filming dad in the foot bath at Superior Health Solutions |
What makes this interesting, first and foremost, is my dad’s
hopefulness. There’s a lot of research about placebos and a patient’s
willingness or fight to get better. I’ve read lots on both sides of the
argument and by no means do I think what my dad is doing at SHS will reverse or
cure his Parkinson’s Disease (PD). The greatest thing they’re offering and feel
fairly confident about is pain management. My dad told me today he feels a
significant uptick in the amount of pain he goes through on a daily basis over
the last several months.
“Golf just isn’t much fun anymore,” he said to me flatly over lunch today.
That one line was heartbreaking because there have been two
threshold points we’ve been measuring my dad’s PD with: golf and driving. We
have said for some time when he’s unable to do either, let alone both, we’ll be
looking at all of this quite differently. These things lend to his freedom and
enjoyment of life. Without them, the world as he understands it looks very
different – far less appealing to say the least.
We sat down with Dr. DeMartino and he went over my dad’s
bloodwork. Then dad had three modalities of treatment: 1) Ionic foot bath
(which Dr. DeMatino admitted and a quick search of the Internet will verify is
highly controversial in terms of its efficacy), 2) light therapy, 3)
Chiropractic adjustments – focusing on dad’s misaligned hips via pressuring
points in the neck.
I am not familiar with the foot bath or light therapy enough
to say more than they appear interesting and certainly do no harm. I want to
reiterate a few things: we’re not paying for the treatment (outside of dad’s
travel expenses), he’s allowing (even encouraging) documenting and challenging
everything, the goal here is sustained pain reduction. The outside hope would
be for a halt of PD symptoms but, again, that’s not the main thrust or anything
that’s been promised.
As we were told, the foot bath changes colors as toxins are pulled from the body. |
Here’s what I want: if you think this treatment is bunk or
Dr. DeMartino is a hoax, please sound off here. Let me hear specifically what
you question and why. If you have any research or personal experience, again, I
welcome it. My dad has said that when he’s shared this treatment plan with some
others they’ve looked at him with pity – as if to say, “Oh, you’re really that
desperate, eh?” While I wouldn’t say he’s desperate, he is in pain. Looking
ahead at a life of filled with chronic pain without what have become assumed
freedoms (driving) or enjoyed recreation (golf) has a way of coloring one’s
point of view. So again, I ask: do not pull punches here. Let us know what you
think.
We are still fundraising
for the sequel documentary and we need your help! Please click here to
donate to our film. We will keep a running tab of how much we've raised and
what are expenses are for so you can see where the money goes. Thank you.
No comments:
Post a Comment