Hi........I don't know how I got mycoplasma..........I guess I could have got
when I was in the Philippines.........much like Gulf War Syndrome. I don't
think it is likely to "know" where you got them........they are slow
replicating and are described as being a "stealth" type of disease. I don't
know what all the symptoms are. I would suspect that they are generally much
like an alergic reaction. My symptoms occurred in the following order.
1. patches on my hands that became rough and cracked to the point of almost
bleeding.
2. muscle spasms
3. shortness of breath even when I was very active and should have been in very
good health.
4. watery eyes along with sometimes blurry vision.
5. Progressive joint pain. {this is the wakeup call}
Finally now I am sure to be on the right track. Today I can walk a
little.......but is very painful..........I've started CS treatments again. I
feel that as long as I have them on the run I might as well stay after
them...............I feel that I am somewhat of a pioneer.......since very few
people are actually being treated for mycoplasma.......and almost none are
treating it with CS. today begins week two of this treatment........the only
other thing I am taking is vioxx every other day.....if I didn't take it I
would probably be suicidal with pain......I'm anxious to get rid of them. If
anyone knows of anything else that may work for pain.....I'm all ears....."MSM
doesn't do it for me"..........Robb
----- Original Message -----
From: Wayne Fugitt
To: silver-list@eskimo.com
Sent: Tuesday, July 02, 2002 7:53 AM
Subject: Re: CS>Pain clear to the bone
Morning Rob,
At 12:12 AM 07/02/2002 -0400, you wrote:
Greetings.........Yesterday I took my biggest doses of CS throughout the
day. This morning at 4 am, I woke up from pain and knew something was
happening........I was having the worst rheumatoid arthritis attack that I've
ever had.......I was evidentley killing the nasty little mycoplasma's in large
numbers. I have never followed through with CS treatments before because I was
unaware that mycoplasma requires long term treatments..........
Are you the person that got the mycoplasma from imported products a few
months ago?
I have been talking to the blood lab about the test. Somehow, they always
talk me out of doing the test.
The tech says, "everyone has it" so no need to test.
I understand that many kinds exist and only a few have been identified and
named.
Any good sites I may have missed?
What are all the symptoms of mycoplasma?
