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Re: Wow..Rectal Cancer

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Most frequent site of mets from rectal ca is by far liver

Gubi

[ ] Wow..Rectal Cancer

Hi , I used to post regularly here, briefly...rectal cancer almost 8

years ago, proctocolectomy (had UC for 25 years colon was caput)have ileostomy,

had mets to right lung, thoracotomy...still in remission...did way too many

things to mention alternatively..

That Said: I am currently getting IV high dose Vitamin C to treat a

fungus..gifted me by the Operating Room at Hoag Hospital (Iatrogenic). Also

receiving trace minerals, vitamins etc; IV and doing great.

My best wishes for your successful recovery and remission...as you must know

the usual route for mets on rectal CA is lungs to brain... STOP IT QUICK!

Prayers and healing thoughts,

Dr.

In So. Cal.

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Hello and List,

I greatly appreciate your encouragement. There have so been so many

on the list who have wished me well, I wish that I had an opportunity

to thank everyone personally.

I am fortunate to have been a member of this group long before I was

ever personally diagnosed, I have worked with cancer all my life

(both family and then professionally), so unlike so many others I was

in the fortunate position to experience zero panic. My life did not

pass before my eyes, I made out no will.

There was a feeling of great annoyance that my HMO turned up its

corporate nose at my earlier powerful evidence of cancer, until it

could no longer be denied. Even now they recommend radiation but

deny me the conformal type that their own radiologist recommended as,

to quote them, " What if everyone wanted this?

I weigh all options for myself the same way I instruct clients --

that is, relatively devoid of emotions or blind biases. Radiation

and certain chemo therapies are attractive to the extent that a

positive outcome seems to be very high with rectal SCC. I did want

the option of doing the IGRT conformal radiation, but I certainly

would not commit until I finished exploring what was available in

other parts of the world or what I could make in my own laboratory or

in the immunology laboratories of our board members.

The fact that my cancer is metastatic and painful has put a little

fire under my usual deliberative decision making

process. Fortunately I learned very quickly that the only things

that my HMO oncologists could offer were apologies and

narcotics. Actually the apologies are more like condolences. They

remain quiet when I matter-of-factly confront them with the magnitude

of their ineptness. It has to be fear of litigation.

I will be going to China for three weeks beginning this Monday,

November 16th. I will probably do some photodynamic therapy (PDT)

and neutron beam therapy. I bought an IPod to learn Mandarin while

sitting in the dark for the PDT. My program in Del Mar, CA will be

closed during this time but will resume the week of December

8th. Anyone inconvenienced by this can call my administrator Shirley

at 858-523-9144 as I was told I should not even look at a computer

screen while doing the PDT.

There are any number of synergists and immune therapies that I am

using and will use once I return. I will be bringing a few meds back

from China that are not available in the US. I plan to be very

transparent about everything that I do as I would like everyone on

the list to get well with me.

At 10:32 PM 11/14/2009, you wrote:

>

>Hi , I used to post regularly here, briefly...rectal cancer

>almost 8 years ago, proctocolectomy (had UC for 25 years colon was

>caput)have ileostomy, had mets to right lung, thoracotomy...still in

>remission...did way too many things to mention alternatively..

>That Said: I am currently getting IV high dose Vitamin C to treat a

>fungus..gifted me by the Operating Room at Hoag Hospital

>(Iatrogenic). Also receiving trace minerals, vitamins etc; IV and doing great.

>

>My best wishes for your successful recovery and remission...as you

>must know the usual route for mets on rectal CA is lungs to brain...

>STOP IT QUICK!

>

>Prayers and healing thoughts,

>Dr.

>In So. Cal.

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