Showing posts with label severely ill patients. Show all posts
Showing posts with label severely ill patients. Show all posts

Friday, August 8, 2014

Sophia Mirza and Severe ME/CFS




August 8 is the birthday of Sophia Mirza, a British woman who died of ME at the age of 32.

Sophia contracted ME in 1999 after a "flu."  She never recovered her health, and by June 2000 was bedbound. Like many patients with severe ME, Sophia could not tolerate light, touch, or sound. She developed sensitivities to foods, and was unable to read, write, or even bathe herself. In response to her mother Criona's request for help, Sophia's GP, Dr. Firth, suggested that Sophia had made herself ill so she could "get attention."

Over the course of the next three years, Criona's attempts to have her daughter treated for ME were repeatedly thwarted. Dr. Firth referred Sophia to a psychiatrist, Dr. Baginski, who recommended a clinic that supposedly treated ME. When Sophia discovered that the treatment consisted of Graded Exercise Therapy, she declined.

At that point, the physicians involved with Sophia's case began to threaten Criona.
"I was told that if Sophia refused to go to Oldchurch Hospital in Romford, or if she did not recover within the following 6 months, that she would be sectioned under the Mental Health Act, then added that if I tried to stop this, then he, Dr. Baginski, would go to the courts to have me removed as the nearest relative. Furthermore, if I did not open the door when they would come to take Sophia away, that the police would be called to “smash the door down”. When I asked how much better Sophia would get by these proposed actions, the reply was given that it was “none of your business, that it was for the courts to decide”. The psychiatrist wanted to arrange for me to see a psychologist so that I could understand the good, that he, Dr. Baginski, was doing to Sophia. I refused." (Sophia and ME)
In July 2003, Dr. Baginski made good on his threat. The police smashed down the door and took Sophia to a local mental hospital, where she was placed in a locked room within a locked ward. During the weeks she was confined to the mental ward, Sophia did not receive even the most basic care. Her sheets were not changed, her blood pressure was not taken; she was never washed, and her bathroom was never cleaned. By the time Sophia was  released, the damage had been done. Sophia descended into a "hell-hole" from which she never recovered.

On November 25, 2005, Sophia Mirza died. The official cause of death was listed as acute aneuric renal failure (failure to produce urine) due to dehydration as a result of Chronic Fatigue Syndrome. A subsequent autopsy revealed that 80 % of the dorsal root ganglia of Sophia's spine were damaged. (This is consistent with active herpes infection.) The dorsal root ganglia are responsible for conveying sensory information to the brain, so damage to the ganglia would produce pain, sensitivity to sound, light, touch - all the hallmark symptoms of severe ME.

Other Sophias

Sadly, Sophia's case is not unique. Many patients diagnosed with ME or CFS are not only labeled as psychiatric cases, but are forcibly removed from their families to undergo "treatments" that only make them worse.

In 1986, Ean Proctor, a 12-year-old boy living on the Isle of Man, fell ill with severe ME. By 1988 he was confined to a wheelchair and could no longer speak. In spite of his diagnosis of ME, Ean was removed from his home after Dr. Simon Wessely decided that Ean was mentally ill. He was taken to a psychiatric ward in a hospital, where the staff told the boy that his parents were" letting him die." Because they did not believe he was unable to get out of his wheelchair, they let him soil himself rather than take him to the bathroom. Then they pushed him into a swimming pool, in the belief that he was faking his paralysis. Ean promptly sank to the bottom. After five months of legal battles, the Proctors finally got their son back, but not until they had nearly bankrupted themselves with legal costs.

Karina Hansen, a Danish woman, is still locked in a mental ward in Denmark. After more than a year of "treatment" her health is worsening, but the state will not release her, in spite of concerted national and international efforts.

David, a German boy who was struck with severe ME at the age of 15, was taken to a mental ward after his physician determined that his sensitivities to noise and light were psychogenic. At the clinic, he was forced to exercise. David was "traumatised" by the experience, and never recovered. At age 17 David died of a brain hemorrhage.

