My story and the incredible, little-known-of treatment - for Lupus, Rheumatoid Arthritis, Ankylosing Spondylitis, Scleroderma, etc.

i eat garlic almost every day. straight up or cooked in almost every meal. family tradition i shall pass on to my own children. i rarely get sick and if i do, just the occasional sniffle. i have a ton of energy and have never in 32 years been bed ridden because of a sickness. only called in sick to a job once and that was to witness the birth of my oldest child. we also ingest a lot of horseradish, honey, goat cheese or milk, sunlight and distilled water.

A daily dose may be too much for some people

My treatment began with a large dose one time, then wait a week. A large dose the 2nd week, then wait a week. Then dosing a smaller dose, 3 times a week. I also used other therapies in conjunction with this, such as the peroxide baths, and diet, and some injections at times of other antibiotics. I was very amazed when I began the treatment, at the results. I would not use minocycline for over 18 months without switching to a different antibiotic. It goes fine for some, but in rare cases, as you approach the 2 year mark, you can get drug induced lupus. This is really bad and you don't want that. It is best to have an MD assist you in administering the protocol and monitoring it. Some people have even recruited doctors to help them with it, had them read a copy of the protocol and begin, and others have found a doctor who does the protocol and traveled to them for occasional consult and upkeep.

I don't know anything about that, I just copy and paste. What is a referrer code? Anyway, you are just distracting from the people who really need this information. I don't do this for a living, or you would have heard from me long ago when I came to GLP. I got the idea for this thread when someone else yesterday posted a thread about how Cancer "cures" are being suppressed by big pharma and instead, they push on us medications that don't really cure you and make more money. It has always been my nature to try to help others, I am a very generous person with a merciful heart and I help many people with medical information and natural health information on many many subjects here on GLP. I have spent the past 25 years studying natural medicine for personal reasosn - because doctors never seemed to have anything but pills to offer, and I was allergic to most of them. I have found alternative medicine to be much more effective, and biologically friendly. That nature in me is how I also came to embrace this protocol as a solution to my own health problems. I found it to make so much sense, to be so much less toxic than the steroids and chemo they give us, and I share it with anyone who is interested, like I am now.

I am not saying I am against all medications or that I have not found some useful or necessary, by any means. But for rheumatic disease, I think they fall VERY short.

Do you work for big pharma, or something?

For those who don't want to read the book (I'm not a book person so much, myself, takes too long - read too many when I was young, I guess) - here's a good article summarizing Dr. Brown's history and work. It's 10 pages, minus the reference pages at the end, but a lot shorter than a book, I'm sure:

[link to www.arthritistrust.org]

Oh, yes, someone asked about COLLOIDAL SILVER - I use this when I feel a flare-up, but not daily. It can cause problems if used too much, but I find it pretty harmless when used symptomatically for temporary inflammation issues or infections. I recommend the low-dose, regular medications for administering the full protocol, as they are safer and more familiar in their effects long-term.

Hmmmmmmmm.

I recommend considering again taking the Plaquenil. I take the generic form. It actually does a lot to control my lupus. Lupus left untreated in any way can lead to kidney failure, as it did with me. You do not want this, as this complication in lupus leads to a much higher mortality rate. I take about half the usual dose of the generic for Plaquenil, with no side effects or harm of any type. I was told that my disease was too severe to use the medication, that it would not help me, but it was actually the most harmless of all of the meds they wanted for me, and did me the most good. You just have to get eye checks every 6 to 12 months, and if you are a rare person who gets side effects, stopping the med usually resolves it. Just wanted to mention that to you. As I said before, I don't find all drugs evil, but when the only options are harmful steroids or chemo, it can be worth finding an alternative. If that is not possible, or the alternative treatments don't work for a person, there is no shame in using the normal protocols to at least preserve your life and try to get stable. These diseases are no joke, and should not be left unchecked. I was not diagnosed until I had 7 years of very severe lupus and it did much damage. I did not have access to medical care during that time and did not realize I had something so serious until it was almost too late. I am very lucky to be alive.

That is WRONG when it comes to the mycoplasmas -

Quoting from the link:

Mycoplasmas however, do not have a cell wall, and like a tiny jellyfish with a pliable membrane, can take on many different shapes which make them difficult to identify, even under a high powered electron microscope. Mycoplasmas can also be very hard to culture in the laboratory and are often missed as pathogenic causes of diseases for this reason. [link to www.rain-tree.com]

.........................................................

Mycoplasma is a unique bacteria, and the problem with having it in your system if you have an autoimmune disorder, is that it agitates the defective immune system. It is a trigger, and needs to be controlled to reduce the attack on the patient. Normally, one's body does not attack its own DNA, unless the system is defective. Our bodies are going after this bacterial element, but in the process, creating antibodies that go after us, but cannot kill off the mycoplasmas. So, the cycle never stops until you get the mycoplasmas in check.

I sympathize with your medical issues and would like to recommend you look into DMSO and Dr. Stanley Jacob, keep in mind he has gotten razed by the government over the years because of the wide range of healing effects of this stuff.
check out www.dmso.org

Here is another web site dedicated to assisting persons with this protocol - how to incorporate it as a medical treatment - support groups - protocol information, etc.

[link to www.rheumatic.org]

I did use MSM, which I think is related. I seriously ran the gamut of natural cures and applications, spent thousands of dollars, learned about every immunomodulator, diets, supplements, nothing worked for me in that regard. I did find help for some symptoms at times from different approaches, but as far as improving my lab work and my overall health, this protocol was the only thing that really made a big dent. I had many people suggest many things to me, some of them had miracle supplements from MLM companies, they all had their token lupus patient who'd been cured. I even went so far as to try hyperbarric oxygen therapy, but I had a very bad reaction to that. They didn't even charge me because of it. I was very sensitive and needed something very effective and targeted like this protocol.

