advertisement
Reply
 
Thread Tools Display Modes
Old 10-22-2008, 10:24 AM #1
KarenMarie KarenMarie is offline
n/a
 
Join Date: Jan 2008
Location: southern Maine
Posts: 2,920
15 yr Member
KarenMarie KarenMarie is offline
n/a
 
Join Date: Jan 2008
Location: southern Maine
Posts: 2,920
15 yr Member
Default Spms

How many of us have SPMS - our ages - our medications ??

Last edited by KarenMarie; 10-22-2008 at 10:28 AM. Reason: Capital letters
KarenMarie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Victor H (10-24-2008)
Old 10-22-2008, 10:29 AM #2
KarenMarie KarenMarie is offline
n/a
 
Join Date: Jan 2008
Location: southern Maine
Posts: 2,920
15 yr Member
KarenMarie KarenMarie is offline
n/a
 
Join Date: Jan 2008
Location: southern Maine
Posts: 2,920
15 yr Member
Default

OK - couldn't go back and capitalize - sorry !!
KarenMarie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Victor H (10-24-2008)
Old 10-22-2008, 11:05 AM #3
SandyC's Avatar
SandyC SandyC is offline
Wise Elder
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
SandyC SandyC is offline
Wise Elder
SandyC's Avatar
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
Default

Jim is spms and has been for 15 years. He takes so many meds it's crazy! He takes baclofen, tizanidine, sinemet for muscle spasms, methadone for pain, zocor for cholesterol, zoloft for Beta side effects, zanax for tremors, macrobid for recurrent UTI's, oxybutinin for bladder spasms, and Beta Interferon.
__________________
. . A woman is like a tea bag. You never know how strong she is until she's in hot water. Eleanor Roosevelt
SandyC is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
KarenMarie (10-22-2008), Victor H (10-24-2008)
Old 10-22-2008, 12:25 PM #4
marion06095's Avatar
marion06095 marion06095 is offline
Member
 
Join Date: May 2008
Location: North central Connecticut
Posts: 544
15 yr Member
marion06095 marion06095 is offline
Member
marion06095's Avatar
 
Join Date: May 2008
Location: North central Connecticut
Posts: 544
15 yr Member
Default

I am SPMS, and I am treating with, and having good symptom relief with LDN. My MRIs have been stable for quite a few years. I am 61.
marion06095 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
KarenMarie (10-22-2008), Victor H (10-24-2008)
Old 10-22-2008, 12:32 PM #5
SandyC's Avatar
SandyC SandyC is offline
Wise Elder
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
SandyC SandyC is offline
Wise Elder
SandyC's Avatar
 
Join Date: Jan 2008
Location: Somewhere over the rainbow
Posts: 9,227
15 yr Member
Default

I forgot to mention Jim is 42 and has had ms for 20 years.
__________________
. . A woman is like a tea bag. You never know how strong she is until she's in hot water. Eleanor Roosevelt
SandyC is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
KarenMarie (10-22-2008), Victor H (10-24-2008)
Old 10-22-2008, 12:57 PM #6
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

Hello, my name is Sally and I'm an Alchol..er..SPMSic.

I've been SPMS for about 10 yrs now ( of my 40+ yrs with MS), on LDN for, going on 6 yrs and I'm 68..

And You, KM??
__________________
~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:
KarenMarie (10-22-2008), Victor H (10-24-2008)
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
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
Roll-Call-PPMS and SPMS kicker Multiple Sclerosis 15 01-29-2008 01:42 PM
Possible new tx for SPMS wannabe Multiple Sclerosis 17 05-07-2007 09:03 AM
MBP8298 Enrolling Patients in SPMS Trial pantos Multiple Sclerosis 0 09-18-2006 11:59 PM


All times are GMT -5. The time now is 12:54 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.