she should receive an email alert......i ll open a thread for this maybe more poeple can be interested
are you sure that you want to put the above answers on this thread ?
I have no problem on this, but maybe somebody (e.g. April9903) wait the answers on a different thread.
there are also reports of gcmaf curing autism very fast in months, so this researcher therory that the base of autims and many autoimmune diseases is some kind of infection.be it a virus or bacteria or prion..whatever it doesn t matter, it looks like that decreasing nagalase reactivates immune function and nagalase is probably a pathogen adaptation to survive immune system in the host
Autism
Hello Dr. Bradstreet, After 13 weeks of the GCMAF, we are happy to report that she continues to have tremendous gains in all areas. Increased socialization and speech, better performance in the school as well as community settings, decreased tantrums and less vocal protests, she is able to change activities and transition to non preferred tasks. It has been absolutely amazing, all her therapists, teachers, other parents have remarked about her good behavior in public places (for example, grocery stores, department stores such as Nordstrom’s, Macy’s, The Zoo, Bowling, the library, parks and playgrounds. In the past, we never went to these places in fear of her stimming, or her behavior (45 minute tantrums). Now, she surprises us as well as others with her appropriate comments and follows direction very well. Before she would only eat one thing (french fries) and now she eats everything including vegetables!!!!! I’ve sent some pictures to show her progress. We are so excited to see what more phenomenal things are in the future to come!
Thanks for the clarification.
i guess you should check nagalase and according to the value consider gcmaf or the maf probiotic when available
http://drbradstreet.org/category/autism/
bottom page, this researcher is treating autism and cancer with gcmaf and results are increadible, autims regressed in 13 weeks and breast cancer with bone metastatis in less than 6 weeks........Asthma and osteoporosis included in gcmaf effective tretament
Immune Function is the Ultimate Key to Autism, Alzheimer’s, HIV/AIDS, Asthma, Allergies, Arthritis, Diabetes, Cancer and even Heart Disease
MARCH 29, 2011 BY DR BRADSTREET 6 COMMENTS
If you want to know what ails mankind in the last 100 years its immune dysfunction. I know and believe for many of these disorders we have the tools necessary to treat and prevent them. But what if an individual already has cancer, or autism, or HIV? Can we treat or cure those disease? The answer is yes (in many to most cases) and it doesn’t have to involve toxic poisons and harsh medications. I have to get back to seeing patients, but I promise to finish this story later today. I know we can put this knowledge to work and I have a great association with the laboratories we need to help us with this. However, before you go off in search of this, realize there are unscrupulous people claiming to have products, but they are not standardize or pure like the research I am referencing. One good source does exist and we need to be cautious in how we dose and use this. More to follow.
Here are part of the references for those of you motivated to search the internet.
References:
Vitamin D binding protein-macrophage activating factor directly inhibits proliferation, migration, and uPAR expression of prostate cancer cells. Gregory KJ, Zhao B, Bielenberg DR, Dridi S, Wu J, Jiang W, Huang B, Pirie-Shepherd S, Fannon M. PLoS One. 2010 Oct 18;5(10):e13428.
Glycosylation status of vitamin D binding protein in cancer patients. Rehder DS, Nelson RW, Borges CR. Protein Sci. 2009 Oct;18(10):2036-42.
Immunotherapy for Prostate Cancer with Gc Protein-Derived Macrophage-Activating Factor, GcMAF. Yamamoto N, Suyama H, Yamamoto N. Transl Oncol. 2008 Jul;1(2):65-72.
Immunotherapy of metastatic colorectal cancer with vitamin D-binding protein-derived macrophage-activating factor, GcMAF. Yamamoto N, Suyama H, Nakazato H, Yamamoto N, Koga Y. Cancer Immunol Immunother. 2008 Jul;57(7):1007-16.
Pancreatic carcinogenesis: apoptosis and angiogenesis. Onizuka S, Kawakami S, Taniguchi K, Fujioka H, Miyashita K. Pancreas. 2004 Apr;28(3):317-9.
Immunotherapy of HIV-infected patients with Gc protein-derived macrophage activating factor (GcMAF). Yamamoto N, Ushijima N, Koga Y. J Med Virol. 2009 Jan;81(1):16-26.
Structural modification of serum vitamin D3-binding protein and immunosuppression in AIDS patients. Yamamoto N, Naraparaju VR, Srinivasula SM. AIDS Res Hum Retroviruses. 1995 Nov;11(11):1373-8.
