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    • 4 hours, 45 minutes ago
      LizB likes your comment at
      If you have ever had extra supplies from a device you no longer use, what did you do with those extra supplies? Please select all that apply.
      A familiar story. I've been holding onto my old Medtronic supplies for ten to twenty years. They're still sitting in the closet.
    • 4 hours, 46 minutes ago
      LizB likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      Diagnosed in September, right after Labor Day, in 1946. I'm 88 and still active, driving, and in general living a 'normal' life for someone my age.
    • 8 hours, 8 minutes ago
      Barb Robertson likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      Diagnosed in September, right after Labor Day, in 1946. I'm 88 and still active, driving, and in general living a 'normal' life for someone my age.
    • 8 hours, 36 minutes ago
      Mick Martin likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
    • 8 hours, 40 minutes ago
      Mick Martin likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      May 8th at 4:30pm - I was at work when I got the call from my doctor. I was fired from my job at 5:00 pm. A day that will live in infamy.
    • 8 hours, 49 minutes ago
      sweetcharlie likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was right before my 5th birthday. I returned from sleep away camp and was looking forward to my birthday party with a Baskin Robbin's ice cream cake and my mother's Hershey's best ever brownies, but instead. My mother took one look at me and took be to the hospital where I was diagnosed with T1D. Oh well. As the saying goes, shit happens. At least we have so many new treatments options available to use now. The doctors told my mom that I probably wouldn't make it to the age of 30 or 40 (I forget), and I am now 62.
    • 8 hours, 50 minutes ago
      sweetcharlie likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
    • 8 hours, 50 minutes ago
      sweetcharlie likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      I had been telling my medical professional parent for a month about my symptoms. My mom commented that it could be diabetes since her great-grandparents had it, but no. I was working at my dad's clinic, he was a doctor, and he had me go get a blood draw in the afternoon. After his birthday dinner, we stopped by to get the results. He said my BG was about 450. I started on oral medications right then. About nine months later I needed insulin injections. I was 18 and vowed it wouldn't change my life. It has changed every aspect of it. Every year on my dad's birthday I remember how it started and what's happened over the last 38 years.
    • 8 hours, 53 minutes ago
      sweetcharlie likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      May 8th at 4:30pm - I was at work when I got the call from my doctor. I was fired from my job at 5:00 pm. A day that will live in infamy.
    • 8 hours, 56 minutes ago
      sweetcharlie likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      I do not understand why this data is important.
    • 12 hours, 23 minutes ago
      KarenM6 likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was right before my 5th birthday. I returned from sleep away camp and was looking forward to my birthday party with a Baskin Robbin's ice cream cake and my mother's Hershey's best ever brownies, but instead. My mother took one look at me and took be to the hospital where I was diagnosed with T1D. Oh well. As the saying goes, shit happens. At least we have so many new treatments options available to use now. The doctors told my mom that I probably wouldn't make it to the age of 30 or 40 (I forget), and I am now 62.
    • 12 hours, 23 minutes ago
      KarenM6 likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
    • 13 hours ago
      Jeff Marvel likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      I had been telling my medical professional parent for a month about my symptoms. My mom commented that it could be diabetes since her great-grandparents had it, but no. I was working at my dad's clinic, he was a doctor, and he had me go get a blood draw in the afternoon. After his birthday dinner, we stopped by to get the results. He said my BG was about 450. I started on oral medications right then. About nine months later I needed insulin injections. I was 18 and vowed it wouldn't change my life. It has changed every aspect of it. Every year on my dad's birthday I remember how it started and what's happened over the last 38 years.
    • 13 hours, 1 minute ago
      Jeff Marvel likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      December 1983. Not sure the exact date, but it was about 6 weeks after becoming symptomatic. Didn't know what it was, but felt awful, plus the peeing/thirst thing, which I didn't even know was related to the other symptoms. I was in grad school at the time and it was nearing end of term. I thought student stress might be making me feel so sick. Doc said "Probably your wife wouldn't have been able to wake you up tomorrow if you hadn't come in."
    • 13 hours, 2 minutes ago
      Jeff Marvel likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      April 1. Happy April Fool's Day!
    • 14 hours, 43 minutes ago
      Gary Rind likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
    • 15 hours, 37 minutes ago
      jo likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      70 years. I hope you are doing well. This gives the rest of us hope.
    • 15 hours, 40 minutes ago
      jo likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      The 13th of December 1973, lucky number 13 🍀 and I was thirteen at that time.
    • 16 hours, 5 minutes ago
      Janis Senungetuk likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      Himmm.. About 70 years ago... I am even not sure of the year exactly...
    • 16 hours, 6 minutes ago
      Janis Senungetuk likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
    • 16 hours, 53 minutes ago
      miss.stake likes your comment at
      If you have ever had extra supplies from a device you no longer use, what did you do with those extra supplies? Please select all that apply.
      InsulinPumpers.com does a great job of distributing supplies to those in need.
    • 17 hours, 4 minutes ago
      KCR likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      Himmm.. About 70 years ago... I am even not sure of the year exactly...
    • 17 hours, 4 minutes ago
      KCR likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      70 years. I hope you are doing well. This gives the rest of us hope.
    • 17 hours, 8 minutes ago
      Sue Martin likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      Himmm.. About 70 years ago... I am even not sure of the year exactly...
    • 17 hours, 14 minutes ago
      Bruce Schnitzler likes your comment at
      During which month were you (or your loved one) diagnosed with T1D?
      It was almost 50 yrs ago. I was 4 when diagnosed - my family doesn’t celebrate or even discuss the dx as it was a very sad day for the entire family. They told my parents I would never have children and that I would never live past age 40. In my teens whilst full of surly attitude, I decided to prove them wrong. So I had a baby at 40 and am living a great life (with some restrictions) at 50-something. Celebrating another birthday in a few days. Glad they were wrong!
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    For people who have experience with both an insulin pump and CGM: If you could only choose to use one of these devices, which one would you use? Share why in the comments!

