tag:blogger.com,1999:blog-6032288097291902285.post7426361049596184468..comments2024-03-19T02:43:07.969-04:00Comments on "Time's Up!": For the Love of a Disabled ChildTime's Uphttp://www.blogger.com/profile/09908111385466002389noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-6032288097291902285.post-17629519252778380972012-04-03T23:18:40.622-04:002012-04-03T23:18:40.622-04:00An excellent article on a topic rarely discussed i...An excellent article on a topic rarely discussed in this country, solutions and information for those with special needs. Donna Gore has taught me so much since she began writing here on the blog. Last week I had the great honor to meet her. She is truly, Lady Justice!!!Susan Murphy Milanohttps://www.blogger.com/profile/15671115229818033345noreply@blogger.comtag:blogger.com,1999:blog-6032288097291902285.post-48401101424855041372012-04-03T21:05:43.266-04:002012-04-03T21:05:43.266-04:00Dear "CP Mom" You have touched my heart...Dear "CP Mom" You have touched my heart like you can't imagine! Thank you for your very kind and generous words....In fact, I forwarded this to my own Mom! My friend who encouraged me to write this blog is a wonderful, caring person as well. It makes us so happy if even one family is assisted by what I have to convey. You must never give up on your daughter...as my mother did not...and never underestimate her abilities.... I have written a few other blogs on this topic that you might enjoy. Specifically, this one comes to mind:http://donnagore.com/2011/11/18/coping-with-your-disability-ladyjustice-style/ I hope you'll keep reading.... I thought that perhaps no one would care much about this! You have restored my faith!<br /><br />Thank You!<br /><br />Donna"<br />"Ladyjustice"<br />www.donnagore.comDonna R. Gorehttp://www.donnagore.comnoreply@blogger.comtag:blogger.com,1999:blog-6032288097291902285.post-12358743973661930512012-04-03T19:59:09.042-04:002012-04-03T19:59:09.042-04:00As a mom of a precious girl with cp, I was very sk...As a mom of a precious girl with cp, I was very skeptical about the sensationalism of this story as well. I don't live in TX, I live in the northeast, where, I do have to admit, we have excellent hospitals and therapies available. My daughter's gait is exactly as you have describe yours as being. She won't qualify for surgeries. She uses a walker for daily mobility, a wheelchair for longer distances. However, I'm worried that many people are on a witch hunt for people to treat SN kids poorly, and as we know, witch hunts are never good things. I think I may someday have my daughter follow your blog. I want her to know that she is strong, independent, and that people aren't there to either serve her because of her disability, nor are they there to hold her back. Thank you!Anonymousnoreply@blogger.com