Here's an article on how to approach your doctor about using this protocol for your condition:

[link to www.roadback.org]

mycoplasma is an obligate intracellular parasite. so nothing youve posted challenges that fact. It's only hard to culture on standard agar, it needs the far more complex and expensive, tissue culture, because IT LIVES INSIDE THE CELL, ya loser.

OP, thankyou for this thread, I learn alot from these types of threads. I have lost faith with the organised medical world ( doctors). I feel that most of them are negative people and have no interest in getting people really healed from sickess'. I have become a real devotee of all things natural. I'd much rather try suppliments than take any of the man made pharmaceutical drugs out there. Of course sometimes we will need a drug but I try to just be on them for the shortest possible time.

I have a child that had to take Prednisone when she was little for a disease she has and I agree it should be called "devil drug". I used to feel so bad for her when she was on them, Nobody should have to deal with taking that..horrible medicine..

the whole reason that tetracyclines work in mycoplasma is that they are fairly fat soluable, and can cross lipid cell walls and affect the intracellular space, and in that way get to mycoplasma in significant enough levels, mycoplasmas hide in cells because they have no significant protection of their own like traditional bacteria. Most bacteria poison the body and generate their effects by virtue of the toxins they have in their cell walls.
Even your veggie-vitamin 'doctor' should know that

you must be here marketing your book put up the info or be ashamed of your hypocritical self!i have lupis too and no med works only pot. so before ya post with a cure all put the damn info waste of 5 min.

I have mixed connective tissue disease with overlapping symptoms of lupus, scleroderma, rheumatoid arthritis etc. I basically feel like shit all the time. I have bad days then, really bad days. I take no meds. I tried minocycline/minocin maintenance years ago and although I was taking a chemical cocktail of 8 other meds, I have no idea if it helped or not.

All I know is they will give you meds like lortabs or oxycodone to help you coexist with these diseases...but nothing seems to dissolve it.

So I said fuck it (after I became dependent on the pain meds)
And now at the age of 53...I pop ibuprofen every now & then and live with the discomfort, flair ups and inflammation. It's tough but my mind is tougher and I try to convince myself, 'I feel good'.

Ok, I will grant you that maybe your motives are sincere. But if you continue to take meds, how exactly did taking antibiotics (still a pill and pharmaceutical) cure or even "treat" you? Why would you still require anti-inflammatory meds like plaquenil if the inflammation can be brought under control "naturally"? For the record, as a general rule I don't click on links posted on GLP. It's like abstinence for my computer, the best way to ensure it doesn't come down with a STD virus.

PS I am bitter because I also wasted thousands of dollars on false hope. Too many people out there prey on the sick and desperate. Please don't take my skepticism as a personal attack.

Oh, and prednisone comes from the bowels of satan himself.

Also, won't long term antibiotic therapy (especially starting and stopping) cause antibiotic resistance in these bacteria?

pot doesnt cure lupus. Sucks to have that, it's one of the more nasty of the autoimmune diseases, which in truth are far more of a range, than discrete entities. You owe yourself to consider a trial of ldn, it's easy cheap and safer than most things.
It's not a cure, it helps with various issues, and improves many symptoms that coexist with a range of alleged ai disorders, and other things. It works on animals too, animals that dont know they were taking it or allow themselves to be affected by placebo effect, but still got better when no other alternatives were possible.
In the end none of us are here permanently, so in that regard, look for a treatment, hope for a cure, but be aware the must be a time and a place where any treatment will fail, where you must transition from this plane to the next one.

your story sounds 'familiar',
You should consider what has worked for 'some' with no insurance for the sweet stuff like enbrel or other tnf meds that ib truth work pretty good, if you can afford them.
routine ibuprofen, every eight hour, dose adjusted to your kidney function studies, too bad your strung on narcotics, you create a whole new set of problems. Until you get off narcotics you cant take ldn, it may tend to bring on withdrawl symptoms. ldn is great for getting rid of viral coinfections, dry eyes and rls you probably have too

Since when did spamming GLP become alright?

I would try sodium chlorite activated with lemon juice to form chlorine dioxide. As chlorine dioxide is a gas, it can travel through cell membranes. Google MMS / Jim Humble. Lots of info, i thinks its the perfect tool if this realtion between bacteria and RA/Lupus is true. You can use minimal doses and go up as your body is able to tolerate.

Its cheap, but not easy to get in some parts of the world, as the medical mafia is afraid of this incredible molecule that renders their overpriced shit antibiotics/antifungales/antiparasites worthless.

Ive used it myself for other issues, and recently my grandmother of 88 years cured his cancer spot in the face in less than a month (it literally dropped off)

Best of luck!!!

ibm you said. well pot dose help i been throwing up everyday every week every year sence childhood had mulitiple biapsies ,kidney failure,been on every med dont want emmm,pot helps ... i live in hawaii health care here is hell!!!!!! ive been accused of seeking pain meds by every doctor but they see me for 5 min and cant see what i go threw.i was just diagnose last month which sux cuz ive had this my whole life and people say oh its in your head prior to my titer i had postitive nuclas i think

theres always someone that sees easy money in the ill and desperate. Then again it's information that's being sold, the end result of someones investment of time, intelligence and work.
On the whole the information has some merit, but the information is also out there already for those that seek it,
I was gonna start years ago,but had been doing pretty good till recently so may as well start now...

Riiiight. And why the URL you provided us with leading to Amazon, has an affiliate ID on it? This means that with every book sale from this URL you get a percentage.

Here are a few websites to heal yourselves naturally..hope it helps..God bless

[link to www.earthclinic.com]

[link to www.watercure2.org]