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Communication options | ![]() | ||
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Posted by: sfraz ® 07/16/2011, 19:52:08 |
What helps you communicate other than botox and writing notes? Does anyone use sign language? How did you and family learn? Is there voice amplification equipment to increase sound of whisper? Is there a computer application that can talk for me? Any tips on communicating at social events? Does SD continue to get progressively worse as you age? |
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Re: Communication options -- sfraz | Top of thread | Archive |
Posted by: baystater ® 07/16/2011, 23:07:57 |
I got this information from the National Spasmodic Dysphonia Assocation some time ago but think it is still valid:..warning: This is a long note.
Telecommunication Options
For those living with spasmodic dysphonia, the obstacles of working around a voice disorder are all too familiar, and the phone can be a particularly difficult one. There are options out there to assist vocal impairments via specialized telecommunications equipment and phone assistance programs. The Telecommunications Equipment Distribution Program Association (TEDPA) provides an immensely useful online directory for assisting people with voice disorders. This includes a listing of state-specific equipment distribution programs. The type of equipment that's distributed are TTYs (text telephones), amplified phones, large visual displays, hands free speaker phones, talking phones, and captioned telephones. Living and working with spasmodic dysphonia can be made easier with these products designed to help individuals with vocal impairments. For more information, log on to: http://www.tedpa.org/. Non-Operator Assisted Resources Telephone Access Programs
Other programs, such as the California Telephone Access Program (CTAP), have an equipment loan program and the equipment is on loan to the person at no cost. If a voucher program is not available in a particular state, equipment companies may be able to process the purchase through Medicare, Medicaid, and even some managed care insurances. Sifting through all the retailers in one’s state to find those which collaborate with assistive programs can be an arduous and time-consuming task but TEDPA has a state directory of vendors who offer this equipment.
Sitris
The Speech Assistant
Operator-Assisted Resources Telecommunications Relay Service
The following is a step-by-step guide to using TRS to communicate with people. A relay call can be made by TTY, Internet Relay Service, Video Relay Service, or Speech to Speech Relay Service. A relay call can include Voice Carryover ( VCO ) and Hearing Carryover ( HCO ) service. While there is usually no cost for the use of these services, there may be local and long distance charges for the phone call. For more information on these services in your state, log on to: http://www.tedpa.org/.
Relay Calls On-line
Relay Call via AT&T and AIM
Relay Calls Via Phone
TTY Relay Service
In this call type, typed messages are relayed as voice messages by a TRS (Telecommuctions Relay Service) operator (also known as Communication Assistant (CA), Relay Operator (RO), Relay Assistant (RA)or Relay Agent (Agent) ), and vice-versa. This allows callers unable to use a regular telephone, to be able to place telephone calls to people who use a regular telephone, and vice-versa. When the person who is Hearing is ready for a response, it is customary to say "Go Ahead" or "GA" to indicate that it is the TTY user's turn to talk and "Stop Keying", "SK", or "Ready to hang up" when hanging up, and vice-versa. From standard telephone to TTY:
From TTY to standard telephone:
Hearing Carry Over Relay (HCO)
1. For HCO Relay Service, dial711.
Speech To Speech Relay Service (STS)
Dialing 9-1-1
Disclaimer: The National Spasmodic Dysphonia Association only provides information about these services and products and is not recommending or promoting any one product. |
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Posted by: Renee ® 07/17/2011, 09:23:26 |
I think Mel gave you a very long and detailed explanation, which I will not add to...To answer the last part of your question...My SD HAS gotten worse as I've aged, but I've had it since, probably, high school...Some people's gets better...Like with everything with SD, everyone is different...
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Posted by: irish ® 07/21/2011, 21:32:23 |
Hi there,
Communication is a biggie. Prior to SLAD-R surgery, I did all sorts of things like drop initial letters of words that gave me trouble. I would answer the phone, 'ello. I used all kinds of gestures to get me through conversations or pointed to things. Gestures are great. After surgery I found that I had developed a lot of compensating speech habits that were actually bad, so I picked up some great speech therapy awareness tips and exercises in case you are doing some of those things, like holding your breath or talking on residual air. Email me if you'd like a list of those strategies: trish0@dslextreme.com |
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Posted by: faithrea ® 07/28/2011, 15:51:57 |
I have been learning sign language. I have been taking a course at a local church, which is great. I also go on line a lot to signing savy or ASL pro. This are great sites that can help you learn a lot. |
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