Went to visit Elizabeth today.  Took ages to get there as I did not have the car – still in the garage being repaired.   Elizabeth looked terrible with bruises all over her face – said it was an accident.  I had prior arranged for her to be allowed off the ward and decided to wait in the hallway outside but waited for ages until eventually I had to ring the bell.   A nurse brought Elizabeth to me and then said he would have to check to see if he was needed to accompany us out.   I told him surely I could spend some time alone with my daughter and if he did not trust me I could give him good references as I was up until recently training to be a police officer but could not continue with the course because of all these problems.

 

Anyway we went for a nice meal in a local tapas bar and then went into the local small town and it was soon time to go back.  Elizabeth wanted to go to the cinema but I had to say there was not time as it would have made us too late and then staff may not be willing to allow her out with me again.  Elizabeth liked the pet shop up the road as she adores animals.   She also wanted to see the babies in a special unit near the ward but this was not allowed.   Together we walked through the beautiful grounds and saw the facilities.   The family were not happy with me today and blamed me for putting her on this “dreadful apalling ward”  which is miles away however there is no hope for Elizabeth if she is not responding to medication and desperately wishes to come off it and certainly it is not doing her any good and will kill her on this high dosage. The Professor promised to take her off for a drug free assessment and that is why I agreed for her to go there.  I have previously highlighted at least 9 medications they have given her  under the local NHS mental health team and then on top there was that for her skin as the drugs made her skin itchy and irritable.  Anyway, we had a nice day together despite the poor weather and the rest of the family are threatening to go to their MPs to complain about the ward and her being there but I told them to wait as I have a meeting Friday with the team and in any case, I hope the team listen this time.  Elizabeth once said “why wont they listen, Mum”.   Whilst the ward is not nice and secure like a prison the surrounding grounds and facilities are great.   For the first time I looked around and saw a wonderful art and craft centre, a swimming pool and lovely restaurant and beautiful flowers everywhere.  There was also a lovely church and Elizabeth lit a candle.  Together we prayed – I hoped that Elizabeth did not see that I was in tears.   I believe that if this more specialised hospital listens for a change and maybe takes on board some of Dr Ann Blake-Tracy’s advice then I can only hope and pray that Elizabeth can be free from the hell she is experiencing as a result of these harmful mind-altering prescribed drugs.

Never a drug taker herself or one to drink in the past,  these prescribed drugs can lead to such addictions which is really shocking.

I hope Elizabeth can be saved but if they do nothing then the whole family with come together and we will all complain – that is the first time ever as it has only been me who has complained about the care in the past which is all about drugs as you can see.  At least in terms of facilities there is more at the specialist hospital than anything at local level but local care should also be improved in this respect in my opinion.  A patient should not just be left to go downhill to such an extent as Elizabeth has done.  A patient also needs more support than is given in the community on release from hospital and this is why all too often care in the community fails.  Once a patient has become institutionalised they need a lot of support but social services do not listen and I believe it is down to money. 

On the door of the ward is a picture of a lovely dog.   The dog is a “sniffer dog”  looking for drugs – I joked about this and said there is nothing but drugs on this ward – drugs that are plied by the staff to patients who ultimately suffere the consequences in terms of health later on in life.

 

 

 

 

From the document I attach you can see what the NHS have to offer for care under the mental health.  They are no better than drug pushers and pick on a patient who is weak and vulnerable introducing one drug after another.   In the above document is not all of the drugs that my daughter has been plied with.   It is no wonder she is not well now and can barely speak at times and you can no longer have a conversation with her.    In addition to these drugs despite having about 4 different diagnoses, she has also been given another drug called Lymececlyne – a skin medication until I looked into this and discovered it should only be used for short term purposes but was allowed to continue for far longer than it should have been. 

I understand that the specialist hospital specialise in pushing the drug Clozapine – “its all about Clozapine here” so I was told.    The leading Professor put in writing about a drug free period and I have every intention of naming him and the hospital if this does not go ahead.   The leading professor said he had one or two contacts.  

None of these drugs above which must have cost the taxpayer a fortune have worked and have made Elizabeth worse.  If she is allowed to continue on a high dosage of Seroquel (Quetiapane) – 750 mg then she could die as a result.  She is suffering from serious effects of the drug right now and has begged to come off it and Astra Zeneca the manufacturer say they cannot discuss things with me in a letter – that they are governed by the British Pharmaceutical Industry. 

It would seem like the British Pharmaceutical Industry do not care less as they have not responded to my email.   The Government – Andrew Lansley, David Cameron and Nick Clegg have also ignored correspondence from me but now Elizabeth’s father is so upset having seen the awful ward that he may go and see Mr Lansley as this is the MP responsible for the area he now lives in.

