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To 'TOTO' I have answered your comments as best I can.
Why should the people in this newsgroup particularly be doing
something about *your* problems or the problems of any other person with dyspraxia. You have to realize that some of us have other problems. Atm, I am dealing with my dgd who is in speech therapy because he is not talking at all. My dil and her sister are partially deaf. What are you doing to help people who cannot hear? He may be verbally dyspraxic. If he is, we will be working through therapy and other means to help him be the best that he can be. I will answer your points. First of all my comment F... .... was uncalled for and I apologise for that. I have, and do spent a lot of time doing voluntary work with disabled people such as mentally handicapped (now called learning disability),the homeless, and raising money generally to help people. So I don't just think about my self. I think the point I was making is that sometimes I find it helpful to talk about how I feel. Generally I am quite undetanding with people when they talk about thier problems. In real life people often do by the way but I have come to realise that I also need to talk about mine. Rosalie said something like stop winging, well sometimes I need to wing. Most of the time I don't but sometimes it helps to let of steam. II think there needs to be more awarness of the condiction and I think people should, show understanding and tolerance. Someone may say why should I show understanding and tolerance, to which I guess there is no answer. However I think most people, if they are aware will show understanding. You haven't a clue what Rosalie is or is not doing in real life to help others. But please remember that dyspraxia is not the only problem in the world and others have other priorities. If you want to help, then try a real life group that deals with the specific problem that you have. I agree that I do not have a clue what Rosalie is doing in the real world. I also agree that dyspraxia is not the only problem in the world but as I said i have been involved in various charities. However my life is as important to me as anybody else so for me it is a priority. The reason why i feel more should be done is because many people have not had thier dyspraxia picked up at school and are going through life, drifitng from job to job, suffering mental torture,leading to mental health problems, depression, anger, some drift into drugs, crime. I have never taken drugs mysefl or got into crime because that just makes things worst in the long run and becasue I am would not want to. The thing is because you cannot see someone is dyspraxic people often don't undersand it and misinterpret peoples behavoiour which can lead to people being isolated and marginalised. I often find mysefl being abused becasue I can't do things and people don't understand. So I want to spread the word to try and change things. There are organizations that help people now. You just need to find one. You will not find it on a newsgroup where parents are discussing the day to day issues they have with raising children. Yes, but I can raise the awarness on a site like this. There are probably parents on this site with children who have problmes like dyspraxia etc and maybe raising awarness will mean their childrens dyspraixia will get picked up sooner rather than later. |
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On 31 Aug 2005 08:26:54 -0700, wrote:
Just FYI.... toto currently doesn't have newsgroup access. Nan |
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wrote in message ups.com... ... II think there needs to be more awarness of the condiction and I think people should, show understanding and tolerance. Someone may say why should I show understanding and tolerance, to which I guess there is no answer. However I think most people, if they are aware will show understanding. .... snip... Yes, but I can raise the awarness on a site like this. There are probably parents on this site with children who have problmes like dyspraxia etc and maybe raising awarness will mean their childrens dyspraixia will get picked up sooner rather than later. www.apraxia-kids.org |
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