    Home > LC Polls > For people who have experience with both an insulin pump and CGM: If you could only choose to use one of these devices, which one would you use? Share why in the comments!
    Previous

    If you had T1D before attending college, did the quality of a university’s healthcare facilities and their services for people with T1D factor into your decision of which school to attend?

    Next

    From which healthcare provider do you receive the majority of your diabetes care?

    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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    75 Comments

    1. Wanacure

      If I’d been approved and if i could have afforded it, I would also have tried a pod insulin delivery device. For now the CGM is very helpful, even though I’ve just had one printout (for a two-week period) in the past six months.

      1 year ago Log in to Reply
    2. Kevin McCue

      Having the accurate cgm information at hand to make necessary changes so much more useful than having to prick my finger every time I need to get a static reading without knowing the trend also

      2
      1 year ago Log in to Reply
    3. Steven Gill

      The advantage of the CGM is I learned I don’t require insulin 24 hours a day. The advantage of the pump is I can stop the insulin release.

      I think for a newer diabetic the CGM is great, for someone with an active lifestyle and not afraid of adjustments (I make different pump adjustments) there’re definitely advantages of the pump.

      For a newly diagnosed I’d think a CGM for the confidence of knowing the legend. After a year with both in a closed loop system, 3 with only the pump I’d opt for the pump alone.

      It’s kind of up to the confidence of the person and definitely advantage to each.

      But for mr, if only one the pump.

      3
      1 year ago Log in to Reply
    4. Sandra Norman

      Tough question since having closed loop system – it is working so great, but I guess I have to go with the CGM as the pump would not work without that. I would manage but not be happy…

      3
      1 year ago Log in to Reply
    5. ConnieT1D62

      CGM. I use both in a closed loop system and would be very unhappy if I had to give up one or the other. However, I could manage manipulating insulin dosing with long and short/quick acting injections if needed as I have survived living with T1D for nearly 60 years and have managed doing so in the past. I rely & depend on the CGM to alert me of fluctuating trends in real time.

      3
      1 year ago Log in to Reply
    6. KCR

      CGM allows me to live a safer, healthier life.

      1
      1 year ago Log in to Reply
    7. Conniekaycox

      Can best manage defective pancreas with both. Have hypoglycemia issues. Without dexcom would be in er all the time.