The rest of the family are also horrified by the ward and so am I.  It is every bit like a prison and the grandparents were shocked at Elizabeth’s appearance. 

Elizabeth has been on this ward for 2 weeks and already the psychiatrist has tried to persuade her to take Clozapaine which carries 5 black box warnings  for agranulocytosis, seizures, myocarditis for other cardiovascular and respiratory effects and increased mortality in elderly patients.   It was voluntarily withdrawn in 1975 by the manufacturer as it was shown to cause agranulocytosis – dangerous decrease in number of white blood cells that led to death in some patients.  It is therefore not FDA approved for anyone who has a history of heart/breathing problems in the family which would ultimately rule out this treatment for Elizabeth as there is such a family history of these problems and she was herself asthmatic and has complained of chest pains and serious effects on the drug she is currently on.   Dr Tracy of the International Coalition of Drug Awareness highlights more information on the attached document and I am waiting for her book and cd.    I am not paid by Dr Tracy or the CCHR who very kindly gave me free of charge the shocking dvds and literature – I just want people to be aware of the dangers and the fact that the psychiatrists openly admit on the dvd “Diagnostic Statistical Manual – Psychiatry’s Deadliest Scam” that there is no way of proving what causes a mental illness in someone.   In fact some of the psychiatrists were laughing and there was one from a specialist hospital over here – it is absolutely shocking and I would urge anyone to look at the site of Dr Tracy and her publications and presentations to the FDA as well as this dvd which contains actual interviews.

Anyway Elizabeth is unhappy on this awful ward.   The rest of the family are extremely unhappy and so am I especially in light of the fact I have just received a letter from the PA of the Professor stating he is no longer in charge of the ward.   Having promised my daughter in his letter about a drug free period there is no way on earth that I am going to sit back and do nothing.   This Professor should never have promised in the first place and he is responsible for referring my daughter to this awful ward which she describes as “prison”.

I have the day off next Friday to go to the CPA.  I will be sitting there quietly taking the minutes as I am never given a copy of the minutes by any team.   I am even thinking of doing a PowerPoint presentation with handouts to the team as these meetings are of little benefit to my daughter.    Elizabeth gets agitated when surrounded by lots of people firing questions at her and has openly told me that she feels pressurised to go along with the team’s decisions.   A patient should be entitled to an advocate and I had to point this out to previous teams as this is in accordance with NICE guidelines.    Nice guidelines are not adhered to from my experience and I had to print off a copy to show a psychiatrist under the previous local team.   The only thing good about the local care was the fact she was near to the family however we all accepted that if they did not have the facilities to take Elizabeth off the drugs which are causing serious side effects then the only solution would be for her to go in somewhere more specialised where they could do just this but now I am told “we will have to weigh up the safety of other patients” – well it looks like they do not intend to do anything but I will soon see when I go to the CPA next Friday.

I am going tol request Elizabeth be moved elsewhere if the only treatment there is drugs which requires a signature on a disclaimer form.  I will also quote the fact that according to Nice guidelines she should have an advocate who sees her alone and not in the presence of a team who are watching every second.   This kind of intrusive care should only be given for a patient who is coming off the drugs, whose behaviour is that unpredictable.  Even then I believe that if there was a beautiful place provided such as on www.earthhouseinc.org then this would be the answer.    Unwittingly a friend of mine signed such a consent form for Clozapine and did not realise what she was siging at the time.  Now her daughter has heart problems.   She has warned me that is what they could try to do.   Elizabeth is now in no fit condition to sign such a form in any case but the team could turn around and say otherwise – she is 25 and weak and vulnerable.   She is already distressed at them offering her this awful drug when she thought she was going in to be reduced off medication.  She is distressed at being in such an awful place which by the way is surrounded by the most beautiful grounds and in a lovely area.  The only good thing is the dogs that come on the ward –  Elizabeth would like a dog.  Elizabeth needs to be in a peaceful area where there is fresh air and nice surroundings not a ward that is like Hell on Earth and all about drug pushing.

THIS IS HOW CRUEL THE NHS CARE IS.  THIS IS NOT CARE AT ALL IT IS NOTHING BUT DRUG PUSHING BUT ANYWAY I AWAIT TO HEAR WHAT THIS SPECIALIST HOSPITAL HAS TO SAY FOR THEMSELVES AND WHAT OTHER THINGS ARE ON OFFER IF ANYTHING APART FROM HARMFUL DRUGS WHICH DO NOT WORK AND EVEN IF THEY DO TEMPORARILY GIVE A PATIENT A FEELING OF WELLBEING THEY ARE A TIMEBOMB IN THAT THEY CAUSE SERIOUS PHYSICAL HEALTH PROBLEMS AND AFFECT THE HEART, LIVER, KIDNEYS AND LUNGS AND HOW MANY TIMES HAS ELIZABETH BEGGED TO COME OFF THEM YET THE TEAM IGNORE  AND EVEN SOCIAL SERVICES GET INVOLVED IN TRYING TO PUSH DRUGS.

