The answer is doctor KOPIC my worlds favourite oncologist.
I have started on tarceva, as of saturday with avastin. prelimenary research indicates its got merit.
http://www.tarceva.com/patient/considering/about.jsp
Tarceva may also affect medications you are taking. It is important that you tell your healthcare provider (HCP) if you are taking any other medications or supplements, including vitamins and herbal products (such as St. John's wort or antacids). DO NOT start taking any new medicines or herbal supplements before talking with your HCP.
Serious side effects of Tarceva, including death, may include:
OH GREAT HERE WE GO AGAIN.
http://news.cancerconnect.com/avastin-plus-tarceva-shows-promise-in-advanced-hepatocellular-carcinoma/
I am learning from the genius, he prescribes and i fill in the blanks, god i am blessed to be treated by the worlds bravest oncologist. the rest of the profession needs a good strong viagra. I want to live, as long and as well as I can, and joyfully to boot, with an excess of love in my life.
Now dont go following in my footsteps, make your own path. Whats worked for me, may not work for you. this is a clear example of the german advantage, our backward, conservative bullshit health system down under makes me sick. this clinic is full of aussies who want life, death is for the dead, its a long time.
life is simply too precious to risk trusting your oncologist. play it safe on the golf course, but when it comes to cancer i say take some big risks.
what you afraid of ? dieing, well thats a certainty for us all. I will stop being so critical of oncologists when i see real improvements in the patients who come to hallwang.
the distinct impression i get is, is that if you escape your state or government based health system alive and make it in the door of a german clinic, well thats the first miracle.
dont stop asking for miracles ! i have not. I just get so emotional when i realise the merit of the therapies i am pivileged to try, while so many others die.
Kopics genius is not just avastin and tarveva, what sets him aprt is the strategy for pete.
my immune system has been hammered, so targetted low dose chemo is the go for now.
intensive care is what i get at hallwang, tomorrow i am being unfaithful and am getting some more ipt and high dose vit c for 3 days. i will run this past asir ! i expect a frown.
the cocktail of drugs and supplements and therapies in the rat is getting seriously scary. what crazy is that i feel fantastic, just had the most magnificent bbq dinner with a glass of red and talked the evening away with Grace gawlers new bunch athallwang.
I got a shot of placenta extract.
also this afternoon I got a copy of my biocentaur report all negative except HPV18 count =29, this is still a low level.
http://nar.oxfordjournals.org/content/27/7/1585.full some examples of the science behind hallwang antisense protocols. if you understand this article your a genius. it gives me faith in the therapies,
again the strategy is removing viral load, so your immune system can eat tumour cells.
indian gold, hpv viral strategies. http://icmr.nic.in/ijmr/2009/september/0911.pdf
I wonder if my hpv levels, are related to the level of tumour cell growth or death. getting the immune system to take out the remnants of the hpv virus an interesting clinical target.
I should raise these results to nesslehut about the vaccine effectiveness, especially asir concerns re ndv and solid tumour efficacy!
http://www.esmo.org/Conferences/World-GI-2013-Gastrointestinal-Cancer/Press-Releases/Immune-Boosting-Colorectal-Cancer-Drug-Shows-Promise
so yes, i am having a minor joyful breakdown, jumping from targetted therapies, metabolic therapies, holistic therapies. the science is a pleasant distraction. I missed out on the sauna tonight. buti had amazing summers eveningbbq, the heart of the kitchen at hallwang tanya is away for 3 weeks holidays, she deserves the rest. godbless her.
tomorrowi got to siebenhuners http://www.hyperthermie-zentrum.de/home.html
he has a unique form of iv curcumin, i will try it for its hvp 18 treatment role.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357525/ ipt clinical study
fromindian gold
C) Natural/herbal derivatives:
In this age of targeted therapy, the failure of most
current drug –discovery efforts to yield safe, effective,
and inexpensive drugs has generated widespread
concern. Successful drug development has been
obstructed by a general focus on target selection rather
than clinical safety and efficacy. The very process of
validating the targets themselves is inefficient and in
many cases leads to drugs having poor efficacy and
undesirable side effects not only for HPV-related
diseases but cancer in general. Since any given cancer
carries an estimated 300 gene alterations, this raises
an important question about how effective these
targeted therapies can ever be against cancer. Thus,
it has become necessary to rethink drug development
strategies and emphasis is being given to natural and
herbal derivatives that are safe and possess multi-hit
capability not only to target against the viral oncogenes
but also to inhibit the co-operative signaling and
dysregulated gene expression of the host cells.
