YAY!! You should start a TR for him! He is going to have so much fun!!
You can edit it in your settings. Yep...Jake is my wish kid!! I love that name haha.
I am curious to know too. My kids would LOVE to go to Lego Land. But I dont know how much time to devote to it because we have never been there before. Then I have to figure out what to take out of our trip so we can put in lego land...haha.
Hi! I have been lurking around this site for awhile, waiting to be "official" enough to post. We just found out last week that my daughter, Maddie, will be granted a wish and today we found out that her Wish Granters will come visit us on Wednesday! It's only been about a month since she was referred to MAW, so things are moving quickly! Her exact wish is yet to be determined, but right now she wants "to go to Disney and be in a parade." Not sure if the parade part can happen! I'll work on a PTR soon, but just wanted to introduce myself Mom2M07 said:
Mom2M07 said:
Mom2M07 said:
Sheri21596 said:Wow - its been a week since my last post! Been so busy but wanted to thank everyone for the advice on Kara's upcoming port surgery. We will be at Hopkins on Feb 20th for it. Very nervous but I know this is what needs to happen for to beat this cancer!
Kara had her wish grantors come over last Sunday and she made her wish to see the princess castle and get her make up done at the BBB!
We turned in all paper work and gave our dates - anywhere between September to December. We want to give Kara some time on her chemo cycles before we travel.
I will let everyone know how she does on Wednesday!
We just got the call on Friday that our two year old adopted son would get his Make-A-Wish. We've been to Disney before we adopted him but this will be his very first time and we are thrilled to be there to experience this with him!!
I'm going to start reading - he has several things that may make it a bit harder for him to get on and off attractions (feeding tube, wheelchair, pulse ox machine, etc.).
He's 2 1/2 so for now, we're showing him videos and pictures of Disney (he's obsessed with Mickey and Buzz) so that he'll have some idea of what it may look like when he gets there!!!
Our other children are so excited to make this trip special for him
Wow - its been a week since my last post! Been so busy but wanted to thank everyone for the advice on Kara's upcoming port surgery. We will be at Hopkins on Feb 20th for it. Very nervous but I know this is what needs to happen for to beat this cancer!
Kara had her wish grantors come over last Sunday and she made her wish to see the princess castle and get her make up done at the BBB!
We turned in all paper work and gave our dates - anywhere between September to December. We want to give Kara some time on her chemo cycles before we travel.
I will let everyone know how she does on Wednesday!
Our kids LOVED Legoland. It was also a very slow day there. Not very many people. We don't have any Legoland anywhere near us, so for us, it was a must see. There wasn't a lot of shade, which can become a problem. Our wish child just melts in the heat so we had to quickly change courses. All rides we were able to walk on. I will agree with PP, not the greatest for mobility. We had to back track a few times with our strollers as some places had stairs and weren't marked. We also did not do everything.
So, if you are very much into Disney/Universal, I am not sure it would be worth it. But we did not do Disney or Universal. We did Animal Kingdom and Sea World. The lack of special treatment didn't bother us. But if you go to the other places, I can see why it would be a bother.
Kennedy Space Center....we thought about that but thought, with our age range of kids, it wouldn't be a good idea. So no help there
We will be heading to the hospital in the morning at 5:30 check in for Carter's MRI. They will be putting him totally out, since there is no way he would be able to do it awake. I guess the official MRI will be at 7, so hoping we will be home by noon. The last time he was put under he had a bit of trouble with his breathing after. That was before he started treatments, so lets hope it will be easier this time!
We will be heading to the hospital in the morning at 5:30 check in for Carter's MRI. They will be putting him totally out, since there is no way he would be able to do it awake. I guess the official MRI will be at 7, so hoping we will be home by noon. The last time he was put under he had a bit of trouble with his breathing after. That was before he started treatments, so lets hope it will be easier this time!