I am going to visit Elizabeth today and will write later.       

I was told my visit unsettled her and that the entire staff and patients thought I was rude.   I was upset at hearing from a  nurse that the care was all about Clozapine and that I should have done my research first.   Now I feel that Elizabeth is stuck in a prison environment and to top it all that the team will pressurise her to take this drug despite a history of heart problems within the family and she has suffered asthma in the past and allergic reactions due to asthma.  The FDA clearly state this drug should not be given in these circumstances.  She has also complained of some very serious side effects from these drugs like fever, sweating, dizziness, anxiety and confusion.   I am so glad that I am in regular contact with Dr Tracy of the International Drug Awareness Coalition.   I heard through someone I know that a form has to be given to a patient to consent to being on this drug.   Elizabeth shouted out in front of my friend who was witness “NO I DONT WANT TO GO ON CLOZAPINE”.  I hope this team listen although it is hard to trust anyone when they respond in such a way towards you and then they say that my visit upset her as well as everyone else on the ward, when in fact the truth is she wanted to go out with us and then you get a scenario where the whole team stick together to support one another.    THIS IS NHS CARE FOR YOU AND WHERE IS THE PROFESSOR – NOONE SEEMS TO KNOW.   THE PROFESSOR PROMISED IN WRITING SHE WOULD COME OFF THE DRUGS AND I M ADE SURE THE REST OF THE TEAM KNEW ABOUT IT BY SHOWING THEM THE LETTER.  ELIZABETH’S WORDS WERE “PLEASE DO WHATEVER IT TAKES TO GET ME INTO ………………HOSPITAL..”  PLEASE MUM PLEASE HELP ME COME OFF THE DRUGS – DO WHATEVER IT TAKES”   SHE WANTED TO COME OFF THE DRUGS NOT BE EXPERIMENTED ON ANY MORE. 

SHE IS NOT ON A SECTION YET SHE WAS NOT ALLOWED OUT!  

 

THE REST OF THE FAMILY ARE VISITING AT THE WEEKEND AND ARE VERY UPSET AS WELL.  LETS HOPE THEY DO NOT PUSH THESE DRUGS ON HER AND THEN MAKE OUT SHE IS  HAPPY AS I WILL LINE UP WITNESS AFTER WITNESS IN THIS RESPECT AND HAVE WRITTEN NOTES TO THE TEAM WHICH HAVE BEEN IGNORED AND NO END OF PEOPLE HAVE HEARD HER SAY “PLEASE HELP ME COME OFF THE DRUGS”. 

 

SHE WAS NEVER ON DRUGS BEFORE – NEVER TOOK ALCOHOL WAS A PLACID, POLITE GIRL WHO HAD A JOB.  SOMETHING BAD HAPPENED TO HER AND SHE SHOULD NOT HAVE BEEN PUT ON THE DRUGS IN THE FIRST PLACE.  THEY HAVE RUINED MY DAUGHTER AND THEY WILL KILL HER ON A DRUG THAT IS VERY VERY HARMFUL NEEDING REGULAR BLOOD TESTS.   I HAVE ASKED DR TRACY FOR HER SUPPORT AS SHE REPRESENTS PEOPLE IN COURT AS EXPERT WITNESS IN SOME OF THE MOST HIGH PROFILE HOMICIDE CASES.   I WOULD URGE ANYONE IN A SIMILAR POSITION TO LOOK AT HER  DRUG AWARENESS WEBSITE AND THAT OF THE CCHR AND REVELATIONS UK.

CLOZAPINE OTHERWISE KNOWN AS CLOZARIL AZALEPTIN, LEPONEX, FAZACLO FROIDIR DENZAPINE, ZAPONEX, KLOZAPOL AND CLOZAPINE IS AN ANTI-PSYCHOTIC DRUG USED FOR TREATMENT OF SCHIZOPHRENIA AND BIPOLAR.   IT WAS VOLUNTARILY WITHDRAWN BY THE MANUFACTURER IN 1975 AFTER IT WAS SHOWN TO CAUSE AGRANULOCYTOSIS, A CONDITION INVOLVING A DANGEROUS DECREASE IN THE NUMBER OF WHITE BLOOD CELLS THAT LED TO DEATH IN SOME PATIENTS.   STUDIES SHOWED IN 1989 IT WAS MORE EFFECTIVE THAN ANY OTHER ANTIPSYCHOTIC FOR TREATING SCHIZOPHRENIA.  THE FDA APPROVED IT FOR TREATMENT RESISTANT SCHIZOPHRENIA ONLY BUT THE FDA REQUIRES BLOOD TESTS TAKEN FOR PATIENTS ON THIS DRUG AND FOR IT TO CARRY 5 BLACK BOX WARNINGS FOR AGRANULOCYTOSIS, SEIZURES, MYOCARDITIS AND FOR OTHER ADVERSE CARDIOVASCULAR AND RESPIRATORY EFFECTS AND FOR INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA RELATED PSYCHOSIS.  IT IS USED AS A LAST RESORT TREATMENT AND AT FIRST BLOOD TESTS ARE CARRIED OUT CONTINUALLY WITH WEEKLY CHECKS FOR THE FIRST SIX MONTHS AND THEREAFTER THE CHECKS ARE REDUCED.

