ALSFORUMS.COM   - ALS/MND Support Group   - Fibromyalgia Support Group   - PLS Support Group   - PBP Support Group   - PMA Support Group   -  
Old 11-25-2007, 04:59 PM   #1 (permalink)
New Member (Say Hi)
Registered Member
Join Date: 2007
City: nc
State: nc
Country: usa
Diagnosed: 00/0000
Posts: 56
peanut78 is on a distinguished road
Unhappy Hand Twitch/Speech slurring

I'm really freaking out now. I have had this hand twitch off and on for a week now. It's on the top of my hand between my thumb and index finger. It started about a week ago, then stopped for a couple of days. Now it's lasted all last night (even in my sleep) and today. Does this sound like an ALS twitch? Would it be off and on like this? I started out with twitching everywhere and now more localized twitches. I'm so scared and don't know what to do.

I also feel like I've had speech slurring today. Would I already be having all of these symptoms suddenly at once?

peanut78 is offline  

Old 11-26-2007, 03:52 PM   #2 (permalink)
Al
Extremely Helpful Member
Registered Member
 
Al's Avatar
Join Date: 2004
City: NW of Toronto
State: On
Country: CAN
Diagnosed: 10/2003
Posts: 8,020
Al is on a distinguished road
Send a message via Yahoo to Al Send a message via Skype™ to Al
Default

How do you know it lasted all night, even in your sleep? Have you tried tape recording your voice when you think you are slurring and playing it back for others to see if they notice it?
AL.
Al is offline  
Old 11-26-2007, 03:58 PM   #3 (permalink)
New Member (Say Hi)
Registered Member
Join Date: 2007
City: nc
State: nc
Country: usa
Diagnosed: 00/0000
Posts: 56
peanut78 is on a distinguished road
Default

Hi Al,
Thank you for replying. Yes, I could feel it twitch even in my sleep. It is still twitching today, so it's been about 2 days now. It's kind of an off and on twitch. It won't twitch for a while, then it will twitch about 20 times in minute. Is that odd?
As far as the slurring, I think that's all in my head. No one has noticed it, and I think it would be very uncommon to have all of these symptoms, all of a sudden. I have a lot of anxiety about my health, and this has by far been the worst ever. I tried to get another appt with my neuro and they don't have an opening until Jan 30! I can't wait that long, I will go insane. Any suggestions? Thank you!
peanut78 is offline  
Old 11-26-2007, 04:05 PM   #4 (permalink)
Al
Extremely Helpful Member
Registered Member
 
Al's Avatar
Join Date: 2004
City: NW of Toronto
State: On
Country: CAN
Diagnosed: 10/2003
Posts: 8,020
Al is on a distinguished road
Send a message via Yahoo to Al Send a message via Skype™ to Al
Default

Well, anti anxiety meds might help. Starting and stopping twitching is not common with ALS as a rule. Once the muscle starts to twitch it is usually 24/7. My wife would see me twitching in my sleep so that's how I know that.
A whole lot of symptoms don't usually come quickly together.
AL.
Al is offline  
Old 11-26-2007, 04:06 PM   #5 (permalink)
Very Helpful Member
Registered Member
Join Date: 2007
City: philadelphia
State: pennsylvania
Country: united states
Posts: 1,227
crystalkk is on a distinguished road
Default

Peanut,

I was just reading somewhere , the most common places for muscle twitches in normal people
are in the hand between the thumb and index finger and in the foot. They named a couple of other spots
which are common I think the eyelid was listed. I can't remember where I read it for the life of me.
If I come across it again I will send it to you.
crystalkk is offline  
Old 11-26-2007, 04:18 PM   #6 (permalink)
New Member (Say Hi)
Registered Member
Join Date: 2007
City: nc
State: nc
Country: usa
Diagnosed: 00/0000
Posts: 56
peanut78 is on a distinguished road
Default

Thanks you Crystal. That makes me feel a little better. But is it normal to last for this long? I had an EMG 2 weeks into twitching, which didn't show anything, but I feel I got it done too early asmany people here have had normal initial EMGs.
peanut78 is offline  
Old 11-26-2007, 05:08 PM   #7 (permalink)
Very Helpful Member
Registered Member
Join Date: 2007
City: philadelphia
State: pennsylvania
Country: united states
Posts: 1,227
crystalkk is on a distinguished road
Default

Peanut,

Anxeity, stress, and caffiene can all cause muscle twitching or make it worse.
Are you taking anything for anxiety?
Do you have anyother symtoms beside twitching?

