linda Pease

      I used Medtronic because it was the only one insurance approved at first but when I could changed to the one I used now because it for my insurance and my needs

      3 years ago Log in to Reply
    17. Bob Durstenfeld

      I tried a clinic pump, I could not see the real time data until I returned it to the clinic for down load. It was more than 20 years ago.
      I went on to use Autosyringe, Disetronic, Minimum, Animas and now a Tandem pump.

      3 years ago Log in to Reply
    18. Russell Buckbee

      I had a prior one and could only switch to a Dexcom to use the CGM system.

      3 years ago Log in to Reply
    19. terrih57@msn.com

      I wish I could have tried all the available options before committing to one. I was on Medtronic’s for 16 years before switching to Tslim. I was able to do a trial with Omni pod. Just would have been nice to try all the other options.

      3 years ago Log in to Reply
    20. lis be

      Insurance only covered medtronic

      1
      3 years ago Log in to Reply
    21. Molly Jones

      I used different Medtronic models for extended periods of time, I tried Omnipod, but it didn’t deliver the small amount of insulin I needed back then. ‘Decided to trial a new Medtronic before switching to Tandem which I like most aspects of, mostly it’s compatibility with Dexcom and now Control IQ. If Medtronic had been compatible with Dexcom or had a better sensor, I probably would have stayed with them.

      1
      3 years ago Log in to Reply
    22. Amanda Barras

      Getting a trial run on a machine that expensive seems like more work than it’s worth. Wish it was an option tho!

      3 years ago Log in to Reply
    23. Sherrie Johnson

      I started on the pump almost 34 years ago it was a new life first time I felt somewhat normal. Medtronic was the only one available and was so welcomed.

      3 years ago Log in to Reply
    24. Janis Senungetuk

      No, I wasn’t offered any free trials. After 60 yrs of MDI I went to my first PWD conference where I was surrounded my 90+ adults wearing many varieties of of diabetes devices. There was a short Q and A with a Medtronic rep, a conference member wearing an Animas Vibe and another conference member who was involved in the development of the iLet pump. I returned from the conference knowing that I wanted to switch to a pump but knew nothing about any of the details. I researched low income assistance, found that Animas offered a substantial discount and that was the deciding factor.

      1
      3 years ago Log in to Reply
    25. Kristine Warmecke

      When I started pumping in 1997 the endocrinologist I was seeing due to insurance only used MiniMed. I wanted a pump & at that time they were the best & latest on the market so I was okay with it. I have done an Omnipod trial, I like the idea of no tubs but it was hard to keep on, for me.

      3 years ago Log in to Reply
    26. Henry Renn

      My Endo C-PA reviewed choices with me. I had no choice since Johnson & Johnson would no longer support my Animas Vibe.

      3 years ago Log in to Reply
    27. Chris Albright

      I did not try out other pumps before getting the one I wanted, but my previous pump was a different mfg and I knew I did not want another pump from that manufacturer….

      3 years ago Log in to Reply
    28. ConnieT1D62

      When switching from Medtronic to a different pump and cgm system, I wore a saline trial of Tandem with Dexcom G4 and a saline trial of Omnipod with Dexcom G4 … gave me the information I needed to make a decision. I chose to go with Tandem.

      3 years ago Log in to Reply
    29. T1D4LongTime

      I went with my endo’s recommendations. My very first pump was Medtronic and infused saline for a few days to get used to having the pump on. I’m now on Tandem and switched right over.

      3 years ago Log in to Reply
    30. AnitaS

      No. I had already started using Dexcom CGMs and I went to a type-1 diabetes convention in the Cleveland area in the spring/summer of 2019. I was checking out the different pumps as I was planning on starting pump therapy. After seeing that the Tandem pump was already communicating with Dexcom CGM, I decided to go with Tandem as opposed to Medtronic. I remember sitting at a table for lunch with a lady who had an omni-pod and remember her complaining about the size of it (it did look unusually large on her arm so that was off-putting to me). I also had a nurse who told me that Tandem was a much wiser choice than Medtronic.

      3 years ago Log in to Reply
    31. Jodi Greenfield

      My Endo has a person on staff that knows about the pumps available and helped me determine which one I would try first. I am still an OmniPod user.

      3 years ago Log in to Reply
    32. Janice B

      I have used 3 different pumps over the last 12 years. So much better than injections. I try to stay on top of all of the developments and I also read user reviews so that when it is time to upgrade I am prepared to either stay with what I have or make the jump to a new device.

      3 years ago Log in to Reply
    33. Steven Gill

      Ironically a FB group and even here some seem real critical of MEDTRONIC, my only concern is their target range (120), otherwise everything about it is exceptional. The only benefit of my last endocrinologist was leading me to pumping, MEDTRONIC was the only option for me. Refused pumping several times because of fears of damaging it but the rep/educator assured if I would be replaced. Cracked it nut worked perfectly, but a battery issue got a new one within 24 hours and an offer for a prescription of Lantus sent to the pharmacy. Great technical support and customer service.

      3 years ago Log in to Reply
    34. Jeff Balbirnie

      The clown who sold me the pump got a larger kickback from particular companies. Can’t prove it, but 100% sure of it, he’s still making his living from selling them and the business they produce, training, psychology, education….

      A good living

      3 years ago Log in to Reply
    35. Stephen Woodward

      I wish this was an option over the last 30 years, you buy it you’re stuck with it, choose carefully.

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

      No. We were not even aware that there were choices. Endo ordered pump while our son was still in the hospital, and he started on it two months later. That being said, he was diagnosed at 18 months of age (9.5 years ago), and Medtronic 530g was the only pump available that delivered .025u.

      3 years ago Log in to Reply
    37. George Lovelace

      In 1998 a rep for Disetronic gave me a Sample Pump and Saline to try it out, the Rep from MM said they would Not lend me one to try, he was so cocky about having “the Best” and I{ have Never gone with MM/M but have lost so many friends who did :'(

      3 years ago Log in to Reply
    38. PamK

      This was not an option when my doctor suggested Medtronic. I went with her suggestion. Once the pump was out of warranty I chose to switch to Tandem and am very glad I did! In fact, my warranty was just up again and I got another Tandem!

      3 years ago Log in to Reply

    If you use an insulin pump, did you try out any pumps before you committed to using one? Cancel reply

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