Reply
 
Thread Tools Display Modes
Old 06-22-2016, 01:30 PM #1
TXBatman's Avatar
TXBatman TXBatman is offline
Member
 
Join Date: May 2008
Location: Houston, TX
Posts: 702
15 yr Member
TXBatman TXBatman is offline
Member
TXBatman's Avatar
 
Join Date: May 2008
Location: Houston, TX
Posts: 702
15 yr Member
Default

Nancy gave good advice above. The key you want to look at is the McDonald Criteria. If you only have a couple of lesions, they typically want to see either new lesions more than 6 months apart from the previous ones, or more than one episode of clinical symptoms separated by time in order to give a diagnosis of MS. I don't know for sure, but I doubt they would give you a dx of progressive MS if you did not meet the RRMS criteria, because it is likely the lack of defined progression (either via new lesions or new symptoms) that is keeping you from getting a RRMS dx at the moment.

Right now, they probably have you Dxed as CIS or clinically isolated syndrome...meaning you have had one episode of symptoms and one set of lesions visible on an MRI to go with it. Until you either see new symptoms, significant progression of you existing symptoms, or new lesions, you are likely to stay stuck in that limbo area. Therefore, if you think there are changes occurring to your symptoms, it is VERY important to record those changes and track when they happen and how long they last in a diary of some sort. Then provide that information when you see your neurologist. That list of symptoms or changes is what they will need to define the change in clinical condition that would form part of the diagnostic criteria.

It is hard to say good luck...because nobody wants to hope for an MS dx...but I hope you get some resolution and clarity for whatever it is that is causing your symptoms!
TXBatman is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
agate (06-22-2016), NurseNancy (06-24-2016), tkrik (06-27-2016)
Old 06-22-2016, 03:07 PM #2
agate's Avatar
agate agate is offline
Senior Member
 
Join Date: Aug 2006
Location: Wild West
Posts: 1,021
15 yr Member
agate agate is offline
Senior Member
agate's Avatar
 
Join Date: Aug 2006
Location: Wild West
Posts: 1,021
15 yr Member
Default

Hi kell.steve@bigpond,

I'm not understanding something, I guess. You mention having "multiple lesions on the brain" as shown on an MRI and yet there is no MS dx. These were some other kinds of lesions, or they weren't clearly MS-type lesions?

Usually if there are multiple lesions on the brain and they're in the locations favored by MS and look like MS lesions, the neurologist will give at least a tentative MS dx. Maybe the clinical exam didn't show any signs even though you'd been having symptoms? Even then you'd probably be tentatively diagnosed with MS.

As TxBatman said, you may be classified as CIS for clinically isolated syndrome. It would be useful if you could get a copy of the doctor's notes on your office visits and any reports about the MRI. If you're listed as CIS, many doctors now will start prescribing one of the MS disease-modifying drugs because it's been shown that these are most effective if started early.

You might not want to worry about whether it's PPMS or RRMS just now. You may have heard that PPMS is a "worse" form but actually many people with PPMS live out a normal life span and aren't so severely afflicted as you might think while those with RRMS have to wonder when the next relapse is coming their way and how bad it will be.

These categories (RRMS, PPMS, SPMS) are a bit fuzzy anyway. The experts aren't always sure which category you're in.
__________________
Repeal the law of gravity!

MS diagnosed 1980. Type 2 diabetes, osteoarthritis, osteopenia.
Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Currently: Glatopa (generic Copaxone), 40mg 3 times/week, 12/16/20 - 3/16/24
agate is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
NurseNancy (06-24-2016), tkrik (06-27-2016)
Reply

Tags
brain, lesions, months, ppms, prove


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
TBI Recovery Information Needed - Newbie DanielsGirl New Member Introductions 2 07-23-2013 01:51 AM
Information needed concerning Drexel stay... keep smilin Reflex Sympathetic Dystrophy (RSD and CRPS) 6 02-17-2010 11:15 AM
Help Please--SCS information Needed johnthepainter Reflex Sympathetic Dystrophy (RSD and CRPS) 8 09-13-2007 09:32 PM
Information Needed! Dmom3005 General Health Conditions & Rare Disorders 3 06-28-2007 03:40 PM
Off topic but needed information for lthe coming cure for neurological diseasestheoui Thelma Community & Forum Feedback 1 10-15-2006 02:15 PM


All times are GMT -5. The time now is 05:46 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.