      1
      1 year ago Log in to Reply
    8. Marsha Miller

      I would miss either so much! But I decided I would keep my pump. I could go back to fingersticks multiple times a day. I did this for several years and my A1C can still be normal.

      5
      1 year ago Log in to Reply
    9. Chrisanda

      I had to think hard, but I would go with just the pump. Finger sticks to check my BS is preferable to trying to adjust two kinds of insulin to cover the daily and bolus requirements. Being able to adjust my insulin to different foods, activities, etc with a few buttons, not having to carry syringes or pens…. I pray I never have to make a decision like this!

      6
      1 year ago Log in to Reply
    10. Gary Taylor

      I choose pump without the CGM. It is a tough choice because I really love knowing the data, but the alarms with the CGM are annoying enough, especially at night, that at times I feel I might be better off without it.

      2
      1 year ago Log in to Reply
      1. AnitaS

        I very rarely get alarms at night. If you are getting alarms because of low blood sugar, you really should appreciate those alarms.

        1 year ago Log in to Reply
    11. GLORIA MILLER

      I would not want to live without a pump. I have been on a pump since the early 1990s and have been T1 for 64 years. Before the pump I would have convulsions at night after a lot of hiking. Those are not pleasant experiences! Not a one after getting a pump. I do love the freedom the CGM offers me but I managed for over 50 years without one. But I do NOT want to have to give up either!

      3
      1 year ago Log in to Reply
    12. Rob Smith

      Actually made this decision. Went off pump (many reasons) and kept CGM.

      1
      1 year ago Log in to Reply
    13. Lawrence Stearns

      The insulin pump was the single most life changing device in my diabetes care. For 21 years before I got my first pump, I lived in a constant fog with multiple hypoglycemic episodes, every day. My life changed and improved instantly, as soon as I got onto an insulin pump, and off of the NPH, regular insulin syringe routine. My head cleared up immediately, my social interactions improved immediately, my ability to perform my work improved immediately.
      I love my CGM system with Tandem/Dexcom G6 Control IQ, It has also improved the quality of my life. But, I could never go back to injections. I believe, at my age, injections would probably shorten my life, and definitely severely worsen the quality of my life.

      4
      1 year ago Log in to Reply
    14. Janice B

      A CGM is the only way to see what your blood sugar trends are, have alerts which for me are crucial.

      1 year ago Log in to Reply
    15. kristina blake

      I answered CGM only, but I think I’ve changed my mind. Prior to Dexcom I was a 15-20 fingersticks a day person, and I ‘spose I could go back. Most of my insulin doses are small fractions – can’t do that on MDI, and having different basal rates throughout the day, I would probably need to have at least 4 different Lantus injections of varying amounts. Ideally, I wouldn’t have to give up either one. Together my Tandem X2 with BIQ (not interested in CIQ) and my Dexcom G6 allow me to be aggressive in my D mgt

      1 year ago Log in to Reply
      1. AnitaS

        I am always interested in why people aren’t interested in CIQ. I know it helps me from climbing too high. Why aren’t you interested?

        1 year ago Log in to Reply
    16. Rose Lentzke

      I started with only the pump years ago and would not give it up. You can always do finger sticks for glucose measurements. However, I would give neither up at this point!

      3
      1 year ago Log in to Reply
      1. Patricia Kilwein

        Yes, same for me. But also very thankful for cgm. Both together are life savers for me. I had just the pump for 2 years before my insurance would OK cgm. Both are important to me. So grateful to not have to poke fingers 7x a day…..

        1 year ago Log in to Reply
    17. Sahran Holiday

      Very ignorant question. Both, no one should go back to horse and buggy. Close to unsubscribing if the questions don’t stop insulting people’s intelligence.

      5
      1 year ago Log in to Reply
      1. Kathleen Amper

        Many people do very well without a pump so your horse and buggy statement is what is ignorant. Just because a pump works well for you doesn’t mean it’s the obvious choice for all.

        5
        1 year ago Log in to Reply
      2. AnitaS

        They aren’t insinuating that you should only use one. They are just asking which one you find helps you better control your diabetes. That is how I interpret the question.

        7
        1 year ago Log in to Reply
      3. NancyT

        I totally agree about this being a very pointless and insulting question. Hopefully, you’re intent is to lower costs and increase insurance coverage so that all PWD can access these benefits.