FILED UNDER AUTISM, CANCER, HIV AIDS, INFLAMMATORY BOWEL DISORDERS, ME/CFS (CHRONIC FATIGUE), XMRV
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Dr Bradstreet
The study used all of the products combined, and the University referred to the protocol as HepTech - so my previous post was a false supposition.
in the presentation poster it is state "The Heptech anti-fibrotic supplements ..." so i think that they refer to Hep Tech: http://www.hepatitistechnologies.com/store/product/68408/HepTech
thanks for the link, i didnt see it yet.....the kimeric mice have human livers so results ae the same as in human livers
it is very surprising that heptech treated livers have lower collagen than uninfected ones, collagen is the main part of fibrotic tissue
there is an answer on their faq about this:
Three of the products focus on different components of liver health maintenance. HepTech, FibroGuard and HeptoShield act in a complementary or synergistic fashion, while HeptoBoost focuses on intracellular glutathione production and is partly overlapping with HepTech. No one knows the exact weight of these component systems on the overall effect. For a minimum, FibroGuard could be used together with HeptoBoost; however the full benefit of this synergistically designed protocol will not be realized unless the complete system is taken together.
hosteoporosis can be cured by gcmaf, so do keep an eye on it or maf 314 when available
i am very happy heptech is helping more people and i could never thank enough hepatitis researcher for letting me know about it and making cirrhosis regression, if not reversal possible
I don't know that, but if I found out I will post this.
Thanks for the great study and all the info. I m just wondering if by heptech they refer to one specific product or all the 4 products in the document? Is hep tech the main anti-fibrosis product?
Dr. Lorne Tyrrell - the one that conduct the above study I think that is the same doctor who invent Lamivudine (even if now is not so used it was the first HBV drug ) and has a huge background on HBC and HCV research.
Anti-Fibrotic study which recently was presented at the AANP national conference by hepatitistechnologies:
http://www.hepatitistechnologies.com/Posters2-4.pdf
study was conducted at the University of Alberta under the direction of Dr. Lorne Tyrrell, (co-investigators Dr. Peter Schmid and Dr. Michael Joyce).
At the moment I have no plan how long I will take HepTec products. But if I see the improvements in September test results I'll continue for some time. Around the time I started taking HepTec products I started Vit D3 5000iu and Vit K (MK-4) also, and my asthma is about 85% better I don't know which vit made my asthma better but I am very happy with this anyway. It's been about 6 weeks now. BTW, I have asthma as well as osteoporosis besides hep b. I always try to avoid asthma medication because my alt gets very high whenever I am on those medicine. Sometimes I think I would die from asthma not from hep b. But now I can take deep breath and my breathing is not easily disturbed.
I live in Canada and Fibroscan is paid by our government health system, so it is free in the hospitals, of course we pay taxes to benefit from the health system services. Not all hospitals offer it though, I had to go to Montreal to have it done.
I was using whole package for a month and the pain I had in right side stopt after 2 weeks ,I will do labs next week and post results.If any improvement I definitly will continue.
Where you live and where did you have fibroscan done? I was in europe on vication and I was trying to have it done there but I needet to be they patiente and do a lot of tests so it was very expensive.Is fibroscan FDA aproved in US yet?
Is there any time period you are planning on having these supplements? Is there a minimum period to get results or should it be a lifetime thing? The package is expensive at around 300$ monthly...
I am taking the whole package, all 4 types.
April, are you taking the whole package or just HeptoShield which is known to reduce Fibrosis, I believe?
4est, yes they are FDA approved according to Stef even though I couldn't find any info online about that.
On the hepatitis technologies website, their recommendation for people with inflammatory diseases like HBV is to exercise, have a good diet and have supplements.
I'm also curios about this subject.
On the other hand, I've read somewhere on this forum that Hepatitis technologies was accepted at a liver conference in November this year and they will present some results. Did anybody know something about this ?
Hep Tech products are antioxidants so they would be good not only for liver but also for other organs I guess. My fibroscan result was 3.5kpa last year but it was 4.2kpa in April 2011. I am taking Hep Tech products now. I'll post the results after my fibroscan test in September.
i think that if one can afford heptech with no trobles due to the cost it is always good for all general health and to prevent both cancer and liver fibrosis, the single research on cucurmin tumerics and reservatrol is increadible as prevention of al todays diseases correlated to older age
i am giving fibrogurad to my father with great improvment, he had a stroke year ago with no detactable damage because took the pill within 5-10min from it but now about 3-5years after he was having a decline of brain function (couldn t play cards, drive car safely, always pains and irritability) well this is all gone in about 4 months.....it is mainly cucurmin tumerics that are reported by many studies to cure brain damage
if you can afford it but it is expensive for your income use only in case of fibrosis already developped, and in case of f3-f4 (>7-8kpa) use absolutely
it wont have any effect on virus or alt but will have an extremely good effect on liver functions and fibrosis, so even if alt are not normal due to the hbvdna detactable your fibrosis will regress, platlets, bilirubin and others will improve