Home Menu

Site Navigation



NeuroTalk Support Groups > > >

SPMS How/when do you know?

Reply
 
Thread Tools Display Modes
Old 02-03-2013, 01:05 PM #1
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
My Neuro told me that I was most likely SPMS, when I stopped having
regular exacerbations. I have been SPMS for about 15 years now
and started progressing slowly but surely, from that point.

10 years ago, when I started LDN, my progression stopped and I
plateaued and pretty much stayed the way I was 10 years ago. I
have had heat and stress caused mini flares from time to time, but
with no lasting damage.

SPMS is the natural slower progression of MS for most RRMS Peeps.
__________________
~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:
Kitty (02-03-2013), Natalie8 (02-03-2013)
Reply

« Previous Thread | Next Thread »

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 05:18 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

All posts copyright their original authors.

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.

Home