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Marilyn's
Report
I went downhill on canned tuna fish in 1998 (my prognosis was post partum
multiple sclerosis). I have kept a food diary for years and when I started to walk
into walls after a few cans of tuna, a food I did not normally consume, (I was
trying the Zone diet for hypoglycemia and looking for easy/quick protein), the
light bulb came on and I thought $%^&*%, it's mercury, you are mercury
poisoned...every now and then an article show up in the paper telling pregnant
women to limit tuna consumption due to methylmercury content... I also got
muscle twitches from the tuna, the same as B-12 shots of cyanocobalamin...(B-12
is a methyl donor to mercury, something I now know but my MD did not have a CLUE
as to why B-12 shots had all kinds of side effects for me....)
So I did my research and had my amalgams safely removed and did research
etc. on chelators and the whole medical-field denial that MS is ever amalgam
induced, etc. I am the type that
reads, reads, reads.
Anyway, my dentist recommended DMPS as the way to go and gave me the
names of some Nds in the Seattle area that were administering it.
At that time (July-Oct 1998) I didn't see a lot of warnings even on the
Internet about DMPS - one German fellow on a dentists' newsgroups warned me to
re-think my approach, but the majority of the info I saw said it was safe and
side-effects were minimal...
So a la Klinghardt protocol, I got an IV infusion the same day as the
last amalgam came out. The ND did not pre-test my reaction to DMPS, did not test my
mineral levels, ignored my revelation that I have "3" kidneys and
urinary dysfunction... he assured me that DMPS never hurt anyone... so I let him
pump that stuff int my veins though my intuition was ringing cathedral-sized
bells in my head.
When I got home I sat on the chair and could not move. This basically
lasted until I had a bowel movement - then regained some functioning.
Later I would realize that DMPS had a constipating effect on me - duh,
just what one needs when you are trying to eliminate mercury... when I told the
ND it seemed to constipate me he didn't seem to think this was much of a problem
- he said the Hg would come out in the urine.
Like a fool I listened to the ND's insistence that I was going to feel
worse before I felt better, he said mineral infusions would make me feel better
(at $95.00 a pop)... and I took a total of 7 DMPS infusions with accompanying
mineral infusions 2 days post DMPS...even with the minerals I got sicker with
each IV until my already limited leg mobility was practically non-existent.
Climbing stairs became an Everest challenge.
I felt like my organs were going to shut down. I finally woke up and
stopped the treatments.
It took 8 months to even begin to feel human again.
I had to do some colonics which I did not react well to and I discovered
at this time that I had stopped making stomach acid (no wonder my mineral levels
were abysmal). Nutritionally, I was
a basket case. It took me a long
time to regain lost ground and I have come to feel my experience was totally
unnecessary. j
I have been reluctant to write an anti-DMPS diatribe because I know it
helps a number of people. But this is not a totally safe compound that never hurt
anyone and if I had to do it over again, I would have listened to my screaming
intuition and passed on this chelator... |
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