This is the email I rec’d from Audeo a few months
ago: Margaret: What is being transmitted: the signal that the brain sends
to
the vocal cords to move (make sound). So, there does need to be some
activity
in the muscles (that is the signal) that control the vocal cords. In other
words, a patient cannot simply think of what they want to say but actually
attempt to say it. You can try and put your fingers just to the patient's
left
of their voice box (Adam's Apple). Have the patient attempt to say
something.
No sound (residual speech) needs to be produced . If you can feel some
movement
on your fingers, it is likely the device will work. Beta Testers: We are still preparing for testing. We are
very
limited to testing patients who are close to us. We are located in east
central
Illinois. Our first phase of development was just successfully tested on
Augie
Nieto in California. However, we still have some work to do. Each patient
will
need to go through a testing/trial and referral process with their health
care
professional/therapist before buying a device independently.
I hope this helps! Thanks! Kimberly Beals Hi Kimberly- Thanks for your response- I appreciate
it. Would it be possible to ask some questions about the Audeo?
There were some things I wasn't clear about. 1. I wasn't clear about exactly what was being
transmitted. If a person has advanced stage ALS, and most of the nerves
and
muscles for speech are atrophied (and essentially dead) would the Audeo
still
work? 2. Are you currently using any beta testers?
3. Does the person still have to have some residual
speech in
order for the device to work? Thanks for your help with this- Margaret Cotts, MA, ATP Margaret Cotts From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On
Behalf Of Wright, Amy Hey Alisa – I have heard similar comments from several of our ALS
patients. The technology sounds exciting but I am concerned that
their
claims may be misleading. To that end, I have emailed the folks at
The
Audeo requesting additional information. Thus far, I have
received
one email back – it is attached. Supposedly, it will be available to a limited number of ALS
patients in the US in December of this year. I am not sure how those
patients will be chosen. Here’s an ALSTDI forum link with some
info: http://www.als.net/forum/topic.asp?TOPIC_ID=3310
Keep me in the loop and I’ll be sure to do the
same! Amy Amy Wright, MCD, CCC-SLP Speech Therapy Coordinator Carolinas Neuromuscular/ALS Center (704) 355-0867 From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On
Behalf Of Alisa Brownlee
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