Yeah! My trip report is unlocked and I can post again. I am not sure what caused it to get locked in the first place. I will add more updates soon!![]()
I think the Mod was trying to move it over to the Trip Report board (from the Pre-Trip board) and it landed on the Completed Trip Report board instead!
It is all good!
I love the pics you have posted!!I couldn't post all of my comments earlier...I think you take GREAT pics!
Can't wait to hear more about the magic!!![]()
I just found your TR and I LOVE it! You kids are adorable and all the magic you got on this trip has made me tear up a few times! What a wonderful experience you guys have had so far! I cannot wait for more!
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No. Way.
I LOVE those characters! What an awesome picture...all 3 of the kids each with one of them!!!!! That is so awesome!
I can't wait to see even more from PhotoPass!Fantastic!!!
Here is the link: http://www.rarechromo.org/informatio...ons FTNW.pdf .
Then he said the most profound thing. He said, "God must have given us this baby since he knew we could take care of him and love him whereas a parent on drugs could not handle him so he gave them the perfect child". It is so true. I did not think I had the strength to deal with a special needs child when he was born, but I have learned so much and I have become a much stronger person because of him. Besides one little smile from him melts my heart!
Wow! Your timing on this trip is fantastic on the character meets! I love all the Pooh, Tigger and Eeyore pictures too. My favorite is the one with all three characters with the entire family. Tyler got to play with Stitch again. Yeah! The gingerbread carousel is fantastic this year. Love all the pictures you took to capture all the details.
Day 2 was another full day for the family! Can't wait for day 3!![]()
Wow, you guys got to do soooo much and meet so many characters! I can't wait to see your next installment, the kids are just beaming in all the pics!
I'm just now going back to the beginning...I was wondering if you have ever heard of CDO? Chromosome Deletion Outreach? (I think their site is CDrg but don't quote me on that). They are US based and raise money for research (no money is solicited from members or required to join) and offer a database and support group for families. They even offer a list of families in your state/area that are working with a chromosomal abnormality (that have approved their info be shared). It sounds like your son's is extremely rare but certainly his challenges are shared by other kids with "syndromes". My daughter is still undiagnosed, but every doctor in several states have agreed she seems to have a genetic syndrome. It was actually her geneticist who submitted her paperwork for MAW, even though she is undiagnosed. Okay, sorry for that rambling. Didn't know if you knew about CDO and I can tell you are the type of parent that does her research.
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Your story also made my eyes water. You have an amazing gift in your daughter. I figure that God knows more than I do so if he chose me to accept and take care of Tyler then there is a greater reason than what I can see before me right now. He has been a lot of hard work and a lot of road blocks with doctors and insurance, but one little smile from him and all is right with the world. He has no idea that anything is wrong with him and he is just happy being alive. I wish everyone could see life the way he does. We all would be so much happier!Oh geez, maybe I should've just stayed where I was with all the happy pictures.You made my eyes water, which is a hard thing to do anymore. Your husband is wise, and it took us a little time to come to terms with this. We were/are infertile and after desperately wanting a baby to love it ripped my heart out every time someone found a baby in a dumpster. I was very bitter towards women who were able to have children but did not appreciate them. When we finally realized that adoption was our path to parenthood it was another blow to find out that our daughter had pretty severe disabilities. We loved her from the minute we saw her. Probably before. We had no doubt that this unborn child was meant to be ours, and no one knew that there would be anything "wrong" with her. Around the time it started to become obvious that she was behind in everything and her medical issues were continuing, we finalized her adoption and immediately were told we were amazing and wonderful people for going through with it. WHAT?!?
She was OUR daughter! If someone had given birth to a baby like her no one would ever say how wonderful you are to keep her....it boggled our minds. It was a challenge to adjust our dreams for her, and grieve the loss of the daughter we expected, but she was nothing but a bundle of pure love. An angel straight from heaven. Even now with all the docs and therapies and worries about the future, we call her the "easy" one.
Phew. Sorry for all of that on your TR, but I just had to share what a nice feeling it is to find people who understand. That's one great thing about our kids... I have found that even without a specific diagnosis we have made amazing friends and can relate to so many of the different challenges out there. Okay, 'nuff said.
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