We have been trying to save our money to pay for our Disney Trip in December 2014, but as of today we have a whole whopping $0.00 saved. As I said, we just are not good at saving money. Plus with the added expense of Nicholass therapies, we now have more outgoing money than incoming. We have applied for SSI for him, but as of today have not heard anything back yet. If we are approved, that money will help a little bit.
And to make matters worse, Chris was laid off work for eight days over the last two weeks, and there are rumors of permanent layoffs after their inventory time is completed next week. We are praying that this does not happen.
We also have medical bills coming out our wazoos. We have all of the bills from Nicholass medical evaluations. Mary fell off her bike and had to have stitches in her knee in May. Then she fell off her friends
scooter in September and broke her arm. I was in the hospital with acute bronchitis in July. CJ injured his shoulder playing football and now has to have physical therapy once a week. Somehow, Noah twisted his knee over the summer. Were not sure how, though. He says he was just walking and he tripped over his feet because they are too big.

The only one who has not had some major medical problem this year is Chris Sr. knocking on wood that he stays healthy.
In late July, my mom told me that she had found a place online called the Sunshine Foundation. She said it was like Make-a-Wish, but they work with all children with medical conditions, not just the ones who have life threatening illnesses. So she had sent Nicholass name to them to request an application in hopes that maybe they would send us on a trip to Disney World. A few days later I received the application in the mail. So I filled it out and sent it back, but I didnt really believe that they would grant a wish to Nicholas.
Before filling out the application, I had gone to their website and done some more research online to try to find out as much about them as I could. I found out that they will work with moderately to severely autistic children, but not mildly autistic. At the time, Nicholass doctor at CCH had not told me if his autism was mild, moderate, or severe, and I never asked. I figured since she didnt tell me, it must not be that important to know. Although, I did have a few people ask me about the severity. As I said earlier, it is hard for me to think of him as having a disability at all, so I just told people I thought it was mild. His therapists have also said that most of his delays are mild. So I didnt think the Sunshine Foundation would even consider Nicholas.
But, when the doctors report that had to be sent in with the application came back from CCH, it said that Nicholass autism was severe. Not even moderate to severe, just severe. This came as a total shock to me, but then again, I hadnt bothered to ask, so I guess I deserved to be shocked. But, even so I still didnt expect for Nicholas to be approved because I feel like there are surely other kids out there who are more deserving of something like this than Nicholas. Not that Nicholas is not deserving, but I know that medically there are other children out there with worse conditions than his.
But earlier this month, I received a call from a lady at the Sunshine Foundation, and she told me Nicholas had been approved to receive a wish. I am so grateful that they think Nicholas is deserving of a wish, because as much as I hate to say it, I dont think we actually would ever make it on our own.
So we will stay at the Sunshine Foundations Dream Village for a few days, and we will get three days worth of tickets to either Disney World, LegoLand, Universal, or SeaWorld. Right now we are considering one day at the Magic Kingdom, one day at Islands of Adventure, and one day at SeaWorld. I would like to see all the Disney parks, but knowing that this may be the only trip we ever get to go on as a family, I think it would be nice to experience a little bit of everything.
We do not have our dates yet, but it may be up to two years before we can go, depending on if they can find someone to adopt Nicholass dream. We are hoping to go sooner than that so that CJ can still go with us for free. If he is 18 by the time we get to go, we will have to pay for him. We will also have to pay for our moms separately.
So we are now trying to get our living expenses, medical bills, therapy costs, and especially our spending habits under control. Our goal is to save as much money as we can between now and the time we get to go so that everyone can go with us. We are hoping that it will turn out to be about a year so we have time to save, but no longer so that CJ will still be 17. We are also going to ask if we can drive so that we dont have to pay airfare for the extra people. Our plan had always been to drive anyway, plus, Im not sure I could handle flying with my brood.

So
Wish us Good Luck, Charlie. Well probably need it.
Thanks.