Parkinson's Disease Tulip


advertisement
Reply
 
Thread Tools Display Modes
Old 08-24-2013, 02:03 AM #1
e-barua@hotmail.com's Avatar
e-barua@hotmail.com e-barua@hotmail.com is offline
New Member
 
Join Date: Aug 2013
Posts: 3
10 yr Member
e-barua@hotmail.com e-barua@hotmail.com is offline
New Member
e-barua@hotmail.com's Avatar
 
Join Date: Aug 2013
Posts: 3
10 yr Member
Question PD and VOICE

One on the long list of PD symptoms is change in voice. Has any one dealt with that?:
e-barua@hotmail.com is offline   Reply With QuoteReply With Quote

advertisement
Old 08-24-2013, 03:38 PM #2
Jomar's Avatar
Jomar Jomar is offline
Co-Administrator
Community Support Team
 
Join Date: Aug 2006
Posts: 27,687
15 yr Member
Jomar Jomar is offline
Co-Administrator
Community Support Team
Jomar's Avatar
 
Join Date: Aug 2006
Posts: 27,687
15 yr Member
Default

Dad's voice gets soft & weak at times.

Did you want your email showing as username?

Post back or use the contact us @ bottom of page if not.
__________________
Search NT -
.
Jomar is offline   Reply With QuoteReply With Quote
Old 08-24-2013, 04:02 PM #3
slashman48's Avatar
slashman48 slashman48 is offline
Junior Member
 
Join Date: Feb 2013
Posts: 77
10 yr Member
slashman48 slashman48 is offline
Junior Member
slashman48's Avatar
 
Join Date: Feb 2013
Posts: 77
10 yr Member
Default

Undiagnosed, but think I found a movement disorder specialist about 50 miles away, which I might make an appointment with. Anyway I do have weak/soft voice issues. Along with not being able to whistle anymore. Also keep rubbing my thumb & finger, open/closing right hand all the time and walk slow & flat-footed, especially when turning.
slashman48 is offline   Reply With QuoteReply With Quote
Old 08-26-2013, 05:16 PM #4
ParkiWife ParkiWife is offline
Junior Member
 
Join Date: Aug 2013
Location: So California
Posts: 8
10 yr Member
ParkiWife ParkiWife is offline
Junior Member
 
Join Date: Aug 2013
Location: So California
Posts: 8
10 yr Member
Default PD and voice

Quote:
Originally Posted by e-barua@hotmail.com View Post
One on the long list of PD symptoms is change in voice. Has any one dealt with that?:
One of my friends who has PD, and has had two DBS, has a problem speaking. Both the ability and the volume have been affected. He was told it was because they passed thru the speech center of the brain while performing his DBS. The docs are considering botox injections on the vocal chords to help him.

My husband with PD has more trouble because he mumbles, perhaps more from never being able to stand up straight, and his voice goes straight down to the floor. My favorite word now is, "What?".

It's frustrating, I know. As our friend says, "Can't walk. Can't talk. Can't pee. Can't see. What next?".

Gotta keep laughing!
ParkiWife is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
slashman48 (08-26-2013)
Old 11-09-2013, 02:50 PM #5
slashman48's Avatar
slashman48 slashman48 is offline
Junior Member
 
Join Date: Feb 2013
Posts: 77
10 yr Member
slashman48 slashman48 is offline
Junior Member
slashman48's Avatar
 
Join Date: Feb 2013
Posts: 77
10 yr Member
Smile

Diagnosed 10/25/13 with Parkinson's Disease by MDS. Am on Carbidopa-Levodopa which has made a remarkable difference. It was a big relief just getting a diagnosis. Am also setting up appointments with speech, physical & occupational therapy. He also wants me to have a swallow test done. Feel better than I've had in at least a year or two.
slashman48 is offline   Reply With QuoteReply With Quote
Old 11-09-2013, 06:52 PM #6
Rob Rob is offline
Junior Member
 
Join Date: Oct 2013
Location: North New Jersey, USA
Posts: 21
10 yr Member
Rob Rob is offline
Junior Member
 
Join Date: Oct 2013
Location: North New Jersey, USA
Posts: 21
10 yr Member
Default

Quote:
Originally Posted by e-barua@hotmail.com View Post
One on the long list of PD symptoms is change in voice. Has any one dealt with that?:
I noticed my voice has changed. (More hoarse, most of the time.)
So far, not dealing with it at all...