AGRANULOCYTOSIS IS AN ACUTE CONDITION INVOLVING A SERIOUS AND DANGEROUS LEUKOPENIA (lowered white blood cell count), most commonly of neutrophils causing a neutopenia in the circulating blood.  It represents a severe lack of one major class of infection-fighting white blood cells.  People with this condition are at very high risk of serious infections due to their suppressed immune system. 

ELIZABETH IS VERY UPSET – SHE HAS BEEN OFFERED THIS AWFUL DRUG SO MANY TIMES AND HAS REFUSED IT.   SHE REFUSED IT AGAIN TODAY IN FRONT OF THE LEAD NURSE.

I COMPLAINED ABOUT ELIZABETH BEING OFFERED THIS AND SAID THE PROFESSOR PROMISED SHE WOULD HAVE A DRUG FREE PERIOD AND SHOWED HIM THE LETTER AND ALSO ELIZABETH’S EMAIL BEGGING TO COME OFF THE DRUG.   THE LEAD NURSE TURNED ROUND AND SAID “YOU SHOULD HAVE DONE YOUR RESEARCH FIRST – IT IS ALL ABOUT CLOZAPINE HERE”.  I WAS EXTREMELY UPSET AND ELIZABETH SHOWED HER DISTRESS IN HER BEHAVIOUR AND I LEFT THE WARD TO GET HER A MCDONALDS AND HER NEW FRIEND SHE APPEARS TO BE LOOKING OUT FOR ON THE WARD.  

I WILL NAME THE HOSPITAL AND THE ENTIRE TEAM IF THEY ABUSE HER HUMAN RIGHTS IN COMING OFF THE DRUGS AS I HAVE IT IN WRITING FROM THE PROFESSOR WHO LIKEWISE WILL ALSO BE NAMED.

Elizabeth is now at the new specialist hospital under a new team however there have been the following developments: 

I received a phone call Friday from Elizabeth and I can hardly bring myself to say how upset I am.  Apparently the new Psychiatrist has mentioned about her taking Clozapane and this is despite her making it clear she does not want to go on this no end of times at previous CPAs – this must surely be documented in the files.    Now it is hard for me trust the team as a result who I have not even met yet.     I will be visiting Elizabeth tomorrow for the first time and will request to see the files as she has already given me permission.  Clozapane is an extremely dangerous prescribed drug that involves monthly blood tests as it affects the white blood cells.  Elizabeth does not want this.  What is so good about Clozapane which involves having monthly blood tests as it affects the white blood count and causes heart defects as I know from several people who have been on it and become affected.   There is no way this is some kind of wonder drug and Elizabeth did not want the blood tests.   I intend to take matters to court if this new psychiatrist goes ahead and changes the medication to this as it has been promised by the professor that she is going to come off the drugs all together.  This is what Elizabeth wants and the heading of this blog is what she requested me to do before her admission.

Elizabeth who can hardly write any more as she is too ill on these chemicals, who once enjoyed writin, wrote the following about the drug Seroquel which she is currently on and I am publishing this with her permission:

Dear …………….” I dislike the dosage fact that I am  not sure what dosage meds am on from rehab.  I’d like to come off it poss.  Please get back to me”. 

This short email was written without my prior knowledge or any encouragement by me – solely by Elizabeth and sent by email from the scheme where she was living to her social worker.   Her social worker responded with visits on more than one occasion trying to get her to go on Clozapane.   Social Services first of all denied this but I confronted the social worker and it was true just as Elizabeth had told me.  What on earth are social services doing getting involved in drug pushing to my daughter – I told the social worker it had nothing to do with her and I requested a new social worker but the team refused and my daughter was upset over this whole incident and told me all about it and how she had been ignored. 

