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Morgellons the Crying Wolf Disease

Aug 18, 2008 - 6 comments
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MORGELLONS

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skin infection

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Skin infections

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Morgellons disease is a growing epidemic in America and abroad.  It is an unknown disease which is said to cause uncontrollable itching and symptoms of feeling like bugs are crawling all over your body.  It also creates a host of painful lesions, rashes, and sores on your body which are said to never heal.  Reported cases of the disease are commonly tracked to California, Texas, and Florida.  The remarkable thing about the disease is that a large percentage of doctors do not recognize Morgellons as a disease and claim that inhabitants of the disease are delusional who suffer as hypochondriacs.  

Under a microscope and/or with the naked eye the disease shows bizarre fibers either clear, white, blue, or red.  Other symptoms include muscle pain, contractions, anemia, enlarged liver, and spleen degeneration.  There are also neurological symptoms associated with Morgellons disease such as memory impairment, confusion, deep depression, chronic fatigue, and attention deficit disorder (brain fog).  The lesions, sores, and skin rashes created by Morgellons disease are reported not to heal well, therefore leaving large discolored marks and blemishes on your skin.

The fact that doctors and medical pathologist refuse to recognize Morgellons and ignore reports of the disease is making life unbearable for many, simply because they are not getting any meaningful treatment for this disease.  To add injury to insult, patients are considered to be crying wolf when constantly trying to prove to their physicians that Morgellons is real and exists.  Some physicians have refused to tend to their Morgellon patients claiming doctors have dropped them as a patient altogether because they are unable to prescribe any medication for Morgellons disease.  Morgellons disease is commonly misdiagnosed as being Lyme disease, staph infection, or a fungal disease – but untreatable.   Morgellons disease is said to mimic scabies and lice, yet again it is untreatable.

Patients of Morgellons are left no other choice but to do self research, self diagnosis, self medication, and self treatment, since medical professionals refuse to believe their cry for help.  This is seemingly a hopeless disease.

There are non-profit organizations such as Morgellons Research Foundation which have propped up to bring awareness to the Morgellons disease.  There are also treatments such as Nutrasilver that relieves most of the symptoms in a relatively short timeframe.

Some people despise these companies for capitalizing off of someone else's pain and suffering.  Well, I see it like this: if you rely on your major pharmaceutical companies to come up with a solution which they currently are not even investigating, then expect to pay high rates through insurance for your care.

This disease is so unbearable that it is reported to be the cause of suicide for many.  The small companies who capitalize today from Morgellons disease are making far less profits than if the major pharmaceutical companies take notice.  I applaud the efforts of Nutrasilver and the like.  There are many testimonials about the product saying that it does heal the lesions and eliminate the cognitive issues with Morgellons disease and other rare skin diseases, so in my eyes at least it is working, while our Congress and government are doing nothing. Unless you consider $338,000 to fund a study from funds from the CDC who has refused to investigate Morgellons with more complaints than any other disease for over six years.




About the Author
An advocate of Nutrasilver products.  Nutrasilver http://www.nutrasilver.com help treats Morgellons disease as well as other rare skin diseases.


Keywords
morgellons, morgellons disease, morgellon, morgellons treatment, morgellons treatments


Comments
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Avatar universal
by tonnie1982, Oct 02, 2009
I TOO BELIEVE I HAVE MORGELLON'S AND I HAVE HAD THIS THOUGHT FOR NEARLY A YEAR.I WISH SOMEONE COULD HELP ME,THE DOCTORS THINK I AM OF COURSE CRAZY.JUST LIKE I HEAR THEY CALL MOST PEOPLE WHO CLAIM TO HAVE PARASITES.MY OWN HUSBAND HAS IT TOO BUT DENIES IT AND SAYS I NEED HELP.I AM 27 AND I HAVE 3 KIDS AGES 5,6,AND 8 AND THEY TOO HAVE WHAT I BELIEVE TO BE MORGELLONS,I KNOW WE ALL HAVE SOMETHING!IT IS VERY PAINFUL MENTALLY AND I AM AFRAID FOR OUR BODIES,I FEEL AS THOUGH THEY MAY BE SLOWLY MAKING US VERY ILL,AND THERE'S NOT A DAM THING I CAN DO ABOUT IT.I MYSELF DO SUFFER FROM SOME MEDICAL CONDITIONS ALREADY,BUT NOW I THINK THIS COULD BE LINK TO THESE PARASITES.DEPRESSION,FIBROMYAGIA,NARCOLEPSY,HYPERTENSION AND A FEW OTHER SMALLER THINGS.I LIVE ON HARD MEDS AND WOULD LOVE TO NEVER HAVE TO TAKE THEM AGAIN.WHAT DO I DO I AM HURTING IN MY HEART WAITING AND WATCHING AS TIME PASSES BY AND WE ALL JUST LIVE WITH THESE THINGS,I FEEL THAT ARE EATING US AWAY.I TOO AM NOW REALLY GOING CRAZY AS I SEARCH FOR ANSWERS AND HELP.I JUST WISH SOMEONE WOULD BELIEVE ME ANYONE AT ALL,THERE IS A HEAVY WEIGHT IN MY CHEST AS I TRY TO FIND HELP AND DO NOT CIGSEED.ALWAYS I AM SEARCHING MY HOME FOR ANSWERS,AS I BELIEVE THERE IS SOMETHING INSIDE MY HOME THAT HAS CAUSED THIS OR IS CONTRIBUTING TO IT.THIS HAS NOW TAKING OVER MY LIFE AND CONSUMED MY LIFE! (MY POOR KIDS) IS WHAT I THINK ABOUT,KNOWING THEY NEED THERE MOM AND I AM NOT REALLY THERE FOR THEM.THIS IS SAD AND I DO NOT KNOW HOW LONG THIS WILL GO ON,PLEASE IS THERE ANYONE THAT CAN HELP?THANK YOU FOR YOUR TIME.

