Cancer Vaccines/Fibrosarcoma

Fibro Sarcoma is a notorious rare cancer. It is the cancer that claimed my Father.

Last week I picked up a client who had large sarcoma lesion on her forehead. Dermatofibrosarcoma. The Sarcoma was CD34 positive which increases its mobility and ability to spread.

The lesion has progressed into her eye socket and surgery is not going to get 100 percent of that lesion, will require skin grafts and will disfigure this person. Since she is a model and has a model agency, surgery has been resisted.

Since FibroSarcoma has shown that it can burn glucose via oxidative and anaerobic pathways we don't feel oxygen therapies will offer much benefit.

Most of these sarcomas utilize tyrosene kinase pathway she is starting on a natural TK blocker.

We have instructed our client that her immune system must be the focus in order to beat this dreadful form of cancer.

She has tested positive for Epstein Barr, Mycoplasma in the intestine plus a parasite of unknown origins.

She is doing topical applications of ascorbate, aloe, coq10, dmso to the cancer site. Alternating with peroxide warm packs and has noticed softening of the lesion.

Since her vitamin d has been chronically low we suggested the GcMAF vaccine which she has already started and we asked her to look at the Dendritic Cell vaccine, along with Lymphocyte activated killer cell vaccine.

She may start Oleandrin but waiting for the doctors to rule out contraindications. Since these doctors are non traditional we dont expect any political BS from them.

She will be getting Coleys toxin, hyperthermia, iv ozone, iv vitamin c as adjunctive therapies. We feel the ozone will kill mycoplasm and help with the EBV.

She is currently taking silver, aloe, pectin, enzymes, has been doing bowell detox using chlorophyll enemas. She was getting Meyers cocktail and ascorbate to try and raise her red blood cell count and white cell count.

After two weeks of these IV's her white cell count returned to normal but the RBC is still lagging behind.

So we then encouraged her to get the immune therapies.

We had originally described these vaccines as limited because they jump over a tagging process that recruits killer cells to the lesion site. Without tagging by Macrophages, typically these vaccines have temporary results because the entire immune cascade cannot be initiated. The trained cells would still be susceptable to histocompatability disguise and would not all congregate at the lesion site.

The killer lymphocytes have recently been combined with interferon and that seems to have improved this therapy.

The dendritic cell vaccine has been improved in two ways.
A photopheresis of the blood and extended application. In other words the client will be taking the vaccine home with her and will continue doing these for six months or so.

The immune oncologist were uncomfortable with overlapping GcMAF vaccine with their vaccines because they do not know much about this GcMAF. I explained to them that this vaccine may be crucial to setting up an entire immune response and giving her permanent immunity. Reluctantly they consented after doing research on the GcMAF.

We will be aggressively pursuing the insurance company to reimburse the client for these therapies of which one of the vaccines is FDA approved and chemo/radiation/surgery really has no true benefit with this cancer.

She is an awesome lady with a supportive and caring husband who will be traveling with her.

I would just like one or two people to say a prayer for her.

Will keep you updated on how this treatment works.

If it does work, she will experience crippling migraines, toxicities, fever. She is in for a very rough ride.

Thanks for your prayers.

Bret Peirce
American Cancer Advocates