advertisement
Reply
 
Thread Tools Display Modes
Old 05-29-2009, 07:00 PM #11
Kitty's Avatar
Kitty Kitty is offline
Wisest Elder Ever
 
Join Date: Jan 2008
Location: Deep South
Posts: 21,576
15 yr Member
Kitty Kitty is offline
Wisest Elder Ever
Kitty's Avatar
 
Join Date: Jan 2008
Location: Deep South
Posts: 21,576
15 yr Member
Default

My right hand has been numb now for a couple of years. Recently (well, within the last 6 months) it's begun aching and then I get the "zaps" that feel like an electric shock. But, I have gotten back some use of that hand even though it's still numb. I still haven't figured out how something can be numb and hurt at the same time.
__________________
These forums are for mutual support and information sharing only. The forums are 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.
Kitty is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Friend2U (05-29-2009), SallyC (05-29-2009)

advertisement
Old 05-29-2009, 09:06 PM #12
ewizabeth's Avatar
ewizabeth ewizabeth is offline
Elder
 
Join Date: Sep 2006
Location: northern Illinois
Posts: 5,258
15 yr Member
ewizabeth ewizabeth is offline
Elder
ewizabeth's Avatar
 
Join Date: Sep 2006
Location: northern Illinois
Posts: 5,258
15 yr Member
Default

I've had instances of days when I'd be walking with excruciating shooting pains in my legs, then later in the day it would be numbness, and around it goes. I think it just depends on whatever sensation the brain wants to "read" from stress or whatever. You know what I mean, the crazy miscommunication of the signals.

It's happened in different areas too, hands, feet, arms, etc...
__________________
Wiz

Turn Left at the next election.
.


RRMS DX 01/28/03 Started Copaxone again on 12/09/09
ewizabeth is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Friend2U (05-29-2009), SallyC (05-29-2009)
Old 05-29-2009, 10:47 PM #13
Erin524's Avatar
Erin524 Erin524 is offline
Elder
 
Join Date: Dec 2007
Posts: 5,020
15 yr Member
Erin524 Erin524 is offline
Elder
Erin524's Avatar
 
Join Date: Dec 2007
Posts: 5,020
15 yr Member
Default

Quote:
Originally Posted by SallyC View Post
Boy, you really have to be careful with the way you say things here...My Bad.

Not everyone automatically progresses from RRMS to SPMS. I believe I said that is the usual way it happens. Noone's MS is the same as another's.

Usually when your relapses stop and you have lasting SX with more spasticity(pain), you have, more than likely, progressed to SPMS. That is the way it happened for me and I believe that is the way it happens for most..not all, RRMSers.

So Sorry, Friend2U, if I didn't make myself clear.
I dont think she was originally asking about how you progress from one form of MS to another, I think she was asking about the particular symptom (at least that's how I read her question) and how you can go from being numb to having the normal feeling back and how it comes back...does it go from numbness to pain to normalishness.
__________________
~ Never do anything that you wouldn't want to explain to the paramedics. ~ Author Unknown ~

~ "Animals have two functions in society. To taste good and to fit well." ~ Greg Proops, actor ~
Erin524 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Friend2U (05-29-2009)
Old 05-29-2009, 10:56 PM #14
Friend2U's Avatar
Friend2U Friend2U is offline
Senior Member
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Friend2U Friend2U is offline
Senior Member
Friend2U's Avatar
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Default Cherie,

Quote:
Originally Posted by lady_express_44 View Post
When I have had a spinal lesion attack, it has started with numbness/tingling in my feet, and by the time it gets to my knees, the burning, aching, swollen feeling and "shocks" get in on the party. It goes up my body like that, until it stops where it wants to . . . and the rest of the sensations do too.

When I recover, it occurs generally in the same order that it came on, bit by bit.

SPMS implies that this is not a relapse (or it is one of your last relapses, as relapses eventually stop with SPMS). I don't think there is any indication you are in this category, because you are still relapsing. If you are ultimately left with many of these ongoing symptoms, ii.e. you don't recover much from this attack, then you might start contemplating that you are advancing to SPMS. It is premature to think that way now though.

If this attack runs it's full course, you may find that the numbness and other sensations continue to climb, to the level where the spinal lesion must be. IF this happens, these attacks seem to escalate over 4 - 6 weeks, and most of the recovery occurs over the following 4 - 6 weeks.

I hope this stays in your feet/legs though ... which can happen depending on where the lesion is.