Rob.
Rob is offline   Reply With QuoteReply With Quote
Old 07-03-2014, 09:39 AM #7
jenndcody jenndcody is offline
New Member
 
Join Date: Jul 2014
Location: Dallas, TX
Posts: 4
8 yr Member
jenndcody jenndcody is offline
New Member
 
Join Date: Jul 2014
Location: Dallas, TX
Posts: 4
8 yr Member
Default Speech difficulty common with PD

Hello! I am a speech-language pathologist that specializes in helping people with Parkinson's with their speech.

Voice changes are very common with Parkinson's. About 89% of people diagnosed will experience some changes in their voices... common symptoms are soft, weak voices, hoarseness, slurred speech, and monotone speech.

The good news is that speech differences are typically very responsive to therapy! Vocal exercises coupled with practice with using strategies while speaking can make a huge difference in the strength, quality, and intelligibility of speech. Seek the help of a speech-language pathologist who has experience treating people with Parkinson's so they can guide you in developing an exercise program and teach you strategies to improve your speech.

I use a treatment program called SPEAK OUT! that was developed at the organization I work for, Parkinson Voice Project. We have trained therapists all over the United States to help people with Parkinson's... there may be a trained therapist in your area.
jenndcody is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
badboy99 (07-04-2014)
Old 07-05-2014, 06:43 AM #8
Aunt Bean's Avatar
Aunt Bean Aunt Bean is offline
Member
 
Join Date: Sep 2009
Location: East TN
Posts: 782
10 yr Member
Aunt Bean Aunt Bean is offline
Member
Aunt Bean's Avatar
 
Join Date: Sep 2009
Location: East TN
Posts: 782
10 yr Member
Default

My voice definitely changes according to my level of l-dopa in my system. Guess I do my own therapy...sing as much as I can.When low in l-dopa, voice is lower pitch and cracks when I sing...sounds lousy. When l-dopa is a good level and I am not under any stress to perform, my voice goes back to where it was in 7th grade before my diving acccident..a very nice tone/ relaxed and a higher range. Humming at times seems to help . Making very loud Lion-type yawns. Also patting face and massaging face and neck to try to keep muscles more functional...lots of neck stretching. Got to keep everything mobile.
Aunt Bean is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Lana (07-05-2014)
Old 07-07-2014, 03:59 PM #9
jenndcody jenndcody is offline
New Member
 
Join Date: Jul 2014
Location: Dallas, TX
Posts: 4
8 yr Member
jenndcody jenndcody is offline
New Member
 
Join Date: Jul 2014
Location: Dallas, TX
Posts: 4
8 yr Member
Default

Quote:
Originally Posted by Aunt Bean View Post
My voice definitely changes according to my level of l-dopa in my system. Guess I do my own therapy...sing as much as I can.When low in l-dopa, voice is lower pitch and cracks when I sing...sounds lousy. When l-dopa is a good level and I am not under any stress to perform, my voice goes back to where it was in 7th grade before my diving acccident..a very nice tone/ relaxed and a higher range. Humming at times seems to help . Making very loud Lion-type yawns. Also patting face and massaging face and neck to try to keep muscles more functional...lots of neck stretching. Got to keep everything mobile.
Regular exercise like singing is great! We have a singing group at our clinic for our PWP to get good exercise for their voices.

One important note tho, it's always a good idea to get an evaluation from a professional as there is a sensory awareness component involved in speech disorders with PD, meaning that the PWP is not always aware of the extent of changes in the voice. Getting an objective eval will help you know that you're doing everything you can do!
jenndcody is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Your voice? Anacrusis Myasthenia Gravis 11 10-29-2012 03:21 AM
TV: The Voice Jomar Books, Movies, Music and TV Talk 3 05-26-2011 10:04 AM
Man With No Voice Has A Lot To Say BobbyB ALS News & Research 1 11-15-2008 12:53 AM
Voice weakness! Megan Peripheral Neuropathy 1 02-28-2008 07:40 AM
A voice all their own BobbyB ALS News & Research 0 02-24-2008 08:31 AM


All times are GMT -5. The time now is 07:21 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.