Now to top it, all the new Psychiatrist at the leading hospital is trying to do the same and get her off Seroquel onto Clozapane.   There is no way I am going to stand by and do nothing.  I gave Elizabeth my word I will help her and will go to any lengths to do this.   Elizabeth has signed an Advanced Disclosure to the hospital saying that she wanted no further experimentation – that includes medication or ECT and it is clear that either the Professor has not passed this on or else the psychiatrist has not properly read the files.     I am furious about this as you can imagine.  I wrote back to the psychiatrist and told him that it was against my daughter’s human rights and he should not put her on Clozapane otherwise there would be legal implications involved.

I obviously cannot trust this specialist hospital and now I shall want to see the files every week to make sure what they are doing.   I was told nothing would be changed for 2 weeks as regards the medication and then I propose to  attend a meeting at the hospital in a week’s time.  I was first of all impressed by what I saw as good communication on the part of this hospital but it seems they are drug pushing as regards Clozapane which is extremely dangerous and I know of people who suffer heart defects as a result.    The Professor promised he would take her off the drugs and now I am hearing this. 

Thank God I have signed up to www.drugawareness.org and am getting good advice from a professional doctor who knows a lot about these drugs and attends court as an expert witness in high profile homicide cases.  I would urge anyone in a similar position to do the same.  At the next CPA I am going to take along with me all the tapes I have from the CCHR including many interviews of laughing psychiatrists who make no secret of what kind of “care” they dish out without having any scientific evidence to back their claims.

I have already shown my daughter the shocking dvds.

I have also approached Astra Zeneca and complained to the FDA about the harmful drug Seroquel (Quetiapane).  Here are some extracts from their letter:

 “We are sorry to learn your daughter has experienced these symptoms and recommend that she consults her doctor on the matter.”   ——-well I have on many occasions consulted the local team of various psychiatrist, all of whom have ignored my complaints and that of my daughter and tried to offer Clozapane instead.

The letter goes on to say the following:

“As I hope you will understand we are prohibited from discussing your daughter’s individual treatment with you by the ABPI (Association of the British Pharmaceutical Industry) Code of Practice.”   I DO NOT UNDERSTAND – SO I THEN CONTACTED THE BRITISH PHARMACEUTICAL INDUSTRY CHIEF EXECUTIVE WHO HAS NOT EVEN HAD THE COURTESY TO REPLY TO MY EMAIL SENT DIRECTLY ON THEIR WEBSITE.

Also, I contacted Andrew Lansley, David Cameron and Nick Clegg – not one has had the courtesy to respond to my email.     It would seem there is close connection with the British Pharmaceutical Industry and the Government.  They make a fortune out of the misery of people like my daughter stuck on harmful chemicals they cannot just come off and need professional help in which to do so.   The drug awareness website above gives such advice and you have to come off them very very slowly and over a period of a year or more.  It is supposed to be more risky to come off these drugs than remain on them BUT THIS IS WHAT ELIZABETH WANTS AND SHE HAS NO QUALITY OF LIFE AS IT IS AND I SUPPORT HER FULLY.

I WILL WRITE TOMORROW TO LET YOU KNOW ABOUT THE CONDITIONS AT THE NEW HOSPITAL AND HOW I GET ON IN GETTING THE FILES FOR WHICH I HAVE MY DAUGHTER’S PRIOR WRITTEN CONSENT.   BY THE WAY THE LOCAL TEAM FLATLY REFUSED TO LET ME SEE ANY MORE FILES DESPITE SEVERAL OF THESE FORMS SIGNED BY MY DAUGHTER BEING SUBMITTED TO THEM.   THEY MUST BE SCARED STIFF.  YOU CANNOT IMAGINE HOW I HAVE BEEN DESCRIBED IN THE FILE BUT I DO NOT CARE – AT THE END OF THE DAY, I FEEL LIKE NAMING EACH AND EVERY ONE OF THE TEAM WHO ARE ABUSING  MY DAUGHTER.

I will only  hope that this new psychiatrist takes note of what I am going to say at the next meeting in a week’s time and that he listens.  I fully intend to go and visit the British Pharmaceutical Industry in person and Parliament to see Mr Lansley on my next day off from work. 

For any information about the  harmful effects of Clozapane or any other harmful anti-psychotics or anti-depressants, I would recommend people to turn to the sites of drugawareness as mentioned above and also CCHR/Revelations UK.

 

 

 

 

 

 

 

  

  

 

At long last the day has come and the move went well.  I was not there to take her and my car is being fixed in any case but I have spoken to her and she says the place is very nice and spacious.  It is in a quiet area.   Whilst the grounds surrounding the local hospital are very nice too, unfortunately the wards need to be improved drastically.   With this specialist hospital staff have already been in touch with  me and wanted to listen – this is communication – at long last!   Meanwhile Elizabeth has invited everyone to join her at the ward but this care is not readily available and it should be in my opinion available to everyone.  The acute wards should only be used for very short term stays and if a patient is not getting better then they should be moved to this specialist unit without having to speak up to the extent I have had to and fight for this to be in place whilst all the time watching her deteriorate. 

