Hi,
I have IBS-d and pretty severe asthma which unfortunately the heat doesn't help. I have been granted a DAS pass for the upcoming trip but have a couple of questions. Fried food or high fat content food is a big no no for me as it will result in a guarnteed IBS issue ( if you know you know) which can come on so quickly it literally means running to the toilet. Other foods can do the same and sometimes its completely random, eating too much at the one time does the same thing and often I don't know how much that is. The cramps, bloating and flatulance are also nasty and so embarrising. My first question is to ask if there are many quick service /snack places in the park that sell non fried food or would I be better bringing my own lunch? I have checked the menus for all the TS meals we have booked and they all have options which are reasonably safe. The fatigue from the asthma and IBS will limit our parks days to a max 4-6hrs and maybe less if I start to feel ill. We were at Universal lst year and I had to sleep for 2hrs in the afternoon if we wanted to go out again at night.
My other question is about using the DAS. My conditions are invisible and unless I'm having to exit a line quickly or use an inhaler no one would know anything is wrong with our family. I'm anxious enough about posting this on a public forum but also anxious about using the DAS. I don't want people to think we are abusing it and don't want to have to explain to every cast memeber why we can't queue. Does anyone else with invisible conditions relate do this or have experience negative or positive? Thank you.
I have IBS-d and pretty severe asthma which unfortunately the heat doesn't help. I have been granted a DAS pass for the upcoming trip but have a couple of questions. Fried food or high fat content food is a big no no for me as it will result in a guarnteed IBS issue ( if you know you know) which can come on so quickly it literally means running to the toilet. Other foods can do the same and sometimes its completely random, eating too much at the one time does the same thing and often I don't know how much that is. The cramps, bloating and flatulance are also nasty and so embarrising. My first question is to ask if there are many quick service /snack places in the park that sell non fried food or would I be better bringing my own lunch? I have checked the menus for all the TS meals we have booked and they all have options which are reasonably safe. The fatigue from the asthma and IBS will limit our parks days to a max 4-6hrs and maybe less if I start to feel ill. We were at Universal lst year and I had to sleep for 2hrs in the afternoon if we wanted to go out again at night.
My other question is about using the DAS. My conditions are invisible and unless I'm having to exit a line quickly or use an inhaler no one would know anything is wrong with our family. I'm anxious enough about posting this on a public forum but also anxious about using the DAS. I don't want people to think we are abusing it and don't want to have to explain to every cast memeber why we can't queue. Does anyone else with invisible conditions relate do this or have experience negative or positive? Thank you.