Many who suffer ADRs from meds, vaccines, environmental and iatrogenic illnesses are relentlessly persecuted in the UK. Most are given a diagnosis of ME/CFS - lack of both medical and social care, often leading to tragedy.
It should be simple to show toxicity from most drugs. Tests of DNA adducts would show traces of the offending medication, tissue samples, toe nail clippings, or even a hair sample, would probably show traces of the offending toxic medication. Yet, it is impossible to find a laboratory to test for residues of Lariam/Mefloquine or Fluoroquinolones in tissue samples.
The story of Sophie Mirza, diagnosed with ME/CFS is very significant. Many of us are diagnosed with ME/CFS. Sophie Mirza died after relentless persecution from UK health officials. Many are threatened by psychiatrists, psychologists of being sectioned. Medieval and cruel, it does not stop there. Sophie Mirza may unknowingly have suffered from an ADR to medication or vaccines.
Those chronically ill, specially those labelled with ME/CFS, are ground to a pulp by social security, social services, lack of medical care, denial by health professionals. This leads to fear, stress, and worsening of health. UK medical doctors no longer provide sick notes, clinical reports are misleading, omitting disabling symptoms, concealing positive results or blatant denial about the level of disability.
The welfare system and disability premiums are the lowest amongst the EU richest countries. It is barely sufficient and does not cover electricity, gas and other utilitiy bills. (Highest costs in the Western world, there is no regulatory price control). We have the highest rate of cold related deaths in the Western world!! The choice is between eat or heat, poor diet, leading to malnutrition makes it unlikely to recover from illness. Some countries in the EU cite the UK as the country where most chronically ill patients are unlikely to recover, (very low standard of socialized medicine) sinking even into deeper poverty (lowest social security amongst EU richest countries), and high cost of living.
Who would want to pretend to be ill under such draconian welfare system? Yet, many are "accused" of deception.
Despite being very weak and disabled, many are forced into physio leading to relapses and even more serious health issues.
As from October 2010, the criteria for being qualified as too ill to work will be very stringent, making most chronically ill patients "fit for work."
Unless paralyzed from head to toes, it will be very difficult to prove being too ill for work. The incentive is to force cheap labor for those too ill to work. If unable to go to work, we are told, work will come to you. Not accepting offer of work, will result in benefits being cut. Doctors no longer write sick notes. Clinic letters from hospital doctors are economical with diagnosis. It is a fight with clinicians, social services, and welfare. We are told, we have to "earn" welfare and disability. If forced to work from home, it will be equivalent to being paid $1 per hour.
Recently published in local regional newspapers, a man found dead in his apartment. He was unable to feed himself, social services refused care. Similarly, a woman was found dead on the floor of her kitchen. She was also refused care by social services.
A woman with a brain tumor was forced to work or face withdrawals of her welfare. She collapsed and could not continue to work.
A woman in her sixties, diagnosed with two cancers, underwent chemotherapy. Despite severe symptoms, doctors told her she was fit to work.
A man with cancer was told he had six months to live. He was told he had to work, and did not qualify for welfare.
Who would choose to be sick and ground to a pulp by a relentless pressure and a society increasingly hostile towards those who are ill - too ill to be productive? Who would choose to barely survive on minimum welfare and threats of dying of cold related illness during cold months?
Campaigners are muzzled, there is little free speech, the press is censored. Oh, and there is NO legal recourse. The UK opted out of the EU Social Charter.
Letters have been sent to Neurologists requesting that patients whose tests are negative, should be referred to a psychiatrist. Now, most of these tests are flawed. For instance, Mitochondrial diagnosis is very difficult to diagnose, tests are not specific with very low accuracy. There are metabollic syndromes caused by medications and vaccines, and environmental pollution, which are not identifiable, for which there are no tests.
Moving on to more persecution.
The told dying daugher she was lying, says mother Criona Wilson
Criona Wilson with a picture of Sophia, who died of ME aged 32
This week, a mother was acquitted of murder. The question here is not about assisted suicide, but how could the so called fourth richest country in the world, allow ME/CFS patients be persecuted with such vehemence, and ignored by all?
Trapped by ME, Lyn Gilderdale made it clear she wanted to die
Lynn Gilderdale, who was struck down by ME after a BCG vaccination at the age of 14. Photograph: Sussex Police/PA
Live Journal was the one place where Lynn Gilderdale felt safe uttering her deepest, most troubling thoughts. Using a specially-designed handheld computer, and adopting the pseudonym Jessie Oliver, it was on the internet networking forum that she shared her desire to die with her closest friends.
After suffering a severe form of ME which left her bedridden and unable to speak or feed herself for all of her adolescent and adult life, she had decided she was never going to recover, and wanted to ensure her life would end before total degeneration robbed her of all dignity.
The revelations about her decision were made to her parents, Kay and Richard, and her small group of friends in the last two years of her life. To those who were invited to share her innermost thoughts it was a painful, yet understandable, choice.
Many of them were girls and young women who suffered the same illness; some, such as Lynn, had been confined to their beds and housebound for years as a result of ME.
"She did mention to me and very few others that she had an overwhelming desire to die," said Emily Levick. "I recall the time I first read about it. I cried, and then immediately texted her, as she was so afraid that her friends would think badly of her for it, and I wanted to reassure her that I could never think badly of her.
"She had battled for so many years, and was so desperately tired. It was quite literally heart breaking to read something like that, but I did understand her reasons. I believe I would have felt exactly the same if I were in her situation."
Her mother and father were kept well informed of her decision. A Do Not Resuscitate note was placed on her medical notes under her own wishes and she later went a step further and directed that a "living will" should be drafted in which she stated her wish not to be resuscitated or subjected to any medical intervention if her quality of life was too poor.
"She knew it was very difficult to talk to me about that subject because no one wants to hear it coming from their daughter," said Richard Gilderdale, a former policeman.
"I always used to say to her I was a coward because I listened to what she said and then she would always look at me with a knowing look in her eyes and say, 'Look, it's never going to go away, dad.' Her feelings were that she had made up her own mind that she couldn't carry on."
Yet despite this clear statement of her intentions, and fresh guidelines from the director of public prosecutions to reassure relatives who help the terminally ill end their own lives, Kay Gilderdale was brought before the criminal courts this month charged with the attempted murder of her 31-year-old child.
After she was acquitted of attempted murder today amid applause in court, the trial judge joined campaigners, friends and lawyers to ask why was she ever prosecuted? http://www.guardian.co.uk/society/2010/jan/25/lynn-gilderdale-me-assisted-suicide
