Agree with all you say jollypirate and so glad to see the "voice of reason" on here - also interesting posts from you Cory as usual. Thanks dilemma for providing the Guardian link. The content of that link is a little extreme but certainly gives the flavour of the sorts of things that cp social workers face on a regular basis. I think one of the problems is that unless you have experienced these kinds of parents, you just cannot imagine or believe these things can happen. I am 7 years out of l.a. ssd but it ws bad enough then and I am sure it has only got worse.
To try to "paint the picture" on another thread where I was getting somehwat frustrated, I gave anonymous details of a particular scenario involving child protection in which I had been involved. Th is was met with allegations that I was making it up, one poster asked all sorts of questions and when I responded she began pointing out what she perceived as "inaccuries/inconsistencies" in the details! After this she began criticising the action I had taken - "why did you do this/not do that" ect etc. All this from someone who had aboslutely no idea of how cp investigations are conducted.
Hobgoblin - I think you are underestimating the professionals involved in parents with LD and the abilities of the Judge to make the right decision. The sad fact is that for many parents who suffer from moderate to severe learning dificulties, this disability means that that are not able to meet all the aspects of a child's development through the age ranges. This is not the fault of the parent - it is a sad fact of their disability. I don't understand why people can't understand that. All I can say is that many of these people who are up in arms about this case and others like it, willhave no idea of the major stumbling blocks that parents with LD face in trying to care for babies and children. It isn't fair to them and it most certainly isn't fair to the child involved.
I think people must imagine someone who is "not very clever" as this is what the gutter press likes to talk about. This is nonsense - it is nothing to do with "not being clever" it is to do with a serious congenital disability that prevents parents afflicted in being able to acquire the skills for safe and nurturing parenting. We all know what parenting takes and to expect parents with mod/severe LDs to safely parent is like expecting someone with mod/severe physical disabilities to do a hill climb, if you will accept this analogy.
I feel sad for Leonie as she (like others) will never change her view, based on her eown experiences and so there is little point in trying to engage with her. Agree with you Cory that people have a right to their opinion, but when it does not seem to have any rational base I get frustrated but that of course is the nature of these views, they do tend to be irrational and my trying to be rational of course not only falls on stoney ground but provokes further frustration and possibly anger for the poster.
Poshsinglemum - you talk of support and a mentor for the mother. This would have some benefit as an idea if we were talking about a short term condition, but we arenot. For a parent with mod/severe LDs they will need support on a 24/7 basis throughout the lifespan of the child, through all the age ranges IF this child is to be kept safe, and that is just not possible or appropriate. Again I think people need to be more aware of how a parent with mod/severe LDs is prevented becasue of their disability from offering safe and nurturing care to their chil, which like it or not is what the child deserves.
Have probably said too much...........