My friend has been diagnosed with atypical
tn, and she is contemplating mvd as you
can see the nerve being compressed on the
mri - so hopefully the surgery will stop
the pain.
However, thanks to the pain she isn't
employed and has no insurance. So we're
looking for funding advice. Currently
based in england, but desperately wants to
go to usa for surgery.
So has anyone here received help for the
funding of such an operation? The cost of
the op is about 70,000 us dollars - but if
something goes wrong... We know it will
be much more than that.
If anyone has any advice for finding
funding - or has received funding
themselves, please get in touch!
