This past week and a half has been a lesson in
being thankful. I have learned my lesson, I’ll be happy to eat my veggies, or
anything else for that matter, from now on. No more complaining about not being able to eat what I want.
Sometime
early last week I began to experience extreme discomfort after eating. Over the
course of a few days this turned into excruciating pain when anything hit my
stomach, even water. It made it next to impossible to eat how I need to in
order to heal my body. I wouldn’t eat because I knew that when I did I would be
doubled over in pain for hours afterward. It just wasn’t worth it. Eventually,
I would get so hungry that I would have to eat and deal with the pain that
inevitably would follow. Eating foods that I simply found to be not so
appetizing would have been welcomed at this point.
Imagine if
someone inserted a bicycle pump directly into your stomach and began to pump.
Pump, pump, pump. The stomach expanding to the point it felt like it might
burst. This is the only way I can describe how I felt. My stomach hurt. It hurt
to even place my hand on it.
Then in
addition to being hungry, doubt and worry starts to set in. Wonder if it has
spread? I had two rounds of chemo. Have I detoxed too quickly? Do I have damage
to my liver or pancreas or gallbladder? Ulcers? Yeast over growth? Parasites
from raw food? The possibilities were endless.
I was hesitant to seek help from conventional medical professionals before all this
started, and even more so now. I don’t have much faith in their abilities to
diagnose in every situation. Their knowledge, in my opinion, is limited and
narrowly based mostly on prescription drugs, which would be counterproductive
in my current situation, and treating symptoms, without treating the primary
causes.
Antibiotics,
while they have their purpose, are extraordinarily overused. What people don’t
realize is that it can take your body up to two years to recover from one
course. It not only kills the bad bacteria, but it also kills the good
bacteria. A very large percentage of your immune system, something like 70%, is
contained within your gastrointestinal tract, and is dependent upon healthy gut
flora, something antibiotics would destroy. Since my chosen therapy is based on
boosting my immune system, taking antibiotics would be out of the question. And
taking any other prescription drugs would only be masking a bigger problem, not
fixing it.
I thought of
other possible scenarios if I elicited the help of medical doctors and
ultimately decided that going to the emergency room, while not completely ruled
out as unnecessary, would be my absolute last resort.
First, I was
going to try to fix it alone, well not completely alone. I had Bob to help me.
He’s been like my own personal Dr. House.
I have some
theories about what may have been causing the pain, but I can’t say for sure.
There were a number of things that all changed around the same time.
I’m trying some different things. I’m taking
an enzyme and probiotic. I drank apple cider vinegar to flush out my
gallbladder, coconut oil for its multiple, wonderful uses, and trying to eat
more often. So far things seem to be improving. I’ve eaten a few meals and with
each one the pain decreases.
It’s not
just medical doctors I have problems with. After a ridiculous last appointment
with the natural doctor I've been seeing and have for years, I’ve decided to
look for another one. I left his office on Monday feeling as though he was
little to no help. He may be a brilliant man, but his antisocial behaviors have
exceeded my tolerance levels. He’ll serve some purpose as I move forward, but I
need someone I feel as though I can confer with and it’s not him.
Hydrogen
peroxide treatments are going well. I’ve had two so far. I’ll continue with
those on a weekly basis.
The results
from my first thermal images are back. It showed I am estrogen dominance. I
question whether this was the case before all this started or if this is a
result of the treatments I underwent. When I looked up the symptoms of having
excess estrogen, I’m definitely experiencing more now than I was prior to
having chemotherapy. Regardless, it’s my current situation that I have to try
to correct.
I’m
questioning whether thermal imaging is going to be the best way to monitor my
progress. I was told if there wasn’t a palpable lump, they wouldn’t have been
able to even tell that I have c*****, and I’m not sure why that is. I clearly
still have a lump. So I am not convinced this will be the best monitoring tool.
I’m not an expert in thermography, but I wonder if the excess estrogen could be
masking the tumor.
And even
though I don’t think this is the case, the other possibility is that the c*****
cells are dead and just have not been reabsorbed by the body. I have read
stories where this has happened.
I was
surprised to find out that the same facility where I had my thermal imaging
done also offers sonograms. So next month I’ll have a sonogram. I know from
when I had my original sonogram done, before my biopsy, they were able to
measure the lump and tell me the exact size, which at the time was 2.5 cm or just
about 1 inch. So I do feel as though this will be a better way to track
progress.
Hair status:
I am almost
7 weeks post chemo. I was told that hair starts to grow back after a month.
Somewhere in my head I created this scenario where all my hair would all grow
back in at the same time as full as it was before it started to fall out.
WRONG!! My hair is in three stages; the hair that never fell out, the hair that
fell out and has started to grow back, and the hair that has yet to grow back.
It’s obviously going to be a much longer process to grow back hair than I
originally thought. Until that time I'll just continue to wear my headcoverings.
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