        1 year ago Log in to Reply
      4. Ahh Life

        My intelligence is never insulted, umm . . . since the bar is very low. However, Sophie’s choice is the choice none of us ever wants to face. Nor is the choice twixt CGM and pump. But forced into that choice, whether by cost, insurance, or a myriad of other fully legitimate and omnipresent reasons, the analysis and advice of Steven Gill and several others given here, are exceptionally sound.

        1
        1 year ago Log in to Reply
      5. Mary Halverson

        Maybe a few of us are newer-ly diagnosed and highly appreciate the questions and user responses for how others live with this disease?

        4
        1 year ago Log in to Reply
    18. Mick Martin

      I selected “Use pump only, without a CGM” primarily because MDI (Multiple Daily Injections) left me with areas of lipohypertrophy … collections of fatty tissue that builds up from repeatedly injecting in the same area(s).

      Even with testing my blood glucose levels up to about 20 times a day I needed to repeatedly inject correction boluses, which didn’t help matters. (I have gastroparesis, which is delayed emptying of stomach contents, which often led me to experience hypoglycaemic events {hypoglycemic, for my American cousins] which needed treating, and this led me to experience higher than ‘normal’ ranges of blood glucose levels.

      Even with pump and CGM I still experience many episodes of hypoglycaemia [hypoglycemia] but knowing where my blood glucose levels actually are, and which direction they are travelling [traveling] I can decide how to treat my hypoglycaemia [hypoglycemia].

      1 year ago Log in to Reply
    19. Todd Thedell

      I wanted a CGM for the longest time and finally had the insurance to get it 3 years ago. My only problem without my pump is the basal, I get much better results with the constant micro-dose than using a long-term shot.

      1
      1 year ago Log in to Reply
    20. David & Kaleo of Team Nani

      That may be the hardest ? “You” have ever asked. It’s almost like : spleen or xray vision superpower, but I said cgm since it’s so helpful to know w/o finger sticks….but no pump means back to NPH insulin, which sounds brutal. And means harder regulation and more injections.

      “You” are mean, let’s pretend you never asked this.

      1
      1 year ago Log in to Reply
      1. Jneticdiabetic

        Haha! I agree this was a hard one.

        2
        1 year ago Log in to Reply
      2. Gustavo Avitabile

        There are several long-acting insulins, besides NPH. They are quite good.

        1
        1 year ago Log in to Reply
    21. Andrew Aronoff

      I am a pump user (Medtronic 640G), but I’m currently taking a “pump vacation” to let my abdomen skin heal. I am maintaining acceptable BG control via my CGM, the Freestyle Libre 2, and MDI using both slow-acting (Lantus) and fast-acting (Humalog) insulin administered via pen injectors. The CGM provides me with trends, which is essential to maintaining good BG control. The hour I spend every two weeks waiting for recognition of a new sensor allows me to appreciate the CGM’s importance. My time-in-range has barely changed since I switched from the pump (80-85%) to MDI (75-85%). The only pump feature I miss is the square-wave bolus. It’s also nice to be able to bolus without using a pen, but that also favors frivolous food consumption. Between the pump and the CGM, there’s no contest – the CGM romps.

      1 year ago Log in to Reply
    22. Patricia Kilwein

      I had to start out using insulin pump only. The CGM was added about 2 years later. Insurance was the hold up. If I had to choose between the two, I’d go with CGM.

      1 year ago Log in to Reply
    23. Jneticdiabetic

      This one was hard. I chose keeping my pump over CGM. I’m insulin sensitive, and had lots of severe hypoglycemic episodes on injections. Having a large amount of long acting insulin on board that I can’t take back gives me flashbacks of those unpredictable times. Switched to pump therapy 21 years ago. Adjustable basal rates, ability to deliver microdoses & suspend insulin delivery made all the difference for me. CGMs have been icing on the cake I shouldn’t be eating. 😉

      2
      1 year ago Log in to Reply
    24. Sue Herflicker

      I chose the CGM because I like knowing what my sugars are with out testing. I rely on the arrows to help me make proper decisions! I hope the day never comes where I would have to choose. I love my tandem Control IQ along with my Dex 6.

