Home | Contact Us | FAQ | Search & Site Map | Link to Us
Sign In | Join | Other 45 Sites in Network
Home
Discussion Groups
General
GeneralCardiologyVisionDentistryPharmacyLaboratoryNutritionAlternative
Diseases and Disorders
AIDSAlzheimer'sArthritisAsthmaCancerBreast CancerDiabetesEpilepsyGlaucomaHepatitisHerpesLupusProstate BPHProstate CancerProstatitisSinusitisTinnitus

Medical Forum / Diseases and Disorders / Breast Cancer / June 2006

Tip: Looking for answers? Try searching our database.

Vitamin C Infusions for Cancer?

Thread view: 
Enable EMail Alerts  Start New Thread
Thread rating: 
su-texas@webtv.net - 25 Jun 2006 05:58 GMT
Vitamin C Infusions, Vitamin C Chemotherapy

I've heard about this, read a bit, & plan to speak with doctors/etc
about it. Try to get more info.

Has anyone tried it?

It's one of the therapies that the molecular research biologist & doctor
(PhD MD) suggested, when I met her in late 2002. She didn't take
insurance, so I couldn't afford the treatments.

She also stressed diet. No sugar at all, ever.

I'm also trying to get a referral to a doctor in Tyler, that might do
integrative medicine, & does take insurance.

I'm also trying to find a good source of Artemisinin. And will speak to
Allergy Research Group (which I've found on the internet) about it,
probably on Monday.

Any opinions or comments on Vitamin C infusions?

Please note that infusions have a different effect, than the oral use of
Vitamin C.

Susan Wms, Su_Texas  my opinions
LT - 25 Jun 2006 16:23 GMT
> Vitamin C Infusions, Vitamin C Chemotherapy
>
[quoted text clipped - 22 lines]
>
> Susan Wms, Su_Texas  my opinions

Hi,

How are things going with you?

I don't know anything about vitamin C infusions but everything I've read
about the effect of the vitamin on cancer has been negative - in the sense
that it apparently does not inhibit it.

However this article on the possible cancer fighting effects of berries
suggests it might be the phytochemicals in these foods with high levels of C
that may be operative - not vitamin C itself.

http://www.msnbc.msn.com/id/13484206/

Lois
su-texas@webtv.net - 26 Jun 2006 02:03 GMT
Hi,

How are things going with you?

Lois, LT

=============

Hi Lois,

Things are as tough as heck, but I'm hopeful, still struggling hard to
survive in primitive conditions, trying to get legal help, trying to
find any legit medical care for cancer.

The oncologist's lying to & betraying me (2002-2006), deliberately
harming me with the chemo (then doing the same to my Mom, major CHF from
Adriamycin/etc), .... his sitting back & watching me struggle & suffer
so desperately for years, his now admitting to & boasting about it, ....
has caused more damage (both emotional & physical) that I have to learn
to live with.

Such is life. Nothing's fair. Crime rules, money & meanness.

------------------

At least, we have the internet now, & can inform others of our
experiences, give them a better chance at life & living, learn from
their experiences. Knowledge is power.

At least, we're not alone.

I'll keep asking about & checking out cancer treatments, trying to see
if they might have some value, work some.

I now know there's no "cure". Cancer is a chronic disease. It's
important to find things that slow it down, improve health & quality of
life.

-----------------

I now know from experience, that the current chemotherapy
(Adriamycin/Cytoxin & Taxol) is NOT safe, viable, well-tested,
well-documented, .... nor are there any tests to see if they've worked
or not.

If these chemos don't kill you outright, then you're declared "cured of
cancer" & "in remission". ?! This is stupid beyond belief.

And the docs would rather cut off both their arms, than order the tests
necessary to show the damage these chemos do, than help you, care.

The docs flat-out refuse to test for, diagnose or report harm done, like
major CHF.  

It took me about two & a half years to get a diagnosis. I was in an ER,
almost dead from it, & the ER doc still didn't want to order testing or
diagnose. Finally he said CHF, gave me some sheets of paper, & had me
wheeled out. In my truck, I read that major CHF was congestive heart
failure. The ER doc made no referral to a specialist, no attempt to
help.

I have health insurance that pays 100% to any doctor anywhere. There was
no reason to refuse me med care, other than to cover-up the frauds &
crimes of the Medical Industry, PHARMA companies, doctors.

Cancer "care" has been a major betrayal, a nightmare.

I'd advise people to avoid these chemos.

Susan Wms, Su_Texas   my opinions
su-texas@webtv.net - 27 Jun 2006 19:27 GMT
Vitamin C Infusions

Steven B. Harris wrote:

"Remember, you don't want to be giving loads of vitamin C to people with
iron overload [excess iron], due to the Fenton reaction.

Give them RDA, and wait until they've been phlebotomized to the point of
iron deficit.  THEN you can give them all the vitamin C you like."

[???]

Susan Wms, Su_Texas   my opinions

PS  I'll try to post bits & pieces of what I find about this & other
treatments, as I find them.
 
Sign In
Join
My Latest Posts
My Monitored Threads
My Blog
My Photo Gallery
My Profile
My Homepage

Start New Thread
Enable EMail Alerts
Rate this Thread



©2010 Advenet LLC   Privacy Policy - Terms of Use
This website includes both content owned or controlled by Advenet as well as content owned or controlled by third parties.