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Insurance paying for treatment (was Light Sensitivity)

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Tetrad

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Mar 1, 1996, 3:00:00 AM3/1/96
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Len Ochs wrote:

>Most of the time (except for managed care) the use of the system is
>reimbursed for the treatment of both physical and emotional injuries. The
>codes we use are either 90908 (EEG biofeedback) or 97770 (cognitive
>rehabilitation).

Today (3/1/96), the Philadelphia Inquirer had an article about health
insurance in the Business Section (http://www.phillynew.com) It said that
3/4 of the people in the US who get health insurance through their employers
are in managed care.

So to say that something is reimbursed except for managed care unfortuately
says that MOST people will not receive the care.

Therefore, IMHO, if we as survivors want access to treatment and the
professionals want to be paid, somehow, the scenerio of managed care NOT
paying for treatment has to be changed.

The sticky wicket, however, is how?

As a survivor, I haven't a clue I'm still dealing with an HMO that, in
spite of neuro-psych tests, acceptance into the PA Head Injury Program, and
an experimental treatment program at Temple for TBI, still says that I'm
just "depressed." (That's better than a few years ago when an insurance
adjuster told my doctor, without ever reading my chart, that I didn't have
headaches [news to me!], I had repressed memories of childhood sexual abuse!
I know some people on this list have been, but I can say without doubt that
I have NEVER been sexually abused as a child, teenager or adult! Of course,
if I had been, they wouldn't have paid for it either because that was
"mental health.") Even when my husband's employer called up the HMO and
told them to let me go to the rehad hospital, they merely took the phone off
the hook and refused to take THEIR calls! The only reason I received
treatment is that my primary care physican told the HMO that she was
directing HER PRACTICE's lawyer to investigate. I had a referral within the
hour!

IMHO, the TBI professionals, who have the access to professional societies,
peer-review journals, and the latest research must take the time to organize
and do whatever scientific studies and the follow-up public relations
necessary to get the managed care organizations to pay for treatments.

Without it, the survivors (except for the financially well-off) will not be
treated and the professionals will not be paid.

As a survivor, I am willing to do my part, but if the TBI professionals do
not take the time to advocate and publicize both their plight and that of
the survivors, we will all be tossed aside as "too expensive" in a society
that continues to emphasize dollars over human suffering.

If I have offended anyone with this post, please let me know, because I do
not mean to. However, I welcome any comments or insights on this subject.
Our lives, literally, depend on it.

Dinara

Francoise Frigola

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Mar 1, 1996, 3:00:00 AM3/1/96
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Dinara,

That was a very good post! as sad as this may be!

I do not know how long Medicare and Medi-Cal will let us choose
our own MDs. So far so good, otherwise I would be in great trouble!

Francoise

-------------------

Dinara

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