      1 year ago Log in to Reply
    25. Dave Akers

      Using a pump BOUNDS you to 100yr old insulin technology. Injectable insulin will not get any faster. Inhaled insulin is simply revolutionary! It’s easier to use this and longer-acting basals than it is to manage a pump.

      And regarding my CGM… “From my cold Dead hands!” Is the only way I would maybe get rid of it!

      1
      1 year ago Log in to Reply
    26. AnitaS

      I put I would use the cgm only, however, I must admit that the pump definitely helps me especially during the night because I would have the dawn phenomena and wake up with those high blood sugars if I didn’t have the pump. Being able to increase my bolus as the night goes on takes care of that problem for me

      1
      1 year ago Log in to Reply
    27. Kristine Warmecke

      I currently use atSlim Control IQ. While I love my G6, I can give it up easier than my pump. I started pumping in Feb. 1997 with Medtronic 507, it was a different quality of company then, it changed my life for the better. I refuse to give it up & will never do so willingly.
      The couple of times I have had to be without, due to waiting for a replacement, I feel like a part of my body has been amputated.

      1
      1 year ago Log in to Reply
    28. StPetie

      I would choose cgm right now. However, it was a difficult decision as I value them both so closely and highly. If asked that question tomorrow the answer may be different.

      1 year ago Log in to Reply
    29. NancyT

      I’ve lived with T1D for over 60 years. From injections and urine “dipsticks” to test glucose, to pumps and CGMs I remember years and years of being without either! You can live without these devices BUT I would not choose give up either device!

      2
      1 year ago Log in to Reply
    30. M C

      I was doing well with just the pump before adding in the assistance of a CGM, so I could easily give up the CGM again. I find the CGM makes testing/checking much more frequent than when just using the finger pricks for testing, but my A1C measures were just as constant with the CGM as without.
      Whereas the pump changed everything for me with regards to much better BG control… So I would not want to ever have to give up the pump.

      5
      1 year ago Log in to Reply
      1. Amanda Barras

        SAME!

        2
        1 year ago Log in to Reply
    31. Dan Heller

      CGMs are the game-changer. T1D Exchange published a study in 2019 showing that CGM use outperforms non-CGM use by an order of magnitude. The study is titled, “State of Type 1 Diabetes Management and Outcomes from the T1D Exchange in 2016–2018”
      https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061293/
      Among CGM users, those using a pump slightly underperformed MDI users for ages > 26. (See Fig 3 chart.)

      According to the CDC, the MOST COMMON CAUSE of diabetic DKA is an insulin pump.
      https://www.cdc.gov/diabetes/basics/diabetic-ketoacidosis.html

      I don’t mention these things because I’m against insulin pumps. Not at all–they’re great for people who understand them and know how to master their nuances. Most important, people have to love them. It’s a lifestyle choice, not a medical necessity. Too many T1D’s falsely believe pumps can do more for them than they actually can. People should not be *encouraged* to use a pump–rather, to propose it as a potential alternative to pens (ideally, bluetooth connected) if their lifestyles accommodate it.

      2
      1 year ago Log in to Reply
      1. Jan Masty

        I absolutely agree. I’ve only been on a pump for a couple months, but so far it sure hasn’t made my life easier! I’ve been using dexcom for a few years and it definitely helps but also has issues. Sensors that quit often for sometimes a couple hours, or give wildly different numbers than my meter. We always have to be aware and ready to compensate, tech has a way to go to be truly lifechanging!

        1
        1 year ago Log in to Reply
    32. Donna Clemons

      Hate my current pump. Medtronic 680 G. CGM prefer.

      1 year ago Log in to Reply
    33. Mary Ann Sayers

      I use BOTH a CGM AND PUMP!!! AND I WOULDN’T have it any other way!!! Having the CGM, I can see the changes taking place (bg) and the direction it’s heading ON MY TANDEM CONTROL IQ PUMP!!!
      I love having a closed-loop pump and CGM! I’ve come a long way, baby, since 1954 age 7!!! All my mother had was urine tests and monthly trips to the hospital for fasting bgs!!! 67years later I have an artificial pancreas, thank God.