 

I will not be able to visit until the weekend as it is too far away but I am happy that I believe the are is better however I am still worried what they are going to do about the drugs.   These harmful chemicals are the cause of my daughter’s behaviour and she needs to come off them.   They are going to take her off them as far as I am concerned but just to  make sure this is done properly I am signing up for membership to www.drugsawareness.org – on this wonderful site is expert advice on how to come off these chemicals safely.   It is a good thing to have knowledge about this when you are dealing with any teams.

 

 

This is the last weekend for Elizabeth in the area where she was born.

Next week she faces being transferred quite a distance away to the specialist hospital. 

Today I saw her and took her off the ward and we went to a place that is so high up you can see wonderful views of London.  Elizabeth went ice skating and after this we made our way back and stopped off to have a meal.    Throughout the day Elizabeth was unsettled and you could not have a conversation with her at all.    By the end of the day it was best not to say a word to her – that was how bad things were and at times her behaviour was quite unpredictable.   One thing for sure is that Elizabeth is extremely upset at her whole situation and there is no doubt about her feelings on the drugs that are being given and how much she wants to come off them.

 

I have all these papers from the specialist hospital but whilst they look impressive, I just do not know how or what they are going to do about taking her off the drugs – the whole business is extremely risky but I have to say Elizabeth has no quality of life on them and they do not work so now I am so concerned for her but at the same time happy if this hospital can do something to help her and listen to her wishes for once.  

 

YES IT CAN BE DONE – YOU DO NOT HAVE TO REMAIN ON THESE HARMFUL DRUGS FOR THE REST OF YOUR LIFE –  PRESCRIPTION DRUGS SUCH AS THESE MIND ALTERING ANTI-PSYCHOTICS ARE EXTREMELY HARMFUL.  ANTI-PSYCHOTICS DEHUMANISE SOMEONE AND CAN CAUSE SEVERE AGGRESSION AND SUICIDE/HOMICIDE.   I HAVE NO DOUBT ABOUT THIS.  I JUST HOPE EVERYTHING GOES WELL AS COMING OFF THESE DRUGS IS EXTREMELY RISKY AND YOU SHOULD ONLY DO THIS UNDER MEDICAL SUPERVISION.

I will not be around to help Elizabeth move things – the local hospital will deal with that however she will be near to where I work so I can visit her and see her at the weekend.   It may unsettle  her if I am there on Tuesday in any case.     I have no idea what to expect.

 Meanwhile, a patient on the ward wanted to write something.     During the week I will post some words from this patient who is extremely intelligent and has a lot to offer in terms of ideas of improvement for patients.   

 

I have received papers asking me whether I want to be a Governor of the local NHS Trust –  I believe they should be asking the patients and getting the patients involved as they are the people who know best and have experienced how awful if is to be on the acute wards

 

Next week I will write about the wonderful ideas that should be on offer for all the patients and you should not have to fight for decent care or alternative care – there must be changes made as patients are not getting better at all and patients should be listened to. 

The following was written by Elizabeth – the first piece earlier on in her treatment, the latter piece is up to date and you can tell from the writing and thoughts how she has deteriorated due to all these powerful mind-altering drugs that have done her no good whatsoever.

I have the permission of Elizabeth to display this on my site:

 

“Being on the Ward”

“Dear Sir/Madam

I can say that I don’t like being stuck on this horrible ward.   I have recently got a bit frustrated from the amount of people on the ward when I threw a book and a chair and threw water everwhere.   I can say that it is horrible because of my small room.

 

I really need to be moved on because you know my life is stuck and I feel confused.   I am currently waiting for Rehab that means moving somebody somewhere you know.   Please help me get a room at Rehab.   I have a good friend at Rehab called …………………

 

Thank you for reading this.

 

Yours sincerely”  

 

