advertisement
Reply
 
Thread Tools Display Modes
Old 08-31-2011, 09:54 AM #1
ItsWonderfulLife ItsWonderfulLife is offline
Junior Member
 
Join Date: Aug 2011
Posts: 22
10 yr Member
ItsWonderfulLife ItsWonderfulLife is offline
Junior Member
 
Join Date: Aug 2011
Posts: 22
10 yr Member
Default Does the weakness ever go away? And is it a relapse when you are?

Im new to all of this stuff and still in limbo waiting to figure out whats wrong with me, but if it does turn out to be MS i was wondering if this extreme weakness in my legs will ever subside? I used to exercise heavily daily and now its difficult to walk up a flight of stairs...Could this just be an exaserbation or is this my new norm? Thanks for any responses
ItsWonderfulLife is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Kitty (08-31-2011), SallyC (08-31-2011)

advertisement
Old 08-31-2011, 10:18 AM #2
Blessings2You's Avatar
Blessings2You Blessings2You is offline
Elder
 
Join Date: Jan 2008
Location: Vermont
Posts: 6,726
15 yr Member
Blessings2You Blessings2You is offline
Elder
Blessings2You's Avatar
 
Join Date: Jan 2008
Location: Vermont
Posts: 6,726
15 yr Member
Default

Hi there, welcome to the neighborhood!

So hard to answer that question, especially without a definite diagnosis! For me, the weakness waxes and wanes depending on the temperature, my exertion level, and who knows what else! Some days it's hard to pull myself up the steps, other days I feel almost normal. It's not the same for any two people!
__________________
*
*
*

**My flesh and my heart may fail, but God is the strength of my heart and my portion forever. (Psalm 73:26)
Blessings2You is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Catch (09-15-2011), ItsWonderfulLife (09-01-2011), Kitty (08-31-2011), SallyC (08-31-2011)
Old 08-31-2011, 10:20 AM #3
Snoopy's Avatar
Snoopy Snoopy is offline
Magnate
 
Join Date: Sep 2006
Posts: 2,280
15 yr Member
Snoopy Snoopy is offline
Magnate
Snoopy's Avatar
 
Join Date: Sep 2006
Posts: 2,280
15 yr Member
Default

Hello ItsWonderfulLife and welcome to NeuroTalk.

In regards to MS: Exercise has been shown to be beneficial. A Physical Therapist (PT) can help get you started. Weakness, for some can be improved but it can take time, effort and frustration on the part of the patient. Unfortunately, a person with MS will not know if their weakness can be improved without making an effort.

Not everyone or every case of weakness can be improved but it is important to continue exercise/PT. What exercises depends on the persons ability.
http://www.nationalmssociety.org/liv...ise/index.aspx
__________________
Dx RRMS 1984
Snoopy is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ItsWonderfulLife (09-01-2011), Kitty (08-31-2011), SallyC (08-31-2011)
Old 08-31-2011, 10:22 AM #4
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

Well, for me it's my new norm. I avoid stairs like the plague! Weakness is especially prominent in my left leg and my right arm. But......MS treats everyone differently and some may have no obvious weakness in their legs but lots of visual issues. Or no visual issues but lots of numbness and/or pain in their arms and legs. And some of us are blessed with all of it!

It's hard being in limbo and not knowing what's causing all the strange symptoms. Have you been to a Neuro that specializes in MS? What testing have you had? Sometimes it takes quite a while to narrow it down and get that diagnosis. Lots of other things mimic MS so it's not a quick process.
__________________
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:
ItsWonderfulLife (09-01-2011), SallyC (08-31-2011)
Old 08-31-2011, 10:44 AM #5
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

Welcome Itswonderfullife, nice to meet you. You have found a nice supportive place to be, while waiting for your DX.
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ItsWonderfulLife (09-01-2011)
Old 08-31-2011, 03:10 PM #6
Judy2's Avatar
Judy2 Judy2 is offline
Senior Member
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Judy2 Judy2 is offline
Senior Member
Judy2's Avatar
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Default

Hi WL and Welcome to NeuroTalk. It's good to meet you, but I really hope you won't have to be here forever.
__________________
_____________________________________________

