
Very appropriate

This book was beyond excellent. It is a MUST read for all parents of children with disabilities,the children themselves, for ALL educators, and anyone who wants to be more informed about how to fairly treat people with disabilities. It is not just for those with Tourettes.
Normally it takes me weeks to read a book. I couldn't put this one down. Living with a child who has a disability is a constant struggle daily. Reading this book confirmed much of what we have been living for the past 11 years. My child's disability is no where as severe as Cory's, however, you often feel like you are all alone in your quest to find answers. You feel no one understands what is going on, doctors keep pushing pill after pill, and yest some of them do make the disability worse. One doctor will tell you one thing when the other tells you the exact opposite. Your friends and family have all the answers but are scarce when you need assistance.
I applaud Cory and his parents for writing this book and sharing a very personal, painful part of their lives with us. Thank you for helping me to see that when I fight at a special education meeting to get what my child should have, it is all worth it.
I would love to meet Cory and his parents and have my chld meet Cory. I think Mrs. Freidman and I have much in common. Then end of the book when Mr. Friedman said his wife always told Cory, "you can do whatever you want in life" brought tears to my eyes. That is the exact thing I have been telling my son for years.
Never give up and always, always follow your heart. This book definately confirmed that what I am doing and have done in the past are on target. Thank you for valadating me and what I have and will continue to do for my child.
Advocate, advocate, advocate. Our children deserve the best and if we need to fight to get it then it is all worth it. Thank you for giving me the strength to continue in the fight for my child.
Review ID: 10000000010285084

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