Unfortunately it was after nearly 2 years Elizabeth got moved on to another ward – supposedly for Rehab purposes.   The friend she mentioned got moved into supportive housing and she was the only girl amongst about 9 men on a mixed ward that had separate sleeping accommodation – a recipe for disaster for a vulnerable patient.  On this ward I noticed patients just lying around not doing much at all – it was on this ward she started to smoke and this was allowed on the patio area outside the ward.  I did not want her to end up like the others, inactive, lying there on the sofas or half asleep so I booked Elizabeth on a floristry course at a local college myself and this caused uproar amongst the team.  I also tried to get her involved with a team sport (netball) which was her wish at the time and this was completely outside of the mental health, also in addition I was taking her to running and special olympics.   She was an excellent runner and once was fit enough to go running with my gym members which is more than I could have done.  Anyway, once a week when I worked part time I would pick Elizabeth up and take her to the college.   Most evenings she would go into the class but there were one or two she flatly refused to go as she did not feel well enough.   Almost every time she suffered from panic attacks before going into the class and could not breathe.   However, you should have seen her when she finished the class and came out with lovely flower arrangements that some of the nurses themselves wanted to purchase and every bit as good as what others made. She was happy, laughing – like a different person altogether.  Clearly Elizabeth has artistic talent and enjoys this sort of thing. but needed help with her written work and unfortunately although help was available if she wanted it the problem is that once someone says “no” after that no-one bothers.    “No” could have been said at a moment when Elizabeth was feeling particularly bad and no-one pursued this any further or gave any encouragement.   As a result she has no certificate to show for all her efforts – the college were upset and so was I.   The psychiatrist who was furious at the time actually said it was a good thing what I did to take her to college.  

 

As far as Rehab goes – everything is “in-house” – patients are not encouraged to mix outside of mental health services and I think this is totally wrong.  Her social worker said for instance that “she was happier mixing with her own kind”  How wrong this is – how can someone be integrated into society effectively.  There are lots of groups designed purely for mental health patients and some of them are good but it is not a good thing to mix solely with other patients who all have serious problems of their own.    I think there should be a mentoring scheme available where say university students, particularly those studying for nursing qualifications/psychology got involved on a one to one basis with patients like my daughter.  They could learn from meeting the families and encourage someone to do things.  A young person is more in tune with someone like my daughter than a psychiatrist for instance.   When I tried to do this and appointed someone I knew well around her age who was studying for nursing –  it caused uproar amonst the team- by this time Elizabeth was living in the community.   Patients are left to go downhill.  Elizabeth not only referred to the ward as being “like prison” but said she did not feel stimulated and also commented on being “institutionalised”.   When she was first admitted on the acute ward again I did not want her to end up like the rest and tried to get her a job – the job was working with old people where my father went to a day centre as this is what Elizabeth said she would like to do.   She got on extremely well but when they asked for a reference from the team this was not forthcoming at the time so she missed out.   Not only did Elizabeth get on with the staff but also with the old people as she was used to seeing her grandfather who had Alzheimers and by the way was on anti-psychotics – Rispiridon and Seroquel.   When you as a parent try to get involved and to help someone you get called pushy, overbearing, abusive – you name it – I have the files and have read them!

Now Elizabeth feels she cannot do anything – she has lost her confidence, suffers from panic attacks amongst other things, has no energy, no enthusiasm – does not care any more after being labelled with the serious condition of Schizophrenia but how many other diagnoses are in the files –  For instance I have the files and there is not only that condition but also Aspergers.  Who is right and who is wrong?    One expert says one thing but the majority of the experts stick together and say the other and that is why I do not trust any of them and have challenged them all.    I believe the current behaviour of Elizabeth is caused directly by the drugs and have sought outside private professional help who have confirmed this with a fully qualified Orthomolecular Psychiatrist and have taken her to a private clinic –  I am also in touch with other experts and have signed up to www.drugawareness.org.

People are not aware of the dangers of these drugs and what it does to people and once on them you are chemically brainwashed, weakened and they have the effect of dehumanising a person.  Many people trust these professionals and do  not know what is going on in reality.   Elizabeth has not got over bad things that have happened to her therefore the drugs have not worked but when you ask to come off them – no-one wants to know and the psychiatrists just ignore a patient who begs to come off them which is cruel and abusive to continue to ply a patient with these awful drugs against their wishes.  There are no facilities for patients to come off psychiatric drugs safely in this country and Yes it can be done but it is only when things get really severe like in the case of Elizabeth that the teams are forced to listen and do something about the situation.

Alternative care should be available for everyone in my opinion to give choice to patients.  Every NHS hospital should employ an Orthomolecular Psychiatrist.

By the way – thank you so much Dina for your contribution to the site in writing about the shocking care available – Drugs and psychiatrists are like drug pushers who experiment on a patient without having any scientific evidence behind their claims of diagnosis.    Patients and carers believe what is told to them as I once did but now I have found out the truth –  IT IS ALL DOWN TO MONEY AND THE MORE PRESCRIPTIONS THE MORE MONEY.

 Now for the second and most recent piece of writing from Elizabeth:

“Today Sun 8 January Mum’s been talking to me about having my cat live with me but unfortunately I dont feel well.  I’m still on the medicine – I have the devil attack me a lot unnecessarily.  I don’t hate the devil only the ones that expectme to respond and I cant  – not I …..dont want …..but I sometimes simply haven’t got any words to say.   I feel forced against my will.   I will only do what I need to – I have had troubles recently – people staring at me at the shopping centre.  This makes me paranoid.   I love my cat though he is very nice.