Keep us updated, won't you?

Cherie
Thank you for the explanation. I seem to stay a little confused about it all. But this makes some sense to me.

I've never had a spinal mri. And I maybe don't fill in my neuro enough at my check ups. Because I'm so glad I haven't had a really bad attack to land me in the hospital since a year ago. So I guess I figure some of this stuff isn't as important. But then as it gets worse I wonder if I should have mentioned it or if it just doesn't matter. It's hard to not really have any control over it.

I can tell though that my feet have become quite numb and hurt more and it has moved up to my knees. It has all been VERY gradual it seems. Nothing sudden. Also my hands and arms are becoming numb where they use to just tingle.

Something else that is getting worse is when I move my head down, I have burning go down my entire body. I use to think it was disc problems in my neck, but I really don't know if it is.

Boy, I better shut up this whining!
__________________
~ Friend2U
.


.

HANG IN THERE!

If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici

MS/dx2006
BETASERON (Quit May 2011)
COPAXONE (Began June 2011)
Friend2U is offline   Reply With QuoteReply With Quote
Old 05-29-2009, 11:02 PM #15
Friend2U's Avatar
Friend2U Friend2U is offline
Senior Member
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Friend2U Friend2U is offline
Senior Member
Friend2U's Avatar
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Default

Quote:
Originally Posted by SallyC View Post
Boy, you really have to be careful with the way you say things here...My Bad.

Not everyone automatically progresses from RRMS to SPMS. I believe I said that is the usual way it happens. Noone's MS is the same as another's.

Usually when your relapses stop and you have lasting SX with more spasticity(pain), you have, more than likely, progressed to SPMS. That is the way it happened for me and I believe that is the way it happens for most..not all, RRMSers.

So Sorry, Friend2U, if I didn't make myself clear.
lol Not a problem!!! No apology needed. I can't remember today if I was confused yesterday, but if I was you didn't cause it!I keep myself confused enough for everybody!

I just so appreciate the responses. I don't really have anyone in my 'real world' to talk to about it, or at least who is experienced it. So I appreciate getting to talk to the cyber world!!!!
Thanks.
__________________
~ Friend2U
.


.

HANG IN THERE!

If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici

MS/dx2006
BETASERON (Quit May 2011)
COPAXONE (Began June 2011)
Friend2U is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
AfterMyNap (05-30-2009), SallyC (05-30-2009)
Old 05-29-2009, 11:06 PM #16
Friend2U's Avatar
Friend2U Friend2U is offline
Senior Member
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Friend2U Friend2U is offline
Senior Member
Friend2U's Avatar
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Default

Quote:
Originally Posted by Kitty View Post
... I still haven't figured out how something can be numb and hurt at the same time.
Isn't that the truth?! It doesn't make much sense, but it sure happens doesn't it?!

Lucky for us....Misery loves company! Just kidding!
__________________
~ Friend2U
.


.

HANG IN THERE!

If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici

MS/dx2006
BETASERON (Quit May 2011)
COPAXONE (Began June 2011)
Friend2U is offline   Reply With QuoteReply With Quote
Old 05-29-2009, 11:08 PM #17
Friend2U's Avatar
Friend2U Friend2U is offline
Senior Member
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Friend2U Friend2U is offline
Senior Member
Friend2U's Avatar
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Default Wiz,

Quote:
Originally Posted by ewizabeth View Post
I've had instances of days when I'd be walking with excruciating shooting pains in my legs, then later in the day it would be numbness, and around it goes. I think it just depends on whatever sensation the brain wants to "read" from stress or whatever. You know what I mean, the crazy miscommunication of the signals.

It's happened in different areas too, hands, feet, arms, etc...
I hadn't thought of it that way, but it makes as much sense as anything!
__________________
~ Friend2U
.


.

HANG IN THERE!

If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici

MS/dx2006
BETASERON (Quit May 2011)
COPAXONE (Began June 2011)
Friend2U is offline   Reply With QuoteReply With Quote
Old 05-29-2009, 11:12 PM #18
Erin524's Avatar
Erin524 Erin524 is offline
Elder
 
Join Date: Dec 2007
Posts: 5,020
15 yr Member
Erin524 Erin524 is offline
Elder
Erin524's Avatar
 
Join Date: Dec 2007
Posts: 5,020
15 yr Member
Default

Quote:
Originally Posted by Friend2U View Post
Thank you for the explanation. I seem to stay a little confused about it all. But this makes some sense to me.

