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sobota, 17 czerwca 2017

co moze powodowac nieskutecznosc leczenia Boreliozy.?

Protomyxzoa  jest infekcją która tworzy biofilmy - może być główną przyczyną problemów z leczeniem Boreliozy.

kleszcze i komary są nią zarażone.(przekazują w trakcie ugryzienia )

Chorzy na Sla, Parkinsona, przewlekłe zmęczenie, fibromialgia, cukrzyca 1, cukrzyca 2, choroby Alzheimera, toczeń, CCSVI ... .. lista jest długa. Dr Fry nie mówi o tym, ale jest wiele dowodów na to, że to przewlekłe zapalenie również powoduje raka.

http://www.cpnhelp.org/dr_fry_and_ms


Leczenie:
Eliminacja wszelkich tłuszczów - McDougall diet
Eliminacja pieczywa, produktow zawierajacych arginine
Wit D nie powinna przekraczać  poziomu - 70
Alinia, Artemisin, Ivermectin, Plaquenil, Tetracykliny, Metronidazol, Tinidazol, czasami Makrolidy
Dieta bogata w bioflawonoidy
Nie jeść tłuszczów
Minerały
Stosować detox - nerki, watroba, układ limfatyczny

Preparaty:

Bab-2 z Beyond Balance

Ziola:

Artemisia, Cryptolepis, Coptis, Cumanda

Jednocześnie  trzeba stosowac 3 lub 4 preparaty z wyzej wymienionych naraz!

Enzymy na biofilmy -Protomyxzoa jest  organizmem , ktory produkuje ogromne ilosci biofilmow a wiec enzymy to konieczność:

 - bolouke - lumbrokinase
- nattokinase
- serrapeptase
- interfase plus
- interfase
- plant enzyme digestive formula
- digestzymes
- wobenzyme
- intestazyme
- marcozymes

Zazwyczaj stosowana:

lumbrokinase, nattokinase, serrapeptase lub plant enzyme digestive, interfase plus.
Alinia lub Metronidazol lub Tinidazol 500 mg x 2 przez 2-5 dni i 2-7 dni przerwy

Reakcja Herx:

W trakcie leczenia występują silne herxy.

 W takiej sytuacji zwiększyć dawke enzymów oraz stosować detox.

www.betterhealthguy.com/dr-stephen-fry-on-fl1953
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http://christavanderham.blogspot.ca/2011/01/mysterious-devastating-curable-fl-1953.html#!/2011/01/mysterious-devastating-curable-fl-1953.html

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  • Protomyxzoa rheumatica is a protozoan parasite sometimes referred to as FL1953.  
  • Its existence is ancient, still it is largely unknown due to it's discovery being within the last twenty years.  
  • Although its DNA has now been mapped the CDC does not yet recognize it as a disease.
  • Information is not readily available pending establishment of patents and credits.
  • Detection is proprietary and 99% of doctors will have no clue to it's existence or where to go for testing.  (Fry Labs, Scottsdale, AZ)
  • Its symptoms are most often diagnosed as other illnesses.  
  • It is believed by some researchers that it will eventually prove to be one of the most common infections.  
  • It is a vector born parasite, meaning it can be passed by animal or insect, usually through direct contact with blood— most commonly, ticks and mosquitoes..
  • Being a blood hosted organism, it is reasonable to assume that until it is widely known and tests are licensed that transfusion will be a source of infection.
  • It may be dormant for years, making point of infection difficult to determine. 
  • It is difficult to treat and nearly impossible to eradicate. 
  • Treatment will take months or years to show results at which time it will be reduced but remain life long.
  • -----------------------
    A New Protozoa looks like Babesia or immature Malaria but is a fully new Protozoan by DNA, Behavior and CDC

    http://www.personalconsult.com/posts/FL1953.html

    -------------------------------------------------------
    Protomyxzoa Rheumatica is a newly-discovered infectious organism that causes chronic disease. Protomyxzoa was discovered by Fry Laboratories of Scottsdale AZ. Although they have published no scientific papers on the organism, they offer a polymerase chain reaction (PCR) DNA test for the organism, and they have done substantial work on culturing, characterizing and sequencing the DNA of the organism. Unfortunately, all this work remains unpublished.

    Fry Labs says that protomyxzoa is in the “malaria family” of protozoans, along with babesia and malaria, based on DNA sequencing of the 18s ribosome subunit. Protomyxzoa, babesia and malaria have a multi-stage life cycle. Like malaria and babesia, protomyxzoa appears to have an immature form that infects red blood cells (erythrocytes), and a mature form that remains in the blood. It does not appear to invade other tissues. Mature protomyxzoa surrounds itself with thick, copious biolfilm substances to protect itself from the host immune system. It is believed that this biofilm contributes to various symptoms depending on its location and quantity. Protomyxzoa will cause capillary inflammation and reduced blood flow in locations where it accumulates. It is also believed that the biofilm can harbor secondary infections (e.g. other bacteria) which can cause further variations in symptoms and test results.
    I was diagnosed in February 2012 by the Fry labs PCR test, after years of persistent symptoms suggestive of a chronic infection. I was initially quite skeptical of the claims by Fry labs of this new organism. I was eventually convinced of the reality of protomyxzoa by 1) negative test results for many other possible infections (e.g. chagas disease, mycoplasma, toxoplasmosis, E Hystolytica etc), and 2) positive responses to drugs generally effective only against protozoans (e.g. ivermectin, artemisinin, miltefosine). Antibacterial or antifungal drugs were not effective. Together these facts suggested  I was infected with an unusual protozoan.
    ---------------------------------
    FL1953 or Protomyxzoa Rheumatica:
     
