Monthly Archives: June 2016

Elizabeth is now in a community scheme. The residents are very nice but my concerns are for Elizabeth because she is being forced to attend meeting after meeting – Safeguarding meetings which is against her wishes. She has not had one advocate present so far which is appalling. Nothing has been provided at all for her to do in all […]

via MESSAGE FROM ELIZABETH — Psychiatric Abuse UK


Elizabeth is now in a community scheme.   The residents are very nice but my concerns are for Elizabeth because she is being forced to attend meeting after meeting – Safeguarding meetings which is against her wishes.   She has not had one advocate present so far which is appalling.   Nothing has been provided at all for her to do in all this time just like at home.    I drew to the attention of the scheme manager today the fact that Elizabeth needs help with cooking and storage of food.  Just like in the other scheme I have had to throw lots of food away and I think that this is a health hazard and I bet no mention of this is being made at the safeguarding meetings.

In her own words this is what Elizabeth has to say about it:

“I’m getting lots of meetings.  I wish I didn’t have all those meetings.  I don’t want to go to meetings every week. I definitely don’t want meetings pushed at me.  I just want a night out and I was planning to go to the shops.”

Today I got a call from Elizabeth to ask me to come round as she wanted to go out shopping.  Today is Saturday not Sunday – that says it all.

“The social worker was not very nice considering I wasn’t feeling well.  She was asking me about things.”

“I was not very happy with this meeting.  I need my Mum – she is helping me.  I am not wishing to take part in any more meetings”

The above message was typed by someone else –  Elizabeth does not type.   I don’t know who has typed this but these are not Elizabeth’s words.

Dear Mum

I will be grateful if you can visit me once a week only on Sundays so that we go to church together and give me my allowance as well.  I will prefer you call before coming to visit me at ………………………..”

Yours faithfully”

The above words are not Elizabeth’s words – she would never use the word “allowance” for a start or say “I will prefer you call before coming to visit me”.

My carer who is now banned from the scheme because he made mention about the microwave oven not being healthy – he  also got a message from Elizabeth that she wanted him to visit in order that they could go out this evening.   This carer is like part of the family – someone we all trust 100% and has provided help in the absence of any assistance or care provided by ENFIELD mental health over a period of more than 2 years whilst Elizabeth was home and I would add it was her choice to come home as she was unhappy at the care home in Northampton.  It was only when I went to the Council’s Scrutiny Meeting that suddenly the Consultant Psychiatrist got in touch.  I accused the Councillors of not doing anything when I was trying to get the chemical Clozapine and I had to go to Harley Street in the end on the fourth day having been told that I would not get the drug anywhere not from any hospital in the local area and to get her back to the care home as they were paying for it.  I of course refused as I knew she would be sectioned as a matter of convenience and they were trying to arrange the funding for this – extra money for the taxpayer to pay out.  This was exactly what they were all planning and all the time I offered to drive all that way to pick up the chemicals.   So I presented the meeting with my story called “Get Her Back We Are Paying For That” to the Scrutiny meeting.

I have spoken to the wonderful organisation Liberty that I have joined as I would like all my carers to be applauded and highly recognised for their wonderful support in the absence of any care at all over the past years.   There are others too I would like to mention and say thanks to and hope I will be chosen.   It was good to see such a turnout at Liberty’s AGM and I was really impressed by their last award ceremony.   I would welcome the chance to talk openly about the state of mental health care in the UK and I am in touch with the most shocking cases of abuse in the UK.   How on earth can all this be allowed to go on in a so called civilised country and none of it appears in the press.

I remember previously at a hospital, (they made out it was Elizabeth’s decision for me not to be allowed on the ward or to phone at an allocated time)  I was allocated a slot to have a supervised phone call once a week but this happened to be at a time I could not ring.  All this time Elizabeth was in touch with me by text message and the letter was written by a manager there who once looked on the floor in shame when I asked what she had against me and so did one of the doctors when I asked why she had been prescribed Metformine and Clozapine which are contra indicated.   There have been so many instances like this where Elizabeth has been treated not like a person but like an object – a possession and her wishes disregarded altogether whilst a team will do everything they can to discredit you – the family – or family member as in my case and go behind your back making you out to be a terrible person, someone who is abusive, cruel, hostile, aggressive, suffering from mental illness you name it!  They even try to put words in the head of a vulnerable person putting pressure on that person and worse of all try to carry out a mental health assessment on you using your GP and accuse you of being mentally ill.    I suppose that would enhance their argument that you are not a fit mother and therefore should be banned.