I've never had a spinal mri. And I maybe don't fill in my neuro enough at my check ups. Because I'm so glad I haven't had a really bad attack to land me in the hospital since a year ago. So I guess I figure some of this stuff isn't as important. But then as it gets worse I wonder if I should have mentioned it or if it just doesn't matter. It's hard to not really have any control over it.

I can tell though that my feet have become quite numb and hurt more and it has moved up to my knees. It has all been VERY gradual it seems. Nothing sudden. Also my hands and arms are becoming numb where they use to just tingle.

Something else that is getting worse is when I move my head down, I have burning go down my entire body. I use to think it was disc problems in my neck, but I really don't know if it is.

Boy, I better shut up this whining!
The burning when you move your head down is probably L'hermitte's sign (Lear-meets is how my neuro pronounced it) I've had that before from a lesion in my neck.
__________________
~ Never do anything that you wouldn't want to explain to the paramedics. ~ Author Unknown ~

~ "Animals have two functions in society. To taste good and to fit well." ~ Greg Proops, actor ~
Erin524 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Friend2U (05-29-2009)
Old 05-29-2009, 11:16 PM #19
Friend2U's Avatar
Friend2U Friend2U is offline
Senior Member
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Friend2U Friend2U is offline
Senior Member
Friend2U's Avatar
 
Join Date: Jan 2008
Location: Great Midwest, USA
Posts: 1,370
15 yr Member
Default

Quote:
Originally Posted by Erin524 View Post
The burning when you move your head down is probably L'hermitte's sign (Lear-meets is how my neuro pronounced it) I've had that before from a lesion in my neck.
Thanks Erin. I think I will mention this next visit at the neuro's. I was wondering how that was pronounced...so thanks!
__________________
~ Friend2U
.


.

HANG IN THERE!

If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici

MS/dx2006
BETASERON (Quit May 2011)
COPAXONE (Began June 2011)
Friend2U is offline   Reply With QuoteReply With Quote
Old 05-30-2009, 12:39 PM #20
AfterMyNap's Avatar
AfterMyNap AfterMyNap is offline
Wise Elder
 
Join Date: May 2007
Location: Right here. Duh.
Posts: 9,213
15 yr Member
AfterMyNap AfterMyNap is offline
Wise Elder
AfterMyNap's Avatar
 
Join Date: May 2007
Location: Right here. Duh.
Posts: 9,213
15 yr Member
Default

Friend, the most fun part of this disease is all the unanswered questions. Like Sal said, there is no designated or natural path for every case. That means that you're special.

I strongly recommend that you at least call this in to your neuro, tracking your symptoms is very important to the overall treatment your neuro can offer you.

Having had both neuropathic pain and profound numbness, I can tell you for sure, the pain is no picnic and I hope it doesn't come to that for you.

Like Cherie pointed out, many MS patients have relapses that put symptoms into action on a temporary basis. Sometimes, after a relapse, those symptoms remain, in smaller proportions.

When/if the SP factor appears to be the case, the relapses cease for the most part and a slower, steadier decline takes over. Not all RR patients become SP patients.

The buzzing sensation in your neck is probably L'hermittes and it is pronounced, luh-herm-i-tease by the three doctors with whom I've discussed it.



Quote:
Originally Posted by Erin524 View Post
I dont think she was originally asking about how you progress from one form of MS to another, I think she was asking about the particular symptom (at least that's how I read her question) and how you can go from being numb to having the normal feeling back and how it comes back...does it go from numbness to pain to normalishness.
Holy cow!
__________________
—Cindy

For every day I choose to play,
I set aside a day to pay.
—AMN


"Sometimes plastic wrap just won't cling, no matter how much money you put in the meter."

—From the Book of True Wizdom
AfterMyNap is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Friend2U (05-31-2009), pud's friend (05-30-2009), SallyC (05-30-2009)
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
Burning/tingling pain barb02 Multiple Sclerosis 7 06-25-2009 06:56 PM
Tingling and Numbness Evonne Parkinson's Disease 3 10-13-2008 01:05 PM
tingling with coldness ssteague Peripheral Neuropathy 7 09-01-2008 10:46 PM
**** tingling tongue! neuromess Multiple Sclerosis 3 06-01-2008 03:57 PM
Tingling optimumeg Peripheral Neuropathy 11 05-07-2007 01:24 PM


All times are GMT -5. The time now is 01:47 PM.

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.