    The Babesia-Like New Protozoan
    This protozoan was sent to the CDC, which reported that it was a protozoan and not malaria or Babesia. The agency could not identify it. Dr. Stephen Fry reports that many studies are being conducted with the goal of publication in a close time frame. We believe that the DNA sequencing done by the Fry Laboratory genetics experts shows a new form of protozoan that is a biofilm engine. For more information, see my summary article at :
     
     
    -----------------------------------
    I believe the way to approach this Protozoa is a 3 step process. 1. No fat diet (STRICT) 2. Spend a month or two building up on powerful biofilm dissolvers 3. Hit it with pulsed doses of Artemesinin and other meds like Ivermectin, Albendazole, et al.

    http://www.ladyoflyme.com/blog/protomyxzoa-fl-1953
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    http://forum.gazeta.pl/forum/w,26140,148348869,148348869,Protomyxzoa_FL1953.html#A
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    http://protomyxzoa.org/
    ------------------------------------
    Quick quick re. testing for FL 1953
    My LLMD has suggested I get the following tests done to determine if I have it, all can be provided by Fry labs as far as I know
    Smear for Fl1953 and Hemobartonella
    A test for biofilm
    PCR for Fl1953
    It's a costs quite a bit
    I was wondering if anyone knows about the accuracy of these tests?
    ---------------------
     I spent $600 for the smear and traveled all the way there to talk to him. He told me what they saw was "probably some kind of protozoa". I went there because I believe I was re-infected with bartonella but he refused to test me, saying he can't prescribe the test himself. He wouldn't use IGENEX either. He gave me a test kit with the recommendation to get about $1500 more testing done. I decided to order the drugs I need from India and to try to pursued an NP I have been seeing to do the tests I need at IGENEX.
    If you get any test, just get the PCR. Don't do the smear. Then if you have it, try the low fat diet.

    http://www.mdjunction.com/forums/protomyxzoa-rheumatica-discussions/general-support/11030515-accuracy-of-testing-for-fl1953
    -----------------------
    When you talk to a real scientist about PCR testing it is like discussing a great love or superior life experience. However, my concern is some feel the testing for tick, flea and other insect vector infections is the same as DNA testing from the television show “CSI.” You get a disposable cup from the criminal and you have the DNA from the infinitesimally tiny residue in lip marks. This is not the case in reality. My conversations with other researchers and other clinicians, and my patients’ intake information and follow up calls to them show that most PCR results report a false negative with tick and flea borne infections. Therefore, while I suspect the PCR test for FL1953 is “good,” I do not have an opinion on the percentage of patients positive for FL1953 who would be detected. I must be frank about my bias. Unless you are able to cause infection debris to be very high before the test, I feel it is not worth the money unless you are affluent. PCR is likely a very good test, as long as you do not conclude that a negative result means your obviously positive smear is worthless. Just as Babesia and Bartonella have many species, might not there be another cousin of FL1953 that is also a super biofilm maker?
    So my opinion is that it would be unwise to reject an enriched-stain blood smear that shows positive for FL1953 Protomyxzoa.

    http://www.personalconsult.com/posts/FL1953.html

    -------------------------
    Dr. Fry is doing some exciting work on a new biofilm-forming protozoan previously referred to as FL1953 and only recently renamed to Protomyxzoa rheumatica, a highly immunosuppressive microorganism. He refers to it as the premier pathogen.
    I recently had the opportunity to attend a lecture by Dr. Stephen Fry MD as part of Dr. Klinghardt's recent "Beyond Lyme" conference. I'm still working on my notes from that event and will post them soon. .... ,,......

    Some of the key points from the the radio interview:
    • FL1953 is a new, unique protozoan organism that is found in people with CFS, Fibromyalgia, Multiple Sclerosis, ALS, and Rheumatoid Arthritis.
    • People with Morgellon's also have evidence of the organism. In Morgellon's, Dr. Fry talked about this new protozoan possibly suppressing the immune system such that a fungal/mycelial condition then develops leading to the symptoms of Morgellons.
    • Dr. Fry discussed the use of Tetracyclines, Zithromax, Plaquenil and other options, but more interesting were his other recommendations. One of the future projects his lab is working on is to complete sensitivity testing of various therapies for this new protozoan.
    • He shared that diet is very important. The protozoan loves lipids (fats) and that lipid restriction via low-fat diets has been a very powerful tool. Lipids and fatty acids also play a role in the formation of biofilms which seem to collapse with lipid restriction.
    • He discussed the benefits of a whole food, plant-based diet full of bioflavanoids; which themselves act as an antibiotic.
    • He suggested that many people with chronic illness may struggle with wheat not due to the gluten content but due to the high arginine which the FL1953 protozoan thrives on.
    Many of these concepts are still emerging, but it appears that Dr. Fry's protozoan may be an important piece of the puzzle. I recently had blood drawn to test for this organism and biofilms with Dr. Fry's lab and will post a blog about my results on my site when they are available. For information on tests available from Fry Labs

    http://www.betterhealthguy.com/dr-stephen-fry-on-fl1953
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    protomyxzoa.

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