Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 01-20-2010, 11:03 AM #11
poochie poochie is offline
Member
 
Join Date: Jan 2009
Posts: 129
15 yr Member
poochie poochie is offline
Member
 
Join Date: Jan 2009
Posts: 129
15 yr Member
Default

How on earth do you know if it is SPMS, when the neuro can't even tell you, I've been on LDN for 5 years now and I don't have anymore attacks, but I think I have progressed somewhat, I have never fully recovered from the first attack, which left me with partial paralysis, 15 years ago. It's so hard to tell about this disease.
poochie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dejibo (02-24-2010), SallyC (01-20-2010)
 


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
RRMS or PPMS? Thumper2 Multiple Sclerosis 5 04-13-2009 11:43 PM
Nik-Key's support thread ---- lets keep her glass FULL!! Addy Survivors of Suicide 42 10-02-2008 10:39 AM
my mother and PPMS Natalie8 The Stumble Inn 4 09-28-2008 09:12 PM
Roll-Call-PPMS and SPMS kicker Multiple Sclerosis 15 01-29-2008 01:42 PM
hello out there -- new with PPMS bbarbick New Member Introductions 7 01-27-2008 11:29 PM


All times are GMT -5. The time now is 04:53 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.

 

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.