MorgellonsUSA.com

In a June 2'nd, 2006 News Article within the
"San Fransisco Chronicle"
a Spokesman for the "CENTERS FOR
DISEASE CONTROL"
Spake a few words.

HERE'S THE LINK TO THIS STORY

After more than a year of pressure from patients convinced they have
Morgellons, the Centers for Disease Control and Prevention will begin
investigating the ailment for the first time and determine, once and for
all, whether it exists. The CDC started organizing a committee this
week for that purpose.
Actually after SEVERAL years of people reporting these
symptoms to their Physicians and to the CDC, they have finally
formed a "Task Force" to look into the Disease.  Well after
thousands have been ridiculed, mocked, ignored, shunned,
diagnosed DOP, lost jobs, became disabled without any
disability benefits, mates have left spouses, taking children
away, lost medical insurance and coverage, some confined to
mental institutions, pushed into the Deepest forms of
Depression, some committed suicide, and many have since
died from complications of the Disease.  
Because of the Past denial of this Disease amongst Doctors
and the Centers for Disease Control, and the absolute ridicule,
mockery and "forcing sufferers out of the doors of the Medical
Establishments and shutting them upon them",    Many people
believe that the CDC amongst other Organizations have
purposely swept this under the carpet, and are
"HIDING SOMETHING"  Waiting for the Infected souls to "DIE OFF
AND DISAPPEAR INTO THE STATISTICS!!!"
"TO COVER UP WHAT THEY KNOW"

"Not a day passes when I don't talk to somebody who claims to have
this," said CDC spokesman Dan Rutz. "In the absence of any objective
review, people have jumped to conclusions and found each other on
the Internet and formed their own belief structure. We really need to
debunk this if there isn't anything to it or identify if there is indeed a
new, unrecognized disease that needs attention."
It's a shame that what Dan Calls "jumping to conclusions" is
nothing more than patients "knowing their own bodies better
than their Doctors" and Diagnosing themselves "BECAUSE
THOSE WHO SHOULD HAVE WOULDN'T!!!"  
(Let's see, if I saw Fibers or Objects come out of my skin did I jump
to conclusions?)
It's a very good thing that we've got the Internet to Self
Diagnose, because the Medical Community has tried to
convince these people that they're "basically crazy" and
secondarily "convincing" many of the afflicted' family members
that they're indeed "Crazy!!!"  What of the thousands suffering
who Don't have Internet?

This has been truly astonishing, and yet relieving... that people
from various Cities, States and "Countries" have written here
saying, things such as these,...........       "Thank you very much
for being there!"  "Now I know what I have!"  "Thank goodness
I'm not crazy!"  "That is the exact same thing that the Doctor's
showed me in their Microscope, and told me that it's ONLY
yeast!"  One recent stated she was in 2 Mental Institutions of
recent, until family scanned the Internet for Morgellons.
We're sick Dan and we don't want to die.  We'd like to try to
live...
The ONLY REASON that we have to do it this way Dan, is
because YOUR EMPLOYER and the Medical Communities as a
WHOLE..... WOULD NOT DO A THING!!!  (except make matters
WORSE!)

THIS HAS BEEN A CALL FOR HELP BECAUSE THERE WAS NONE
OTHER WAY,  (I myself talked to CDC about this in February 2005  
and was told that they're not an enforcement agency and then
ignored.)
NOW ALL EYES ARE ON THE CDC to see if their Concern and Care
is Real, and to Debunk THEM if they are NOT!  
It's a good thing the sick have found one another on the
Internet because the CDC and the Medical Community had
'jumped to conclusions and formed their own belief structure"

NOW ALL EYES ARE WATCHING THIS......
(see Next Column)...
Being pretty much disabled for the past several years, not
able to work at all, or minimal part time work.
In the very beginning of 2005 I was fortunate to learn of
Morgellons on the Web.  After registering as a sufferer and
counseling by phone and e-mail I was convicted to buy a
microscope and a wood's lamp.  After turning the lamp on I
saw in a darkened room "very fine white Fibers" growing
out of the skin everywhere, hundreds and hundreds... Some
had light bluish tint...  And shedding off of my face and onto
my clothes.   I mostly wore dark blue or black shirts at the
time so it definitely wasn't coming from my clothes.  My
wife was there beholding all of this in wonder, and we took
the light and shone it upon her...   No white Fibers were
coming out of her face, nor protruding from her skin.
Looking much more closely I could see beneath the surface
of the skin "glowing pustule like structures" and looking yet
closer... I could see hundreds to thousands of tiny bright
orange/red spots, also, white starry dots beneath the skin's
surface.  
While showering I began to sweep the floor prior.  I installed
screens in the shower and sink drains.  Then I would bathe
with a firm bristle scrubbing brush and a clear shampoo.
Because of the results found I became truly astonished.
So "MorgellonsUSA was born" to help get the word out.
Then April 2005 I began a Medicine regimen.
After 5 months the small white Fibers with the pustules
were mostly gone.  Only few of the starry dots remained.
By experience "I found these to be very helpfull"
(Also See Page 14 for Treatment Hints)
#1) Terramycin Ointment on trouble spots or open sores
and lesions.  Mix with:

#2) Pure Peppermint Oil (Do NOT get around eyes or the
Private area's.  Even vapors will irritate eyes, etc.

A). SeptraDS: 2-3 Tabs taken daily for 1 to 2 years.  (Note
some persons are allergic to Septra.  May need Hormone
for Cerebral Inflammation)

B). Albendazole (taken with fatty foods), 400mgs. Twice
Daily for 28 days, 14 day breaks in between, with 5 or more
continuous courses, with low dose hormone for Cerebral
Inflammation (Occasional liver panels)

C). Diflucan 400-800 mgs. per day for scalp and eye
infections, etc. (Take as needed during 14 day interval
breaks from Albendazole)
(After Initial Treatments these 3 Meds may be taken
Occasionally for Shorter Intervals)
I'm very much better, although I am disabled, having
permanent "Neurological and Endrocine Damage."  It's a
good thing, because there could be no Disability Benefits
for a Disease that doesn't exist in the eyes of the Medical
Community.  (Quite a quandary)
On Page 13 are some VIDEOS of my
newer work!  Note:  If you've
constantly dismissed this Disease,
and  work in the Medical and
Science Field, and are now telling
yourself, "These are just a bunch of
fuzzy pictures, unscientific."  
That's True!  It should have been
YOU Publishing this.  Not me.....   
Sincerely,
Greg Vigil
"STATEMENT"
from
Oklahoma
State University
"Click Here"
For Professor
Randy
Wymore's
Comments
"Click Here"
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