Most clinical studies aren't worth a bucket of warm spit. To find
out if a therapy is useful it is best to avoid preset
notions. Reread your message and count the number of absolutes that you used.
Over the years I've learned to isolate our work from anything that
would skew the quest for truth. Number one is the pursuit of
money. When a treatment brings the cash rolling into the clinic it
is hard to think of it as anything but wonderful. We made our
operation non-profit to avoid this. It works. Ten years ago I was
convinced that mu-trioxobiscarboxyethylgermanium (sesquioxide) had to
be one of the world's best cancer killers, but it was just too
expensive to use.
As a non-profit we had a contributor who donated multiple kilos. We
could use it whenever we felt like it with no consideration to the
cost. Over the years we noticed that it tended to stay on the
shelf. We might use it in a nebulizer for certain lung cancers, but
that was about it.
On the other hand we started using pau d'arco tea about the same
time. Over the years we found ourselves reaching for it more and
more. It often seemed to work as a stand alone, it seemed to help
most other therapies and hindered none that we noticed.
Another example is the use of Zometa. Most clinics switched from
pamidronate. It allowed a 15 minute infusion instead of a two-hour
infusion and the profits were higher. We noticed that often cancers
that were in remission started to grow again. We switched back to
the earlier drug. The same with dosage. As long as there are no
dental problems we use pamidronate weekly, though often in smaller
doses. We get much better results than those who use it monthly. It
has been known for over ten years that it prevents mets to the
bone. Insurance won't pay for it until bone mets are proven. This
is because it will typically cost insurance $1,000 to $2,000 per
injection. We give it away free to anyone doing our program.
Antineoplastons will cost as much as $8,000 per month to obtain this
in Texas. We gave it away free for years. I have slowed on this as
I don't consider it very effective.
I remember when someone from your own country, Manju Ray, was
attacked unmercifully for using methylglyoxal with vitamin C. None
of her critics could claim that it didn't have value. They were
outraged because it did have value and a researcher outsmarted them
in putting together a clinical trial. Manju's husband also works at
the Institute in Kolkata. He donates his entire salary back to the
institute. I am convinced that part of the reason their work is so
successful is that they are not in this for the money and they will
do whatever it takes to stop cancer no matter how the industry
protests. Twice now she has been an honored guest at our Center in
Del Mar, California.
I do think that medicine would progress at lightning speed if both
arrogance and the pursuit of money were removed from the equation.
Vincent
At 10:25 AM 8/7/2008, you wrote:
>I would appreciate quote some clinical studies in your practice
>where you have found results with Ascorbic acid infusions in cancer
>patients. We see both for and against intravenous ascorbic acid
>efficacy in cancers. When it comes to individual cancer patient in
>your office and you have used this therapy and if it has shown
>results kindly share. We see many many theories and studies that are
>never reproducible in spite of all structures used in virtual
>practice. Ascorbic acid is one among them. I am still searching for
>one cancer patient that is put into remission with VitC. Using other
>therapies like menadione is another therapy by itself. Monotherapy
>with VitC and remmission so far doesn't exist. G6PD deficiency is
>risk by itself before you give VitC. This is another risk factor. If
>not checked you woould kill the patient by massive haemolysis.
>-Chakra.
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