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    • 4 hours 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, 1 minute 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, 2 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 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 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 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, 1 hour 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, 2 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, 3 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, 15 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, 15 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, 15 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, 20 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, 20 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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    Do you currently have a kit containing the T1D supplies you would need in case of a natural disaster or emergency?

    Home > LC Polls > Do you currently have a kit containing the T1D supplies you would need in case of a natural disaster or emergency?
    Previous

    If you wear a CGM, do you look at the Glucose Management Indicator (GMI) available in many CGM reports? If so, is your GMI typically higher than, lower than, or equal to your A1c?

    Next

    Which foods/drinks do you prefer to use to treat a low? Share your favorites in the comments!

    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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    16 Comments

    1. LizB

      I have a small case that I carry in my bag when I’ll be away from home for more than a couple of hours, but not for days. It has an extra infusion set & reservoir for my pump, my current vial of insulin, some batteries for the pump, some syringes and a few alcohol & prep wipes. It was what I always had in my bag in the days when I went to/from the office everyday. So I could have that in an emergency but it wouldn’t get me far. My meter is in its own case and is kept on my desk, I don’t have any sensors or other CGM supplies ready to go.

      1
      2 years ago Log in to Reply
    2. Kristen Clifford

      It’s not assembled, but I do have what I need to put one together, including a bag the right size.

      2
      2 years ago Log in to Reply
    3. Sherolyn Newell

      Never thought of doing that. It’s a good idea.

      2 years ago Log in to Reply
    4. Sahran Holiday

      I have a small bag with the vial of insulin currently using to fill my Pod, always carry whenever I’m leaving the house further than walking distance, several pods with a frozen water bottle. There’s a spare Dexcom G6 sensor in my car.

      2 years ago Log in to Reply
    5. Anthony Harder

      I don’t know if my answer is yes or no (this I answered other). My daily T1D supplies are in the medicine cabinet with other medicines. I have reserves I keep in a different spot. Disasters will be a headache regardless where one keeps T1D supplies. However, keeping a “kit” and dragging that with me everywhere will soon become its own headache.

      1
      2 years ago Log in to Reply
    6. Richard Vaughn

      I would have a hard time keeping track of a “kit”. When I go shopping or take a several hour trip, I wear cargo pants. My diabetes equipment are in the 5 spacious pockets on my pants.

      2
      2 years ago Log in to Reply
    7. Bill Williams

      I don’t have an assembled kit but I keep a list on the refrigerator that I could put together in a few minutes.

      2 years ago Log in to Reply
    8. George Lovelace

      Being on Medicare I do have a ‘collection’ of necessary supplies, it’s just not in a Kit

      2 years ago Log in to Reply
    9. cynthia jaworski

      My answer depends upon what youmean. I have a small “pancreas” bag that goes from my dining room table to my purse, etc. It contains my cgm reader, spare needles, short-acting insulin pen, and sugar tablets. It goes with my everywhere. Everything else that I use on a daily basis, but not during the daytime hours, is together and could be packed up in a mater of seconds.

      2 years ago Log in to Reply
    10. ConnieT1D62

      I always keep extra “just in case” pump change and hypo treatment supplies with me in my everyday carryall bag. I also have a designated compartmental travel case made for diabetes self-care supplies that I stock with enough extras for 10 to 14 days in case of a natural disaster or emergency. The only thing I have to do is grab extra insulin from the fridge on my way to safety. I have Frio pouches in the kit to keep insulin cold. Periodically I check to make sure everything hasn’t passed the expiration date.

      2 years ago Log in to Reply
    11. Henry Renn

      With Medicare I only have supplies for 30 days at a time. I would have to throw all supplies (whatever is on hand) into duffle bag to evacuate or shelter in place.

      2 years ago Log in to Reply
    12. Amy Nance

      No, to contain everything I would need for a natural disaster or emergency it would need insulin – more than just the one vial I am currently using. I assume natural disaster means my house is demolished by fire, flood, tornado and that could mean I need more than one currently used vial and those are in my fridge. In addition, everything else, including a go bag, is at home-if it happens when I’m out and about In the community and can’t return home, I do not have a kit in my car, as storage in the car has extreme fluctuations in temperature and could or would ruin the supplies in the vehicle. I’m not without plans and ready to pack bags, but all emergent situations are not possible to plan for.

      2 years ago Log in to Reply
    13. Mike S

      I’m lucky enough to have several vials of back up insulin at the moment, but they are naturally in the fridge. I do have an extra G6 sensor and a few Omnipods in our go bag (along with an old finger prick meter), so if we were able to grab that it might help. BUT I’d only have the one semi-used insulin vial that’s in my every day kit…unless I could get to the fridge in time. Good reminder to replace the “emergency” Omnipod that I usually keep in my everyday kit too. (I actually used it last week, but not for the sort of emergency you’re talking about, just a randomly failed pod.)

      2 years ago Log in to Reply
    14. Sally Numrich

      Yes! A plastics storage box with handles in the cabinet right outside my bedroom. It has everything I would need. I rotate the Dexcom sensor when I get a new shipment so it doesn’t expire. Spare syringes, pump supplies, spare meter w/strips,glucose tablets, alcohol wipes etc. I of course do not have insulin but that stockpile is in the refrigerator & can grab when evacuating for wildfire, earthquake, tsunami (whatever natural disaster is coming our way). I figure I can never be over prepared and if I am someone in the evacuation center might not be.

      2 years ago Log in to Reply
    15. KarenM6

      Rotating out batteries is a bit of a nuisance, but important.
      What I figure is, if the natural disaster is bad enough, all regular stores and ways to get supplies will be affected. So, I think of the disaster plan/kit as if I am going back to treating my diabetes as if it’s 1970 again… shots instead of pods, no CGM, meter only, glucose tabs… i.e. enough “analog” diabetes to live. If I can also have the “digital” diabetes for long enough to get through the disaster, that is going to be a bonus.

      1
      2 years ago Log in to Reply
    16. Patricia Dalrymple

      Somewhat. I’ve learned living through this pandemic that it is difficult to plan for every type of emergency. My worst nightmare is running out of insulin, and I can’t plan for that because insurance controls it. I have a large makeup type plastic insulated bag with my pump supplies. I keep tablets handy. My glucometer is always within reach. My strips are with my pump supplies. My pump supplies are in a box. I have a Yeti that I’ve used in hurricanes (live in FLA). I have a Frio that I use on trips. It all makes me nervous.

      2 years ago Log in to Reply

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