posted
After years of symptoms associated with Lyme, I finished one year of treatment this past summer under the supervision of my LLMD(consisting of antibiotics, supplements, diet).
Over the past few months, my C3a C4a test came back normal, muscle testing indicated no active Lyme disease, and energy testing indicated no active Lyme or co-infections.
Nevertheless, symptoms persist. They have again increased with the colder weather. Current symptoms include achy knees, pain on left elbow, pressure/tingling on left temple, fatigue...
I am currently taking supplements and I also see a classical homeopath. I don't have an appointment with my LLMD until January.
I'm not sure what I should do next. I've read about MMS, Colloidal Silver, and also Bionic 880 treatments. The earliest I could go to Germany would be this coming summer.
A local Naturopath stated that she recently successfully treated a man for Lyme (who had also used antibiotics) with MMS. He apparently went from intense pain to no pain in a few months.
Any suggestions?
Posts: 83 | From Minnesota | Registered: Dec 2006
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If he/she is a god LLMD they'll look for answers and will find them for you.
Be well.
-------------------- simplify.... Posts: 96 | From Rhode Island | Registered: Jan 2008
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seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
I hope you find answers. I wouldn't bet the bank on muscle testing for all answers.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
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djf2005
Frequent Contributor (1K+ posts)
Member # 11449
posted
muscle testing says no lyme but you still have symptoms???
hmmmm...
id def look into treating it still with abx or alternative means.
look into azc (advanced cellular zeolite) and the collodial silver product the same company puts out. they are both very good. i think the silver is acs200 or something.
good luck
there are many ways in which to treat lyme.
were metals, adrenals, endocrine, etc etc sufficiently worked up?
derek
-------------------- "Experience is not what happens to you; it is what you do with what happens to you."
posted
Dr. K put my son on MMS as a miracle cure and swore by it.. He did not have any improvement. Sorry, maybe different for you tho.
Posts: 38 | From Seattle | Registered: Nov 2008
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lymie_in_md
Frequent Contributor (1K+ posts)
Member # 14197
posted
I think Dr. MacDonald discovered something called biofilm in lyme patients. Which I believe protects lyme and other pathogens in a lipid caccoon. So no matter how much ABX you use or how much MMS you use it may not work. If you use a combo of monolaurin and oregano you might have a better chance at removing the biofilm and disabling the disease.
I believe instead of ABX use MMS and freeze dried garlic. Do this for about a month or two. You might be surprised at the combination and how well it works. At least ask your llmd about it.
Of course mercury adds yet another big wrinkle to the problem. And yeast/fungi/candida -- one reason I wouldn't use ABX. ABX gives rise to candida/yeast/fungi making it very difficult to get rid of biofilm in the body.
-------------------- Bob Posts: 2150 | From Maryland | Registered: Dec 2007
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Hoosiers51
Frequent Contributor (1K+ posts)
Member # 15759
posted
You might also want to think about mycoplasma, babesia, or bartonella.
Posts: 4590 | From Midwest | Registered: Jun 2008
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