Medical Eugenics - How to format an ME patient (part 2)
Posted by: admin / Category: food intolerance test
Ingredients:
Deny the illness (Most important)
Blame the patient
Blame the mother
Blame the carer
Blame the family
Ignore past medical tests
Block future medical tests
Lie about test results that are positive
Invent false patient history (Lie)
Invent patient mental illness (Lie)
Evoke ‘plan’ to treat this mental illness and stick to it
Use Psychological theories you read in books by British Psychiatrists
Self anoint yourself as a CFS/ME ‘expert’
Never allow the word ‘ME’ to be used
Get fellow sadists to join you to
produce false research together
Present this as ‘evidence’ to the MRC/DOH/NHS & Pro-Psychiatric CFS charities
Refuse patient basic human rights such ability to open bladder in bed (make them walk)
Refuse patient basic human rights such as food in bed (make them walk)
Refuse patient basic human rights such as ability to open window in 28c heat
Refuse patient basic human rights such as access to a Medical Doctor
Refuse patient basic human rights such as access to pain medication, or other medications usually taken
Refuse patient basic human rights such as access to visitors (make a claim that visitors ‘distort’ patients mind and ‘interfere’ with the ‘treatment protocol’
Make sure to produce LOTS of ‘research’ that prove your theories by using ‘OXFORD Criteria CFS’, which cites ‘No Specific Symptoms’ as a criteria for diagnosing CFS
Don’t tell anyone this
Refer to CFS, as ME - but inform the patient ME does not exist anymore, and instead ‘we call it CFS/ME’
Exclude anyone with genuine ME in your research as they’ll alter the outcome, thus invalidating your claim ME is a mental illness
Make sure to do newspaper, radio, TV appearances, or better still - obtain bogus CFS patient to masquerade as ‘ME’ patients on your behalf - further guaranteeing ME patients never will get basic medical care, and certainly no treatment
Block all bio-medical research into ME by ociating on a ‘professional basis’ with those who steer funding into Psychiatry
If caught deny you know them or that you have a common cause
Deny any quote of your research or say you ‘don’t remember’ saying that
Claim the only ‘treatment’ that works, belongs to you, or those of your mind set
If busted, claim the patient is intellectually unable to understand what he/she reads - so it must be ‘The Internet’s fault’
If busted, claim the patient is a failure with the opposite sex to further embarrass/shame them
If busted, take away any social contact the patient has - thus isolating them more, and making them more vulnerable/desperate to your manipulative techniques
Whenever possible - humiliate the patient or falsely ‘befriend’ them - in order to get them to talk
Whatever they tell you, exaggerate, or lie.
Ask the patient if they want to be ‘resuscitated’ if they die
Tell the patient if they don’t sleep - they could die
Tell the patient they are plenty other ways to ‘treat’ ME patients - including ‘drugging them heavily’
Tell the patient their mother is mentally ill because she had 5 miss-carried pregnancies before you were born
Make lots of money by doing this
Ignore
Repeat for the perfect manufacture of the non disease ‘CFS’ and perfect cover-up for the Internationally recognised neurological disease ME
When backed into a corner and/or threatened with legal action for killing or harming your patient, or inducing suicidal thoughts….
Simply retire on significant Government pension with a clear conscience you never did a thing wrong - and only devoted your life to ‘helping’ ME patients
Get your colleagues to award you a medal for your services to ME CFS patients
Duration : 0:8:22
Tags: CFIDS, CFS, Chalder, Cleare, dysautonomia, Encephalomyelitis, Hoptoff, intolerance, M.E., Myalgic, orthostatic, postural, pots, SYNDROME, tachycardia, Wessely
June 6th, 2009 at 12:56 pm
sad thing for me is …
sad thing for me is, i actually was being treated for anxiety BEFORE i got sick with this…. i should have just went on with life and overcame my anxiety instead of telling every doctor how anxious i got because now they have something to lean on instead of actual medical tests.
i am really really sick, and it all sees to have started from a upper respiratory infection, which spread to my intestines, ect.
June 6th, 2009 at 12:56 pm
i too was sent off …
i too was sent off to a behavioral unit after first coming down with symptoms of M.E. i had my doctors and various family members telling me i was crazy and then when i was in the unit, i realized something…. i am NOT crazy…. i am sick and need medical help. i got out, only to find a never-ending web of “i don’t know” excuses from my doctors and run-arounds to different specialists who all seem to jush rush in and rush out saying “everything looks good!” no explanations to why i am twiching!
