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First official death from chronic fatigue syndrome
NewScientist.com news service ^ | June 16, 2006 | by Rowan Hooper

Posted on 06/16/2006 8:22:50 AM PDT by aculeus

Chronic fatigue syndrome has been given as an official cause of death – apparently for the first time in the world.

On Tuesday, coroner Veronica Hamilton-Deeley of Brighton and Hove Coroners Court, UK, recorded the cause of death of a 32-year-old woman as acute aneuric renal failure (failure to produce urine) due to dehydration as a result of CFS. The deceased woman, Sophia Mirza, had suffered from CFS for six years.

CFS, which is also known as myalgic encephalomyelitis (ME), has a variety of devastating symptoms ranging from extreme weakness, inability to concentrate and persistent headache. Sufferers can have the disease for years, but its cause remains controversial, with fiercely opposing views from psychiatrists on one side and biologically minded physicians on the other.

The coroner’s verdict is a breakthrough for those who argue that CFS is a physical condition, possibly with its roots in the immune system. Dominic O’Donovan, a neuropathologist at Oldchurch Hospital in Romford, UK, who gave evidence at the inquest, said that Sophia’s spinal cord showed inflammation caused by dorsal root ganglionitis - a clear physical manifestation of the disease.

Overactive immune response CFS specialist Jonathan Kerr of St George's, University of London, says he is not surprised that inflammation in the spinal cord has been found in someone with the disease, as it is known to be associated with it. He says that the immune system tends to be over-activated in people with CFS and this may underlie the inflammation of the neurological tissue.

“People have been reluctant to subscribe to the biological side because of the power of the psychiatric lobby,” says Kerr. “Doctors are sceptical about the existence of CFS and there is controversy about its underlying cause.”

Abhijit Chaudhuri, a consultant neurologist at the Essex Centre of Neurological Science who worked with O’Donovan on Sophia’s case, says the changes to her spinal cord may have resulted in symptoms of chronic fatigue.

“Sophia’s case sheds light on CFS because there were changes in her dorsal ganglia – the gatekeepers to sensation in the brain – and we know that fatigue depends on sensory perception,” he says. “What we need to understand is what happens that makes fatigue more persistent, without there being an obvious systemic disturbance.”

Rigorous inquest

The inquest was rigorous, Chaudhuri says, and considered all other potential causes of death consistent with the post-mortem results, such as sleep apnoea and drug use, and rejected them.

The verdict was welcomed by Sophia’s mother, Criona Wilson, who had to fight for recognition that her daughter was physically - rather than mentally - ill. Sophia was sectioned for two weeks under the Mental Health Act in 2003.

“I’m extremely pleased that CFS/ME was identified on the death certificate as one of the primary causes of Sophia’s death,” she says, “because this can be used to reinforce the need for biomedical research into the disease.”


TOPICS: Extended News
KEYWORDS: chronicfatigue; health; unexplaineddisease
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To: Old Professer
To you and those whose posts echo yours it might be wise to consider that not every day can be a great day and that going to a doctor is not always the best first course.

My case wasn't caused by doctors, but it was one of those things that wasn't fixed by doctors, either.

41 posted on 06/17/2006 1:04:57 PM PDT by Pearls Before Swine (Is /sarc really needed?)
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To: LadyDoc
Believe me, fibromyalgia is a real disease. Mine has really gotten worse with all the stress I am under right now. It feels like a have one or two elephants on my chest.
42 posted on 06/17/2006 1:14:02 PM PDT by MamaB (mom to an Angel)
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To: MamaB

It's raining right now, isn't it?


43 posted on 06/17/2006 2:38:17 PM PDT by Old Professer (The critic writes with rapier pen, dips it twice, and writes again.)
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To: Old Professer

No, these are people who say they are allergic to the fillers that are used to make up the pills. Makes treatment more difficult, to say the least.

One of us seems to end up angry. I think their personality disorder rubs mine the wrong way.


44 posted on 06/17/2006 9:34:58 PM PDT by hocndoc (http://www.lifeethics.org/www.lifeethics.org/index.html)
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To: Old Professer

I'm glad you found a good doc.

Lisinopril and similar BP meds cause cough, but Toprol can lead to depression.(lack of energy).
Ask your doc if it's okay to switch to Losartan or other ACE-2 BP medicine. Now, if you have irregular heartbeat, you might need Toprol, so check first.

Second, check the thyroid.
Low thyroid is a common cause of depression/low energy.

And if you are over 60, try B12. There are tablets but drops and shots work better. They can do a B12 level to check if you have insurance. If you have a lousy diet, add a "stress" vitamin.

And try to eat a balanced diet: I tell my men to eat a Turkey sub instead of a cheeseburger and fries, and drink orange juice instead of coke.

I'm glad they found your pressure was up before you had a major stroke.
BP medicines are lifesaving: I date before they existed.


45 posted on 06/17/2006 10:26:12 PM PDT by LadyDoc (liberals only love politically correct poor people)
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To: hocndoc
Hey! It could be valid. I, myself, am allergic to corn in all forms so when they put corn starch in a pill, it affects me.

I was taking generic claritin and my allergies got worse then we realized they were putting corn starch into the allergy pills.

46 posted on 06/19/2006 9:28:53 AM PDT by Freedom Dignity n Honor (There are permanent moral truths.)
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To: LadyDoc

No wonder the leading cause of deaths for CFIS/ME is suicide with doctors (are you really?) like you. Interesting enough, after being diagnosed with CFIDS/FIBROMYALGIA the last 13 years, it has finally been PROVEN via lab work that I have CVIDS (Common Variable Immunodeficiency). Neurotic?? Your comments leave me speechless and irritated because it is people like you who have DELAYED the much needed medical resolution to this DISEASE. I am glad that my doctors ARE NOT like you - I would be dead by now.


47 posted on 06/21/2006 8:48:08 AM PDT by Fightingforthecause (Thank God for "REAL" csring doctors!)
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