Guest guest Posted December 16, 2005 Report Share Posted December 16, 2005 What???How is that different from the person who has seizures gets a device to stop them and is asked questions about things we have no answers for? How is a recovered kid different from anyone who has overcome a great set of barriers? I do not understand your comment. It's our moral duty to help as many people as we can. My daughter still has Autism and if I found one cure that helped her function 100% in this world, I would be screaming it from the mountaintops! I would be having aparty everyday for the rest of my life! Iknow my daughter would be so excited and feel so blessed that she would share her experience in hopes that she could help answer the un answered questions so she could help other children in the world. Your comment just really blows me out of the OCEAN- embarrassed? No way! Let's celebrate a cure! Candis Autism Research Survey online at: http://www.inclusioncommunitytrainingcenter.org Candis Firchau,MA,TLPC Director Inclusion Community Training Center Advocacy, Behavioral Interventions, Counseling and Training 979.826.8568 This email is intended exclusively for the person to whom it was addressed. This email is confidential. If you have received this email by error, please disregard it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 16, 2005 Report Share Posted December 16, 2005 I think we've all made our point here, which is this... some children would be happy and proud to get up on stage, some would rather not be there. Some parents would be glad to have their children represent recovered children publicly, and some would prefer to provide support in other ways. At every holiday school program when he was in elementary school, my NT son looked so miserable to be on stage that he looked like he might pass out... and that was in a large group of children.... he would inch his way back so that he was completely hidden by the other kids standing on the risers. He hated it. He would not be one to choose to get up in front of a crowd. He ran for mayor of his class and threw up at home (nerves) before he went to school to give his speech. He won, by the way... but he absolutely hated giving that speech. My NT daughter, on the other hand, will put on a never ending show for anyone who glances her way. At the holiday program this year, even though she is the smallest one in her class, she elbowed her way to the front and did her best to thrill the audience. She sang a solo at the school talent show in front of more than a hundred people. She would be thrilled to get up in front of a crowd for almost any reason. Different strokes for different folks... that's what makes the world interesting. Caroline Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2005 Report Share Posted December 17, 2005 Candis - while I agree with celebrating a cure and it being our moral duty to help as many people as we can, despite what you think your daughter thinks now, she might not want this screamed from the mountain tops if she were blessed with a cure or recovery. Some of our children have been so severely bullied and harassed during their recovery, that all they want to do is act, be and be treated as normal - especially when they are in their more formidable teen years. Screaming about recovery from this disease might just not figure in their agenda yet. In 10 - 15 years time with adult maturity - and others around them in their peer group have reached a maturity to accept, then they might want to be more open about it. RE:recovered & embarrassed by past What???How is that different from the person who has seizures gets a device to stop them and is asked questions about things we have no answers for? How is a recovered kid different from anyone who has overcome a great set of barriers? I do not understand your comment. It's our moral duty to help as many people as we can. My daughter still has Autism and if I found one cure that helped her function 100% in this world, I would be screaming it from the mountaintops! I would be having aparty everyday for the rest of my life! Iknow my daughter would be so excited and feel so blessed that she would share her experience in hopes that she could help answer the un answered questions so she could help other children in the world. Your comment just really blows me out of the OCEAN- embarrassed? No way! Let's celebrate a cure! Candis Autism Research Survey online at: http://www.inclusioncommunitytrainingcenter.org Candis Firchau,MA,TLPC Director Inclusion Community Training Center Advocacy, Behavioral Interventions, Counseling and Training 979.826.8568 This email is intended exclusively for the person to whom it was addressed. This email is confidential. If you have received this email by error, please disregard it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2005 Report Share Posted December 23, 2005 Thank you, . I completely agree. I absolutely feel that I have a moral obligation to spread the word that recovery is possible. I have had countless converstions via email and telephone with strangers, sharing my experiences and story. I have even invited people into my home so they could see the miracle with their own eyes. However, my recovered 10 year old remembers being teased and taunted in preschool. She remembers how much she hated being pulled out of regular kindergarten for adaptive phs ed. and speech. (she would cry and ask why the other kids didn't have to go). Another story that comes to mind happened in grade 1 when little nasty formed a girls " club " during recess times and all the girls in the class were in it. went out of her way to make sure my daughter wwas excluded. My daughter was crushed. Although pretty much recovered at that point, she didn't understand why anyone would be " mean " , nor did she know how to stick up for herself. Now, she's an honor student in regular 4th grade with many friends(even nasty ended up a good friend). She's on a swim team and is a girl scout. She just wants to live her life and be a normal kid. She understands her disease and appreciates all it took to get her here. However, she is not interested in sharing any of this information with her peers or anyone else. They accept her as one of their own, and that's all she's ever wanted. I was a teacher for a long time in an inclusion school. I've seen absolute angels embrace sped kids and make them feel accepted, and part of the group. I will never forget the expressions on the faces of these sped children who were treated with such love. Unfortunately, I've also seen lots of exclusion and downright cruelty, and the resulting heartbreak . Before recovery, I rememeber my desperation and my thoughts of what I would do(including screaming from mountaintops) if only she would " make it " . It didn't occur to me at that time that my child wouldn't like that idea. I do want to help in any way I can- especially in spreading the word of . I would welcome any one of you into my home to meet my family and witness our blessing. Not a day goes by when I don't appreciate how lucky we are. I hope someday, my daughter will want to share her story with the world -but that will be her decision. Happy Holidays to you all. Never give up. __________________________________ for Good - Make a difference this year. http://brand./cybergivingweek2005/ Quote Link to comment Share on other sites More sharing options...
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