stephen55
Literotica Guru
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- Jan 6, 2010
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Our two Canadian apologists are singing in two-part-harmony, crooning seductively about social democracies and Universal Health Care just as a 'Death Panel' in Canada has sentenced a 13 month old child to death against the will of its' parents to a point they are fleeing Canada to the free United States of America.
Go figure.
Amicus
edited to add: http://www.rightpundits.com/?p=8294 account of Canadian Death Panel...
I thought I'd do a follow up on Baby Joseph. I've already vented at length on ami's ignorance of all things Canadian. I've already given what I felt was a fair reflection of what I thought was going on back in London, Ontario from a retired doc's point of view. As for Canadian Death Panels, they exist only in ami's fevered brain.
14-month-old Joseph Maraachli has had a tracheostomy done at the Cardinal Glennon Children's Medical Center in St Louis, Missouri.
When I first read about this poor child, I had a suspicion that the diagnosis, not at first made public, was Leigh's Disease. The whole story rang a very painful bell. When I was a resident, I was involved in the care of a one year old boy who was dying of this exceedingly miserable condition. I've just read that little Joseph does have Leigh's Disease, the same neurometabolic disorder that took the life of his sister.
Leigh's Disease, or Subacute Necrotizing Encephalomyelopathy is a very rare inherited disorder that usually effects children before they are two years old. It is 100% fatal. There is no cure or even partially effective palliation. Life expectancy is usually about one year following onset of symptoms.
It is characterized by movement disorder which progresses to dystonia, rigidity, tremor, chorea, hypokinesia and myoclonus. Other symptoms include loss of appetite, vomiting, irritability, continuous crying (in infants), and seizures. Later problems can also be episodes of lactic acidosis, which can lead to impairment of respiratory and kidney function. Brain function deteriorates, coma ensues and finally a persistent vegetative state is followed by death. Once the child can no longer eat or drink, the child's life can be prolonged by assisting ventilation, IV fluids and parenteral nutrition, but the neurological condition is irreversible. The brain continues to deteriorate and death is inevitable.
http://i.dailymail.co.uk/i/pix/2011/03/22/article-1368559-0B49405600000578-781_306x354.jpg
This is Joseph Maraachli. That "chubby cheeks" you see is not a sign of health and vitality. It is the irreversible edema of irreversible kidney failure. Those eyes are never going to open.
http://i.dailymail.co.uk/i/pix/2011/02/28/article-1361593-0D6A674C000005DC-174_634x432.jpg
His father, Moe Maraachli wants his son to live as long as possible. I don't blame him one bit.
http://i.dailymail.co.uk/i/pix/2011/03/21/article-1368559-0B2EC85C00000578-174_634x404.jpg
The priest is father Frank Pavone of the Priests For Life charity, who are footing all the bills for both hospital care and the air ambulance that brought little Joseph to St. Louis. I'm not going to argue with a Catholic priest about when a patient with a terminal illness and in a persistent vegetative state should be allowed to die of their disease as opposed to be kept going by heroic measures.
I will argue a bit with the hospital spokesperson who had this to say...'It is our hope that this procedure will allow Joseph and his family the gift of a few more months together and that Joseph may be more comfortable with a permanent tracheotomy.
'As with any of the children we help, our primary focus must remain on the patient and what is best in his or her individual circumstances.'
Joseph is comatose. He is not more comfortable with a tracheostomy and the last thing that tracheostomy will ever be is permanent. It's a judgment call, but I'm not at all sure that the docs at Cardinal Glennon Children's Medical Center have done Joseph any favors. They certainly have made his parents happy but his parents aren't the patient.
Having spent the better part of my three month rotation in paediatrics dealing with a baby dying of Leigh's Disease, all I can say is that I'm very grateful that the parents of my patient did not wish any heroic measures taken to prolong their baby's life. I was in the room when their baby died. I was fighting back tears then and I'm losing tears now. Sometimes life really, really sucks.
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