Guest guest Posted January 8, 2009 Report Share Posted January 8, 2009 Hi Sandy, I have a friend who has a little boy with asd. Whilst at Disney he had a huge seizure - the first ever. They had terrible problems as they did not speak French and the hospital staff didn't either. I am not sure why the hospital didn't arrange an interpreter. Cards with explanations sounds like a very good idea! Jane Sandy and Tim wrote: Hi, We are looking into going to Eurodisney too - we've not been before. Thinking about early April. Eddie is anaphylactic (badly so and to wheat and egg) and very allergic too so he can never eat anything except our food. We plan to drive so we can take all the food etc. I rang Eurodisney 2 weeks ago to ask if Eddie would be allowed to eat in the restaurants there (they said we would have to ask ourselves in each - but it would probably be OK). We will make up cards in French to help the explanation. We were told that there are lockers by the main gates so you can leave food bags and not have to carry them around all the time. We are looking at the Addagio self-catering apartments. I didn't know the Davy Crockett had kitchenettes - and I'd asked about cooking facilities in the hotels. I rang the anaphylaxis campaign and they said that they'd had very mixed reports of Eurodisney - some had a great time and found everyone very helpful and others had a very different experience. (Mandi - what did you have in the kitchens there? Was there a full size fridge?) Sandyx Quote Link to comment Share on other sites More sharing options...
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