And on the home front, the recent case of Justina Pelletier's incarceration in a mental ward made national news. Her physical deterioration while locked in the ward could be documented, because the press got involved. Justina became a cause célèbre, to the point that two Congressmen have introduced a law that would prevent medical experimentation on children in hospitals.

These cases, while striking, are not isolated. How many ill children - and adults - have been stuck away in locked mental wards, to be abused, drugged, and ignored? And how many people have died, after years of medical neglect, from complications due to their illnesses?

What Really Killed Sophia Mirza

When doctors are unable to make a diagnosis they almost always place the blame on their patients. Perhaps in a society in which doctors were less arrogant, this would not be the case. But in our society - which has given almost god-like status to physicians - if a patient does not get well, it is because the patient does not want to get well. The subsequent psychiatric diagnoses saddled on these patients are numerous - somatoform disorder, factious disorder, Munchausen's - but they all amount to "I cannot figure out how to fix you, therefore you are to blame."

Once people are branded with a psychiatric disorder, they cease to be human beings. Their civil and legal rights are revoked, and they can expect no compassion. Psychiatric patients are isolated from friends and family, who are almost universally considered "enablers." They are drugged into a state of compliance. And rather than attend to their needs, which are considered part of their "illness," staff members can, on doctor's orders, legitimately engage in active abuse, which is justified by relabeling it as "therapy."

Cases like Sophia's, or Ean's, or Karina's, or David's, or Justina's raise some very important questions, one of which is "Should anybody, under any circumstances, be treated like that?"

Another question is "Who decides what is real?" What special training qualifies social workers, school nurses, and petty bureaucrats to determine what is and is not real? For that matter, which course in medical school trains physicians in the finer points of reality?

Sophia's decline can be directly attributed to active medical neglect. But as long anyone in an official capacity is allowed to make the determination of what is real and what isn't, the physicians and bureaucrats responsible for contributing to Sophia's demise will never be held accountable.

Who Decides What is Real?

The idea that an illness is not "real" arises from the concept that people whose illnesses cannot be easily diagnosed by physicians must be faking it. There is an inherent problem with this line of reasoning.

With a few exceptions, mental illnesses are "all in your head." There is no identifiable physical cause for the majority of them. They cannot be confirmed by a medical test, and there is no cure. The treatments are, at best, palliative, and, at worst, fatal.

Yet, insurance companies pay for treatments for mental illness. Why do they spend money on illnesses that are imaginary? And why do therapists have a 991-page manual describing these "not real" illnesses? If all one has to do is convince the patient that he or she does not have a real illness, why are there hospitals, clinics, hefty fees, and a pharmaceutical industry built around these illnesses?

Furthermore, if these illnesses are "all in your head" then why aren't evil eye and spirit possession included in the DSM V as well? If physicians actually believe that physical symptoms can somehow be created by the mind, why isn't there a diagnostic code for voodoo? Are there levels of unreality in which some unreal illnesses are more unreal than others?

Even more bizarre is the notion that if you believe that you have an organic (real) illness, but the doctor can't find a test to confirm it, then your belief that your illness is organic proves that it isn't.

That brings us back to Sophia Mirza. Sophia was diagnosed with ME, a neurological illness her doctors did not believe was "real." Eventually, Sophia's "unreal" illness killed her. Her autopsy revealed that there had been a real problem all along. Yet nearly ten years after Sophia's death, doctors still don't believe in the reality of ME/CFS. Nor will they ever as long as cultural myopia is permitted as an acceptable basis for medical opinion.


Friday, August 2, 2013

Severe Myalgic Encephalomyelitis Understanding and Remembrance Day - August 8

Press Release: The 25% M.E. Group, August 8, 2013

By Simon Lawrence

'I am a ghost in the land of the living – forgotten, ignored and drifting on the edges of life, whispering my message in the ears of the lucky ones who can participate in life. I have Myalgic Encephalomyelitis. I call it paralysis, muscle and cardiac failure, brain injury, a living plague that kills only slowly, but does kill..." ~Aylwin (Jennifer) Catchpole, who died in August 2010

Why have an Understanding and Remembrance Day highlighting the plight of the severely affected?

