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Surviving Against All Odds: Analysis of
6 Case Studies of Patients With Cancer
Who Followed the Gerson Therapy
A. Molassiotis, RN, PhD, and P. Peat, RGN, DiplPallCare
Case 6
A 44-year-old woman (born in 1962) was diagnosed
with fibrillary astrocytoma following stereotactic
biopsy in August 1993 after 3 seizures in a swimming
pool. The plan was for no immediate active treatment,
and the patient commenced carbamazepine
400 mg.
Three months later (November 1993), there
were further seizures, and the patient commenced
Chinese herbal medicines. In May 1995, MRI scan
revealed evidence of increase in the tumor size, and
the decision was made to resect the tumor.
Pathology
from the resection showed it to be an anaplastic
astrocytoma. The treatment plan was to proceed with
radiotherapy (27 fractions), which was given over
June and July 1995.
In September 1996, she complained
of frontal headaches, and after an MRI scan,
it seemed that the tumor had recurred in the left temporal lobe, showing a very large cyst behind the
area of craniotomy together with some abnormal tissue,
but no active treatment was planned.
Two consultant
neurosurgeons agreed with this diagnosis
based on the radiological progression without clinical
progression of the disease. At this time, the
patient discontinued the herbs she was taking and
commenced Gerson therapy. She continued to have
occasional seizures.
A review in June 1997 showed
that the cyst had decreased quite considerably in size,
with no evidence of any active tumor in the surrounding
area of the brain. A review in November
1998 showed no increase in size.
In 1999, the Gerson
regimen was scaled down (maintenance phase of the
Gerson regimen), and the homeopathic remedy pulsatilla
was added. A review in November 2000 showed
no increase in size from the previous year.
She has
since had annual reviews with no increase in tumor
size, although symptoms of headaches and seizures
continued throughout. The patient has continued
on carbamazepine.
The patient remains well and stable
at present.
Integr Cancer Ther 2007; 6; 80
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