Since productive life cycle of HPV is tightly
linked with the differentiation programme of infected
epithelial cells, various leads are being tested for their
activity at different stages of HPV’s life cycle in the host
cell which include virus binding and entry, presence of
viral DNA in episomal form and its replication in host
cells as well as host cell-dependent expression of viral
oncogenes following integration of its DNA into the
host cells. The noncoding upstream regulatory region
(URR) of HPV consists of myriad of transcription
factor binding sites like AP-1, SP1, NFκB, NF-1,
TEF-1, TEF-2, Oct-1, AP-2, KRF-1, YY-1, STAT-3
andglucocorticoid responsive elements85. During
differentiation, these upregulated cellular transcription
factors bind to the HPV URR and facilitate the
expression of viral oncoproteins and late structural
proteins. As these cellular transcription factors serve as
a major link between oncogenic host cell transcription
and also the viral gene expression, transcription factors
provides a unique target for development of anti-HPV
therapeutics86. Theoretically, preventing binding of
these transcription factors will eventually leads to the
suppression of HPV oncogenic gene expression and
stop assembly of virion particles. In past few years,
several herbal compounds, derivatives, antioxidant and
smallpolyphenol plant compounds have been used for
selective suppression of host cell transcription factors
like AP-1, and NF-κB in HPV infected cells87-91. The
selective suppression and alteration in composition
of these factors has been shown to be associated with
downregulation of HPV gene expression and induction
of apoptosis in infected cells91. Here, in this section we
have described some of the potent anti-HPV activities
which are in process of development for being used as
anti-HPV therapeutics (Table IV).
Curcumin: Curcumin is a potent antioxidative agent
(diferuloymethane) and an active compound of the
perennial herb which also exhibits anti-inflammatory
andantitumour activity110. Recent studies using this
I have started on tarceva, as of saturday with avastin. prelimenary research indicates its got merit.
http://www.tarceva.com/patient/considering/about.jsp
Tarceva may also affect medications you are taking. It is important that you tell your healthcare provider (HCP) if you are taking any other medications or supplements, including vitamins and herbal products (such as St. John's wort or antacids). DO NOT start taking any new medicines or herbal supplements before talking with your HCP.
Serious side effects of Tarceva, including death, may include:
OH GREAT HERE WE GO AGAIN.
http://news.cancerconnect.com/avastin-plus-tarceva-shows-promise-in-advanced-hepatocellular-carcinoma/
I am learning from the genius, he prescribes and i fill in the blanks, god i am blessed to be treated by the worlds bravest oncologist. the rest of the profession needs a good strong viagra. I want to live, as long and as well as I can, and joyfully to boot, with an excess of love in my life.
Now dont go following in my footsteps, make your own path. Whats worked for me, may not work for you. this is a clear example of the german advantage, our backward, conservative bullshit health system down under makes me sick. this clinic is full of aussies who want life, death is for the dead, its a long time.
life is simply too precious to risk trusting your oncologist. play it safe on the golf course, but when it comes to cancer i say take some big risks.
what you afraid of ? dieing, well thats a certainty for us all. I will stop being so critical of oncologists when i see real improvements in the patients who come to hallwang.
the distinct impression i get is, is that if you escape your state or government based health system alive and make it in the door of a german clinic, well thats the first miracle.
dont stop asking for miracles ! i have not. I just get so emotional when i realise the merit of the therapies i am pivileged to try, while so many others die.
Kopics genius is not just avastin and tarveva, what sets him aprt is the strategy for pete.
my immune system has been hammered, so targetted low dose chemo is the go for now.
intensive care is what i get at hallwang, tomorrow i am being unfaithful and am getting some more ipt and high dose vit c for 3 days. i will run this past asir ! i expect a frown.
the cocktail of drugs and supplements and therapies in the rat is getting seriously scary. what crazy is that i feel fantastic, just had the most magnificent bbq dinner with a glass of red and talked the evening away with Grace gawlers new bunch athallwang.