MY nickname used to be Peanut.
crystalkk is offline  
Old 11-26-2007, 05:34 PM   #8 (permalink)
New Member (Say Hi)
Registered Member
Join Date: 2007
City: nc
State: nc
Country: usa
Diagnosed: 00/0000
Posts: 56
peanut78 is on a distinguished road
Default Thank you Crystal and Al!

Al,
When you say twitching with ALS is usually 24/7, and doesn't stop and start, what exactly do you mean? Do you mean that it's a non-stop pattern? Or would a twitch be all day, but a few times a minute, hour? thanks!
peanut78 is offline  
Old 11-26-2007, 05:49 PM   #9 (permalink)
Al
Extremely Helpful Member
Registered Member
 
Al's Avatar
Join Date: 2004
City: NW of Toronto
State: On
Country: CAN
Diagnosed: 10/2003
Posts: 8,020
Al is on a distinguished road
Send a message via Yahoo to Al Send a message via Skype™ to Al
Default

Mine would look like a bag of worms wriggling under the skin. It would be a ripple every few seconds.
AL.
Al is offline  
Old 11-26-2007, 06:04 PM   #10 (permalink)
New Member (Say Hi)
Registered Member
Join Date: 2007
City: nc
State: nc
Country: usa
Diagnosed: 00/0000
Posts: 56
peanut78 is on a distinguished road
Default

Hmmm. I'm not sure my twitches look that way. Mine are more like a flutter or heartbeat. Thank you Al!
peanut78 is offline  
Old 11-26-2007, 08:36 PM   #11 (permalink)
Member
Registered Member
Join Date: 2007
City: Cardiff
State: Wales
Country: UK
Diagnosed: 10/2007
Posts: 164
Steve100 is on a distinguished road
Default

My mother say's the same, that her twitches are like 'heartbeats', and I certainly don't think its 24/7. She's been diagnosed with ALS. I wish I knew what on earth was going on
Steve100 is offline  
Old 11-27-2007, 07:54 PM   #12 (permalink)
Member
Registered Member
Join Date: 2007
City: Cardiff
State: Wales
Country: UK
Diagnosed: 10/2007
Posts: 164
Steve100 is on a distinguished road
Default

How common are fasciculations with MND? Are they just a pointer towards it, or is the absence of these a sign that you are unlikely to have it?

Thanks

Steve
Steve100 is offline  
Old 11-27-2007, 07:59 PM   #13 (permalink)
Member
Registered Member
Join Date: 2007
City: Seagoville
State: Texas
Country: US
Diagnosed: 07/2007
Posts: 155
delb is on a distinguished road
Default

I have always had fasciculations all my life. And had problems building muscles no matter how much I did to build muscle. Makes me think I have been fighting off ALS all my life. This was long before my mother died of this horrible disease. This is also why the fasciculations I have now don't bother me. I have overcame the feeling long ago.
delb is offline  
Old 11-27-2007, 08:01 PM   #14 (permalink)
Moderator
Registered Member
Join Date: 2006
City: Anytown
State: New England
Country: USA
Diagnosed: 00/0000
Posts: 3,559
CindyM is on a distinguished road
Default

A lot of conditions cause twitching. It is common with ALS but other signs must be there too before they can say for sure it is MND. Most ocnditions that have twitching are treatable. Some people just twitch. That is called BFS and that is what everyone wants to have because it is completely benign.
CindyM is offline  
Old 11-27-2007, 08:14 PM   #15 (permalink)
Member
Registered Member
Join Date: 2007
City: Cardiff
State: Wales
Country: UK
Diagnosed: 10/2007
Posts: 164
Steve100 is on a distinguished road
Default

Hi Cindy, the doctors have diagnosed my Mother with MND, and though she does have a few twitches, they are not very frequent and have more of a 'pulsing' rather than a 'rippling' appearance. If only things could be straightforward eh?

Thanks

Steve

Steve100 is offline  
Closed Thread

Tags
als, night, scared, sleep, speech, symptoms, twitch, twitches, twitching


Currently Active Users Viewing This Thread: 1 (0 members and 1 guests)
 
Thread Tools


Similar Threads for: Hand Twitch/Speech slurring
Thread Thread Starter Forum Replies Last Post
fasciculations in hand kristine21 Do I Have ALS? Is This ALS? 4 10-21-2007 06:19 PM
Index finger twitch RAidanM General Discussion About ALS/MND 4 10-16-2007 05:58 AM
Slurring Speech LONGSAM2 People With ALS - "PALS" 13 04-25-2007 11:14 AM
The solution about ALS is only in your hand kirsten General Discussion About ALS/MND 2 05-08-2005 08:36 PM


    
   
   
   
   
  ALSforums - Get help and support with ALS/MND