Home Menu

Site Navigation



NeuroTalk Support Groups > > >

Foot problems

Reply
Page 2 of 2 1 2
 
Thread Tools Display Modes
Old 01-12-2009, 01:41 PM #11
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
Quote:
Originally Posted by Jalee View Post
Thanks, Miss Sal. How have you been?
I'm doing okie dokie, for an older Babe with MS, JL. Thanks for asking. Are you still in Florida?
__________________
~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
Old 01-12-2009, 05:02 PM #12
tovaxin_lab_rat's Avatar
tovaxin_lab_rat tovaxin_lab_rat is offline
Elder
  
Join Date: May 2007
Posts: 7,009
15 yr Member
tovaxin_lab_rat tovaxin_lab_rat is offline
Elder
tovaxin_lab_rat's Avatar
 
Join Date: May 2007
Posts: 7,009
15 yr Member
Default
Quote:
Originally Posted by Jalee View Post
Sorry you have something similar. It is maddening, isn't it? Did you have problems when you first started Sinemet?

I've been titrating my dose of Mirapex for a month now. I take a single dose in the morning, then a double at night. I've had some nausea off and on, hence the slow escalation.

I can see that if I don't get this under control, it could be quite disabling.

I've missed you too.

I've been trying to concentrate on RL and staying well. Most of the time I can't stand to talk. It is difficult to find the words I want to say. It is easier not to.
No problems with the Sinemet. No titrating up either. I take 2 25/100 tabs at night b/c that's when I have the most problems. It's a parkinson's drug so you might take a look in the parkinson's forum and see what that group has to say about the drug. There's a CR form and different combinations. It's a combo drug of levidopa/carbidopa.

RL is good to concentrate on sometimes! But staying well is more important! I do understand about the "silence" thing....LOL!

You have my number...it hasn't changed!
__________________
Cheryl
Dx: MS 2001 CRPS 2009
“When everything seems to be going against you, remember that the airplane takes off against the wind, not with it.” - Henry Ford
tovaxin_lab_rat is offline   Reply With QuoteReply With Quote
Old 01-13-2009, 08:19 AM #13
Jalee Jalee is offline
Junior Member
  
Join Date: May 2007
Location: Florida
Posts: 43
15 yr Member
Jalee Jalee is offline
Junior Member
 
Join Date: May 2007
Location: Florida
Posts: 43
15 yr Member
Default
Quote:
Originally Posted by SallyC View Post
I'm doing okie dokie, for an older Babe with MS, JL. Thanks for asking. Are you still in Florida?
Still in the same place, and after seeing the weather in the rest of the US, loving every minute of it!
Jalee is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
SallyC (01-13-2009)
Old 01-13-2009, 08:22 AM #14
Jalee Jalee is offline
Junior Member
  
Join Date: May 2007
Location: Florida
Posts: 43
15 yr Member
Jalee Jalee is offline
Junior Member
 
Join Date: May 2007
Location: Florida
Posts: 43
15 yr Member
Default
Quote:
Originally Posted by Av8rgirl View Post
No problems with the Sinemet. No titrating up either. I take 2 25/100 tabs at night b/c that's when I have the most problems. It's a parkinson's drug so you might take a look in the parkinson's forum and see what that group has to say about the drug. There's a CR form and different combinations. It's a combo drug of levidopa/carbidopa.

RL is good to concentrate on sometimes! But staying well is more important! I do understand about the "silence" thing....LOL!

You have my number...it hasn't changed!
Mirapex is a Parkinson's med also. I've done a bit of research on it. I've been having some problems with the side effects, so I tried to titrate slowly. It didn't seem to matter because the side effects haven't abated.

I may be calling my neuro today to report in just in case.
Jalee is offline   Reply With QuoteReply With Quote
Reply
Page 2 of 2 1 2

« 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
Foot Num... PatriciaQ Multiple Sclerosis 4 07-10-2008 06:57 PM
Had fusion and now foot is hot corisimo Spinal Disorders & Back Pain 1 05-26-2007 11:00 PM
My RSD has spread to my foot. Bronco4586 Reflex Sympathetic Dystrophy (RSD and CRPS) 3 04-10-2007 06:42 PM
Gait related foot problems made it up Parkinson's Disease 4 01-24-2007 01:48 PM
Foot spasm? petpuppy Multiple Sclerosis 2 11-02-2006 10:45 AM


All times are GMT -5. The time now is 04:02 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