We are going on our first family trip to disney world in 10 days. We have lots of travel experience and the kids have been to 12 different countries but Disney seems to require a whole new level of planning which is a challenge for this disorganized mom! I have type 1 diabetes and as of 5 days ago, all 3 of my kids have it as well. My 3 year old and 5 year old were diagnosed 2 years ago and then my other 5 year old was just diagnosed. The kids all have Animas Ping pumps and I have an Animas Vibe pump and we all have dexcom CGMs. However, despite the helpful technology we are still in crisis mode here but I can't really tell the kids we are not going to Disney so the trip is on. I have searched but I still have questions and would appreciate any assistance.
1. Are the fridges reliable enough to store insulin? Not a huge issue but ideally I would be able to keep the back up insulin cool. I have had issues in the past with hotel fridges freezing insulin. We are staying at the Grand Floridian in the outer club level building in a suite.
2. How does it work in terms of bringing bags on rides? Will I be able to keep a small cross body bag with glucose with me at all times? I can't imagine we will be going on any roller coasters so just the small rides.
3. 2 of the kids also have Celiac which I have noted on our dining reservations. Is it correct that there is no reason to notify them of diabetes since we don't restrict carbs? It would be awesome if they had carb counts but since I read they do not I am not sure what assistance we could possibly need.
4. I previously had no intentions of getting a DAS but with the newest diagnosis I think it may be helpful to have on hand just in case. I am very confused about how it works with the 4 of us. Can I just get one and use it if needed? I read the FAQs on here but I am still confused (sorry!). I know it is related to need not disability but are DAS's typically granted for concerns about needing to leave the line suddenly? I guess my largest concern with this would be waiting for an hour in line, and then needing to leave because of a kid having a low and then needing to go through the waiting process all over again. Is there any pass that could help with that?
5. Last question.... What is the best place if I need a quiet area to change a pump site? My newly diagnosed son is still very anxious about site changes so it is not possible to just quickly pop it in. Would it be the family restrooms or the first aid stations?
Thank you so much for any and all advice
1. Are the fridges reliable enough to store insulin? Not a huge issue but ideally I would be able to keep the back up insulin cool. I have had issues in the past with hotel fridges freezing insulin. We are staying at the Grand Floridian in the outer club level building in a suite.
2. How does it work in terms of bringing bags on rides? Will I be able to keep a small cross body bag with glucose with me at all times? I can't imagine we will be going on any roller coasters so just the small rides.
3. 2 of the kids also have Celiac which I have noted on our dining reservations. Is it correct that there is no reason to notify them of diabetes since we don't restrict carbs? It would be awesome if they had carb counts but since I read they do not I am not sure what assistance we could possibly need.
4. I previously had no intentions of getting a DAS but with the newest diagnosis I think it may be helpful to have on hand just in case. I am very confused about how it works with the 4 of us. Can I just get one and use it if needed? I read the FAQs on here but I am still confused (sorry!). I know it is related to need not disability but are DAS's typically granted for concerns about needing to leave the line suddenly? I guess my largest concern with this would be waiting for an hour in line, and then needing to leave because of a kid having a low and then needing to go through the waiting process all over again. Is there any pass that could help with that?
5. Last question.... What is the best place if I need a quiet area to change a pump site? My newly diagnosed son is still very anxious about site changes so it is not possible to just quickly pop it in. Would it be the family restrooms or the first aid stations?
Thank you so much for any and all advice
