Within the first week of Caden's diagnosis, when we were still unsure if our son was going to live, we were approached by a representative for Make A Wish.
I remember telling him about the company before telling him that he could make a wish, making sure to say that it was many different people that donated many different things so that children could have something special to look forward to. We looked online at many different stories where he told me some of his favorites.
About halfway through our online search, Caden's breath caught in his throat, and with tears in his eyes, he said, "This is a cool thing." I couldn't have felt more excited to be the one to tell him that he would get to make a wish. The tears came even faster. And then he started asking.
Caden has never been one to jump into something important without much thought. He steps back, reviews every angle, and makes sure he has all of the information. He asked everyone, including the representative that approached me, what they would wish for. He asked nurses, friends, patients, and his siblings. He never asked me, but I wouldn't have said, anyway. I wouldn't want him to try and grant me my own wish. He is that selfless. As it stands, he already did grant me my wish- he is still here. We researched more wishes online, and then researched each place traveled, each person that he wanted to meet. You name it, we researched it. For weeks.
During this time, we stopped worrying about cancer so much, and started worrying about recovery. He had a Wish to get fulfilled. His first choice was the meet Brian Regan. And then that happened, without the help of the Wish Granting Machine. So what to choose now? I would say it took him to the end of Round 3 to decide.
We were going to Disney World as a family!!
He chose there over Disney Land because of the longer flights. Yay!!! (Cringe) We'll see how he feels about long flights when we get back. Caden could go any time it was cleared with his doctors. He could have gone as early as July. However, wanting to make sure that everything was perfect, MAW recommended a few options. "The weather is SO hot in Florida until about September. We could go, but remember you will swelter." "Halloween is an absolute blast, but it is SUPER crowded. Same with Christmas." "However, if you go the first week of December, they will have started decorating for the Holidays. It is also, statistically, the least busy week of the year. That leaves many volunteers and staff to watch out for Make A Wish participants." And so it was set.
And, as if this incredible trip we get to go on isn't enough, Make A Wish threw Caden a party to present him with his packet. He got to choose every detail. And it was tonight.
Jamie has some amazing tools, so I asked her to help me make some decorations. I didn't want to go all out, but I did want to make a banner. My own Mickeys.
I hate that the lighting is so horrible. This is Sri and Dorothy, his Wish Granters. They kept monthly contact with us, bringing our kids gifts, and keeping the excitement fresh in our minds. Make A Wish gave Caden, and our other kids, excitement for something wonderful
during the rough spots. I will forever love them. Words are not enough.
Not perfect, but better than before.
Caden was given a choice of whom to invite. He invited the Scouts and Leaders, plus three friends from school. He was
surrounded with love!
I didn't get many pictures, mostly because I wanted to be present. To watch the excitement on his face, to hear the sound of his laughter, to revel in his health. My son is alive. And he is
living that life. And I don't want to miss a thing.
I was able to capture this little cutie. Look at that face!!
In addition to Winco providing a bunch of the food, Michelle Walker providing the fountain, Make A Wish providing the other portion of the food,
Game On also donated one hour to Caden.
That is a huge trailer full of video equipment, enough for 28 people to play!!! And,
I kid you not,
dance!! And even though he has to have surgery tomorrow, the owner, Robert Lenzi personally came to our home for our party. They donated the hour, outfitted Caden with a t-shirt, and showed his party guests the time of their lives. Just one more amazing couple that have given us such kindness.
(L to R) Kade Harrison, Hunter Peterson, Caden, Logan Powell, Mason McShane, Spencer Hammond, Nathan Haggard (from Caden's Crew) Zachary Bagley, Zachary Graves, and Satch Berkey. Missing from the photo, Brother Bagley, Brother Elsberry, Brother Haggard, and Brother Walker.
Tonight was magical. My heart is full to bursting. Our week of Wishes begins on Sunday with a 6:00AM flight, returning the following Saturday at 11:59PM. This is going to be a week to remember.
We are completely open about cancer in our home. We talk about it often. The kids ask questions, we remember times of hardship and blessing and talk about them, and we always have the kids tell us their feelings about things. We asked Caden if he wishes his life had been different. His response, "I'd keep it exactly the same." Cancer was HARD. Cancer SUCKED. But we are all stronger because of it. And this upcoming miracle week, we get to bask in the luxury of health. Our son is going to be given a gift that was granted at a time of mortal uncertainty. And now we can enjoy it fully, knowing that our son is cancer free!