I want to tell you all that I do not visit the scheme during the week daytime as I work.  I am not there every second of the day.   I am not there to “interfere” as they like to say.  It is the team who are putting words in Elizabeth’s head right now, excluding the family once again and having constant secret meetings behind everyone’s back.  They play on confidentiality and use a vulnerable person like a tool to get back at you when they dislike you and from what I see from the files they certainly dislike me a lot  but it is all wrong.  These professionals are publicly funded and there is absolutely NO accountability as no-one likes to admit if something is wrong or apologise to you about the treatment of the family and person cared for especially when very serious things have happened under their care.  They are truly above the law, protected and untouchable especially some doctors – mainly psychiatrists who are a law unto themselves.

I want to tell you that Elizabeth is very upset about all of this and does not like all their constant questioning as to whether she is being abused by me or worse.   Then they make up their sorry notes and even the past history is wrong in the files.    It is not just myself but others in the family who have complained and I have so many witnesses as many people helped me when the Clozapine had to be retitrated from scratch involving team members coming into my home twice a day reporting back to the Community Rehab Team.    Elizabeth has since told me she was “persuaded” or rather pushed to continue these distressing meetings and that there are  further meetings planned next week and she has felt forced to go along with this and is not at all happy understandably so.   Why is there no advocate present?  This is so very wrong and in itself abusive of a team of professionals as Elizabeth is finding all of this very upsetting.

Safeguarding seems to be  a once- sided exercise where a team question and question and question –  they put pressure on Elizabeth to say things against people in the family especially me who they don’t like and afterwards she feels very sorry that she may have said one or two things and all of this is being recorded in their files behind our backs.  At least I am saying things openly and honestly here.   We have most of the files to see for ourselves what goes on. This is not care this is abuse by professionals to force a vulnerable person against her family and if a whole gang of professionals say things against you as a mother for instance then it is all very biased and unfair. Who is going to believe someone who is just a mother.   So Elizabeth has attended a Safeguarding Meeting  where at least   I bet there are many professionals are in attendance and not one single advocate.    Not a fair situation at all.  At the Bethlem there were 9 at a meeting and Elizabeth often did not feel well enough to attend.  One of Elizabeth’s diagnoses is Aspergers and no one in Enfield wishes to let her have an assessment and the other diagnosis is PTSD.  I’ve got reports and other professionals are being ignored here.   Surely under the Equality Act 2010 Elizabeth has a right to be treated fairly and have an Advocate present.

I wish so much there was Open Dialogue in the local area as none of this would go on and openness and transparency which would mean I could trust the people are involved in the “care”  – but unfortunately there is nothing like this in ENFIELD.

I wish to express my thanks to the Court of Protection for acting fairly in the past not just for my daughter but for my father who had Alzheimers.  I kept him out of a home for many years and provided carers to look after him too.    Elizabeth was so terrified of going to Court.  They wanted to sever contact and deprive liberty and force her back to a care home hundreds of miles away where she had no food at the weekend.  All is written in the files.   £30 to manage on and if the money ran out they she had to go without.  Elizabeth was in bed at 6.00 pm –  what kind of care is this?

Tomorrow I am taking Elizabeth to church and I am going to tell every single church about all of this abuse.  Let God be the judge of them all as it is not my place to as they like to judge me.  I know that members of a team just go along with things as they have bills to pay and families to support –  I personally could not work in such a profession that likes to tear families apart and treats vulnerable people in the most despicable way.  They make out they know the family but they do not know anything about the family at all and there are so many mistakes in the files you would not believe it.











Gaslighting is an attempt of one person to overwrite another person’s reality. Yes I’m afraid this does go on – I would also use the word “brainwashing”.

I am sad to say they are at it again – the team of ENFIELD Mental Health are holding lots of “safeguarding” meetings.   A vulnerable person like Elizabeth should never be put under pressure to attend meeting after meeting with no advocate present. There should always be an advocate present.  All this is happening to my daughter Elizabeth right now as, unfortunately, she is in the “care” of a scheme run by Craegmoor part of the Priory Group.  She wanted to be independent but there are more restrictions than ever before and when you pay for a tenancy within reason you should not be under excessive control – it is more like RESTRICTIVE SUPPORTIVE HOUSING THAN SUPPORTIVE HOUSING.  The scheme is a small scheme situated  just down the road from where I live and consists of six people.     Sadly, when Elizabeth came out from Cygnet on 20mg (one of the most highly dangerous drugs Elizabeth has been on so far) this left her unstable.  Abilify, is manufactured by Otsuka and they sent me an email when I contacted them saying this drug is licensed for Schizophrenia and Bipolar only and should only be given for 12 weeks. Well what about the other diagnoses.  What about if Elizabeth has been misdiagnosed which we all think she has been.  Elizabeth has suffered an adverse reaction on this drug which I have had to report.     It is all down to drug metabolism and the problem is that  Elizabeth cannot metabolise the drugs – that is the problem.  She is multiply diagnosed.