Avatar universal
by speciallady73, Apr 26, 2011
I TOO SUFFER FROM THIS CONDITION, I HAVE DRIVEN THE DOCTORS, NURSES, DERMATOLOGIST, ANY, AND EVERY BODY YOU CAN THINK OF.. I HAVE DRIVEN MYSELF IN THE GROUND BECAUSE I'M AT THE EMERGENCY ROOM EVERY FOUR TO SIX MONTHS AND NOBODY HAS CAME UP WITH NOTHING BUT "ITS A STAPH INFECTION", "ITS A BACTERIAL INFECTION", "ITS MRSA 85% OF THE POPULATION SUFFERS FROM IT", DO YOU KNOW WERE AM GOING WITH THIS. I HAVE A FRIEND THAT SAYS I SUFFER FROM HYPOCHONDRIACS. I HAVE BASICALLY ALL THE SYMPTOMS HE DESCRIBED.WHY ISN'T IT RECOGNIZE AND ITS ONLY REPORTED IN THREE STATES. DOES ANYONE HAVE ANSWERS TO THESE QUESTIONS OR DO WE GO ON LIVING WITH THIS DISEASE.
  



Avatar universal
by RaeRaeM, Aug 03, 2011
Thank you for posting this!  I have also had horrific experience with doctors, even top notch specialists at Univeristy hospitals. Every dr. that I saw or was referred to eventually dropped me from their care as well. They all come to the same conclusion that I have OCD that is manifesting as neurodermitis and am causing the lesions myself!  I was even accused of being on drugs and/or trying to obtain prescribtion pain killers!!  I have lost several people in my life due to the fact that they also starting thinking I was crazy!!  After awhile a person starts to wonder if they really are!!   I am sorry for your loss and the inablity of the medical professionals to take her seriously. By sharing this information you are going to help many many people!  Thank you!

Avatar universal
by Lmac42, Dec 07, 2012
I too have this ...I have more info for treatment

Avatar universal
by Lmac42, Dec 09, 2012
Take action...call Radio, TV, Senators,Congressional officials, Bombard them with call...others need to hear about this..so they won't think they are alone...but the government, CDC won't help unless me all complain at the same time.....but, there is all kinds of info on the net and you tube...research, I am helping myself...find a Naturopathic doctor who wants to help...they should not be that expensive...but lots of info on youtube....GET RID of all cotton...clothes and sheets..it spreads Morgellons.  I is in the dust all over the place...in our water...Get a cheap microscope and you will see it.  It looks like a  tiny cotton lint on your black clothes.  It appears to be white when on black clothing...but in the microscope it is very black.  Don't buy "modal" either....it is the new cotton.  ....where these Nanno fibers nest.  Then we buy these clothes from all over the world...and they are infecting people that sew these clothes as well....Even our patches, bandades and qtips have morgellons fibers.  I even checked all my clothes...all these fibers have wrapped through the cotton weave in them as well....Lmac42

Avatar universal
by Cmsstar, Oct 23, 2015
I want to tell people about it but I am afraid to go public because four years ago I was ridiculed by an emergency doctor and two dermatologists and I saw I could get nowhere. Now I see where the CDC investigation went nowhere. I got so angry I am writing a three part book in fiction form about this "unknown dermopathy". I am on the third and supposedly last part of the mini novel series. That is my way of putting it out there without putting myself under. I am experiencing a block in my attempts to complete the story since every waking day new information emerges that changes my intended outcome. Is there any end in sight?

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