We have been coming here for a few years now, so we do have a pretty basic routine for coming and going. We are blessed that my sister's family will go when we do. The boys know that we will stop for a break, then stop for breakfast - all together. They also know after breakfast it's off to Disney. We get our hotel room, unpack the car, have a snack and head to the park the first day. Even though it's months between visits, they know the routine. We keep the morning routine the same as home - wake, eat, meds, dress and head off for the day. (At home it might be for school or errands.)
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We keep a time for snacks, lunch, snacks - again, supper, etc. Food routine seems to be crucial for us. There is nothing worse (to me) than a hunger meltdown - why? because it's usually the easiest one to prevent. Going back to the hotel room late afternoon, early evening usually proves a little more difficult. They boys (and us) are usually a little "over-tired", which makes for the very likely scenario of a "big" meltdown by one or both boys. So, we finally realized that if we vocalize the: medicine time, walk time, bath, relax and bed-time.
Hopefully the whole week will go well. I'm sure we'll have the usual "ups and downs", but it will be ok - just a different location. We will have a good vacation.
For those who've heard about the new Disneyland and Disney World rules that go into effect tomorrow, the 9th of October, regarding the special needs pass, I will try to write again tomorrow (otherwise as soon as I'm able) to let you know what we find out.
From a mother's heart - may we all be blessed with a little time to get away, and may our kiddos on the spectrum - not receive such a shock that they can't - enjoy it.
God Bless!
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