If there is a genetic component it may be auto immune. LDN
is helpful
in many auto immune disorders. It has been show to stop the
progression
of MS including demyelinations in at least 70 - 80% of
patients.
Starting with a very low dose just twice a week is a great
way to ease
into the therapy.
There are a number of Yahoo lists and info sites.
http://groups.yahoo.com/group/Very_Low_Dose_Naltrexone
Discusses very low dose and interval dosing.
Information is spread out over many sites and lists because
there is not
enough formal dose response data across all conditions so
that patient
reports are the main source of info, not unlike CS.
Personally I take 0.5 mg twice a week, very low and spread
out but
it is working for my allergies and I will slowly increase,
but some
go right to 4.5 mg every night. Depends on your individual
reaction.
Worth looking into since it is cheap and low tox, also has many
fringe benefits of preventing cancer, colds, flus, improving
general
health.
www.alldaychemist.com sells 50 mg tabs without an Rx, which can
be diluted in 50 ml of distilled water to produce a 1 mg/ml
solution.
Many people use these tablets for years with great results
in their
severe MS and other conditions.
Garnet
------------------
http://groups.yahoo.com/group/Very_Low_Dose_Naltrexone
http://groups.yahoo.com/group/LDN_Information
Dr Chris Steele, ITV's This Morning supporting LDN
http://www.youtube.com/watch?v=CVpjsDK0LPA
Marshall Dudley wrote:
My son in law has this disorder: *http://www.hnpp.org/whatis.htm
My granddaughter is now showing signs of it. Does anyone have any
information on this, or a remedy? It is caused by **demyelinating.
thanks,
Marshall
*
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