Help get my son off Cytoxin!
How about YOUR question here?
Read below or choose another question.
Dear Karl,
Please send us the following free report: #6, Let's Kill Stones.
Also, I have a question. I've been reading about EDTA Chelation, and it seems that most people take so many treatments, say 20, and then they are able to leave it off for a year or so and then take maintenance treatments thereafter. Is it the same with oral chelation or must you take 30 pills of Life Glow every day for the rest of your life?
Another question. Our son, age 25, came down with something last year. At first the doctors thought it was Lupus, but tests didn't confirm this and so they finally settled on Vasculitis and he's been on a drug called Cytoxin, along with a Steroid, Prednisone, for about 8 months now. We'd like to get him off this.
Any recommendations?
Thanks, Ken and Beverly
Texas
Dear Ken and Beverly,
Thanks for the response. Report #6 will be on its way to you later today, by mail.
The concept behind continued I/V treatments and continued use of oral chelation is the same.
You will get the most dramatic improvement in the first batch -- in the case of I/V in the first 5 treatments -- in the case of oral chelation in the first 30 to 90 days.
After those periods, for either way, you are looking at the likelihood that you will no longer notice change, but you are also very likely to continue to receive benefit and improvement.
I've had several customers get on Life Glow for some months, cut back, or quit, and then, after a few more months, decide that they don’t feel as good now that they have quit.
It is NOT just the "chelation" which provides continuing benefit, of course, but in the case of oral chelation you get 51 other ingredients, at super high dosage levels, so you are getting the all-around general value of many vitamins that don't relate to "chelation."
Incidentally, it is only 10 tablets of Life Glow, but 30 capsules of Super Life Glow that we recommend. (The new Life Glow Plus requires 20 capsules per day for an initial dosage and 10 capsules later, as a maintenance dose.)
Getting your son off that stuff!
Metatoxin: Here is what the stuff does:
Here is a comment I found about Cytoxin on the net. Click Here to go to the same source where I found this. It is amazing that there are so many angry people out there -- people who have been duped into taking drugs and then found themselves hurting. Some of these people start publishing their stories. All I had to do to find this story was to enter "Cytoxin" in the Yahoo Search Engine, and there were many references to people who are hurting or angry because of Cytoxin.:
There are two kinds
of this disease. One is genetic. Alpha was told when he was diagnosed that he
would only live for six months. At 27 this was very hard for him to accept. The
only other treatment that could be helpful is Cytoxin. This is a chemo-drug that
is sometimes used with this disease. It suppresses the immune system and stops
the T-cells from attacking the scar tissue. But I have to warn you that Cytoxin
can be fatal.
It can either help or kill. If it helps it may make the girl very sick, but that can be treated.
I cannot stress this enough. It's not for everyone. If you read through this forum you will see some of the things people have gone through that took the Cytoxin.
It's not a pretty picture. I hate to be so down right now but there are decisions that her
family and her will have to make. From what you wrote I take it she's already in lung
failure.
When Alpha got to 33% lung capacity he made his own mind up that he was going to take the
chance
The disease was going to kill him anyway, he might as well see if this would work. It did
work for him. The other thing to remember that if she has not had an open lung biopsy they would
not know if she has the genetic type or not. If she has than a close eye should be kept on her son
as he will have some of her genetic make-up. It's not known if the disease skips generations or
not.
Again, I'm sorry to bring such news to you.
I agonized about writing you back at all, but then I felt that you should know the truth. Then you can decide what to tell the family. For the most part this is an old person's disease. But I'm seeing more and more younger people on here that have it.
The problem is the doctor's aren't sure how to treat it with out a lot of
complications.
Older people usually have something more wrong with them than just their lungs.
Vital!
Probably most important is to change doctors. Any doctor who prescribes that stuff is NOT a friend, and is probably too close-minded to ever listen to a vitamin therapy.
So, either disconnect, at least intellectually, from that guy, or find another.
I've learned that new solutions usually don't work while bad solutions are still accepted.
But, what WILL help is:
After those are true, ask for more help, but before those are in, you would be spinning your wheels.
Karl Loren
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