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?