The severity of this illness often makes it impossible for people to have contact with loved ones, doctors, or the outside world. This is a group of thousands of people in the UK who are generally invisible. People with the severe forms of this disease can no longer pursue their careers, hobbies, or everyday lives.

In helping us to make visible the stories of people living with severe M.E., and of those who have died as a result of the illness, you can help end years of misrepresentation about M.E. and increase the understanding of the general public, who often underestimate the seriousness of the disease.

This ignorance causes much suffering to those with M.E., who have a double battle, not only with the disease itself, but also to get the illness taken seriously by those around them. There is an urgent need to raise awareness.

What's the significance of 8th August?

This is the birth date of Sophia Mirza. Sophia was bed-bound with severe Myalgic Encephalomyelitis and was a victim of medical abuse.

Her doctors did not believe that Myalgic Encephalomyelitis was a physical disease and so she was forcibly taken from her bed/home by social workers, police officers and doctors, and kept in a psychiatric facility where she received inappropriate treatment and care.

Sophia subsequently died of M.E. at the age of 32.

Her post-mortem revealed widespread inflammation in the spinal cord. This same inexcusable abuse still goes on.

Emily Collingridge - 17th April 1981 - 18th March 2012

“When our daughter, Emily, died in 2012, my husband and I were overwhelmed by the hundreds of messages of sympathy we received, even from people we did not know.
They came from friends, from those expressing gratitude for her endless campaigning to spread awareness of ME and from readers of her guide to living with severe M.E., many of whom said it had changed their lives.”

The inquest into Emily’s death took place on 24th May 2013. In her summary the Coroner referred to ME as a condition which is not understood, and expressed the need for more research.

She was echoing an appeal made by Emily in 2011 highlighting what she described as “the scandalous lack of research into the most severe form of M.E. and the lack of appropriate support for those suffering from it.”

A final plea in Emily’s own words: “Please put an end to the abandonment of people with severe ME and give us all real reason to hope”.

Emily may have lost her personal battle, but her battle on behalf of all those still suffering from severe ME should not be ignored.

What is Myalgic Encephalomyelitis?

Myalgic Encephalomyelitis literally means muscle pain (myalgia) with brain and spinal cord inflammation (encephalomyelitis). It is a complex neurological illness.

The most characteristic distinguishing feature is that symptoms are exacerbated by activity and sensory stimuli beyond the patient's limitations.

Activities that trigger flare-ups can be tiny by healthy standards, depending on the severity of the illness. Simple things like talking, watching a TV programme, or eating a meal, can cause an exacerbation.

Dysfunction has been found in all the major systems - neurological, immune, endocrine, cardiovascular, musculoskeletal, gastrointestinal, respiratory, and genito-urinary, which is why people with Myalgic Encephalomyelitis can have such a wide range of symptoms.

Common symptoms include widespread pain, cognitive dysfunctions (e.g. problems with concentration and memory), disabling sensitivities to everyday stimuli (such as light and noise), difficulty being upright (including sitting up in bed), sleep disorders and gastrointestinal problems.

You can read Sophia's story here: www.sophiaandme.org.uk

Her story also features powerfully in the film 'Voices from the Shadows' which is available from: www.voicesfromtheshadowsfilm.co.uk

Emily also wrote an informative book entitled:

'Severe ME/CFS: A Guide to Living' which can be found at: www.severeme.info

Further website information can be found at: http://tinyurl.com/oasltvy

The parents of those mentioned in this Press Release are happy to be contacted by members of the Media. This can be arranged through contacting the 25% ME Group, (the national support group for severely affected ME Sufferers).
Contact details below.

25% ME GROUP
21 CHURCH STREET
TROON
AYRSHIRE, KA10 6HT
Tel: 01292 318 611
www.25megroup.org
E-MAIL: enquiry@25megroup.org

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