I just visited Tori's website. My daughter, Mackenzie, was diagnosed with a brain tumor the day after her 8th birthday in September of 2011. Today marks one month since we departed for our Wish Trip to Disney. It seems like it was so long ago but we had a wonderul time. Tori is beautiful and I look forward to hearing more about your trip!
Shawna Roach
Shawna Roach
Hi everyone, my name is Michelle and I am new. I just posted my "Team Tori" PTR in that forum, I think I did it right.
My daughter Tori is 6 and she is my wish kid. She wants to be a REAL princess at Disney World. We are waiting for confirmation, but I think we are going July 21 to 27th.
Tori has a genetic disorder called neurofibromatosis. She is adopted from foster care and her biological mother has the disorder and passed it on to Tori. Her biological brother Jon was also adopted by us but he does not have it.
I began fostering Tori at 21 months and she was adopted four years later. She is the most amazing little girl! She is always smiling and making friends with everyone.
During an MRI in February, they found three brain tumors. They removed one in an 8 hour surgery in February and now she is undergoing fifteen months of chemotherapy. She has a website which I can't post but if you google Tori Gaga, you'll find it.
I'm looking forward to learning more and more!!!