This is an 'overshare' post, but deals with
something I have become increasingly frustrated and confused by: the line
between medical care as a need and medical care as a business. I'd love if
anyone with a similar experience or knowledge of sifting through the health
care system could provide their advice!
While I was around 28 weeks pregnant, my OB
recommended I see a geneticist. I was a bit confused about why – DORV is not
linked to any genetic cause, 28 weeks is too late for an abortion if I wanted
one, and the test they can run for informational purposes, an amniocentesis, carries the small but still possible risk of harming or killing the fetus.
Nonetheless, even after making it clear I was not interested in the amniocentesis,
my doc insisted it would be a good idea, and I naively believed that doctors
know best. Instead, I showed up to the geneticist office and wasted my morning
and my copay on a doctor who knew zilch about DORV and had nothing to recommend
beyond the one test she had known in advance I refused. I was thoroughly
annoyed and said so to my OB, who then admitted the referral is a standard
practice to cover their backs, so I can’t later claim I didn’t get the option.
In other words, this is the business end of medicine: “selling” services and
tests. My next, high-risk, OB added to the cycle by redoing the same blood work
the first OB had done, insisting she wanted her own office to check, and
hitting me with a $300 bill for tests that weren’t medically necessary.
Now, I’m wondering if I’m being squeezed again. James
sees 2 doctors regularly every few weeks, his cardiologist and his
pediatrician. At his last appointments, we were encouraged to set up visits
with a Nutritionist as well. Well, I called today to set that up and was told I
must see a gastrointestinal doctor in the same department before the
Nutritionist. That's 2 visits, 2 specialist copays, and... for what?
James isn't gaining much weight, and the NICU did
assign him a feeding specialist during his initial hospital stay when he was
born. However, his pediatrician has him on a special high-calorie diet already
- as juiced up as she thinks he can handle - and his weight gain issues aren't critical. She tells me she's already spoken
to the nutritionist, and the nutritionist agrees that his diet is pretty much
at the max. So, 2 new consultations only serve to cover the bases, as no one
expects that a change will be in order.
I feel like this is deja-vu; I sense my geneticist-induced rage
appearing all over again. Do I feel guilted into consulting new doctors because
“what if” they come up with a new idea; I should try anything for my kid’s
health? Or do I assume this is ‘covering their bases’ too, and I refrain from
jumping through hoops until/unless there is reason to think there is a problem
they can fix?
Ughhhhh. We have had top-o’-the-line care, and we appreciate our
proximity to such a reputable hospital and medical team. However, I am sick of
our health care system as it is organized. You can only see whomever your
insurance likes, even if it’s not the closest or best for you; you must pay up
front copays for consultations even when the doctor has nothing to offer you;
medical care is sold as a commodity with better care going to those with deeper
pockets.
It’s a dysfunctional “store”: higher costs for quality care suggest you
get what you pay for, yet up-front costs for doctors who then provide no
service says you’re gonna pay anyways. You're charged just to
walk through the door.
OH my Kirsten... I will send you an email! It sounds like a bunch of hooey to me! And I will share my own high-risk pregnancy fiascos as well. Did I tell you I had 15... yes 15 ultrasounds?? They also wanted to do an amnio on me and I also refused. They can actually give a bloodtest (of course VERY expensive) that gives MORE info than an amnio... obviously no risk to the fetus. Okay... lots of ranting more in my email :) xoxo
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