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Help mother get her son back home

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My name is Joan Campbell, I have a son 21 year old son I am manager to Autism Mothers and  I want to help the plight of this mother over her disabled 24 year old son, who from the judgment I can see has actually been taken into care by the local authority against his wishes.  So I am reaching out to you all for donations please. 

 It is clear this mother did not start this legal action, the local authority did this to her as they wanted to remove her son and the Deputyship [Guardianship] she had for him. She had already won in the Court of Protection to keep her son and the Deputyship, so they took it to the High Court because they have endless supply of public money to do that.

She has no history of mental health illness so they had to make it up to remove her son from her and to do that they used the MMR vaccine litigation she was involved in (1996 – 2004). Her case was nothing to do with the MMR that she did not want brought up in court, she had no MMR papers to rely on and she was only one of nearly 2,000 families in that legal action but she was not able to defend herself against this as she was not legally represented and not because she chose not to be but because she had run out of money. She is in debt as that local authority has targeted her for years since she won court action against them, to get them to fund what her son needed when he left school at 18.

 To make this fabricated mental illness stick the court had to claim that she imagined her son had been damaged by the MMR, so it could say that alternative therapies and biomedical interventions did not work for our adult children but she used them anyway. Worse than that she was told that these alternative therapies and biomedical interventions were dangerous and she was mentally ill to use them, so the court could also condemn those professionals who provide them.

 There are 100’s and 1000’s of us all over the world who use a gluten-free/casein-free diet and use prescribed natural supplements with complementary therapies to help our children to cope better in the world we live in and this is all she did, this is all she is guilty of!

 Most of us do this alongside medical doctors as she did because the NHS is very limited and restricted in what they can do to help make our adult children’s lives more bearable, so complementary works.

 Will this now mean we will all be diagnosed as mentally ill if we continue to do this for our children? or do we let our children suffer because legal people with no idea of what our lives are like tell us to?, when we have known our children all their lives so we know what will help them to feel better and how dangerous is it for local authorities to be allowed to behave like this to families? does this give them the green light to do this to all other families?

 This diagnosis wasn’t even given by a Psychiatrist but what NHS Psychiatrist will overturn it to risk being treated like Andrew Wakefield? will a private one be brave enough? but that costs money.

 It is shocking to think this is actually happening and to a vulnerable young adult, who I read does not have any capacity so he cannot speak, object or defend himself and whatever he can manage to say is being ignored. To do this the local authorities are using as much public money as they want to, to do this to a loving close family so it could happen to any of us, especially parents who are pro active and make demands for care, support and services or who object when things go wrong as they do and their loved ones are neglected.

 We all need her to appeal this decision because if this judgment stands it could be used against us all, as families trying to support their vulnerable and disabled loved ones but as she has exhausted all avenues for monies to appeal this she cannot do this without help, our help.

 The judgement is here http://www.bailii.org/ew/cases/EWCOP/2014/33.html and I hope my take on it explains the plight of this mother better, thank you very much!

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Joan Campbell
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