Saturday, November 19, 2016

LYME IS


The Model is TRUE if you've seen it written in Play-Doe :)
http://www.actionlyme.org/EAT_OSPA_GO_LIMP.jpg
1) You saw the latest thing on EBV (activated with Malaria, too)? (See ActionLyme.org near the top if you missed it).
The way EBV causes disease is in the first step, INHIBITION of the "auto-kill" kinases (apoptosis means, "I will kill myself," says the cell, "if I am infected with something I cant control"), or BCL2 (stands for "B Cell Lymphoma"- clue) genes.
I will say that again: The way EBV causes disease, in the first step, is that it *stops* the cells infected by it, from killing itself, or "undergoing apoptosis."
So, in a way, the way EBV starts to cause disease (again) is to STOP the cell from killing itself, which is what the BCL2 class genes do - the BCL2 class genes say "DO NOT COMMIT SUICIDE"; it's like having TOO MUCH BCL2 gene expression. Then it starts replicating and pouring out little EBV-babies.
OspA or other fungal antigens do the same thing. They *act* like too much BCL2, or cause the cell to not kill itself. Fungal antigens INHIBIT APOPTOSIS. [You can verify that independently, it's also well-reported in the scientific literature.]
So, imagine, B cells in the Lymph nodes are where both Borrelia and EBV *BOTH* hang out. [You can verify independently.]
You can also have a genetic abnormality where you have a duplication (imagine a rope lying on the ground with a loop in it, and that loop recombines with a straight strand of DNA). This is called a reversed-duplication, and happens in "nerve overgrowth syndromes" (that's a thing) such as the kind of Autism Einstein had, and where Neurofibromatosis co-occurs with "the Autism Spectrum," - also now a well known thing.
Why. Too much BCL2, or not enough "natural neurodevelopmental synaptic pruning." These kinds of Autism kids have too many nerves, or tumorish nerve endings (Neurofibroma), and large brains.
Why. They have a reversed duplication of a BCL2 class gene, which STOPS the nerve cells from dying on schedule.

So, too much BCL2 *STOPS* the normal process of a cell killing itself when it should. EBV also PROMOTES the expression of BCL2 class genes (assuring that it can continue to replicate, which is BAD), which is bad. And the Osps, like OspA *ALSO* tell the cell not to kill itself. You saw even Gary Wormser say this.
If you want that "Osps or fungal antigens inhibit apoptosis" data it is on an Actionlyme dot org page followed by /101016.htm Search for the term "apoptosis."
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2) Same thing with childhood vaccines: Live attenuated viruses injected together with immune suppressing fungi, *** reactivates the "live, attenuated viruses."*** [THIS IS IN THE LITERATURE.]
3) This is a real thing. We see it everywhere. We hear about it in the Humira and Stelara commercials (immune-suppressing) - they talk about the "risk of LYMPHOMA" which comes from reactivated EBV - which is nearly the first thing if not 100% the first thing that happens in all kinds of immunosuppression cases.
Because there are so many parallel models, we call that an "Occam's Razor" ("it *MUST* be *THIS*").
4) In AIDS, people die of the opportunistic infections, like Karposi's scarcoma, which is caused by what? A HERPES VIRUS!!
Immunosuppression ALWAYS results in the reactivation of latent viruses.
5) How about organ transplant victims? Yes, "risk of lymphoma (EBV)" because they have to take immune suppressing drugs. Happens all the time. A lot of transplant patients end up with cancer, this is a well-known thing...
6) Hospital Sepsis? YES, well known now: reactivated latent herpes viruses. (Dual or multiple infections, cytokine storm, boom, the immune response STOPS to keep the human alive.)
Fungi cause immunosuppression. Cant have that with live viruses in the vaccine vial.
LYMErix was fungal. The diseases - Lyme and LYMErix - are mainly caused by the reactivated herpesviruses (Great Imitator was really the Great Detonator of EBV, et al.)
7) Thimerosal was *EXACTLY* invented to prevent LYMErix.
They call mercury (Thimerosal) a "preservative." Why. Because it prevents FUNGAL growth, which is the worse immune suppressor.
True Story.
8) Rituximab is a mab (monoclonal antibody) that targets CD20 on B cells. It is a "B-cell depleter." Where does EBV hang out? Right. B cells.
It seems to help the CFIDS/ME people. Why. Because THAT disease is also an immune suppression disease, spoken of as Post-Sepsis Syndrome, and spoken of by who?
WHO?
9) ANTHONY FAUCI in a 1995 patent (5,696,079).
"....Illustrative of specific disease states in treatment of which the present invention can be applied are HIV infection and other diseases ***characterized by a decrease of T-cell immunity, for example, mycobacterial infections like tuberculosis and fungal infections such as cryptococcal disease.*** This method also can be used in the treatment of secondary infections that occur in patients with suppressed immune systems, such as the opportunistic infections that occur in AIDS patients. ..."
MYCO or fungal diseases, well known to cause immune suppression. They put Thimerosal in vaccines to prevent fungal antigens like LYMErix or the Osps on the shed blebs of spirochetes, all spirochetes, Syphilis too.
Stop making me say the same gallblammed thing every day. You already have all this evidence in the criminal charge sheets which we developed 2 years ago. The new evidence only supports this model, and NOTHING has detracted from this model.
Something is considered TRUE if it passes the requirements of the Scientific Method, which states that the model must repeat, or is VALID. Not only does the model of Pam3Cys as a fungal antigen causing immunosuppression repeat, we show the science proves this phenomenon occurs in other disease conditions, and with other drugs and vaccines.
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Tuesday, November 8, 2016

