advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-03-2013, 08:29 AM #1
Lynn's Avatar
Lynn Lynn is offline
Member
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Lynn Lynn is offline
Member
Lynn's Avatar
 
Join Date: Sep 2006
Location: Australia
Posts: 660
15 yr Member
Default SPMS How/when do you know?

Hi everyone

This may sound like a really dumb question, but something I have often wondered about.

Is there a definitive sign that you have reached SPMS? Do you get lots more lesions, but no clear relapses - or is it a general decline - no lesions, no relapses, but lots more symptoms?

I don't have lots more lesions, but I am sure that my general capabilities and functions are on a (relatively slow) decline. I have been RRMS for 12 years now - and I may just be paranoid (but hey, that isn't a shooting offense with this stupid illness - I absolutely defy anyone to be totally calm).

My walking, weakness, vision, strength, memory, and fatigue just seem to be slowly drifting down down down.

So, do you have lots of definitive evidence in order to decide whether that progression is happening, or is it based on clinical findings?

Thanks and sorry to be a pain.

Lyn
__________________
Lyn
.



Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993.
Lynn is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
ANNagain (02-03-2013), Blessings2You (02-03-2013), jprinz99 (02-04-2013), Kitty (02-03-2013), Natalie8 (02-03-2013), SallyC (02-03-2013)
 


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
Spms? Catch Multiple Sclerosis 3 09-12-2012 04:31 PM
Spms KarenMarie Multiple Sclerosis 19 11-03-2008 07:47 PM
does RRMS always become SPMS? Rissa_TX Multiple Sclerosis 8 05-25-2008 02:19 PM
A question for those with SPMS plum tuckered Multiple Sclerosis 3 03-11-2008 01:15 PM
Possible new tx for SPMS wannabe Multiple Sclerosis 17 05-07-2007 09:03 AM


All times are GMT -5. The time now is 06:31 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.