Anyway, I am so concerned as to what is going on right now that I am going to post this to everyone and I want everyone to know which area I live and that is ENFIELD – an area where we have encountered bullying by a team “professionals”.  I am proud to stand up alone against this.  I told my daughter tonight nothing will ever turn me against her.  Not even the nastiest comments that appear in the files.  Other parents should be aware of this tactic by so called “professionals” who do not like you, who act in such a way so as to try to distance/sever contact between you and the person cared for  instead of work together with the family under Open Dialogue.

Sadly we as a family would have benefitted from joining the Open Dialogue UK that has just been put into effect from 4th May through NEL MH Trust but I feel that we have been discriminated against by NHS using “red tape” by saying that we already had a team in place  – well what team?    For the past two years I have had to employ my own team as we have had no care whatsoever.  Care should not be about pushing drug after drug at maximum levels without review.    All I wanted as a mother was to have my daughter on the minimal of drugs but now I can see why they put it up to maximum levels in the hope that this blots out someone’s memory –  no one in the local area would wish to hear that something serious happened under a scheme in the community to my daughter because of lack of supervision and weakened by enormous levels of drugs more than one serious incident has occurred under “care”

Elizabeth is now living in a smaller scheme in the community run by Craegmoor (part of the Priory Group).   In this current scheme it is really designed for someone who is able to stand on their own two feet.  The only thing that makes me happy about this scheme is the residents.  There is a woman there who acts like a mother figure thank God.  I never see staff downstairs but their duties are to take my daughter to the constant safeguarding meetings.  It is a pity that after all this time since her admission on 17 May that not one thing has been provided for her to do and neither was anything provided for over 2 years at home .  I had to provide things for her to do out of my own pocket.

Just to let you know the family currently have had an enormous complaint out against Social Services ENFIELD and this has been “dealt with” by the NHS’s Deputy Leader of Quality.   We are looking forward to another meeting as our complaint has not been properly answered.,

We have Power of Attorney not just myself but other family members not because we wish to control Elizabeth’s life but because we wish to provide for her one day.  She has come out of the system disabled.  Even walking up the road to get shopping is an ordeal for her.  It is a pity this team under ENFIELD have not signed up to  Open Dialogue. Naturally I have no trust in professionals in this Borough because of reading the shocking contents of the files which label me as being “mentally ill” whatever that is?  You can also see how the team tried to set up a MHA assessment for me  through my GP –  I was too busy to attend.  I work, I have a busy life and combine this with caring for my daughter.  I am not with my daughter 24/7 but this is a team who do not seem to care for my daughter and who know nothing about the family.   They just want to control.   They have got past history wrong.  All Elizabeth wishes for is that everyone works together and gets along but this is a team who play on confidentiality to save their own backs.  I am satisfied that I am correct in saying this,  having read so many nasty comments in the files.  There is no accountability.  Most people would not be allowed to get way with this kind of behaviour.

I am so concerned of the recent developments that I feel I should make it public.

At the latest safeguarding meeting Elizabeth told me this evening when I called round with a new chip for her phone she told me she was put under such pressure at the SAFEGUARDING meeting where she is constantly taken that she does not want to go to any other meetings and she was put under pressure by the care coordinator to say the following in a typed letter that Elizabeth would not have done herself as she does not type and these are not her words in any case:












Elizabeth told me tonight she was “put on the spot”

I have said to her that what if I cannot come on a Sunday.  She then told me that she was put under pressure by the care coordinator accompanied by a member of staff from Craegmoor.

Elizabeth had hand written  a letter to the staff member of CRAEGMOOR reading as follows:

Dear F…………. (not sure how to spell)



Elizabeth’s own words.  Take note team and especially care coordinator.


I think they may be trying to ban me and I will keep you all informed.  THIS IS NOT WHAT ELIZABETH WANTS AND NEITHER IS IT HELPFUL TO HER.

We have had all of this in the past from Cambian and now this is going on at Safeguarding Meetings and witnessed by a member from Craegmoor – how nasty can you get!   Elizabeth did not type this letter herself.  The wording is not coming from her.  If she did say once a week she was put under pressure and it is DISGUSTING THAT ENFIELD MENTAL HEALTH ALLOW THIS KIND OF THING TO GO ON.

So our complaint (not just mine by the way) is about the care coordinator who has failed to provide any “care” and neither have social services.  They prefer instead to work against the family trying to destroy us all like they have done in the past.   What kind of people are these who work in what should be a  “caring” profession?

