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David Doherty
Update, June
2000: After 28 months on antineoplaston therapy, David's tumor
is now reduced by a whopping 96%.
David needs
your help. Contributions can be sent to
Coast Commercial
Bank, David's Cancer Fund, 203A Mount Hermon Road, Scotts Valley,
CA 95066
Antineoplastons
have become the life raft that is bringing us safely through the
dangerous sea of treatment for pediatric brain tumors.
In October
of 1995, when David was 16 months old, he was diagnosed with an
astrocytoma in the left thalamus region of the brain. An operation
was performed immediately, and 75% of the tumor mass was removed.
David had surgery at the University of California at San Francisco.
Doctors there recommended 70 weeks of chemotherapy (vincristine
and carboplatin). David could only take it for 30 weeks.
Ethically,
we had problems because we felt we were poisoning our son even
though the benefits promised by the doctors were only vague and
indefinite. We prayed, and our friends prayed, too. At the same
time, we were hearing of other anticancer regimens in the vast
sea of treatments. We tried several that attempt to strengthen
the body in its fight against the devouring disease. Although
health regimens have helped many people with cancer, brain tumors
usually do not respond well to these treatments.
In 1997, David's
brain tumor showed signs of growth. The doctors recommended another
operation. We declined, a decision that appeared foolhardy to
David's doctors but one we had come to after 2 weeks of prayer.
Over the next 10 months, David lived a perfectly normal life.
Then in December of 1997, he began having headaches. We took him
for an MRI, which showed a greatly enlarged tumor mass. Another
operation was necessary. The doctors assumed that David would
have radiation therapy afterward because the tumor mass was still
in his thalamus.
Although the
radio-oncologist was sensitive and very kind, we had to pull and
squeeze out of her a clear statement of the side effects of radiation
therapy. She couched them in the nicest and most positive language
imaginable. "And maybe David will tolerate it well,"
she said. When I asked David's neurosurgeon about the side effects
of radiation therapy, he told us that it was very likely that
David would be permanently paralyzed and that a decrease in his
IQ was almost certain. The doctor said, "But, you know, Mr.
Doherty, that is something he can live with." The answer
that did not occur to me at the time was more the truth: "Don't
you mean, doctor, that it is something he will die with?"
Irradiating David's tumor held little hope for a long-term cure;
however, that was not made clear to us. Only later did we discover
the statistics. David would have begun his journey to death paralyzed.
We were ready
to give up. We began to go through the motions and agony of preparing
to submit David to radiation therapy. Our hopes for a humane treatment
for him seemed to evaporate before our eyes because David continued
having headaches. And, in January of 1998, another MRI showed
that in only 1 month, the remaining portion of the tumor had doubled
in size. While looking at the frightening scans, I said to David's
oncologist, "So it's obviously too big to irradiate safely."
(A small tumor size is much safer to irradiate, and in children,
radiation therapy normally is only successful when the tumor mass
is very small [depending on the tumor type]). The oncologist replied,
"It's never too late to radiate." I felt it was conspicuous
that he left our the word "safely."
I drove home
with David, not knowing how to tell his mother the news, thinking,
"What will we do." As I look back on it, what happened
to me during that car ride was amazing. The idea just popped into
my mind -- follow-up on Burzynski. A holistic doctor from Santa
Cruz had told us about Dr. Burzynski 2 years earlier. Because
David was on chemotherapy at the time and because of the problems
the doctor was having with the FDA trying to indict him, it wasn't
an option for us. It hadn't even been a thought in almost 2 years.
Then, as we drove home, the idea came to me. We were on a plane
to Houston in 1 week.
Before we
went to Houston, I asked the doctors at UCSF what they thought
of Dr. Burzynski. "We can't recommend him," they said.
"It is not normal for a doctor to charge patients so much
money. It seems as if he is taking advantage of patients in their
time of crisis." Somehow, we decided to go anyway.
While in Houston,
I read The Burzynski Breakthrough into the night. To my astonishment
I found that UCSF was conducting its own clinical trials on phenylacetate.
When we arrived home from Houston, I called UCSF and talked to
a doctor involved in the trials. I said "I heard you are
testing phenylacetate derivatives. Do they work?" Dr. Horn
replied, "Yes. On some patients they show anticancer properties,
but our clinical trial is full this month. Perhaps we could sign
up David for next month." I replied, "Actually, we are
also using phenylacetate, but David is being treated by Dr. Burzynski."
I can only
describe Dr. Horn's response as an explosion of jargon, buzz words,
anger, and surprise. She said things such as "He never tells
anyone what is in his drug." "He doesn't submit to peer
review." "He is dangerous and is making a lot of money
from his patients." I later contacted my MediCal worker,
who informed me how much had been paid to UCSF for chemotherapy
and oversight of David's case. The amount turned out to be much
more than what Dr. Burzynski charges.
David began
antineoplaston treatment in February of 1998. Four weeks prior
to that, his tumor had doubled in size. After 11 months of stable
disease on antineoplaston treatments, on January 12, 1999, an
MRI showed a sudden 40% reduction in tumor size. Best of all,
David is still running around, pretty much like a normal boy his
age. We pray that he continues to improve.
Our first
2 weeks in Houston were great. It was a time of hope and encouragement.
Patients must go to the Clinic every day to learn how to care
for and manage administration of the drugs. At the Clinic, we
met people who were doing the 2-week initiation and people coming
back for regular checkups. While there, I met a man whose son
has the same type of tumor David has. His son had been on the
treatment for 18 months. Just as we were talking, a doctor came
into the waiting room to tell my new friend that his son's tumor
could no longer be seen on the MRI. We hugged, cried, and rejoiced
together, right there in the office. That is what I want for my
son.
However, it
doesn't work out like that for everyone. Of the four people (and
families) we befriended who were doing the 2-week initiation at
the same time, all have since passed away. However, all had radiation
and chemotherapy before they received antineoplaston treatment.
It is rightly
said that antineoplastons are generally nontoxic; in contrast,
the treatment is complicated. Those two things should not be confused.
There is a great commitment of time and energy on the part of
David's mother. David also must shoulder the burden of carrying
the pump and bags full of medicine and of having a catheter.
Our personal
recommendation is to try antineoplaston therapy before radiation
and chemotherapy. As people with cancer know, treatment decisions
placed on your shoulders can be brutal. Yet, if we had listened
to our highly paid medical advisors at UCSF, our son would now
be paralyzed and, at best, would have only a couple of years of
life left, a life that would be difficult and "medicalized."
Because we
chose to go to Houston and Dr. Burzynski, we now find ourselves
on a stable life raft that steadily is moving us closer to our
goal, that beautiful island called Remission. Moreover, we are
giving our son the gift of life while maintaining his quality
of life. We will not have to face the guilt of knowing we poisoned
our son and destroyed his brain function. Dr. Burzynski's treatment
corresponds to our ethical ideals of how the human body should
be treated and, as a result, it is cleansing to our consciences,
not to mention curative for David.
Anika and
Michael Doherty
February 1999
This patient
has requested to be contacted through Burzynski Patient Group.
<maryjo@siegel.net>
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