June 6th, 2009 at 12:56 pm
The very troubled ” …
The very troubled “outlaw” branded UNUM CORP’S “Bio-Psycho-Social” model in ACTION throughout the UK…
$ICKO coming to a NHS hospital or GP surgery near you?
“Collusion is also easier to defend if one party gains nothing from the encounter — but when the doctor reaps a “rich reward in fees”, it is harder to claim a moral paternalistic high ground.” Professor Simon Wessely in Unum’s UK CMO Report, 2007
June 6th, 2009 at 12:56 pm
mefmaction(DOT)net, …
mefmaction(DOT)net, I DAMAGED bad repeatedly from psych med’s for neurlogical illness, 10 years, whole body repeatedly, fighting for my rights to neurlogical diagnosis and care for the damage, already 17 year survior of ME/CFS and FM, fIUUing s,
all the best for us in the new year
June 6th, 2009 at 12:56 pm
Thank God she did a …
Thank God she did a test for Lyme disease as well as a routine investigation, which came back acutely positive and I got some (although insufficient) treatment. At least now I know I can get well with long-term antobiotics, although I still relapse again months later.. I probably would be bed bound etc as well by now otherwise, in 3 years when I tried living without treatment I became a virtual recluse (but for the internet..) due to worsening symptoms.
June 6th, 2009 at 12:56 pm
I seem to be really …
I seem to be really lucky, as when my symptoms first started my GP referred me to a neurologist/psychologist. After the first appointment, where she seemed to be sure that I was having a major psychological problem (as she was visibly “upset” when I answered to whether anything worried me in my life that I am usually always happy & optimistic, and the only thing bringing me down in my life where the daily symptoms of headache, tiredness, paraesthesia etc)..
June 6th, 2009 at 12:56 pm
I am appalled at …
I am appalled at the medical profession for psychologizing ME/CFS. They know better. They’re trying to make ME/CFS look like a mental illness so they can benefit the insurance companies. Those of us with this illness know this of course but we need to get the word out to the general public because this needs to change. This happens in the US too but here we also have doctors and specialists who do admit that ME/CFS is a disabling and crippling serious physical illness.
June 6th, 2009 at 12:56 pm
The very troubled ” …
The very troubled “outlaw” branded UNUM CORP’S “Bio-Pyscho-Social” model in action.
$ICKO coming to a NHS hospital near you?
“Collusion is also easier to defend if one party gains nothing from the encounter — but when the doctor reaps a rich reward in fees, it is harder to claim a moral paternalistic high ground.”
Professor Simon Wessely in Unum’s UK CMO Report, 2007
June 6th, 2009 at 12:56 pm
Wow, the way we are …
Wow, the way we are treated is a major scandal
I’ve had 21 years of this cr*p from the medical profession whilst being housebound in intractable pain with M.E. I’ve just found out from private testing that I have Lyme disease and symbiotic cryptostrongylus pulmoni. I can’t have any NHS treatment for them, but am still being offered graded exercise and cognitive behaviour therapies that made me so ill in the past
A few tablets 21 years ago would have saved me from existing in this living .
June 6th, 2009 at 12:56 pm
oh my! this sounds …
oh my! this sounds markedly similar to a report a psychiatrist did on me when he rejected my previous diagnosis with ME and tried to claim I was sufferering from: major depression, atypical depression, generalized anxiety disorder, psychomotor retardation, aspergers syndrome (WTF>!), the diagnosis (and medication) changed everytime. lots of money. lots of drugs. no improvements. if I ever felt depressed it was walking out his door after being treated sub-human.
June 6th, 2009 at 12:56 pm
This is outrageous! …
This is outrageous! WHEN are they going to WAKE up and READ the national and international medical journals!! They have PROVEN time and time again that there is scientific evidence that this disease has a BIOLOGICAL cause! Are they really so daft that they can’t understand that? Oh, and NOW your mother needs psychotherapy due to the fact she too believes you are physically ill?!?!? Sadly, even with ALL of the evidence available, many of us in the US are treated the same way. It’s an OUTRAGE!!!
June 6th, 2009 at 12:56 pm
Wow, that’s a …
Wow, that’s a pretty heavy video. I don’t know how I would handle something like that. I am blessed here in the US that CFS is recognised as a serious real illness. My heart goes out to you.
Sandman cast his spell