Hello everyone,
My PAL’s has reached the point where I’m about the only one who can understand him (and sometimes even I can’t). His hands work fine so don’t need eye gaze etc. wondering if there is a favorite easy to use voice assist device anyone loves? Hopefully one that speaks in...
Could someone explain what you need to do eyegaze and how it works? Also what are the costs involved with it?
My wife has a very noticeable change to her voice although no pain swallowing or the other bulbar symptoms. Is there a chance she won't lose her voice or is it inevitable?
Has anyone used the Speax system or something similar?
Ataiamedical dot com
PALS is now using Bipap almost all day and it’s so hard to communicate with the mask on.
Lee
The demo sounded really good. I don’t know how much work it is and if they can do anything to improve it if already impaired. For US PALS
https://bridgingvoice.org/elevenlabs/
Bridging voice which has done some good work with pals and communication is partnering with eleven labs. I believe...
I finally finished the apple personal voice. It is only 150 sentences and I think someone with no issues could knock it out in one session. I was doing a few at a time and then stopped for a while. It sounds like me but sometimes the emphasis is wrong. Still it isn’t terrible
I can use it...
You can go to Software Update on your iOS device to download it. Personal Voice is the new app that does sort of accelerated voice banking and Live Speech is an app that reads text using that voice. The early reviews are positive.
Once you have downloaded/installed iOS 17, the path to record...
About 8 months ago, I posted regarding voice changes I was noticing.
At that time I was noticing for the first time a weak, raspy, and hoarse voice, plus fatigue. Especially at the end of the day. It was very concerning because prior to that my disease course had been all limb-related...
Hi All,
I first want to thank you for the opportunity to voice my concerns as well as my apologies for any inconveniences.
To start, my symptoms began a year a ago with some twitching on my stomach. I did a quick google search and Lou Gehrig's Disease came up. At first, I quickly brushed it...
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