.....Judy
SPMS -- FIBROMYALGIA -- Ouch! and Ouch!
.
Judy2 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ItsWonderfulLife (09-01-2011), SallyC (08-31-2011)
Old 09-01-2011, 12:04 PM #7
ItsWonderfulLife ItsWonderfulLife is offline
Junior Member
 
Join Date: Aug 2011
Posts: 22
10 yr Member
ItsWonderfulLife ItsWonderfulLife is offline
Junior Member
 
Join Date: Aug 2011
Posts: 22
10 yr Member
Default

Thanks everyone for welcoming me so warmly and for the replies Kitty: I have been to about 6 docs including a neuro and rhemotologist and no one seems to be able to find out whats wrong. I had an MRI with and without contrast which came back clear with no lesions and the nerve conduction tests etc. I havent had a spinal yet but im being refered to another neuro to maybe find some answers. Im not sure when I can rule out MS as being a possible cause. Its difficult because so many symptoms seem to come and go (although some stay) that its hard to talk to a doc without them looking at you like your a loon lol the first question almost every doc ive seen started by asking me what stressful situation happened when this started so im sure theyd love to chalk it up to stress and believe me i would too but i dont think its that simple Hopefully i can find an answer but its nice to be around such kind people, thanks again for your inputs
ItsWonderfulLife is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Kitty (09-01-2011), SallyC (09-01-2011)
Old 09-01-2011, 12:40 PM #8
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 Diagnostic Criteria for MS

Here's a good website explaining the McDonald Criteria and how it's used to diagnose MS:

http://www.mult-sclerosis.org/DiagnosticCriteria.html
__________________
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:
dmplaura (10-18-2011), ItsWonderfulLife (09-15-2011), SallyC (09-01-2011)
Old 09-01-2011, 11:04 PM #9
doydie's Avatar
doydie doydie is offline
Elder
 
Join Date: Aug 2006
Location: southern Indiana
Posts: 5,533
15 yr Member
doydie doydie is offline
Elder
doydie's Avatar
 
Join Date: Aug 2006
Location: southern Indiana
Posts: 5,533
15 yr Member
Default

Welcome to our family. you don't even have to behave here!!!! I agree with the others. I feel better when I can go to the Y. The silver sneakers aqua classes really help. It is surprising how many younger people you may find in there. I used to walk in the mall. My husband would make several laps as I made my one. Or at times it wasn't even one. I remember how happy it was when I could go from one end to the other, wasn't able to go back to the beginning but I was finally able to make it to one end! Make small goals and allow yourself those days when you can't do as well as the day before.
__________________

.
doydie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ItsWonderfulLife (09-15-2011), SallyC (09-02-2011)
Old 09-15-2011, 11:01 AM #10
Catch Catch is offline
Member
 
Join Date: Jan 2008
Location: Sherwood Forest
Posts: 300
15 yr Member
Catch Catch is offline
Member
 
Join Date: Jan 2008
Location: Sherwood Forest
Posts: 300
15 yr Member
Default

Hi and welcome! I wish I knew what was permanent and what isn't. The pains I know are permanent, though I don't hurt every day. But I'm not sure about lead legs. I lived practically lead-leg-free for two years after a 6 mo course of solumedrol, now its back with a vengeance! Both legs and arms too.

The standard rule of thumb for a relapse is unrelenting symtems lasting three days or more. If it keeps up you may need a trip to the neuro, and some steriods.

Good luck, and hope your dx is soon.
__________________
Relax--It only hurts until you die
.


I'm still walking upright and six feet above ground.
.
Catch is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
dmplaura (10-18-2011), ItsWonderfulLife (09-15-2011), SallyC (09-15-2011)
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
Meds and weakness zorro1 Peripheral Neuropathy 3 02-23-2011 07:10 PM
Leg weakness zorro1 Peripheral Neuropathy 10 02-14-2011 04:45 PM
Eye weakness and focusing wondergirl Myasthenia Gravis 1 10-28-2010 01:21 PM
weakness...help !!!!! mommywms Multiple Sclerosis 4 02-02-2008 07:06 PM
Arm Weakness debbiehub Reflex Sympathetic Dystrophy (RSD and CRPS) 4 05-30-2007 09:24 PM


All times are GMT -5. The time now is 01:13 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.