RE: AAC Help antoinette@xxxxxx (15 May 2017 09:54 EDT)
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Re: AAC Help
Jacqueline Gaddis
(15 May 2017 14:26 EDT)
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Kelly, Welcome to the group! I feel for you and appreciate your diligence in wanting to provide the best service for your ALS patients. It is a steep hill to climb, but keep at it! My advice with specific regard to AAC equipment would be to contact all of the eye gaze reps in your area. When it comes to high tech/eye gaze AAC, support is king. Find out which reps will provide good support as this will take some work off of your plate - at least while you work on the other needs. They should also help with any insurance paperwork and provide some templates that you can work off of - it is always intimidating starting with a blank piece of paper. I will let other respond with regard to your other questions, but I would say in my experience, with cognitive intact, literate adults - getting to the point where the PALS is using their device for communication is not a long process - it is more of a function of providing proper access. Once that is established, it is typically not a long process to get communicating - unless you are dealing with some sort of unusual eye issue. Also, as the patients progress, additional support may be needed to help maintain access. This is why early introduction is so important. This way you know that the person understands the system, and you can focus on addressing access issues. Along those lines, you may want to get an OT involved to assist with the access piece - more heads are always better. If it is at all possible, visiting a well established ALS clinic would be of great value - seeing how others have solved these problems will save you a TON of time and effort. Attending ALS conferences and staying connected with the organization is helpful - they have webinars on a regular basis and often address AAC needs - here is a link to the archived ones - http://www.alsa.org/als-care/resources/webinars.html Sincerely, Antoinette Verdone, MSBME, ATP Owner, Rehabilitation Engineer ImproveAbility, LLC Office/Text: 512-522-1705 Cell: 512-497-6026 Email: xxxxxx@improveability.com Web: www.improveability.com Fax: 888-501-1009 3310 W Braker Lane, Suite 300-424, Austin TX 78758 "One cannot consent to creep when one has the impulse to soar" -- Helen Keller Follow Us -------- Original Message -------- Subject: AAC Help From: "Mangione, Kelly" <xxxxxx@SITRIN.com> Date: Sat, May 13, 2017 2:45 pm To: "'xxxxxx@alsa.simplelists.com'" <xxxxxx@alsa.simplelists.com> Hello, I am fairly new to the world of ALS as well as have limited background with AAC. The following topics/questions come to mind: Eye gaze technology: Are there any statistics on rate of use with an eye gaze device (i.e., similar to how many wpm one can type)? Also any thoughts on how long it typically takes a patient to learn how to efficiently use an eye gaze device for basic communicate needs? We have had good luck borrowing eye gaze devices from the local ALS association. Other AAC Options: I am working on an inpatient unit so obtaining new devices is not easy as well as not always time efficient by the time a patient requires care 24/7. In simple terms (remember-I’m a newbie J), what are some favorite quick, effective, and cost friendly communication options that could be purchased to have on hand? I’m also struggling with AAC options that work well with our cognitively impaired ALS patients so thoughts are welcomed. For verbal patients with no bulbar symptoms when should AAC be introduced-again in an ideal world I understand sooner is better but with limited resources, limited staffing, limited staff experience, and varying cognitive statuses I’m trying to prioritize the best I can. I’m trying to understand the norms to help support our staffing needs, set realistic goals for treatment as well as daily time management. Ugh and goals-that is hard to measure too. I am trying to be proactive and do my “homework” but the info is limited in some regards, requires you to be very tech savvy and/or is put in terms of an ideal situations/settings such as being able to have access to all AAC options and/or having time to dedicate the whole work day to ALS and AAC. I greatly appreciate any information, resources, etc that anyone is willing to share. Thank you, Kelly Kelly Mangione, MS, CCC-SLP Speech-Language Pathologist Charles T. 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