      1
      1 year ago Log in to Reply
    34. Mig Vascos

      I chose CGM. Ever since I was put on insulin therapy I dreamed of a day when I could tell what my BG was all the time. So…I wouldn’t give that up.
      I use a DEX G6 and a t:slim 2x with CIQ. THIS SYSTEM WOULD NOT WORK WITHOUT THE CGM.
      CIQ works wonderfully during the night I get almost a straight line during the night but that is not the case during the day when it shuts off the basal and then I run short later in the day and my sugar spikes. I often turn off the CIQ during parts of the day and I my control works well. So the pump still needs quite a bit of involvement on my part.

      1 year ago Log in to Reply
    35. Marie Cardinell-Daldry

      I still prefer the security of the instant results from a CGM. I’ve used 2 types of pumps. The Medtronic was terribly unreliable with it’s sensors.The Omnipod performed well but it has not been approved yet for a CGM

      2
      1 year ago Log in to Reply
    36. Clare Fishman

      I chose CGM because that is the device that changed my life the most. I went from being very reactive to being proactive. Preventing highs and lows rather than reacting to them. I use both in a hybrid closed loop system and would hate to give that up, but could manage ok with basal/bolus and mdi which I did for 38 years before pumping.

      3
      1 year ago Log in to Reply
    37. Bob Durstenfeld

      Data over delivery.

      6
      1 year ago Log in to Reply
      1. Ahh Life

        Best summary. Few words say it all. Good job!

        3
        1 year ago Log in to Reply
    38. Amanda Barras

      The pump itself completely changed my life. I pumped without CGM for 5 years and just adding this therapy and stopped long acting insulin completely stopped my sever , catatonic, and combative low bloodsugar episodes and stopped the need for paramedic calls since 2007! The addition of a CGM just helped improve over all A1c due to me addressing highs and lows quicker. But I was able to keep my A1c below 7.0 with just the pump alone. I wouldn’t trade the pump therapy for anything!

      2
      1 year ago Log in to Reply
    39. Kim Murphy

      I had a pump for years without a CGM and had severe hypoglycemia several times. I am fortunate to be alive. I wouldn’t want to have to choose because the pump has allowed me to avoid other diabetes related complications. They are making so much progress with closed loop systems I am not sure how this is a relevant question. Anyone who has had a pump and a CGM wouldn’t want to give up either of them. If horrifies me to even contemplate living without one of these devices, because I probably wouldn’t live long without them.

      2
      1 year ago Log in to Reply
    40. Karen LeBoulch

      Wouldn’t want to give up either pump or CGM. Hope I never have to choose.

      3
      1 year ago Log in to Reply
    41. kim bullock

      That is great question. If I had to choose it would be a cgm .

      1
      1 year ago Log in to Reply
    42. Jodi Greenfield

      As much as I love my cgm, I would choose my pump because instead of injecting myself 3-4 times a day, I only have to inject the pod every 3 days. The PDM (pump’s remote control) will take blood testing strips and give me a reading that PDM calculates how much insulin I need for my meal, or for correction.
      I feel insulin dosage is more important than saving my fingers.

      1 year ago Log in to Reply
    43. Michael Ratrie

      I find questions like this offensive.

      The better question, IMO, is how can we get affordable access to any of the tools that are available?

      1
      1 year ago Log in to Reply
      1. Karen Newe

        I love this question.

        1
        1 year ago Log in to Reply
    44. Rafaela

      I’ve never minded giving injections. What I did mind was my pump coming “unglued,” falling out, and having to get back on the phone to request an insulin refill, which I got sometimes, but not always.

      1
      1 year ago Log in to Reply
    45. Donna Condi

      My Dexcom CGM is the lifesaver and makes living with diabetes easier while using my pump has lowered my A1c and raised my TIR.

      1
      1 year ago Log in to Reply
    46. Lenora Ventura

      Visibility is everything. These days, insulin delivery comes secondary especially with the newer insulin varieties on the market.

      1
      1 year ago Log in to Reply
    47. Ernie Richmann

      The pump because I can adjust basal rates and reduce, stop, or take more insulin quickly. I am very active most of my waking hours. It would be more challenging to make insulin adjustments while biking, walking, working.

