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Lyme disease.

My cholesterol went from 168 to over 200 over some years, triglycerides were up, inflammation (RA factor) was up, I ate little, and well, but weighed 15 lbs more than I wanted. I was finally diagnosed w/ Lyme disease.


It also made me very sensitive, I had allergic reactions when it got really bad, was afraid to eat anything, had the elisaact.com allergy test done, was told to avoid cheese and other things.


For a while I ate only chicken, fish, fruits, vegetables, brown rice, raw almonds and cashews and tortilla chips, and drank mostly water. Between this and getting antibiotics for Lyme, my weight dropped EASILY for the first time in years, in fact it scared me as I dropped 25 lbs. very quickly. It's balanced out well now, but I hardly eat any prepared or packaged foods, and use healthy oils as I always have.

My cholesterol is 158... and I've been cautioned by doctors and the pharmacist that I don't want it being too low, as it affects hormones.
I'm on cholestyramine (mainly used to reduce cholesterol) to help remove lyme toxins, and I actually came to this site to remind me what I could have to increase it! : 0

Btw, anyone w/ questions about fatigue, pain, fibromyalgia, chronic fatigue, not feeling quite right, and having problems attributed to hormones or stress or depression should look at this:

http://www.ilads.org/files/burrascano_0905.pdf

Most standard doctors know nothing about it, and claim it's not in their area, etc. This is "the" other side of the story! (as well as numerous books of horror stories by families w/ undiagnosed Lyme for years, it's so sad). Some think even M.S., Alzheimers and mental disorders may be undiagnosed Lyme disease.

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Lyme disease.

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Oct 27, 2009
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by: Anonymous

I posted to this site due to the link w/ weight and cholesterol I experienced with Lyme, when I should have been able to lower both, the way I was eating.
I've read that the Lyme test(s) are 50-75% accurate, yet many doctors say a negative test means you don't have it. Not true. It doesn't test for all strains, results can be affected by prior antibiotic use, by the state of the immune system, there can be co-infections, etc.

Even the CDC info. on this subject has been poor, and many doctors (& infectious disease doctors) don't acknowledge 'chronic' or long lasting Lyme disease after a round of antibiotics. (I think they'd change their mind if exposed, not treated early, and experienced the aftermath of lyme hiding in it's cyst form).

PLEASE refer to ILADS and lymedoctor.com for accurate information. He also had it for years, w/out diagnosis, despite being a M.D. in an area with excellent medical care. Any Tan, award winning author, had terrible symptoms associated with it for years, w/out diagnosis or help.... http://amytan.net/.
There are a number of books written by people who were misdiagnosed, or their FAMILY was misdiagnosed, for years.

You do NOT have to have the bulls-eye rash, and many do not find the sesame seed size tick on them. CDC even acknowledges their criteria were for reporting, not diagnosis, and that Lyme is tremendously underreported. That's led Drs to say "we don't have it in this state", perpetuating that myth, not properly treating it, which has led to many ending up on disability (One doctor said "What, deer don't cross state lines?"). Not all cases are the same, some look like tiredness, arthritis, forgetfulness, poor motivation, etc. We've got to get more research, proper diagnosis and help for this disease!

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