I have had to complain recently about the lack of communication leading to Elizabeth being given wrong dosage of drugs at 20mg and not 10. Apparently the care coordinator based at Silver Street ENFIELD does not like to use emails and neither does the Consultant Psychiatrist but instead of sending a letter to Elizabeth they should have copied in the tam at the scheme.

Anyway back to the meeting today, Elizabeth was very upset as she had been put on the spot.  She is multiply diagnosed but I am currently challenging ENFIELD who just do not wish to pay for proper assessments, choosing to ignore the fact that Elizabeth is multiply diagnosed and I have been asking about this for some time now.  There is more than one diagnosis I can see in the files and Aspergers is one of them.   It is absolutely disgusting that ENFIELD do not wish to provide such assessments so I have contacted the National Autistic Society regarding this and I also feel that she suffers from PTSD.


When I visited tonight I asked Elizabeth what she had eaten.    “just a few chips”.   She is likely to go downhill and that is my one complaint.   The mistake in the dosage of medication I would put down to lack of communication from the team at Silver Street as they write letters and do not inform anyone.   If they had properly informed staff at the scheme then this would not have happened.

We as a family are cut out completely and I can see this is AGAINST NICE GUIDELINES.

I think that NICE Guidelines should be enforceable to some extent as it would appear that no notice is taken of them.

The manufacturers of Abilify state clearly no more than 12 weeks on the drug.  Elizabeth has been on this for much longer. and all they have done is change the toxic red dye drug of 10mg that causes tumours in mice and rats to a white tablet again of 10mg.

I feel that Elizabeth would be kept on this drug for life if she is left under that scheme.  At home the team did not wish to revise the drug Clozapine that caused her tongue to go to the back of her throat.

Anyway, it is a good job that I as a mother look into the ingredients of these chemicals thoroughly and am also constantly looking into where there is better care and guess what I HAVE FOUND IT!   I shall keep you all informed as I’m trying to get funding for this..   If it is a manufacturer’s guideline that you should only be on a chemical for 12 weeks as Inspector Brown would say “WHAT THE HELL IS GOING ON” – Sorry for pinching your title Inspector Brown but it is so appropriate for my honest blog.

At the weekend I enjoyed attending Liberty’s AGM.  I really hope I get chosen for my Award nominations  as this will give me a chance to discuss the most shocking abuse going on in the UK to MH and vulnerable people.   Yes, I am in touch with even worse cases.   Good to meet you all at LIBERTY and I support all of your campaigns.  I will be more than happy to help if I can.   I would also be prepared to be filmed and hopefully people will really take notice – there is more than one Winterbourne and I want to bring all this to the public’s attention.

When I called to see Elizabeth tonight she was feeling a bit low.  She can easily get agitated but Dr Joanna Moncrieff has explained to me to say that the drug Abilify is noted for causing Anxiety and Agitation and I remind myself that this is the drug and what it is doing,  not Elizabeth’s character and I said to her today that nothing would ever destroy things between us even if the team have prompted her to say nasty things.  I KNOW WHAT IS GOING ON TEAM –  PLEASE ALSO DO NOT TRY TO ARRANGE ANY MORE MHA ASSESSMENTS VIA MY GP.  I am seeing my GP tomorrow and I will tell him now that never will I attend such an assessment in a million years.  Someone who is a professional said to me that perhaps they should do an assessment on themselves and I could not agree more.

Other people in my family and my carers would like an apology for being called “aggressive” “hostile” –  I have been called a prolific complainant – they failed to name me as “vexatious” .      It is cowardly to label someone behind your back and I would welcome an open discussion with team members on TWITTER in front of everyone.

When I left tonight after seeing Elizabeth she was smiling and happy.   Elizabeth needs help at the moment but hopefully she will be able to get on with things herself one day.   –  there is nothing more controlling than a group of professionals who instead of providing help and support are holding SAFEGUARDING meetings no doubt for the purpose of cutting contact no doubt but now Elizabeth has written in her own words.  This is not a typed letter written by someone else – this is coming from her in handwriting and no way on earth could I have ever forced her to write it:

Dear F…………. (not sure how to spell)



If all that has been done was  meant to destroy the family I am afraid they have brought the family together –  this is because of all the nasty things that have been said for all to see in the files.

Tomorrow I am going to vote and hopefully take Elizabeth.  According to the letter it says every Sunday!   Just like at Cambian –  phone calls – restricted to once a week – not that I used to phone every night but at a time that I could not call anyway.     How very sad that a team of “Professionals” resort to this kind of behaviour and I understand that my emails have been called “annoying” by the care coordinator.  It could be because I know how to communicate effectively and the best way is to copy everyone in so that everyone knows what is going on.







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