About where I live – my Mum is upset and didnt like being banned from the building where I live.  I need to go in somehwere to come off the medication.  Please could you arrange it as I feel terrible.  I get very bad headaches.  At night I get nightmares/hallucinations after I take it.  Please can I come off the medication and go in somehwere nice.”

 

This writing was barely legible with lots of crossings out – you can see the difference between this and the last piece of writing – THIS IS WHAT THE AWFUL DRUGS ARE DOING – ELIZABETH NEVER SUFFERED FROM HEARING VOICES IN THE FIRST PLACE – SHE DID NOT SUFFER FROM HALLUCINATIONS.  WHAT IS IN THESE DRUGS?  WHEN I APPROACHED THE DRUGS MANUFACTURER OF SEROQUEL THEY SAID THEY WERE FORBIDDEN TO SPEAK TO ME BY THE BRITISH PHARMACEUTICAL INDUSTRY.

This weekend is the last weekend ont he acute ward for Elizabeth thank goodness and I hope to see her today and we will go out somewhere as we usually do but it is a nuisance I have not got my car back from being repaired and this will restrict where we go.    

 

I will write later about this.

Today I have not seen anything of Elizabeth but know she is safe and well with her grandparents.   I have had the chance to catch up on things at home and have spent a good deal of the day shopping but when I got back I saw all the details of the leading hospital that Elizabeth is due to go into on Tuesday had been sent to me by post.    I skimmed through them – there certainly is a lot to read.

On the surface it sounds good however I am not going to get too excited – at the end of the day I will not be at all happy if they do not take her off the drugs that do not work in accordance with her wishes and I will become extremely outspoken as this will be against my daughter’s human rights.

I then sat down and watched more of the shocking dvds that the CCHR sent me.  I saw one called “All Fall Down”  – featuring children diagnosed with ADHD and put on Ritalin.   It showed how these drugs are a stimulant rather than drugs that calm someone down.  It contained interviews of people affected.

I then watched a dvd called “Psychiatry’s Prescription for Violence”.  In this dvd it showed the link between major homicide cases and these harmful drugs – in each and every case anti-depressants had been prescribed.

I thoroughly agree with this as I have seen the effects of anti-depressants on my daughter and then anti-psychotics.   It is every bit true that these drugs can lead to extreme violence/aggression/delusions and hallucinations amongst other things.      

Unfortunately my film which I took of Elizabeth’s kitten has not come out well.    However I will still post it on You Tube and will probably get some comments to the effect that I would qualify for the worst photographer of the year.    However just 1 photo came out well of Fluffy which I will post on this site.     No matter how bad Elizabeth is feeling and how awful her moods may be seeing the kitten has a miraculous effect.   There is no doubt that this is better than all the medication in the world.

I am going to sign up to the www.drugawareness.org as this website will give me useful information bearing in mind Elizabeth’s admission into the leading specialist hospital.  

One good thing is the hospital, although a long way from where I live is not too far from where I work so I will get to see her.

I WISH I KNEW IN THE FIRST INSTANCE WHAT I KNOW NOW THANKS TO THE CCHR ABOUT THE HARMFUL EFFECTS OF THE DRUGS AND WOULD URGE ANYONE TO ORDER THESE DVDS ESPECIALLY “DIAGNOSTIC STATISTICAL MANUAL – PSYCHIATRY’S DEADLIEST SCAM” 

I WILL TALK MORE ABOUT THIS WONDERFUL INFORMATIVE DVD IN FUTURE BLOGS AND WILL BE POSTING SOME THINGS WRITTEN BY MY DAUGHTER WHO IS NOW NOT IN A FIT STATE TO DO ANYTHING ANY MORE AND ON A HUGE DOSAGE OF HARMFUL CHEMICALS THAT DO NOT EVEN WORK.

 

 

 

At last good news has come and a placement for Elizabeth with the specialist hospital early next week.  This is the news I have been waiting for over the past months.  The hospital is a long way from home but at the end of the day, if it means something is done then this is wonderful news.

I have made sure that the team there know it takes more than a few months so I have been told by experts to come off powerful mind-altering anti-psychotics on the dosage that Elizabeth is on.   I have been told it could take up to a year and must be done on a gradual basis and very slowly.   I have also been told that coming off such drugs can be more dangerous than staying on them however if a patient is that unhappy and the drugs do not work then they should be entitled to come off the drugs.  If I had not challenged things then Elizabeth would have probably remained on them for the rest of her life.

I will keep you informed of her progress over the forthcoming weeks.