Cryme Disease- Lyme

Friday, November 4, 2016

A MUST FOR WELLNESS

PLEASE WATCH THIS VIDEO FIRST IT IS THE BEST EXPLINATION OF HOW THIS ALL WORKS> https://www.youtube.com/watch?v=5DKgT5Go6sU

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660449/
https://www.google.com/patents/WO2014202956A1?cl=en
https://www.google.com/patents/WO2016072871A1?cl=en
A SIMPLE RECIPE FOR ALL ISSUES AS WELL AS LYME . OUR GUT IS THE KEY TO LASTING WELLNESS.
Just three of many, many examples above.
You can PUBMED searches for COLOSTRUM and KEFIR, thousands of papers.
This drink will AID all.
This is my fourth rebuild with KEFIR. First time a few years back with so called LYME
The last three are chronicled here.

My latest KEFIR experiences Kefir is loaded with lactoferrin and whey. While I still like Rife and Herbs I believe kefir as well played a HUGE role in my so called lyme journey. In about 6-8 months it was an astonishing turn around. I've been using the kefir again now since about February with colostrum, and "add on's" I call them Chondroitin Sulfate, Oleic Acid, Bifidus Culture. This only pertains to home made kefir as store bought is pasteurized.
February I was really going down hill from a knee transplant from May of the previous year. I get hit with vancomycin after a severe mrsa infection from a previous operation, I'm holding at 15 ops so far, half utter failures and unnecessary, but that's another book. Chatting with Mary a light came on concerning colostrum (I'm a Bottle bay from the 50's), microbes etc., and I started back with kefir, yogurt and the goodies. amazingly in a few months I'm gaining lost ground, insomnia, panic attacks leaving, bunch of other things too. The knee replacement went arie, so May 10 this year get another OP on the knee. I'm also getting steroids shots for my back as well. This is “DAMMED IF YOU DO OR DAMNED IF YOU DON"T FOR ME” , I know the consequences of both steroids and abx. So back in I go, more vancomycin and abx. It was supposed to be no big deal but was far worse than the replacement, I'm just now starting to walk. I've been thru months of immobilization and knee draining. Headed back down hill again, I'm beginning to feel the medical yo-yo effect. “I will heal you but they leave out the inevitable, destroy you while I’m at it part". Only the latter seems to be the more accurate prognosis.
So here I go again now using mainly kefir as I really crave the taste. Funny I hated milk my entire life. I guess it was a dominate microbe thing. Cravings are microbes talking to us but, yet is up to us to figure out if is a good guy or bad one, we need them all just in balance. Everything is going good, sleep returns panic disappears just like last time. Enter my next steroid shot again. Right back on my butt again. Back on the kefir and one week later sleep is half way back. Anxiety is lower by a lot. And some little things as usual.
Anemia is gone.
A few things I have learned. Kefir alone is quite helpful and very well tolerated. With the colostrum and "add-ons" it is not. Over the line is an individual tested level of tolerance, starting at a tabespoon and up. Some of my over the line side effects are butterflies, stomach ache, bloat, increased bowel movements, edema and anxiety as well. I would start slow and jump up a little , I try and consume a cup a day now as it is easy for me to make and use, including feeding to dogs, horse, goat's with any extra.
PS Kefir Recipe
Method used 1 pint Kefir (home made) 1 tbs Colostrum
ADD ON'S 600 mg Chondroitin Sulfate 1/4 teas Bifidus Culture ( Can not go over 120 degrees F ) 1/8 teas Oleic Acid (in plants and oils) Add to each dose.
Take finished kefir add colostrum and bifidus culture and blend till smooth, 5-10 seconds., return kefir to jar and second ferment 12-to 24 hours in refrigerator. Swish in mouth for a few minutes at least. Start with a low dose say a tablespoon at a time slowly building up twice a day is a good start. Eventually you can drink as tolerated thru the day. One can flavor it if you choose.
http://www.icnr.org/articles/Fascinating%20Colostrum.pdf
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337124/
https://www.youtube.com/watch?v=zI6Ra-SGZJM
http://ar.iiarjournals.org/content/36/7/3771.long
http://gcmafblogspot.weebly.com/blog/side-effects-of-gcmaf