GAGirlInVA
DIS Veteran
- Joined
- Apr 23, 2010
- Messages
- 1,255
I've debated posting here for a few days.
Our allergist believes that our son has multiple food protein intolerance and has placed our 2.5 year old on an elemental, hypoallergenic formula as his only source of nutrition.
We don't know how long this will be all that he can eat. Our understanding is that once they decide his gut has had a break, we will introduce a single food at a time in multiple food trials while keeping him on the formula for the majority of his nutrition.
According to our allergist, he may never be able to be completely formula free.
I've grieved this quite a bit in the last 5 days and all I can think about is how this will affect everything in his life. Birthday parties, celebrations involving food, snack time at church, dinner parties, vacation, etc.. EVERYTHING is different now.
My husband and I are starting to plan a trip in 2013 to where else, but Disney.
I'm not concerned about the dining plan, or whether he will be charged or whatever. Right now we can't even eat as a family so it is hard for me to imagine being able to eat out with him just drinking formula.
My biggest concern at this point is whether or not they have blenders for us to mix his formula. It is quite clumpy and he won't drink it without it being completely mixed.
I think I remember someone saying that the DVC had blenders..and we could take ours to the hotel or whatever, but what do you do when you are in the park or at a restaurant??
Even if we blend it when we mix it the first time, before he drinks it, it has to be blended again.
Maybe I'm just hyperfocusing on this, because I am seriously wigged out about his MRI tomorrow. (He is also being evaluated for neurofibromatosis..)
I dunno.
I guess I want to hear that we can find a new normal. And that this won't be as big of a deal as it feels right now.
Our allergist believes that our son has multiple food protein intolerance and has placed our 2.5 year old on an elemental, hypoallergenic formula as his only source of nutrition.
We don't know how long this will be all that he can eat. Our understanding is that once they decide his gut has had a break, we will introduce a single food at a time in multiple food trials while keeping him on the formula for the majority of his nutrition.
According to our allergist, he may never be able to be completely formula free.
I've grieved this quite a bit in the last 5 days and all I can think about is how this will affect everything in his life. Birthday parties, celebrations involving food, snack time at church, dinner parties, vacation, etc.. EVERYTHING is different now.
My husband and I are starting to plan a trip in 2013 to where else, but Disney.
I'm not concerned about the dining plan, or whether he will be charged or whatever. Right now we can't even eat as a family so it is hard for me to imagine being able to eat out with him just drinking formula.
My biggest concern at this point is whether or not they have blenders for us to mix his formula. It is quite clumpy and he won't drink it without it being completely mixed.
I think I remember someone saying that the DVC had blenders..and we could take ours to the hotel or whatever, but what do you do when you are in the park or at a restaurant??

Maybe I'm just hyperfocusing on this, because I am seriously wigged out about his MRI tomorrow. (He is also being evaluated for neurofibromatosis..)
I dunno.
