MRSA

Saturday, February 5, 2011

Joni Mitchell Successfully Treated For Morgellons Disease


Joni Mitchell Successfully Treated For 

Morgellons Disease

Joni Mitchell Successfully Treated For Morgellons Disease

Joni Mitchell has revealed publicly that she has had Morgellons disease for the past 20 years. I have spoken with hundreds of Morgellons sufferers during the last three years, so I have a glimmer of how much this gifted singer has suffered. Joni said she has spent hundreds of thousands of dollars on Doctors, pharmaceuticals and every other kind of health-care practitioner imaginable over the years in many different countries including some of the best Doctors and hospitals in the USA as well.
All she got was worse. Until now…
Joni mentioned she was so angry with most of her Doctors, since none of them knew anything at all about Morgellons. All of them took her money and gave her prescription drugs, herbs, potions and lotions. She said “Most of them are out for the money and pretend they know about Morgellons so she would come back for further help.”
Since Morgellons Disease was reported in the mainstream media in 2005, there has been no real progress made in discovering the cause, how Morgellons is contracted and transmitted, if it is contagious or if it is directly responsible for deaths other than suicides. Deaths are increasing exponentially and so is the level of infection in the global population.
The symptoms are right out of a science fiction novel. Most experience ‘brain fog’ (confusion like ADHD), severe depression, deep bone and muscle ache just like fibromyalgia, severe chronic fatigue just like Chronic Fatigue Syndrome (many Morgellons victims sleep 10 to 16 hours a day and are still exhausted), multi-colored fibers grow from their skin that are coated in high-density polyurethane that will not burn until 1,400 degrees Fahrenheit is reached, and most bizarre, they experience animals that relentlessly move and bite the victim under their skin 24/7.
Morgellons victims lose their lives to this disease; MD’s and Dermatologist dismiss the symptoms as Delusions of Parasitosis (DOP), a subset of schizophrenia. The Medical Community treat their Morgellons patients much like HIV/AIDS patients were treated 30 years ago when that disease was new. The idea was simple; if it is not in the ‘book’, than it must be in your head. These victims are shunned by family and employers and are left alone without support and eventually become severely depressed, hopeless and suicidal.
Over forty US Senators and Congressmen has written letters to the Centers for Disease Control, including Senators Obama and Clinton requesting an investigation into this bizarre disease. The CDC began its investigation in Oakland, California at the Kaiser-Permanente Hospital in January, 2008 and was supposed to release its finding in May 2009. Inside sources now say it will be another year before the results are released. The funding for the CDC study was a mere $338,000; barely enough to set up the investigation. These same inside sources say that the remainder of the funding comes from the US Army.
In April, 2007 in the Journal of the American of Dermatology, Dr. William Harvey published an open letter to the Medical community regarding how Physicians should approach Morgellons disease.
In the past 5 years, there has been little financial resources to scientifically explore the cause(s) and treatment(s) to help Morgellons suffers begin to ‘get their lives back’. There are small pockets of individuals who are conducting their own Morgellons investigations with little or no funding. The Morgellons Research Foundation, located at Oklahoma State University, is severely underfundedand has expressed little interest in finding any relief for Morgellons victims, but rather focuses ondiscovering the cause of this mysterious new disease. Meanwhile, Morgellons victims search relentlessly on the Internet for some clue as to how to eliminate their suffering.
Worse, there is no spokesperson to bring to the public eye the incredible torment Morgellons victim’s experience. Most of the scientists that are willing to discuss Morgellons say that there could be as many as 10,000 new Morgellons victims every day in the USA alone. Most will not get diagnosed correctly and will be given a DOP label to labeled in their medical record for life as mental patients.
Included in this number of new Morgellons victims are celebrities, Senators and Congressmen and other public figures. Until one or more of them steps up and shares their Morgellons suffering with the world, the rest of us will remain asleep to Morgellons until each of us becomes the next Morgellons sufferer. Until a celebrity or public figure has the courage and conviction to publicly announce their Morgellons disease and encourage mainstream science to fund and investigate Morgellons disease, the silent suffering will continue.
Morgellons Lesions on elbowIn February, 2009, it became public that Joni Mitchell has Morgellons. I found her manager in Canada and spoke with several people in his office. They were very pleasant and helpful, especially when I told them that I was sending her 8 bottles of NutraSilver without charge and that Joni should expect to heal dramatically in a few weeks. I waited and waited until Joni actually called me to say that many of her worst symptoms had either subsided or were mostly gone. She said she was beginning to feel “like herself” again and that her brain fog was clearing up and she could think clearly once more. She has since bought several hundred bottles for herself.
Many of her lesions have dried up and fell off. The lesions actually consume the skin pigmentation, so where the lesions fell off there are now white areas where the lesions used to be. Joni said she could live with that as long as the lesions did not return. While not yet symptom-free, Joni continues to heal and gain her life back. Joni has since moved away from her relentless suffering towards recovery which has made life easier for her.
As an expression of gratitude, Joni was gracious enough to send me an advanced copy of her up-coming ballet The Fiddle and the Drum. Not being much of a ballet fan, I really was not interested in any form of ballet until I actually saw Joni’s DVD. Joni and her team did an outstanding job creating this entertaining and enjoyable masterpiece. Joni’s singing and writing skills have been honed exquisitely for this very endeavor.
I am happy to have met Joni and I know that if she continues to take NutraSilver, her Morgellons symptoms will leave her alone and she can continue to create music and art for all of us to enjoy. Joni is a brave and courageous woman. I hope she decides to tell her story of how Morgellons disease nearly ruined her life; that she speaks up to publicly proclaim to the world that Morgellons Disease a real disease and perhaps she can lead the charge to raise significant money so real research can occur. In the mean time, Morgellons sufferers sit and suffer and wait.

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