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    • 4 hours, 31 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 4 hours, 32 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 4 hours, 33 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 1 day ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 1 day, 1 hour ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 1 day, 1 hour ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 1 day, 1 hour ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 1 day, 4 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 1 day, 23 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 1 hour ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 2 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 2 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 2 days, 3 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 4 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 4 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 2 days, 16 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 2 days, 16 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 2 days, 16 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 20 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 2 days, 20 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 3 days, 13 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 3 days, 13 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 3 days, 21 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    • 3 days, 21 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Hmmm... I'd almost welcome it, another challenge to enjoy?
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    How satisfied are you with your current health insurance plan?

    Home > LC Polls > How satisfied are you with your current health insurance plan?
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    Do you notice changes to your blood sugar on the weekends, compared to weekdays? Select any that apply to you.

    Next

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    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    21 Comments

    1. Gordon Calley

      I’ve the best plan offered through my wife’s employer with an $11K deductible for my wife & and our best choice was to ALSO purchase a concierge plan with a Dr. dropped by our plan. My lab work today saved me more money than we spend for the concierge Dr.

      3 years ago Log in to Reply
    2. Bob Durstenfeld

      I had a great PPO through my employer, with decent drug coverage and a great mail-order pharmacy. We were dropped in mid-summer after meeting deductibles and were switched to a $4,000 high deductible plan and they told us that we had to start our deductible all over again. I fought that and won. Having T1D is expensive, and our president wants to do away with protection for pre-existing conditions having no idea what real life costs.

      3 years ago Log in to Reply
    3. Mick Martin

      N/A as I don’t have a health insurance plan … unless you count the NHS (National Health Service) over here in the UK. This is financed via direct taxation of all working people, which means that I don’t have to pay for my diabetes-related supplies.

      3 years ago Log in to Reply
    4. Chip Brookes

      I would say satisfied, which is not one of the selections offered. Medicare with United Health Care supplemental. NHS is broke as is our Medicare/Medicaid. In England one is allowed to buy supplemental insurance, ergo not all people are covered by NHS alone. In France it is the same. One may purchase supplemental insurance, I have a friend there with 3 supplemental policies. When has the president said he wants to eliminate coverage for pre-existing conditions.

      3 years ago Log in to Reply
    5. René Wagner

      Neutral. I’m on Medicare for SSDI and have an Advantage Plan. I used the same provider from living in Florida to Texas. The Texas plans don’t cover T1D supplies as well.

      3 years ago Log in to Reply
    6. Mig Vascos

      I don’t know where some people get their information, but our president and all the representatives of the present government has repeatedly said that protecting existing conditions is a prior Edy in any new health care plan.

      3 years ago Log in to Reply
    7. james murphy

      The obamacare debacle stopped letting me use the plan that i liked, that was BS, and even worse when they knew that would happen. i wish govt would get out of trying to provide healthcare for everyone. that is not in our founding constitution. not sure why everybody thinks the govt is better running our healthcare?? i had to purchase the obamacare plan and it sucks because my deductible is $6k and my total premium is $9k.. i use to pay $75 a month for $10k deductible, and just purchase my needles,insulin and finger sticks. i now pay $9k a year, and still have to get all my supplies that never go past $6k

      3 years ago Log in to Reply
    8. Mig Vascos

      Let’s not spread false information. Anyway to answer the question I have Medicare and a supplemental with Anthem through the company my husband retired from. This year I was offered an enhanced plan for a bit of a higher premium and I took it. No deductibles and no copayments except on my prescription plan that has to go through the government run part D. Before Obama care I had an excellent insurance where the prescription plan had nothing to do with the Medicare part D, but that was cancelled. So I was not helped by Obama care on the other hand I had to jump through the hoops to ensure a good coverage that result more expensive and restrictive than before.

      3 years ago Log in to Reply
    9. Trina Blake

      I keep my current plan (an HMO) because the co-pays and Rx coverage are good. But I am not impressed with the medical care/D mgt policies. They have lower standards (i.e. higher A1C, looser D mgt) than I do. I smile sweetly, and then go about my D mgt the way I want to. I have great A1C’s and time in range (a narrower range than they expect) – ergo I feel I am healthier.

      3 years ago Log in to Reply
    10. Sheryl Campbell

      I am Canadian and pay $120/month for my husband and myself. I have some coverage for blood testing strips but it is very limited. This Blue Cross plan we have provides no coverage at all for CGMs. It does provide some coverage for prescriptions, but not for an insulin like Tresiba or Fiasp. It’s like they pick on those who need the meds the most. I do find it really horrible, but we have a terrible premier (who is leading our province) who is also under investigation for voter fraud…

      3 years ago Log in to Reply
    11. Kristine Warmecke

      I would be very satisfied with my Medicare Advantage plan, if my insulin didn’t cost 3/4 of my monthly income. Only issue I really have with it. I’m not sure why people are bringing up pre existing conditions and saying the current POTHUS is trying to protect it? Have you seen the law suites by his Senator yes men to get rid of pre existing conditions? He’s telling you one thing and doing the opposite as usual.