I got a shot of placenta extract.
also this afternoon I got a copy of my biocentaur report all negative except HPV18 count =29, this is still a low level.
http://nar.oxfordjournals.org/content/27/7/1585.full some examples of the science behind hallwang antisense protocols. if you understand this article your a genius. it gives me faith in the therapies,
again the strategy is removing viral load, so your immune system can eat tumour cells.
indian gold, hpv viral strategies. http://icmr.nic.in/ijmr/2009/september/0911.pdf
I wonder if my hpv levels, are related to the level of tumour cell growth or death. getting the immune system to take out the remnants of the hpv virus an interesting clinical target.
I should raise these results to nesslehut about the vaccine effectiveness, especially asir concerns re ndv and solid tumour efficacy!
http://www.esmo.org/Conferences/World-GI-2013-Gastrointestinal-Cancer/Press-Releases/Immune-Boosting-Colorectal-Cancer-Drug-Shows-Promise
so yes, i am having a minor joyful breakdown, jumping from targetted therapies, metabolic therapies, holistic therapies. the science is a pleasant distraction. I missed out on the sauna tonight. buti had amazing summers eveningbbq, the heart of the kitchen at hallwang tanya is away for 3 weeks holidays, she deserves the rest. godbless her.
tomorrowi got to siebenhuners http://www.hyperthermie-zentrum.de/home.html
he has a unique form of iv curcumin, i will try it for its hvp 18 treatment role.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357525/ ipt clinical study
fromindian gold
C) Natural/herbal derivatives:
In this age of targeted therapy, the failure of most
current drug –discovery efforts to yield safe, effective,
and inexpensive drugs has generated widespread
concern. Successful drug development has been
obstructed by a general focus on target selection rather
than clinical safety and efficacy. The very process of
validating the targets themselves is inefficient and in
many cases leads to drugs having poor efficacy and
undesirable side effects not only for HPV-related
diseases but cancer in general. Since any given cancer
carries an estimated 300 gene alterations, this raises
an important question about how effective these
targeted therapies can ever be against cancer. Thus,
it has become necessary to rethink drug development
strategies and emphasis is being given to natural and
herbal derivatives that are safe and possess multi-hit
capability not only to target against the viral oncogenes
but also to inhibit the co-operative signaling and
dysregulated gene expression of the host cells.
Since productive life cycle of HPV is tightly
linked with the differentiation programme of infected
epithelial cells, various leads are being tested for their
activity at different stages of HPV’s life cycle in the host
cell which include virus binding and entry, presence of
viral DNA in episomal form and its replication in host
cells as well as host cell-dependent expression of viral
oncogenes following integration of its DNA into the
host cells. The noncoding upstream regulatory region
(URR) of HPV consists of myriad of transcription
factor binding sites like AP-1, SP1, NFκB, NF-1,
TEF-1, TEF-2, Oct-1, AP-2, KRF-1, YY-1, STAT-3
andglucocorticoid responsive elements85. During
differentiation, these upregulated cellular transcription
factors bind to the HPV URR and facilitate the
expression of viral oncoproteins and late structural
proteins. As these cellular transcription factors serve as
a major link between oncogenic host cell transcription
and also the viral gene expression, transcription factors
provides a unique target for development of anti-HPV
therapeutics86. Theoretically, preventing binding of
these transcription factors will eventually leads to the
suppression of HPV oncogenic gene expression and
stop assembly of virion particles. In past few years,
several herbal compounds, derivatives, antioxidant and
smallpolyphenol plant compounds have been used for
selective suppression of host cell transcription factors
like AP-1, and NF-κB in HPV infected cells87-91. The
selective suppression and alteration in composition
of these factors has been shown to be associated with
downregulation of HPV gene expression and induction
of apoptosis in infected cells91. Here, in this section we
have described some of the potent anti-HPV activities
which are in process of development for being used as
anti-HPV therapeutics (Table IV).
Curcumin: Curcumin is a potent antioxidative agent
(diferuloymethane) and an active compound of the
perennial herb which also exhibits anti-inflammatory
andantitumour activity110. Recent studies using this