As this subject was so new to me, I thought that as a resource for people 
with the condition or have the symptoms but don't know why, and are being 
told they it's in their head (possibly truer literally than the dismissive 
practitioners realise) it would be good to have it mentioned.
I don't think the condition would necessarily respond to CS unless the cause 
is single-celled; they don't seem sure at this point whether the "hairs" or 
"bristles" are debris or crittur.  However, CS would certainly support the 
body systems, while something else such as microelectricity or Rife 
frequencies or coconut oil or FIR sauna or far older methods treated it. 
Here is a condition that one would expect to respond to sauna.  You'll 
notice what treatment was used four hundred years ago!

http://www.morgellons.org/

According to the Morgellons Research Foundation, a number of people who had
been diagnosed with CFS and FMS have after some years discovered the
symptoms of Morgellons, a condition described back in the 1500s and 1600s.

Sufferers find "threads" coming out of lesions in the skin, have unbearable
itching, and little black specks also come from the lesions.
It appears to occur around specific geographic locations.  The threads are
filamentous, branching, and have tentatively been identified as cellulose,
and researchers recently speculated that it might just be dead DNA from the
organism.  They are described by sufferers as fuzzballs or lintballs, as
they are often twisted into what looks like bundles of fibres.  They do not
come from textiles.  They are usually white, but sometimes blue, black, or,
rarely, red.  The black specks are found also to contain fibres.

Some 95% of patients are reported to have been diagnosed by their doctors as
having delusional parasitosis - they are supposedly  imagining parasites in
their skin. They also have brain fog, CFS, FMS, ADHD, Bipolar, mood swings,
depression, joint swelling and pain, rapid visual and aural decline, hair
loss, autoimmune problems, and so on.

Some people have the dreadful itching without any skin lesions.

(When I was working for a CFS doctor, one of his patients rang me up and
said that he had returned to the city and found that he had a child he
didn't know about.  He got back with the mother.  After a few months, both
mother and child had the dreadful itching that had been troubling him for a
long time but "had no cause", there was nothing there according to the
doctors.  "But I know there's something there," he said, "especially since
they didn't have this before I turned up".   - R)

One site with articles linked the problem with damp areas and named an
organism.

The problem was described as existing in Languedoc in the 1600s, and in a
book published in 1544 this conditions was also described.  It was mainly
found in children, in the muscular parts.
http://www.morgellons.org/kellett.html
Draconcia and Dracunculus were names used back then.   Schenkius said that
when the women realised that their children were wasting away from this
condition, they brought them to the sweating chambers.
A 1588 book calls it pilaris affectio, "the hair affection" and the people
treating it back then believed that unless the "hairs" were removed, the
parasite would reach the brain and cause epilepsy.  Another old book says
the Languedoc people called it Masquelon.  Various other people described
them as bristles.
http://www.morgellons.org/updates.html contains updates and description of
the research being undertaken.

Word is spreading, and even Popular Mechanics has had an article about it.

Rowena


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