Morgellons Disease: Virtually Unknown and Dreadful

Morgellons Disease is still pretty much unknown today even in the medical community. I first heard of this Morgellons Disease in 2007 from Allen Galapon, a good friend of mine who has an experience as a Nursing assistant. He was, at that time, looking for rare diseases and called me one day to drop by his place to watch a video he found on Youtube. We watched a few related videos on Youtube dealing with this disease (an unknown nasty worm species actually) whose origin cannot be explained by scientists up to this day.

Now, after doing some more online research on Morgellons Disease, my wife informed me that until this day, there is no clear explanation as to the origin and prevention of Morgellons Disease. She even read an article stating that this condition is man-made (a theory) and the worms that come out of lesions in different parts of the human body do not actually have DNA – the blueprint of life. WTF! I was startled and started to think that it could really be a product of a failed science experiment by some men playing God.

To cut the long story short, watch the video below about a patient’s testimony and how she triumphantly won over Morgellons Disease. I will not post related videos here because I find a lot of them gross and I myself cannot bear to look at those worms which look like filaments in thickness (Note: some are visible to the naked eye though)

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6 Comments on “Morgellons Disease: Virtually Unknown and Dreadful”

  1. Morgellons Suffers Need a “Poster Child Celebrity” To Tell This Amazing Story

    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: ‘brain fog’ (confusion like ADHD), severe depression, deep bone and muscle ache just like fibromyalgia, severe chronic fatigue just like Chronic Fatigue Syndrome (Morgellons victims sleep 10 to 16 hours a day and are still exhausted), multi-colored fibers growing from their skin that are coated in high-density polyurethane that will not burn until 1,400 degrees Fahrenheit, and most bizarre, they experience animals that relentlessly move and bite the victim under their skin 24/7.

    Morgellons victims loose 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. 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 requesting an investigation into this bizarre disease. The CDC began its investigation in Oakland, California at the Kaiser-Permanente Hospital in January, 2008 and is expected to release its finding in May 2009. The funding was a mere $338,000; barely enough to set up the investigation. Inside sources say that the remainder of the funding comes from the US Army.

    In the past 5 years, there has been little funding to scientifically explore the cause(s) and treatments to help the Morgellons suffers begin to ‘get their lives back’. There are small pockets of individuals who are conducting their own Morgellons investigation with little or no funding. The Morgellons Research Foundation, located at Oklahoma State University, is severely underfunded and has expressed no interest in finding any relief for Morgellons victims, but rather focuses on discovering 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. The scientists that are willing to discuss Morgellons at all say that there are at least 10,000 new Morgellons victims a 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 has the courage and conviction to publically announce their Morgellons disease and encourage mainstream science to fund and investigate Morgellons disease, the silent suffering will continue.

    jessie reply on April 8th, 2009:

    Thanks for updating the article with your comment.

    jessie’s last blog post..Homedics Brethe Air Revitalizer BRT 150 – Cheap and Compact

  2. Oh dear..what a scary disease! Have a blessed Holy Week Fren.

    Joyoz’s last blog post..Our little ones 3rd Birthday

    jessie reply on April 10th, 2009:


    Ganun din sa inyo ng family mo. Yeah, the Morgellons disease or Morgellons Syndrome is really scary amiga. Sana wag tayong magkaron nyan.

    jessie’s last blog post..Low Apple 8GB 4th Generation Ipod Nano Price

  3. This is a nice video, giving hope to sufferers of the morgellons disease world wide.

    Thank you.

  4. This disease seems real. I have been seeing doctors, 8 or 9 all together, since 1991. Scabies it is not, but I’ve been diagnosed 3 times with it. Diflucan seemed to get rid of the red bumps, but I can’t get a doctor to prescribe it again, maybe I’ll try harder…
    Anyways, I have posted my microscopic videos online, the black n red moving thread is the best video I’ve got so far, watch the 1st 5 seconds closely…
    YOUTUBE NAME TheRealPhatgrower