      3 years ago Log in to Reply
    12. ConnieT1D62

      I am satisfied with an excellent Medicare Advantage plan that covers everything I need to manage my T1D except for Baqsimi, for which I pay a negotiated out-of pocket price under Tier 3 coverage. It will even be better in 2021 with the cap for insulin coverage.

      3 years ago Log in to Reply
    13. Steven Johnson

      Blue Cross/Blue Shield/Blue Plus has been been my primary coverage while Ilive in MN. Medicare is secondary. As far as office visits, urgent care, labs it has been good. The insulin is covered through PartB of Medicare. The issue is lack of coverage for some of the immunizations is the one I do need. the other situation is withe emergency glucagon kits. . They refuse to pay for them. I cannot afford them without help. I am afraid this situation will not be resolved. Life is good One day at a time. Sweetblood

      3 years ago Log in to Reply
    14. ConnieT1D62

      The Affordable Care Act is not meant as the only health care coverage choice for everyone. Truth be told it does help millions of people gain access to reasonably affordable health care. It is sad, harmful, and shameful that the ACA has become so misunderstood and politicized.

      3 years ago Log in to Reply
    15. Germaine Sarda

      I chose “moderately satisfied” because I have Cigna’s High Deductible Health Plan. The coverage is excellent including customer service which is rare for insurance companies. But I pay a pretty penny for it. I also pay for all medical expenses until we reach our family $6K deductible which is usually met by March of each year due to the exorbitant cost of having Type 1 in the US. If it was more affordable, I’d likely marry it.

      3 years ago Log in to Reply
    16. Jeffrey Slott

      I use Keystone First which covers all costs for my syringes and my NPH. Years ago, I had two doctors who advised me to use Lantus… back in the day when a vial was only a bit above $100 or so. This was long before I had an insurance plan. I was able to pay for the thing out of pocket. Well, we all know what happened next! Lantus now sums for almost 400 smackers. At first, Keystone wouldn’t cover it, probably because of the exorbitant price tag. But last time I checked with them, I found out they changed their policy and WILL cover it… but they won’t cover the new Semglee, a Lantus substitute that is a lot cheaper! Go figure…

      3 years ago Log in to Reply
    17. Stephen Woodward

      I’m using Medicare with supplement plan. If I did not research, question and push when needed, my insulin and supplies would be costing thousands of dollars a year. If you carefully do the work it’s an ok plan combo, if not you can get screwed because of all the rules and regs that have to be followed or challenged.

      3 years ago Log in to Reply
    18. Patricia Maddix

      I have original Medicare and a United healthcare supplement with a Humana part D prescription plan. I selected moderately satisfied as my insulin for my pump, test strips, CGM are all covered under my part B insurance at no charge after the $200 a month supplement premium and annual Medicare deductible. however my prescription drug plan doesn’t cover a lot of the various other medication that I use including glucagon. I always check the good RX website to see if there are discount coupons for medication and have sometimes found this to be a better deal. But, why should I have to do that if I am paying for prescription drug coverage? I wish insurance companies would realize that if they covered all the things that diabetics need to better manage their diabetes it would cost them less in the long run due to better health and if you were complications. It is sad that some people have to pay so much for their diabetic supplies or make decisions to do without or ration.

      3 years ago Log in to Reply
    19. Molly Jones

      I am satisfied with the current insurance plan I am on through my husband’s employer. Many options and abilities to try new ways to control diabetes and epilepsy within a quick time would not be available without it. I have not used a different insurance plan while with diabetes, only with epilepsy. During that time I was without, on Medicare and our current plan, which I again think is the best. I am curious of how our insurance will change with retirement in hmmm…. less than twenty years. Again, hopefully research will have made bounds of helpful new discoveries.

      3 years ago Log in to Reply
    20. ANN GALLUZZO

      Our previous private insurance through employment was better than Medicare. A few months after starting to use Medicare they started covering CGM’s, which had been covered under private insurance for year (for things like hypoglycemic unawareness). But getting Medicare to pay means jumping through hoops that were not helpful. To get a pump, Type 1’s have to see their endo every 3 months. Under private insurance 6 months sufficed. My doctor has limited time and does not enjoy the requirement that he see me more often now. And the pharmacy where I get my insulin never succeeded in getting Medicare to pay for it. I had to file my own appeal, not something 95% of retirees would be able to do. They turned down the claims by CVS at least twice before I submitted my own appeal, which worked. CVS serves a lot of pumpers on Medicare, so it should not have been so difficult. Medicare was paying another provider for my pump supplies, but told CVS they had no evidence that I used a pump!!! Clearly a lot of wasted money for CVS and for Medicare employees.

      3 years ago Log in to Reply
    21. Bonnie Lundblom

      Moderately satisfied, ecstatic that using an insulin pump that my insulin is covered under Part B along with all of my pump supplies. We have United Healthcare as our Medicare Supplement and they pick up the 20% remaining balance.

      3 years ago Log in to Reply

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