Nothing seems more strengthening than liver and onions. I love to cook organic chicken livers with onions, coconut oil, a little bit of balsamic vinegar and lots of lemon juice. This is so crave-worthy and I can't get enough of it. Lately, I've also enjoyed sauteing radishes along with my greens like this ruby chard. Delish!
~a quest for health incorporating lessons learned over two decades with multiple sclerosis
Wednesday, May 10, 2017
Monday, May 8, 2017
I'm Upset About Gadolinium
We spoonies have to trust our doctors. They have what we don’t – years of
training, access to diagnostic clues and the latest treatment options. Trusted physicians are crucial to our
care. I do trust my physicians and
am so grateful for them, but I no longer trust elements of medical research, or
the FDA.
When I was diagnosed with MS in 1996 I did everything my
doctors told me. I got regular
MRI’s and I took medications that ruined my quality of life, with no evidence
of benefit. After the first few
years, I finally learned balance, and began honoring my intuition as much as
the doctors’ advice. I became a
partner in my treatment and, along with my physicians, made wiser decisions
about medications and lifestyle.
But I never questioned the MRI.
It's considered the gold standard in tracking the progress of neurological disease,
and every professional I’d ever come across, over 21 years and in 4 States
where we’ve lived, valued this view into my brain and spine. Heck – I valued it too.
At my last MRI, the technician paused halfway through, as
always, to administer the contrast agent.
I was given a consent form to sign, once again, before the vial of red
liquid was injected into my vein.
For the first time ever, I wondered about it. I asked the technician what it was.
“Gadolinium is a very rare earth element, a heavy metal
that is only found in one place on earth and is very expensive,” she said.
[Heavy metal.
That taste in my mouth – that’s what it was – metal.]
“I taste it, “ I said, “I guess I should drink a lot of
water today to wash it through?”
“Yes, that’ll help, it’ll be fine,” she said.
That was two years ago. It isn’t fine.
I scheduled my next MRI recently, but then I remembered I’d
meant to find out more about gadolinium.
I did some cursory online research. Very quickly I learned that deposits of the heavy metal
remain in our systems. The
National Institutes of Health believed at first that patients with renal
failure (kidney issues) were most at risk, but then they realized that all
recipients of gadolinium are prone to lingering deposits in our brains. The FDA opened an inquiry into “gadolinium
poisoning” in 2015, but they’re not in much of a hurry to finish. They are also not concerned with
informing the Neurological practitioner community in the meantime. My neurologist was grateful for my research and said she had
never heard of the issue. The NIH
article stated that anyone who has received more than 6 lifetime doses is
particularly vulnerable to gadolinium poisoning. I’ve had at least double that amount. The metal settles in the detate nucleus
and the globus pallidus of the brain.
Memory, cognition and gross motor skills are affected (which also happen
to be classic MS symptoms).
Further, the gadolinium sets us up for zinc toxicity. I have no idea if my symptoms are
really caused by MS or if it’s just the heavy metals in my brain.
My neurologist was happy to re-write my MRI order, with no
contrast. She explained the
contrast only helped to show active lesions anyway. Symptomatically, it’s clear to me when my lesions are active,
so there’s never really been a need for the contrast. My neurologist said she can still get a
lot of information from an MRI with no contrast.
I’m angry that anyone ever thought putting heavy metals into
sick people is a good idea. I’m
angry the FDA doesn’t care enough to put their relationship with big pharma
aside in order to prioritize our health.
I’m angry they don’t bother to inform our caregivers that we’re being
poisoned. I’m angry at myself for
my blind trust in the system, and for failing to read every word on the forms
I’ve been signing all these years. Please read the
fine print, everyone.
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