Hello,
I just thought perhaps this may help with commination issues with patients forwarding you some of the basic info we give to our pALS.
The communication partners / caregivers will need to learn a strategy called "partner assisted scanning" Please see instructions in
the attachment. Patient and caregivers can adapt any of these tools to their needs.
1 ) Eye gaze alphabet board w instructions (see attachment below). Be sure to read instructions. They provide good strategies for all
non-verbal communication.
2 ) Make a top ten requests list
example:
1 - Bathroom
2 - Hungry
3-Thirsty / clean my mouth
4-reposition me
5-Bed (back to bed)
etc.
Make a large easy to read chart with the choices. Communication partner/caregiver reads numbers down list. Establish a way to select
that works for the patient (pt looks up or bites teeth loudly). Do not choose blink for selecting - it is too confusing.
3 ) Here is a resource for other low tech communication board that can be adapted for partner assisted scanning (see instruction under
number 1).
4) Consider using a laser pointer with this flashlight holder instead of partner assisted scanning to make choices on a communication
and/ or alphabet board
Nite Ize Headband -
https://smile.amazon.com/Nite-Ize-Headband-Flashlight-Holder-Black/dp/B004YUC71W/ref=sr_1_3_a_it?ie=UTF8&qid=1467393689&sr=8-3&keywords=nite+ize+headband
4 ) If pt. has financial resources to pay out of pocket (approx. $1000). This is a great tool that can be used with communication software
on a windows based tablet (not ipad)
http://www.quha.com/products-2/zono/. It needs to be purchased from an authorized dealer. If she is interested, I can put her in touch with someone.
If she has the means to buy something like this, she would also need to consider the cost of a tablet computer ($500), computer mount ($200-$500) and communication software ($150) Much less expensive than an eyegaze device, but still a lot for most people to
pay out of pocket.
Sarah Hardy Care Services Coordinator
ALS Association Nevada Chapter
4220 S. Maryland Parkway, Building B #404 | Las Vegas, NV 89119
| alsanv.org
office 702.777.0500
mobile 702.884.6301
email
xxxxxx@alsanv.org
From: xxxxxx@alsa.simplelists.com [mailto:xxxxxx@alsa.simplelists.com]
On Behalf Of xxxxxx@improveability.com
Sent: Friday, July 8, 2016 10:15 AM
To: ALS AT Listserv <xxxxxx@alsa.simplelists.com>
Subject: How to have more natural conversations with AAC
Hello AAC peeps,
I got the following question from a PALS that I would like to get additional feedback on:
"I am now effectively at a point where people can no longer understand me when I speak, except when I use individual words like yes. no, hungry, etc. But no sentences;
they come out slow and slurred. I've taken the first step; I have a Tobii-Dynavox and am learning how to use it. But that doesn't address how to actually be part of an interchange with people and even with my wife. I feel like there's this person inside
me bottled up that can't get out.
Maybe this is just a pipe dream but Is there any good literature that is available that would help me and other people to know how to achieve this?"
I already gave him some pointers on how to facilitate AAC use, such as letting people know if it is ok to guess and waiting for him to finish. I also shared with
him some low tech options, but I would like to know others thoughts on this.
Thanks for your feedback.
Sincerely,
Antoinette Verdone, MSBME, ATP
Owner, Rehabilitation Engineer
ImproveAbility, LLC
Office: 512-522-1705
Cell: 512-497-6026
Email:
xxxxxx@improveability.com
Fax: 888-501-1009
3310 W Braker Lane, Suite 300-424, Austin TX 78758
DARS Provider# 1-274278960-0-000
"One cannot consent to creep when one has the impulse to soar" -- Helen Keller