I have always thought that a rolling
mount
would offer more flexibility with regard to repositioning, suctioning, etc
but
it seems these folks are able to work around it. Having the
system
mounted on the chair doesn’t affect their ability to recline, tilt or
elevate legs and if you figure there’s a good 18-24 inches between
them
and the device, there’s room to lean forward or get in there for
suctioning. The mount doesn’t get in the way if pulling someone
up
in the chair from behind either. I will try to survey our eye-gaze
communicators about why they prefer the wheelchair mount and get back to
you!
Like you, I have my own thoughts about it but I’d like to hear what
they
have to say… Amy Wright,
MCD,
CCC-SLP Speech
Therapy
Coordinator (704)
355-0867 From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Margaret Cotts Thanks to everyone who has written
so
far- I really appreciate it. I’d be really curious to know
why
PALS who expressed a preference for wheelchair mounting wanted it expressly
mounted onto their wheelchair. My personal thought had been that on
the
whole, most people would be better served by using a rolling mount.
In
addition to what Mary Jean, Kathleen and Joan mentioned, it seems like a
lot of
my former clients needed a lot of help with positioning (being
straightened,
lifted up in the chair, tilted back, leaning forward for pressure
relief…) It was easier to move a rolling mount out of the way in
order to
help with positioning and saliva management. Off the top of my head, it seemed
like
this is easier to do when you can just roll a rolling mount out of the
way… (but again, I could be
wrong….) Another thought- Earlier in my
career,
when it was more difficult to get an eye gaze system, the only people who
were
really getting them were people who truly were at an advanced stage of ALS.
Now, for a number of different reasons, it’s a lot easier to get an
eye
gaze system. I’m imagining that more and more people who aren’t
at
such an advanced stage will be receiving the system, (and as follows, maybe
more people will be mounting them onto their
chairs?) Just a thought. Thanks to everyone
for
their input Margaret
Cotts From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Wright, Amy Hi
Margaret, I doubt that this is the
trend… Of our advanced stage PALS who are
currently using an eye-gaze system, 7 are wheelchair mounted and 3 are on
rolling mounts. Recently, our patients have verbalized
a
preference for wheelchair mounting when given the option. In some
cases,
we’ve had to spend a considerable amount of time getting the
wheelchair
mount just right for calibration accuracy and to ensure that caregivers can
easily work around it or remove it as needed. We’ve also
done
quite a bit of “rigging” with spare mounting parts.
These are folks who, though they may
be
vent-dependent, are still getting out of bed on a regular basis and spend a
considerable amount of time in their wheelchairs. Since
positioning
can be problematic when trying to calibrate, a wheelchair mount seems to
offer
more stability and consistency. One patient, who does spend the
majority
of his day in bed, has his wife drive his chair over to him and swing the
mount
around so that he can access his system from bed.
I’ll be curious to hear your
thoughts! Amy
Amy Wright,
MCD,
CCC-SLP Speech
Therapy
Coordinator (704)
355-0867 From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Margaret Cotts There
is something I’ve been curious about for a
while.- I’ve
been thinking about eye gaze systems, mounting, and folks with advanced
stage
ALS. I
wanted to take an informal survey - do people think that most folks with
advanced ALS would generally be using a rolling mount for an eye gaze
system,
or a mount attached to a wheel chair? (I
have my own thoughts on what I think most PALS would be using, but I
thought I
would check with the group first ;-) Thanks
for your help with this- Margaret Margaret
Cotts, MA, ATP DynaVox
Technologies & Mayer-Johnson This
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