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Not really vacations, but May 5th we are taking the kids to Disneyland (we live less than 20 minutes from Disney) thanks to my mom and sister who are giving David the Birthday of his life at Disney. Then June 6, we are going on a road trip (me, my mom, and the kids) to Palo Alto for the regional Histio Conference and the kick off event for Hike 4 A Cure thanks to my mom who knows how important it is to me to meet other Histio Families.
We went to Disney World last month, and had a great time. They offer a special pass (GAC) for SN kids (we brought a note from our dr). Kyle doesn't have endurance and can't wait in the heat, so we used a stroller as a wheelchair. The pass gave us access to a special entrance area. He didn't have to wait in any lines for rides, and when we got off - our stroller would be right there. It was wonderful. Disney at spring break would not have been doable for him, without it. The first aid centers also stored his meds and neb pump for us while we were in the parks.
Disney and Sea World (all of the parks) have been amazing with SN kids. I know several kids who have used the special passes. A lot of times, they both just give passes to the parks to kids and their families. I know that a lot of other amusement parks do this as well. Just something to think about if you all live near some parks.
We have nothing planned. We can't really leave our house for more than a couple of hours. We thought about a day trip somewhere, but have no idea if that will actually happen. It's about to be too hot to do anything outdoors for Milo. We have a family pass for a year to a local science center. Kannon loves it. Milo even likes it-there's always something we can do with him to make him enjoy it. There are several parks and the library. As far as the kids are concerned, this is all vacation.