      1 year ago Log in to Reply
    48. Clearblueskynm

      I used to always say cgm is the one I couldn’t live without and I still lean that way, however I had to be without my pump two separate occasions for 2 days and really missed it. I think I’ll say they are both equally important to my life.

      1 year ago Log in to Reply
    49. Sasha Wooldridge

      If forced to choose, it would be the CGM. I can’t do anything with a pump or injections without knowledge and the knowledge it gives is invaluable.

      That being said, I just switched to the t:Slim a couple months ago. Changed my life for the better for sure. I definitely wouldn’t want to be without it. 😉

      1 year ago Log in to Reply
    50. Andrew Stewart

      CGM paired with a pump is a game changer. Once you’ve experienced the benefits of looping there’s no going back.

      1 year ago Log in to Reply
    51. LizB

      I would hate to have to choose but if forced I think I would take a CGM over the pump. I am hypo unaware so being able to see when my BG is dropping is really crucial.

      1
      1 year ago Log in to Reply
    52. PamK

      I have never felt my pump settings are correct. So, I would definitely go with the CGM over the pump. I have tried checking my basal rates, etc on my own and every time I think I’ve got it right something goes wrong. I have not been able to find an endo in my area who can help with this. It’s very frustrating!

      1
      1 year ago Log in to Reply
    53. Laurie Tomer

      Why chose either or?? The technology is there to have both. The CGM makes the insulin pump that much smarter and more benefit to the user. I am a brittle diabetic and CGM is crucial for knowing where my blood sugar is going. The insulin pump is crucial for the very fine tuning of insulin delivery to try to keep me somewhat in good numbers.

      1
      1 year ago Log in to Reply
    54. Bonnie Lundblom

      Hypoglycemia unawareness makes my Dexcom a priority above my pump.

      1
      1 year ago Log in to Reply
    55. brettsmith115

      This was a good question…difficult to answer. For 15 years I used a pump with no CGM. My control was good, not great. I then used the Medtronic CGM for a while, and saw minimal improvement to my control, but I also grew very frustrated by the daily regimen required by that CGM. Now I’m using the Dexcom G6 CGM (its been about 2 years) and I love it. My control has been better than ever, and the Dexcom has improved my daily regimen considerably! With all of that said, I can’t imagine NOT using a pump. However, it’s a question I’d like to ask my endocrinologist: “Could I maintain good control with injections and the Dexcom CGM?” If I could, I’d definitely choose a CGM over a pump. But, my guess is that my control is due to both my pump and my CGM working together. I’m very grateful for the technology advancements I’ve seen in my lifetime.

      1 year ago Log in to Reply
    56. Sherrie Johnson

      The pump changed my life 32 years ago and the CGM changed my life two years ago one without the other it’s a hard choice but I would pick the CGM just to know where I am at all times

      1 year ago Log in to Reply
    57. Molly Jones

      I have to choose pump even though I would hate to give up CGM.
      I could not live with one basal rate/day or deliver it according to my needs.

      1 year ago Log in to Reply
    58. Chris Albright

      I guess it would be (for me) the pump. While the pump is not as useful without a CGM, I used a pump for many years without a linked CGM. While I am sure there are people out there that use a CGM with MDI’s, I don’t think that it is a popular combination.

      1 year ago Log in to Reply
    59. James Cheairs

      In my opinion, the advance in CGM technology is the most important game changer in terms of managing T1D. I was on MDI for over 19 years and started using a pump in 2017. I go back from time to time to MDI to take a break from the pump. I can certainly live without a pump if I were forced to only choose one of the two.

      1 year ago Log in to Reply
    60. Vivian Moon

      I have had very scary experiences with very low blood sugars, so a CGM has save me and my husband a Lot of Grief!

      1 year ago Log in to Reply
    61. Cheryl Seibert

      A CGM can keep you safe from hypoglycemia in the night. If you know your Sensor Glucose, you can easily use a smart pen instead of a pump. Preventing lows is more important than convenience. No pump does take away the ability to auto adjust basal and calculate bolus amounts though. Tough choice.

      1 year ago Log in to Reply

    For people who have experience with both an insulin pump and CGM: If you could only choose to use one of these devices, which one would you use? Share why in the comments! Cancel reply

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